Hepatitis A virus vaccines

Abstract
A live hepatitis A virus adapted to growth in MRC-5 cells, which HAV is preferably characterized by suitable attenuation for effective vaccine administration to humans and animals without inactivation, methods for adapting HAV to growth in MRC-5, vaccine compositions and method of vaccinating humans against HAV infection.
Description

FIELD OF THE INVENTION
The present invention relates generally to the field of vaccinal compositions useful in the prophylaxis of hepatitis A. More specifically, the invention provides a novel live hepatitis A virus (HAV), and recombinant and chimeric HAVs, the genomes of which are modified from that of their parental strain HM-175 to provide them with the ability to propagate in MRC-5 cells and retain appropriate attenuation for use as live vaccines in humans and other primates.
BACKGROUND OF THE INVENTION
In the United States, hepatitis A virus is the cause of approximately 25% of all clinical hepatitis cases, accounting for approximately 150,000 such cases. Populations at high risk of acquiring hepatitis A in industrialized countries include the socially disadvantaged, medical personnel, military personnel, staff and adult contacts of children in day-care centers, male homosexuals, drug addicts, and travelers to endemic areas.
In developing countries, virtually the entire population is infected with hepatitis A virus at an early age. Much of this infection results in subclinical and inapparent infection, but, as countries improve their hygienic conditions, infection with hepatitis A virus occurs at progressively older ages, resulting in a higher proportion of clinical disease. Thus, there is a paradoxical increase in clinical hepatitis A as the overall rate of infection diminishes. To successfully immunize against hepatitis A in the United States and in other industrialized countries as well as in developing countries, it will be necessary to vaccinate the entire pediatric population. There will be an increasing need for hepatitis A vaccines in such countries for the foreseeable future.
Research in HAV vaccines has focused on inactivated, or killed, viruses. However, in vaccine therapy there are several advantages to a live vaccine, rather than an inactivated, vaccine. With a live vaccine, one can use a lower dosage and smaller number of doses, because a live vaccine replicates in the vaccinee to produce more antigen and can stimulate the immune system of the vaccinee to make both IgA and IgM. Inactivated vaccines, such as the Salk polio vaccine which stimulates production of IgG only in vaccinees, do not protect against infection by ingested virus, only against disease.
A major obstacle to the development of live, attenuated vaccine has been the difficulty in adapting HAV to a cell line that supports rapid viral growth and is licensed for vaccine production. Wild type hepatitis A virus (HAV) grows poorly in cell culture.
U.S. Pat. Nos. 4,532,215 and 4,636,469 describe, respectively, a strain of wild-type HAV, designated HM-175 [see FIG. 6 below; also SEQ ID NOS: 1 and 2], initially isolated from human feces of a patient in Melbourne, Australia, and adapted to passage in vitro in African green monkey kidney (AGMK) culture cells and methods for obtaining same by serial passaging. U.S. Pat. No. 4,620,978 describes a vaccine employing the HAV HM-175, triply cloned in AGMK cell culture and attenuated. U.S. Pat. No. 4,894,228 describes the HAV strain, HM-175, Pass 35, passaged 35 times in AGMK, which differs from wild-type HM-175 by nucleotide changes in the genome, is attenuated for chimpanzees, elicits serum neutralizing antibodies, and is suitable for use as an attenuated HAV vaccine. It discloses the complete nucleotide sequence of clone 7 of the HAV, designated HM-175/7 or pHAV/7. See FIG. 6 below; the nucleotide changes in pHAV/7 from wt HM-175 appear above the wt sequence; the amino acid changes in pHAV/7 from wt HM-175 appear below the wt amino acid. See, also, B. C. Ross et al, J. Gen. Virol., 70:2805-2810 (1989); R. W. Jansen et al, Virol., 163:299-307 (1988); and Tedeschi et al, J. Med. Virol., 39:16-22 (1993). The disclosures of these patents and articles are incorporated by reference herein.
N. Fineschi et al, J. Hepatol., 13(4):S146-S151 (1991) describes an HAV isolate, LSH/S, which is a candidate for an inactivated vaccine. It was adapted to grow in human diploid MRC-5 cells, a preferred licensed cell for vaccine development. This document compares only a small part of its nucleotide sequence to that of wild-type HM-175.
Provost et al, J. Med. Virol., 20:165-175 (1986) described the F and F' variants of the CR326 hepatitis A virus strain. While it is reported to be immunogenic in volunteer vaccinees, the F variant also caused abnormal serum ALT levels in a substantial proportion of individuals.
Another publication from this group of investigators has described further work with the F' variant [K. Midthun et al, J. Infect. Dis., 163:735-739 (1991)]. They observed that the immunogenicity of the F' vaccine product is dose dependent, i.e., a 10.sup.7.3 TCID.sub.50 evoked an antibody response in 100% of volunteers within 9 weeks after immunization whereas lower doses were immunogenic in a smaller percentage of volunteers, and anti-HAV was observed 4 to 6 months after immunization. Chinese investigators have also described studies of a potential live attenuated hepatitis A vaccine prepared from the H2 strain of HAV [J. S. Mao et al, J. Infect. Dis., 159:621-624 (1989)]. Twelve volunteers received the vaccine by the subcutaneous route.
A live attenuated hepatitis A vaccine could have a significant impact on the eradication of the disease. It could be anticipated that a live attenuated vaccine which requires minimal purification and no adjuvant would be less costly than presently available inactivated hepatitis A vaccines.
There is a need in the art for methods and compositions for effective vaccination of humans and animals against hepatitis A.
SUMMARY OF THE INVENTION
In one aspect, the present invention provides a live hepatitis A virus adapted to growth in MRC-5 cells. This virus is preferably characterized by attenuation. The attenuated virus may be recombinant or chimeric. More preferably, the HAV is characterized by suitable attenuation for effective vaccine administration to primates or humans, without inactivation. The HAV may be characterized by containing one or more of 16 specific nucleotides which differ from nucleotides in the same position in the genome of HAV HM-175, Pass 35 [SEQ ID NO: 3].
In another aspect, the invention provides a vaccine useful for protecting humans or other primates against hepatitis A which vaccine contains at least one above-described HAV adapted to growth in MRC-5 cells. Preferably, the vaccine is effective in inducing a protective antibody response without adjuvant.
In still another aspect, the invention provides a method for protecting humans against hepatitis A virus infection which comprises administering to the human patient an effective amount of a vaccine composition of this invention.
In a further aspect, the invention provides a method for preparing a live HAV adapted to growth in MRC-5 cells by incorporating into a selected area of the genome of an HAV one or more of thirteen specific nucleotides. The HAV genome so modified is preferably HAV HM-175, Pass 35 [SEQ ID NO: 3] or a related cell culture-adapted mutant.
In another embodiment, the HAV may be constructed using another HAV cDNA clone and inserting appropriate nucleotides into its genome. According to this method an attenuated, MRC-5-adapted HAV is provided without requiring further passaging in MRC-5 or other primate cell lines.
In still another aspect, the invention provides polynucleotide sequences encoding the recombinant or chimeric HAVs described above. Preferably these sequences are cDNAs useful as master seeds for vaccine preparation.
Other aspects and advantages of the present invention are described further in the following detailed description of the preferred embodiments thereof.





BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a graph plotting anti-HAV antibody production vs. time (weeks) vs. ALT and ICD levels for the chimpanzee studies with HAV virus 4380 and subsequent challenge with wild-type HAV, as described in Example 1. These results were obtained from a chimpanzee that was infected with the attenuated HAV at time 0 and challenged with virulent virus at week 28.
FIG. 2 is a graph plotting anti-HAV antibody production vs. time (weeks) vs. ALT and ICD levels for the chimpanzee studies with HAV virus 4380 and subsequent challenge with wild-type HAV, as described in Example 1. The conditions were the same as for FIG. 1.
FIG. 3 is a graph plotting anti-HAV antibody production vs. time (weeks) vs. ALT and ICD levels for the chimpanzee studies with HAV virus 4380 and subsequent challenge with wild-type HAV, as described in Example 1. The conditions were the same as for FIG. 1.
FIG. 4 is a graph plotting anti-HAV antibody production vs. time (weeks) vs. ALT and ICD levels for the chimpanzee studies with HAV virus 4380 and subsequent challenge with wild-type HAV, as described in Example 1. These results were obtained from the chimpanzee that was not infected with the attenuated HAV, and therefore developed hepatitis following challenge with the virulent virus. The conditions were the same as for FIG. 1.
FIG. 5 is a bar graph of endpoint dilutions of several of the chimeric viruses, Viruses #2, 3, 4, 5, and 6, listed in Table VI.
FIGS. 6A-6K illustrate the nucleotide sequence of wt HM-175 [SEQ ID NO: 1] and its amino acid sequence [SEQ ID NO: 2]. Appearing above the nucleotides are the nucleotide changes of HM-175/7 (pHAV/7) [SEQ ID NO: 3] and appearing below the amino acids of wt HM-175 are the amino acid residues which are characteristic of pHAV/7 [SEQ ID NO: 4]. The dashes represent nucleotides present in wt HM-175 which do not appear in pHAV/7.
FIG. 7 provides the genomic map of the mutations that occurred during passage in AGMK cells and MRC-5 cells (both MRC5/9, which is HAV 4380; and the clone MR8 described in Example 5 below), and shows those mutations which differentiate the MR8 clone from the HAV 4380 (MRC5/9) virus. Mutations noted in each successive bar diagram represent only newly acquired mutations and resulting amino acid changes, if any, with absent mutations designed by dotted lines.





DETAILED DESCRIPTION OF THE INVENTION
The present invention provides hepatitis A virus (HAV) adapted to growth in the human fibroblast-like cell line, MRC-5, a cell substrate suitable for commercial production and licensing of inactivated and live, attenuated hepatitis A vaccines. In addition to such adapted HAVs, the invention provides a method for adapting a selected HAV to growth in that human cell line and preparing an MRC-5-adapted, attenuated HAV without passaging in other primate cells. The HAV of this invention and the preparative method also preferably provides the HAV with sufficient attenuation to enable its efficacy as a vaccine for humans and animals.
Although the prior art discloses other candidate vaccine strains of hepatitis A virus which have been adapted to growth in human diploid fibroblasts, the genetic changes in the virus genome necessary and sufficient for such adaptation have not been characterized. Thus, these strains cannot be manipulated in vitro to assure a reproducible and fully-characterized vaccine product.
The present invention is based on the wild-type HAV, strain HM-175, which is described in detail in the above-cited and incorporated art [Cohen et al., J. Virol., 61:50-59 (1987); SEQ ID NOS: 1 and 2]. Briefly described, the wild type, infectious HAV HM-175 virus was previously adapted to growth in primary African green monkey kidney (AGMK) cells at 37.degree. C. After 26 passages in AGMK, the virus was cloned three times in AGMK cells by serial dilution, then passaged three more times to provide passage 32 (P-32). P-32 was found to be attenuated as described in R. A. Karron et al, J. Infec. Dis., 157:338-345 (1988).
The P-32 virus described above was passaged three more times in AGMK, and molecularly cloned. The virus that was cloned was called P-35 and the full-length clone was referred to as pHAV/7 [SEQ ID NOS: 3 and 4]. pHAV/7 is an infectious cDNA clone of the virus that can be maintained in a monoclonal state and amplified at will with diminished risk of spontaneous mutations. The resulting P-35 virus grew well in fetal rhesus monkey kidney (FRhK) cells and minimally in human fibroblastoid lung cells (MRC-5).
U.S. Pat. No. 4,894,228 and Cohen et al., Proc. Natl. Acad. Sci., USA, 84:2497-2501 (1987) provide the HAV nucleotide sequence of wild-type HAV strain HM-175 (see, FIG. 1 of the patent; SEQ ID NO: 1) and the nucleotide differences between HAV HM-175, Pass 35, clone pHAV/7 [SEQ ID NO: 3], and the wild-type sequence. Thus, these documents, incorporated by reference, provide the nucleotide sequence of pHAV/7, P-35 [SEQ ID NO: 3]. The nucleotide numbers used herein to which the mutations of this invention correspond (Tables I and VI below) are the nucleotide numbers assigned to positions of the wild-type sequence of FIGS. 6A-6K [SEQ ID NOS: 1 AND 2] from U.S. Pat. No. 4,894,228 containing the mutations for P-35. Note that the nucleotides which are deleted from wild-type virus to P-35 are assigned the nucleotide position of the wild-type sequence and appear above the wt sequence of FIGS. 6A-6K as dashes (-). Thus, for example, nucleotide position 131 represents a nucleotide that was deleted between wild-type and P-35.
The P-35 cDNA, i.e., HAV/HM-175/7, is on deposit at the American Type Culture Collection, 12301 Parklawn Drive, Rockville, Md. under Accession No. 67495, deposited Aug. 7, 1987. One of skill in the art can readily construct the nucleotide and amino acid sequences of P-35 by use of the above-cited art and its deposit. See, also, SEQ ID NOS: 3 and 4.
Yet another HAV virus was provided as follows. The P-32 AGMK cell-adapted and attenuated virus was manipulated to enable it to be adapted for growth in MRC-5 cells, so that it is available for large scale vaccine production. Passage 32 was double plaque cloned in MRC-5 to form Passage 37. A selected clone 25-4-21 of Passage 37 was passaged once in MRC-5. The resulting Passage 38 was passaged three times in MRC-5 cells, resulting in Passage 41, the master seed, designated 87J19. This master seed virus stock is also referred to as HAV 4380 or MRC5/9 (the latter term reflects its ability to grow in MRC5 cell, as well as the fact that it is 9 passages from P32). This virus is referred to throughout this disclosure by the name HAV 4380.
Live attenuated virus HAV 4380, was deposited on Apr. 4, 1990 at the Collection Nationale de Cultures de Microorganismes, Institut Pasteur, 25, rue du Docteur Roux, 75724, Paris CEDEX 15 under Accession No. I-936 the deposited HAV 4380 virus has a nucleic acid sequence shown in SEQ ID NO: 5.
TTCAAGAGGG GTCTCCGGGA ATTTCCGGAG TCCCTCTTGG AAGTCCATGG TGAGGGGACT 60TGATACCTCA CCGCCGTTTG CCTAGGCTAT AGGCTAAATT TTCCCTTTCC CTTTTCCCTT 120TCCCATTCCC TTTTGCTTGT AAATATTGAT TCCTGCAGGT TCAGGGTTCT TAAATCTGTT 180TCTCTATAAG AACACTCATT TTCACGCTTT CTGTCTTCTT TCTTCCAGGG CTCTCCCCTT 240GCCCTAGGCT CTGGCCGTTG CGCCCGGCGG GGTCAACTCC ATGATTAGCA TGGAGCTGTA 300GGAGTCTAAA TTGGGGACAC AGATGTTTGG AACGTCACCT TGCAGTGTTA ACTTGGCTTT 360CATGAATCTC TTTGATCTTC CACAAGGGGT AGGCTACGGG TGAAACCTCT TAGGCTAATA 420CTTCTATGAA GAGATGCCTT GGATAGGGTA ACAGCGGCGG ATATTGGTGA GTTGTTAAGA 480CAAAAACCAT TCAACGCCGG AGGACTGACT CTCATCCAGT GGATGCATTG AGTGGATTGA 540CTGTCAGGGC TGTCTTTAGG CTTAATTCCA GACCTCTCTG TGCTTGGGGC AAACATCATT 600TGGCCTTAAA TGGGATTCTG TGAGAGGGGA TCCCTCCATT AACAGCTGGA CTGTTCTTTG 660GGGTCTTATG TGGTGTTTGC CGCTGAGGTA CTCAGGGGCA TTTAGGTTTT TCCTCATTCT 720TAAATAATA ATG AAC ATG TCT AGA CAA GGT ATT TTC CAG ACT GTT GGG 771GGT CTT GAC CAC ATC CTG TCT TTG GCA GAC ATT GAG GAA GAG CAA 819ATT CAA TCA GTT GAT AGG ACT GCA GTG ACT GGT GCT TCT TAT TTT 867TCT GTG GAT CAA TCT TCA GTT CAT ACA GCT GAG GTT GGA TCA CAC 915GTT GAA CCT TTG AGA ACC TCT GTT GAT AAA CCC GGT TCA AAG AGG 963CAG GGA GAG AAA TTT TTC TTG ATT CAT TCT GCA GAT TGG CTT ACT 1011CAT GCT CTT TTC CAT GAA GTT GCA AAA TTG GAT GTG GTG AAA TTA 1059TAC AAT GAG CAG TTT GCT GTT CAA GGG TTG TTG AGA TAC CAT ACA 1107GCA AGA TTT GGC ATT GAA ATT CAA GTT CAG ATA AAC CCT ACA CCT 1155CAA CAG GGG GGA TTG ATC TGT GCT ATG GTT CCT GGT GAC CAG AGC 1203GGT TCT ATA GCA TCA TTG ACT GTT TAT CCT CAT GGT TTG TTA AAT 1251AAT ATT AAC AAT GTG GTT AGA ATA AAG GTT CCA TTT ATT TAC ACA 1299GGT GCT TAC CAC TTT AAA GAT CCA CAA TAC CCA GTT TGG GAA TTG 1347ATT AGA GTT TGG TCA GAA TTA AAT ATT GGG ACA GGA ACT TCA GCT 1395ACT TCA CTC AAT GTT TTA GCT AGA TTT ACA GAT TTG GAG TTG CAT 1443TTA ACT CCT CTT TCT ACA CAA ATG ATG AGA AAT GAA TTT AGG GTC 1491ACT ACT GAG AAT GTG GTG AAT CTG TCA AAT TAT GAA GAT GCA AGA 1539AAG ATG TCT TTT GCT TTG GAT CAG GAA GAT TGG AAA TCT GAT CCG 1587CAG GGT GGT GGG ATC AAA ATT ACT CAT TTT ACT ACT TGG ACA TCT 1635CCA ACT TTG GCT GCT CAG TTT CCA TTT AAT GCT TCA GAC TCA GTT 1683CAA CAA ATT AAA GTT ATT CCA GTT GAC CCA TAT TTT TTC CAA ATG 1731AAT ACA AAT CCT GAC CAA AAA TGT ATA ACT GCT TTG GCT TCT ATT 1779CAG ATG TTT TGT TTT TGG AGA GGA GAT CTT GTC TTT GAT TTT CAA 1827TTT CCC ACC AAA TAT CAT TCA GGT AGA TTA CTG TTT TGT TTT GTT 1875GGC AAT GAG CTA ATA GAT GTT TCT GGA ATC ACA TTA AAG CAA GCA 1923ACT GCT CCT TGT GCA GTA ATG GAT ATT ACA GGA GTG CAG TCA ACT 1971AGA TTT CGT GTT CCC TGG ATT TCT GAC ACT CCT TAC AGA GTG AAC 2019TAT ACA AAG TCA GCA CAT CAG AAA GGT GAG TAC ACT GCC ATT GGG 2067CTT ATT GTG TAT TGT TAT AAC AGA TTG ACC TCT CCT TCT AAC GTT 2115TCC CAT GTC AGA GTG AAT GTT TAT CTT TCA GCA ATT AAC TTG GAA 2163TTT GCT CCT CTT TAT CAT GCT ATG GAT GTT ACT ACA CAA GTT GGA 2211GAT TCT GGA GGT TTT TCA ACA ACA GTT TCT ACA GAA CAG AAT GTT 2259GAT CCC CAA GTT GGT ATA ACA ACC ATG AAA GAT TTG AAA GGA AAA 2307AAC AGA GGG AAA ATG GAT GTT TCA GGA GTA CAA GCA CCT GTG GGA 2355ATC ACA ACA ATT GAG GAT CCA GTT TTA GCA AAG AAA GTA CCT GAG 2403TTT CCT GAA TTG AAA CCT GGA GAA TCC AGA CAT ACA TCA GAT CAT 2451TCC ATC TAC AAG TTT ATG GGA AGG TCT CAT TTC TTG TGC ACT TTT 2499TTC AAT TCA AAT AAT AAA GAG TAC ACA TTT CCT ATA ACC TTG TCT 2547ACC TCT AAT CCT CCT CAT GGT TTG CCA TCA ACA CTG AGG TGG TTT 2595AAC TTG TTT CAG TTG TAT AGA GGG CCT TTA GAT CTG ACA ATT ATT 2643ACA GGA GCA ACT GAT GTA GAT GGC ATG GCC TGG TTC ACT CCA GTA 2691CTT GCC GTT GAT ACT CCT TGG GTA GAG AAG GAG TCA GCT TTG TCT 2739GAC TAT AAA ACT GCT CTT GGA GCT GTC AGA TTT AAC ACA AGG AGA 2787GGG AAC ATT CAG ATT AGA TTA CCA TGG TAT TCT TAT TTA TAT GCT 2835TCT GGA GCA CTG GAT GGT TTG GGA GAC AAG ACA GAT TCT ACA TTT 2883TTG GTT TCT ATT CAG ATT GCA AAT TAC AAT CAT TCT GAT GAA TAC 2931TCT TTT AGT TGT TAT TTG TCT GTC ACA GAA CAA TCA GAG TTT TAT 2979CCC AGA GCT CCA TTG AAC TCA AAT GCC ATG TTA TCC ACT GTA ACA 3027ATG AGC AGA ATT GCA GCT GGA GAC TTG GAG TCA TCA GTG GAT GAT 3075AGA TCA GAG GAA GAT AAA AGA TTT GAG AGT CAT ATA GAA TGC AGG 3123CCA TAT AAA GAA CTG AGA TTA GAA GTT GGG AAA CAA AGA CTC AAG 3171GCT CAG GAA GAA TTG TCA AAT GAA GTA CTT CCA CCC CCT AGG AAA 3219AAG GGA CTG TTT TCA CAA GCC AAA ATT TCT CTT TTT TAT ACT GAG 3267CAT GAA ATA ATG AAG TTT TCC TGG AGA GGT GTG ACT GCT GAT ACT 3315GCT TTA AGG AGG TTT GGA TTC TCT TTG GCC GCA GGC AGA AGT GTG 3363ACT CTT GAA ATG GAT GCT GGG GTT CTT ACT GGG AGA CTG ATT AGA 3411AAT GAT GAG AAA TGG ACA GAA ATG AAG GAT GAC AAG ATT GTT TCA 3459ATT GAA AAG TTT ACA AGT AAC AAA TAT TGG TCC AAA GTG AAT TTC 3507CAT GGG ATG TTG GAT CTT GAA GAA ATT GCT GCC AAT TCT AAG GAT 3555CCT AAC ATG TCT GAA ACG GAT TTG TGT TTC TTG CTG CAT TGG TTA 3603CCA AAG AAA ATT AAT TTA GCA GAT AGA ATG CTT GGA TTG TCT GGA 3651CAG GAA ATT AAA GAA CAA GGT GTT GGA TTA ATA GCA GAG TGT AGA 3699TTC TTA GAT TCT ATT GCT GGA ACT TTA AAA TCT ATG ATG TTT GGA 3747CAT CAT TCT GTG ACT GTT GAA ATT ATA AAC ACT GTG CTC TGT TTT 3795AAG AGT GGA ATT TTG CTT TAT GTA ATA CAA CAA TTG AAT CAG GAT 3843CAT TCT CAC ATA ATT GGT TTG TTG AGA GTC ATG AAT TAT GTA GAT 3891GGT TGT TCA GTT ATT TCA TGT GCC AAA GTT TTT TCC AGA ATG CTG 3939ACA GTC TTT AAT TGG CAA ATG GAC TCC AGA ATG ATG GAG TTA AGG 3987CAG AGT TTT TCC AAC TGG TTA AGA GAT ATT TGT TCT GGG ATC ACC 4035TTC AAA AAC TTC AAG GAT GCA ATT TAT TGG CTT TAT ACA AAA TTA 4083GAC TTT TAT GAA GTG AAT TAT GGC AAG AAG AAG GAC ATT TTA AAT 4131CTT AAA GAT AAC CAA CAA AAA ATA GAG AAA GCC ATT GAG GAA GCC 4179AAA TTT TGC ATT TTG CAA ATC CAA GAT GTG GAA AAA TCT GAA CAG 4227CAG AAA GGG GTT GAC TTG ATA CAA AAA TTG AGA ACT GTT CAT TCA 4275GCT CAG GTT GAT CCA AAT TTA ATG GTT CAT TTG TCA CCT TTG AGA 4323TGT ATA GCA AGA GTT CAT CAG AAA CTT AAA AAC CTT GGA TCT ATA 4371CAG GCA ATG GTA ACG AGA TGT GAG CCA GTT GTT TGT TAT TTT TAT 4419AAA AGA GGG GGA GGA AAG AGC TTA ACA TCA ATT GCA TTG GCA ACC 4467ATT TGT AAA CAT TAT GGT GTT GAG CCT GAA AAG AAT ATC TAT ACT 4515CCT GTG GCT TCA GAT TAC TGG GAT GGA TAT AGT GGA CAA TTA GTT 4563ATC ATT GAT GAT ATT GGC CAA AAC ACA ACA GAT GAG GAT TGG TCA 4611TTT TGT CAG TTA GTG TCA GGA TGT CCT ATG AGA TTA AAC ATG GCC 4659CTT GAG GAG AAG GGT AGG CAT TTT TCT TCT CCT TTT ATA ATA GCA 4707TCA AAT TGG TCA AAT CCA AGT CCA AAA ACA GTT TAT GTT AAG GAA 4755ATT GAC CGC AGA CTC CAT TTC AAG GTT GAA GTT AAA CCT GCT TCA 4803TTC AAA AAT CCT CAC AAT GAT ATG TTG AAT GTT AAT TTA GCT AAA 4851AAT GAT GCA ATC AAA GAT ATG TCT TGT GTT GAT TTG ATA ATG GAT 4899CAT AAT GTT TCA TTG ATG GAT TTG CTC AGT TCT TTA GTC ATG ACA 4947GAA ATT AGA AAA CAA AAC ATG ACT GAA TTC ATG GAG TTG TGG TCT 4995GGA ATT TCA GAT GAT GAT AAT GAT AGT GCA GTA GCT GAG TTT TTC 5043TCT TTT CCA TCT GGT GAA CCA TCG AAC TCT AAA TTA TCT GGC TTT 5091CAA TCT GTT ACT AAT CAC AAG TGG GTT GCT GTG GGA GCT GCA GTT 5139GTT CTT GGA GTG CTC GTT GGA GGA TGG TTT GTG TAT AAG CAT TTC 5187CGC AAA GAG GAA GAA CCA ATC CCA GCT GAA GGG GTA TAT TAT GGT 5235ACT AAG CCC AAG CAA GTG ATT AAA TTA GAT GCA GAT CCA GTA GAA 5283CAG TCA ACT TTG GAA ATA GCA GGA CTG GTT AGG AAG AAC TTG GTT 5331TTT GGA GTT GGA GAG AAG AAT GGA TGT GTG AGA TGG GTT ATG AAT 5379TTG GGA GTG AAA GAT GAT TGG CTG CTT GTG CCT TCC CAT GCT TAT 5427TTT GAG AAA GAT TAT GAA ATG ATG GAG TTT TAT TTT AAT AGA GGT 5475ACT TAC TAT TCA ATT TCA GCT GGT AAT GTT GTT ATT CAA TCT TTG 5523GTG GGA TTC CAG GAT GTT GTT CTG ATG AAG GTT CCT ACA ATT CCT 5571TTT AGA GAT ATT ACT CAG CAT TTT ATT AAG AAA GGG GAT GTG CCT 5619GCT TTG AAT CGC CTG GCA ACA TTA GTG ACA ACT GTA AAT GGA ACC 5667ATG TTA ATT TCT GAG GGC CCA CTA AAG ATG GAA GAG AAA GCT ACT 5715GTT CAT AAG AAA AAT GAT GGT ACA TCA GTT GAT TTA ACT GTG GAT 5763GCA TGG AGA GGA AAA GGC GAA GGT CTT CCT GGA ATG TGT GGT GGG 5811TTG GTT TCA TCG AAT CAA TCT ATA CAG AAT GCA ATC TTG GGC ATC 5859GTT GCT GGA GGA AAT TCA ATT CTT GTT GCA AAA TTG GTT ACT CAA 5907ATG TTC CAA AAT ATT GAT AAG AAA ATT GAA AGT CAG AGA ATT ATG 5955GTG GAG TTT ACT CAG TGT TCA ATG AAT GTG GTC TCC AAA ACG CTT 6003AGA AAG AGT CCC ATT TAT CAT CAC ATT GAT AAA ACC ATG ATT AAT 6051CCT GCA GCT ATG CCC TTT TCT AAA GCT GAA ATT GAT CCA ATG GCT 6099ATG TTA TCT AAG TAT TCA TTA CCT ATT GTA GAA GAA CCA GAG AAT 6147AAA GAG GCT TCA ATT TTT TAT CAA AAT AAA ATA GTG GGT AAG ACT 6195TTA GTT GAT GAT TTT CTA GAT CTT GAT ATG GCC ATT ACA GGG GCC 6243GGA ATT GAT GCT ATC AAC ATG GAT TCA TCT CCT GGA TTT CCT TAT 6291CAG GAG AAG TTG ACC AAA AGA GAT TTA ATT TGG TTG GAT GAA AAT 6339TTA TTG CTG GGA GTT CAT CCA AGA TTG GCT CAG AGA ATC TTA TTC 6387ACT GTC ATG ATG GAA AAT TGT TCT GAT TTG GAT GTT GTT TTT ACA 6435TGT CCA AAA GAT GAA TTG AGA CCA TTA GAG AAA GTG TTG GAA TCA 6483ACA AGA GCT ATT GAT GCT TGT CCT CTG GAT TAC ACA ATT TTG TGC 6531ATG TAT TGG GGT CCA GCT ATT AGT TAT TTT CAT TTG AAT CCA GGT 6579CAT ACA GGT GTT GCT ATT GGC ATA GAT CCT GAT AGA CAG TGG GAT 6627TTA TTT AAA ACA ATG ATA AGA TTC GGA GAT GTT GGT CTT GAT TTA 6675TTC TCT GCT TTT GAT GCT AGT CTT AGT CCA TTT ATG ATT AGA GAA 6723GGT AGA ATC ATG AGT GAA CTA TCT GGA ACT CCA TCC CAT TTT GGC 6771GCT CTT ATC AAT ACT ATC ATT TAT TCC AAG CAT TTG CTG TAT AAC 6819TGT TAC CAT GTC TGT GGT TCA ATG CCC TCT GGG TCT CCT TGT ACA 6867TTG CTA AAT TCA ATT ATT AAT AAT GTC AAT TTG TAC TAT GTG TTT 6915AAG ATA TTT GGA AAG TCT CCA GTT TTC TTT TGT CAG GCT TTG AAG 6963CTC TGT TAT GGA GAT GAT GTT TTA ATA GTT TTC TCT CGA GAT GTT 7011ATT GAT AAT CTT GAT TTG ATT GGA CAA AAA ATT GTA GAT GAG TTT 7059AAA CTT GGC ATG ACA GCT ACT TCT GCT GAC AAG AAT GTA CCT CAG 7107AAA CCA GTT TCG GAA TTG ACT TTT CTC AAA AGA TCT TTC AAT TTG 7155GAG GAT AGA ATT AGA CCT GCA ATT TCG GAA AAA ACA ATT TGG TCT 7203ATA GCA TGG CAG AGA AGT AAC GCT GAG TTT GAG CAG AAT TTA GAA 7251GCT CAG TGG TTT GCT TTT ATG CAT GGC TAT GAG TTT TAT CAG AAA 7299TAT TAT TTT GTT CAG TCC TGT TTG GAG AAA GAG ATG ATA GAA TAC 7347CTT AAA TCT TAT GAT TGG TGG AGA ATG AGA TTT TAT GAC CAG TGT 7395ATT TGT GAC CTT TCA TGATTTGTTT AAACGAATTT TCTTAAAATT TCTGAGGTTT 7450GTTTATTTCT TTTATCAGTA AATAAAAAAA AAAAAA 7486
This deposit was made under the Budapest Treaty on the International Recognition of the Deposit of Microorganisms and has not been publicly disseminated. HAV 4380 is a cell culture-adapted and attenuated strain of hepatitis A virus strain HM-175, adapted to growth in a human fibroblast cell line (MRC-5) suitable for vaccine development by incubation at a reduced temperature of 32-35.degree. C. Growth of the virus is determined by detection of viral antigen in a serological assay. The adapted virus is purified by plaque-purification, using an accepted method (radioimmunofocus assay).
As stated above, after a total of nine passages in MRC-5 cells at reduced temperature, the resultant virus was examined for its biological characteristics in cell culture and in two primate species that are considered to be surrogates for man, i.e., marmosets and chimpanzees. See, e.g., Example 1 below. The HAV 4380 virus was found to be temperature-sensitive (i.e., only grew at reduced temperatures) in MRC-5 cells but was still capable of growing at 37.degree. C. in primary African green monkey kidney cells. The virus was further attenuated in virulence, compared to the parent virus HM-175, P-32, when tested in chimpanzees and marmoset monkeys, in which species the virus replicated poorly or not at all. This reduced capacity for replication in primates was further confirmed in human volunteers, as described in Example 2.
A candidate inactivated hepatitis A vaccine was prepared from the HAV 4380 and demonstrated to be safe (i.e., it does not produce hepatitis or other serious adverse effects) and immunogenic in humans. It was also found to induce antibody production without adjuvant. HAV 4380, as it currently exists, grows well in a cell substrate suitable for commercial vaccine production. It also does not infect human beings when administered by the oral or intravenous route at doses of up to 10.sup.7 tissue culture infectious doses, even when not inactivated. HAV 4380 is suitable for use as a live HAV vaccine in humans. However, as indicated in Example 2, vaccine 4380 is believed to be somewhat over-attenuated, because it is not infectious, which characteristic reduces its efficiency when used as an attenuated vaccine.
In order to produce other vaccine candidates which are maximized for desirable levels of attenuation and good growth in MRC-5 cells, the inventors determined the genetic changes that occurred in the genome of the MRC-5-adapted HAV 4380 virus that altered its growth characteristics and made it more suitable for vaccine production than the related AGMK-adapted virus HM-175, Passage 35 [SEQ ID NO: 3]. The discovery of the following mutations in the nucleotide sequences in HAV 4380, when compared to HM-175 Pass 35 [SEQ ID NO: 3; Cohen et al, cited above; and U.S. Pat. No. 4,894,228, FIG. 1], permit the manipulation of the HAV genome by genetic engineering techniques.
Thus, knowledge of the genomic differences between the AGMK-adapted passages of HM-175 and the more attenuated 4380 permit the construction of chimeric viruses having the improved growth characteristics, i.e., rapid and efficient growth in MRC-5 cell culture, but with a level of attenuation of virulence for primate species, including man, that will permit the virus to replicate efficiently without producing hepatitis or other untoward effects. This invention permits the design of a chimeric HAV that can achieve the optimum characteristics for a candidate live-attenuated hepatitis A vaccine. Such a virus will also permit the design of preferred inactivated vaccine candidates, if desired. The present invention identifies the mutations that are believed to have occurred during adaptation to growth of the HM-175 HAV, passage 32, strain in MRC-5 cells. One or a combination of these mutations are responsible for MRC-5 cell adaptation and overattenuation in HAV 4380.
The nucleotide sequence of the MRC-5 cell adapted virus HAV 4380 was compared with that of the AGMK-adapted, HM-175 virus, passage 35, clone 7 [SEQ ID NO: 3]. Nucleotide consensus sequences were determined directly from polymerase chain reaction products.
The inventors have discovered that there are at least sixteen unique nucleotide differences between the Pass-35 HM-175/7 virus and the MRC-5-adapted virus 4380. Table I lists these sixteen mutations by nucleotide differences and resulting amino acid (AA) differences, if any, acquired by the MRC-5-adapted virus HAV 4380. Note that the partial sequence of LSH/S HAV of Fineschi et al., cited above, overlaps with only the mutation observed at position 5145.
In the Table, A represents adenine, G represents guanine, C represents cytosine, and T represents thymine; Leu represents leucine, Phe represents phenylalanine, Ile represents isoleucine, Val represents valine, Ser represents scrine, Lys represents lysine, Asn represents asparagine, Thr represents threonine and Arg represents arginine. Note that the nucleotide positions in Table I correspond with the nucleotide positions of wt HM-175 [SEQ ID NO: 1]; see FIGS. 6A-6K. This is true for all nucleotide positions referred to throughout this specification.
TABLE I______________________________________Difference in Nucleotide Sequence ofMRC-5-Adapted Hepatitis A Virus:Comparison with Sequence of HM-175/7 (P-35)Nucleotide Region ofChange Genome AA Change______________________________________591 A to G 5' nc NA646 G to A 5' nc NA669 C to T 5' nc NA687 T to G 5' nc NA2750 C to T VP1 No change3027 T to A 2A Ser to Thr3196 G to A 2A Ser to Asn3934 A to G 2B Lys to Arg4418 A to T 2C Leu to Phe4563 A to G 2C Ile to Val4643 A to T 2C No change5145 A to G 3A Ile to Val5745 A to T 3C Thr to Ser6908 T to C 3D No change7032 C to T 3D No change7255 A to T 3D Asn to Ile______________________________________
Note that two previously reported changes at nucleotide position 2864 from U to A in VP1, resulting in no amino acid change, and at nucleotide position 6216 from U to C in 3D, resulting in no amino acid change, are nucleotides that were actually present in a subset of HM175 wild-type cDNA clones made from virus before passage in cell culture. These changes occur due to microheterogeneity in some wild-type subpopulations of HM-175/7, as reported in Cohen, Proc. Natl. Acad. Sci., USA, 84:2497 (1987) and Cohen, J. Virol., 61:50 (1987), cited above. These nucleotides were present in the wt HM-175 sequence used to prepare HAV 4380.
The nucleotide changes at positions 2750, 3027 and 7255 were previously unreported. However, all of these nucleotide changes are contained in the HAV 4380 deposited virus.
A nucleotide change at nucleotide position 6383 from a C to a U in region 3D of the HAV genome, which would cause no change in amino acid sequence, has also been detected in some clones. This change is also believed to occur in some HAV strains due to microheterogeneity in the Virus 4380, since it was not present in a PCR consensus sequence, but was present in a subclone used to make a full length virus cDNA.
New HAV vaccine candidates are designed by introducing one or more of the nucleotides mentioned in Table 1 and discussed above into an HAV at a nucleotide position homologous to the nucleotide position in the genomic sequence of the wt HM-175 [SEQ ID NO: 1] or the AGMK-adapted virus HM-175, Pass 35 [SEQ ID NO: 1]. These nucleotides identified in Table I may be introduced at analogous and/or homologous nucleotide positions to those of P-35 in the genomic sequences of other HAV strains and variants to produce a recombinant or chimeric HAV of this invention. By the phrase "analogous or homologous nucleotide position" is meant a nucleotide in an HAV other than HAV HM-175, Pass 35 which is present in the same viral region, e.g., 2C, 3D and the like, at a position in that region similar to that of the nucleotide of Table I. In other words, the nucleotide position may differ in position number due to deletions in other regions of the virus; but one of skill in the art can readily determine its functional similarity to the nucleotide position in HM-175 [SEQ ID NO: 1] or in HM-175, Pass 35 [SEQ ID NO: 3].
While such nucleotide positions may not have the identical nucleotide position numbers corresponding to the wild-type HM-175 [SEQ ID NO: 1], it is anticipated that these analogous and/or homologous positions can be readily identified to enable HAVs other than strain HM-175 derivatives to be modified to create novel HAVs according to this invention.
Similarly, the inventors are able to manipulate the genome of a progenitor or intermediate of HAV 4380 with resort to this knowledge and can thereby `reverse` certain mutations in 4380 to create new chimeric HAV viruses. One or more of these nucleotides, or varying combinations thereof, can be incorporated, by chimera formation or oligonucleotide-directed mutagenesis, into an HAV strain, most readily the cDNA clone HAV/HM-175/7, to produce new viable virus which has acquired the ability to grow in MRC-5 cells. Other HM-175 HAV derivatives are available from the American Type Culture Collection under ATCC designation numbers VR 2089, VR 2090, VR 2091, VR 2092, VR 2093, VR 2097, VR 2098, and VR 2099. These and other HAVs may be employed to derive desired HAVs of this invention. Since there are indications that the MRC-5-adapted virus 4380 may be over-attenuated for humans, it is important to be able to remove or introduce selected mutations into HM-175. The construction of nine exemplary chimeric viruses containing one or more such mutations is described in detail in Example 3 below.
The mutagenic and genetic engineering techniques employed to construct chimeric or recombinant HAVs which incorporate one or more of these mutations are conventional and known to those of skill in the art [see, for example, Sambrook et al., Molecular Cloning. A Laboratory Manual, 2d edition, Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y., (1989)]. Other conventional techniques, including polymerase chain reactions and chemical synthetic techniques may also be used to design HAVs of this invention. Similarly, it is anticipated that homologous mutations may be made using other HM-175 passages. It also may be possible to adapt similar changes to HAV strains other than HM-175 by introducing these nucleotides into homologous regions.
Chimeric and recombinant viruses of this invention may be designed by application of similar techniques and selecting one or more different combinations of the nucleotides (mutations) appearing in Tables I and VI. For example, data from growth analyses of the chimeric viruses of Example 3 demonstrate that one or more of the four MRC-5 specific mutations in the 5' non-coding region (mutations at nucleotide positions 591, 646, 669, and 687 of HM-175/7) and one or both of the MRC-5 specific mutations in the 2C region (mutations at nucleotide positions 4418 and 4643 of HM-175/7) are desirable for optimal growth of the virus in MRC-5 cells.
Additional viruses employing other combinations of these mutations were prepared by conventional cloning and PCR techniques. When acting together and in the presence of the 5' non-coding and 2C mutations of Table I, MCR-5-specific mutations in P3 and VP1/2AB in every instance increased growth efficiency in MRC-5 cells. Similarly it was noted that the mutations in the 5' non-coding region increased growth efficiency in every virus and in different background genotypes. Studies have shown that the 5' non-coding mutations can reduce biochemical evidence of hepatitis. Other mutations may also be involved.
Specific exemplary chimeric HAVs of this invention are characterized by the mutations in the genome of HAV HM-175/7 that appear in viruses designated #2 through #10 in Table VI of Example 3 below. However, other chimeric HAVs may be readily prepared by application of the same methods known to those of skill in the art.
HAVs of this invention may be characterized by the presence of one or more of these nucleotides of Tables I or VI in analogous genomic positions of HAV HM-175 derivatives or other HAV strains. HAVs of this invention may also be characterized by two or more such nucleotides, where one nucleotide in the HAV parent strain is a guanine (G) at position 5145 of pHAV/7 or the analogous position of another HAV strain.
It is further anticipated that additional mutations may appear in a few regions of HAV that have yet to be sequenced. The mutations appearing in Table I may be incorporated in any combination, and/or with other mutations yet to be identified to construct a number of chimeric or recombinant HAVs with desired characteristics for use as live HAV vaccines.
Additional chimeras and recombinant viruses constructed by oligonucleotide-directed mutagenesis may be designed and evaluated for assessment of the individual effects of the mutations and combinations thereof on viral growth in MRC-5 cells and on adaptation to growth in selected cell culture. The attenuation phenotype of these chimeric viruses may be evaluated in marmosets or chimpanzees by techniques such as described below in Example 1 for HAV 4380.
Also provided by this invention are the polynucleotide sequences encoding the HAVs of this invention. Such polynucleotide sequences are preferably cDNA sequences, which can form a master seed for the HAV vaccine. A cDNA sequence of this invention comprises a DNA sequence encoding a selected HAV genome characterized by the presence of one or more of the nucleotides identified as the thirteen mutations in Table I in any desired combination which imparts desired characteristics to the novel HAV. Such cDNAs may be obtained by conventional techniques known to those of skill in the art. See, e.g., Sambrook et al, cited above, and U.S. Pat. No. 4,894,228.
Thus, the present invention provides a live vaccine composition useful in protecting against HAV infection and a prophylactic method entailing administering to a primate, preferably a human, an effective amount of such a composition. This vaccine composition may contain one or more of the HAVs of the invention, including HAV 4380, as well as the chimeric and recombinant HAVs described herein. The vaccine composition may also contain mixtures of two or more of the HAVs, if desired.
A vaccinal composition may be formulated to contain a carrier or diluent and one or more of the HAVs of the invention. Suitable pharmaceutically acceptable carriers facilitate administration of the viruses but are physiologically inert and/or nonharmful. Carriers may be selected by one of skill in the art. Exemplary carriers include sterile saline, lactose, sucrose, calcium phosphate, gelatin, dextrin, agar, pectin, peanut oil, olive oil, sesame oil, and water. Additionally, the carrier or diluent may include a time delay material, such as glycerol monostearate or glycerol distearate alone or with a wax. In addition, slow release polymer formulations can be used.
Optionally, the vaccine composition may further contain preservatives, chemical stabilizers, other antigenic proteins, and conventional pharmaceutical ingredients. Suitable ingredients which may be used in a vaccinal composition in conjunction with the viruses include, for example, casamino acids, sucrose, gelatin, phenol red, N-Z amine, monopotassium diphosphate, lactose, lactalbumin hydrolysate, and dried milk. Typically, stabilizers, adjuvants, and preservatives are optimized to determine the best formulation for efficacy in the target human or animal. Suitable preservatives include chlorobutanol, potassium sorbate, sorbic acid, sulfur dioxide, propyl gallate, the parabens, ethyl vanillin, glycerin, phenol, parachlorophenol.
A vaccine composition of this invention is most preferably produced without an adjuvant. However, where necessary, one or more of the above described vaccine components may be admixed or adsorbed with a conventional adjuvant. The adjuvant is used as a non-specific irritant to attract leukocytes or enhance an immune response. Such adjuvants include, among others, mineral oil and water, aluminum hydroxide, Amphigen, Avridine, L121/squalene, D-lactide-polylactide/glycoside, pluronic plyois, muramyl dipeptide, killed Bordetella, saponins, and Quil A.
Alternatively, or in addition to the HAV of the invention, other agents useful in treating HAV infection, e.g., immunostimulatory agents, are expected to be useful in reducing and eliminating disease symptoms. The development of vaccine or therapeutic compositions containing these agents is within the skill of one of skill in the art in view of the teaching of this invention.
According to the method of the invention, a human or an animal may be vaccinated against HAV infection by administering an effective amount of a vaccine composition described above. An effective amount is defined as that amount of HAV vaccine capable of inducing protection in the vaccinee against HAV infection and/or against hepatitis. The vaccine may be administered by any suitable route. Such a composition may be administered parenterally, preferably intramuscularly or subcutaneously. However, it may also be formulated to be administered by any other suitable route, including orally.
Suitable effective amounts of the HAVs of this invention can be determined by one of skill in the art based upon the level of immune response desired. Such a composition may be administered once, and/or a booster may also be administered. However, suitable dosage adjustments may be made by the attending physician or veterinarian depending upon the age, sex, weight and general health of the human or animal patient.
Similarly, suitable doses of the vaccine composition of the invention can be readily determined by one of skill in the art. The dosage can be adjusted depending upon the human patient or the animal species being treated, i.e. its weight, age, and general health.
The following examples illustrate the preferred methods for obtaining HAVs of the invention and using them as vaccine compositions. These examples are not intended to limit the scope thereof.
EXAMPLE 1
Test of MRC-5-Adapted HAV 4380 Vaccine in Marmosets and Chimpanzees
The attenuation of hepatitis A virus (HAV), strain HM-175, by serial passage in cell culture has previously been demonstrated. Following 32 passages in primary AGMK cells, the virus was completely attenuated for chimpanzees and almost completely attenuated for marmosets. Subsequently, according to this invention, the virus was adapted to growth in MRC-5 cells and recloned by plaque purification.
HAV 4380 was prepared from Volunteer lot 87J19, passage level 41 of strain HM-175 HAV that was derived from previously characterized passage levels of the virus that have also been prepared as volunteer pools. Two such earlier passage pools were shown to be attenuated for chimpanzees and marmosets. However, neither was administered to volunteers because it was recognized that primary African green monkey kidney cells, the substrate for those volunteer pools, would not be available in sufficient quantities to produce an economically viable vaccine. Therefore, the virus was adapted to MRC-5 cells and further passaged to prepare volunteer lot 87J19 or HAV 4380.
The purpose of this experiment is to test the level of attenuation of this virus for marmosets and chimpanzees, prior to phase I trials in volunteers. Lot 87J19 was tested for safety and immunogenicity in four chimpanzees and four Saguinus mystax marmosets. Two additional marmosets served as uninoculated controls. The chimpanzees used in this study were bred and raised in captivity; the marmosets were wild-caught animals. An inoculum of 10.sup.4 TCID.sub.50 of candidate vaccine lot 87J19 was administered intravenously to each animal. Residual inoculum was frozen and the titer reconfirmed subsequently in two different laboratories.
According to the experimental protocol, marmosets identified by the arbitrary ID numbers 570, 572, 566, and 575 and chimpanzees identified by the arbitrary ID numbers 1300, 1333, 1309 and 1313 received an inoculum of HAV 4380 from Clone 25-4-21, Lot 87 J 19575, 17/11/87 at a dose and route of administration of 10.sup.-3 dilution/1 ml/I.V. Marmosets No. 541 and 578 received a diluent at a dose and route of 1 ml/I.V.
A. Infection: Three of four chimpanzees and one of four marmosets were infected, as determined by development of anti-HAV detectable by commercial radioimmunoassay (HAVAB, Abbott Laboratories, Chicago, Ill.). The chimpanzees seroconverted ten to eleven weeks following inoculation; the single marmoset seroconversion occurred eight weeks following inoculation. This marmoset subsequently died on week eleven of the study and another, noninfected, marmoset subsequently died on week fourteen, but neither death was attributable to the inoculum.
All three chimpanzees that seroconverted also developed IgM anti-HAV. Two of these, Chimp 1309 and Chimp 1313, developed IgM anti-HAV on weeks ten and thirteen, respectively, when tested by the standard HAVAB-M (Abbott Laboratories, Chicago, Ill.) at a final serum dilution of 1:4,000. When sera were tested at a dilution of 1:40, Chimp 1313 and Chimp 1333 seroconverted at weeks nine and five, respectively. The HAVAB-M test is a capture assay utilizing anti-human IgM and has not been standardized for use with sera from primates less closely related to man than to the chimpanzee. For this reason, the marmosets were not tested for IgM anti-HAV.
B. Biochemistry: Biochemical evidence of hepatitis was monitored by weekly determinations of serum alanine amino transferase (ALT) and isocitric dehydrogenase (ICD). The former is the most reliable indirect means of diagnosing hepatitis in the chimpanzee and the latter is comparably sensitive for evaluating marmosets. None of the chimpanzees or marmosets had elevation of liver enzymes attributable to the inoculum. All values for chimpanzees were within normal limits. The only infected marmoset, number 582, had normal liver enzymes up to the time of its death. Marmosets 566, 570, and 578 each had one or more abnormal liver enzyme values, but the first two of these animals were not infected by the inoculum, as judged by failure to seroconvert, and the third was an uninoculated negative control.
Marmosets often have less stable liver enzyme values than chimpanzees, in part because they are, by nature, relatively fragile animals and because they are jungle-caught and therefore usually infected with a variety of endo- and ecto-parasites, including microfilaria.
C. Histology: Histologic sections prepared from serial weekly liver biopsies obtained from the chimpanzees and marmosets were evaluated under code for histopathologic changes. Although some animals had a high base-line of histopathologic changes, none of the animals had evidence of histopathologic changes more severe than those seen in preinoculation biopsies. Equally important, there were no histologic changes that were temporally related to seroconversion in infected animals. The two marmosets that died were subjected to more extensive evaluation. Both animals had evidence of systemic disease that was probably etiologically related to their deaths, but histologic changes in the liver were diagnostic of chronic, not acute, disease and therefore not related to the inoculum.
A comparison of histopathologic changes observed in chimpanzees and marmosets with these various volunteer pools and wild-type virus was performed. See Tables II and III below.
TABLE II______________________________________HISTOPATHOLOGY: CHIMPANZEES Liver Histopathology Range ofInoculum* # Inoc. # Infected # Severity**______________________________________W.T. 4 4 4 .+-.-3+P-21 6 6 1 0-3+P-32 6 6 0 0MRC-5 4 3 0 0______________________________________ *Dose: 10.sup.3 -10.sup.5 ID.sub.50 IV **Scale of 0-3
TABLE III______________________________________HISTOPATHOLOGY: MARMOSETS Liver Histopathology Range ofInoculum* # Inoc. # Infected # Severity**______________________________________W.T. 4 4 4 1+-2+P-21 8 8 8 1+-3+P-32 5 5 3 0-2+MRC-5 4 1 0 0______________________________________ *Dose: 10.sup.3 -10.sup.5 ID.sub.50 IV **Scale of 0-3
Lot 87J19 appears to be more attenuated than the other volunteer pools or wild-type virus, based upon infectivity and severity of histopathologic changes.
D. Immunofluorescence: Serial snap-frozen liver biopsies obtained from infected animals were evaluated for expression of viral antigen by immunofluorescence. Only one animal, Chimp 1313, was definitely but weakly positive for intrahepatic viral antigen. This animal was positive for only one week. These results were compared with those obtained in the previous study of other volunteer pools and wild-type virus. As seen in Tables IV and V, intrahepatic replication was further diminished in both chimpanzees and marmosets when compared with the AGMK-grown virus and wild-type virus.
TABLE IV______________________________________VIRAL REPLICATION IN THE LIVER:MARMOSETS (IMMUNOFLUORESCENCE) Mean MeanInoculum* # Inoc. # Infected Peak Duration (wks)______________________________________W.T. 4 4 2.5+ 12.2P-21 8 8 1+ 3.5P-32 5 5 <1+ 2.4MRC-5 4 1 0 0______________________________________ *Dose: 10.sup.3 -10.sup.5 ID.sub.50 I.V.
TABLE V______________________________________VIRAL REPLICATION IN THE LIVER:CHIMPANZEES (IMMUNOFLUORESCENCE) Mean MeanInoculum* # Inoc. # Infected Peak Duration (wks)______________________________________W.T. 4 4 1+ 1.8P-21 6 6 <1+ 0.5P-32 6 6 <1+ 0.6MRC-5 4 3 <1+ 0.3______________________________________ *Dose: 10.sup.3 -10.sup.5 ID.sub.50 I.V.
E. Protection: Although the single infected marmoset on study died, all four chimpanzees were available for challenge with wild-type parent HAV to determine if the levels of anti-HAV present in infected animals were protective. Consequently, the three infected and one uninfected animal were challenged with approximately 10.sup.3 chimpanzee infectious doses of wild-type HM-175 strain HAV (human stool suspension), administered intravenously (FIGS. 1 through 4).
All three previously infected chimpanzees were protected against type A hepatitis, as measured by persistently normal serum enzyme values (FIGS. 1 through 3). All three protected animals had an anamnestic antibody response to the challenge virus, suggesting that there was limited replication. In contrast, the previously uninfected chimpanzee developed high enzyme values diagnostic of hepatitis following challenge with wild-type virus (FIG. 4). Thus, volunteer pool 87J19 produced an inapparent infection in chimpanzees that stimulated protection against subsequent challenge with virulent wild-type virus.
The results of these portions of the experiment demonstrate that volunteer pool 87J19 of HAV 4380, strain HM-175 (adapted to MRC-5 cells) was significantly more attenuated for chimpanzees and marmosets than its parent, HAV, strain HM-175 (AGMK, Pass-32). It is clear from these studies that HAV 4380, strain HM-175 volunteer pool 87J19, is highly attenuated for chimpanzees and marmosets which are accepted surrogates for man in the study of hepatitis A viruses.
EXAMPLE 2
Clinical Study of Volunteers
In this clinical trial, volunteers received increasing titers of the live attenuated hepatitis A vaccine 4380, volunteer pool 87J19, which was previously tested in chimpanzees and marmosets as described in Example 1. These pre-clinical studies demonstrated that the vaccine was safe, immunogenic, and efficacious in experimental animal models.
Volunteers were admitted to a closed clinical ward at the United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Md. Eight volunteers received the live attenuated hepatitis A vaccine (1 ml) by the oral route in the following manner: two received a 10.sup.4 TCID.sub.50 dose, two a 10.sup.5 TCID.sub.50 dose, two a 10.sup.6 TCID.sub.50 dose, and two a 10.sup.7 TCID.sub.50 dose. Six volunteers received the vaccine by the intramuscular route in the deltoid area in the following manner: 2 received a 10.sup.5 TCID.sub.50 dose, 2 a 10.sup.6 TCID.sub.50 dose and 2 a 10.sup.7 TCID.sub.50 dose.
Each volunteer remained on the ward for three days after immunization. Local or systemic side effects were monitored during the admission period and for 12 weeks following the immunization. Volunteers were asked to return at 6 and 12 months for serological follow-up.
Sera were obtained prior to immunization and once a week for the next 12 weeks. In volunteers who completed the appropriate follow-up time, sera were also obtained at 6 and 12 months after initial administration of vaccine. Serum specimens were tested for alanine aminotransferase (ALT) and antibody to hepatitis A. ALT was tested with a Kodak EKTA Chem 700XR analyzer (Rochester, N.Y.); normal values were 0 to 50 IU/ml. Antibody to hepatitis A was tested by four different methods, including a commercial radioimmunoassay (HAVAB, Abbott Laboratories, N. Chicago, Ill.). Second, an enzyme-linked immunoassay developed by SmithKline Beecham (SKB-ELISA), which was more sensitive than the standard HAVAB, in which a level of .gtoreq.20 milli-International Units (mIU) was considered positive. Selected sera were tested by the RIFIT (radioimmunofocus) assay for neutralizing antibody to hepatitis A. With this test, a serum titer of .gtoreq.1:10 was considered positive [S. M. Lemon et al, J. Infect. Dis., 148:1033-1039 (1983)]. Finally sera were tested for IgM anti-HAV by commercial radioimmunoassay (HAVAB-M, Abbott Laboratories, N. Chicago, Ill.).
Stools were collected from the volunteers two to three times per week for the first 12 weeks and were tested for the presence of hepatitis A virus by radioimmunoassay [R. H. Purcell et al, J. Immunol., 116:349-356 (1976)] and molecular biology techniques [J. Ticehurst et al, J. Clin. Microbiol., 25:1822-1829 (1987)].
All volunteers remained healthy during the follow-up period (14 weeks to one year). No systemic complaints were present immediately after immunization or during long-term follow-up. Serum alanine aminotransferase levels remained normal in all 14 individuals during the period of observation.
Antibody to hepatitis A was not observed in any of the eight volunteers who received the vaccine by the oral route or in the two volunteers who received the 10.sup.5 TCID.sub.50 dose by the intramuscular route. The four volunteers who received higher doses of vaccine (10.sup.6 TCID.sub.50 or 10.sup.7 TCID.sub.50) all had detectable antibody by the SKB ELISA as early as 3 weeks after immunization. Detectable levels persisted for the 12 weeks of observation. Selected sera tested for neutralizing antibody had titers ranging from 1:10 to 1:40 in a volunteer who received a 10.sup.6 dose and 1:40 to 1:2560 in a volunteer who received a 10.sup.7 TCID.sub.50 dose. The commercial HAVAB assay detected anti-HAV in only one of the volunteers, who received the 10.sup.7 dose. IgM anti-HAV was not detected in any of the volunteers who received the vaccine orally. Sera from volunteers who received 10.sup.7 TCID.sub.50 I.M. had detectable IgM anti-HAV.
Stools from all volunteers who received the oral vaccine were negative for hepatitis A virus, while those from volunteers who had received the vaccine by intramuscular route are in the process of being tested.
Although only a small number of volunteers received the vaccine orally, it appeared that the vaccine is not immunogenic by this route. This is likely due to over-attenuation of the virus, although other causes, such as inactivation in the gastrointestinal tract or too small an inoculum, should be considered. The vaccine was safe and immunogenic by the intramuscular route at doses of 10.sup.6 and 10.sup.7 TCID.sub.50. The antibody response was prompt: anti-HAV was observed within 3 weeks of immunization, persisted during the period of observation, and did not diminish in titer. Such a response to one single inoculation of a preparation which lacked an adjuvant, is remarkable. If indeed, anti-HAV persists for a long time after one dose, the logistics of administration of this product would be much simpler and more successful than with present hepatitis A vaccines. The presence of IgM anti-HAV in volunteers who received 10.sup.7 TCID.sub.50 without evidence of hepatitis is suggestive of asymptomatic replication of the virus.
EXAMPLE 3
Construction of Chimeric Viruses
Several exemplary chimeric viruses were generated to evaluate the effect of several of the mutations of Table I on host range and/or attenuation in primates. The sequence of the MRC-5-adapted virus 4380 was obtained using reverse-transcriptase:polymerase chain reaction (RT:PCR) to amplify regions of the virus as cDNA prior to sequencing (hence T instead of U in Table VI below). Numbers 2-10 in Table VI designate chimeric viruses made by inserting mutations found in the MRC-5-adapted virus 4380 into the cDNA clone of pHAV/7 encoding the attenuated HM-175 virus, Pass 35, of Cohen et al., J. Virol., 61:3035-3039 (1987) [SEQ ID NOs: 3 and 4]. Mutations introduced by "chimera" means a portion of the 4380 virus genome was amplified by RT:PCR, digested with specific restriction enzymes and the fragment used to replace the homologous fragment in the cDNA clone pHAV/7. Mutations introduced by mutagenesis were inserted by oligonucleotide-directed mutagenesis of the cDNA clone pHAV/7 using the Amersham mutagenesis protocol.
The chimeric cDNAs were transcribed into RNA in vitro and the nucleic acids (both RNA and DNA) transfected into FRhK-4 cells to generate chimeric viruses. Quantification of chimeric virus growth for the exemplary chimeras was performed by slot-blot assay.
Table VI reports the results of the construction and testing of nine chimeric viruses. As used in Table VI, the following terms are defined: Cell culture refers to virus containing indicated mutations selected by growth in MRC-5 cells. Mutagenesis refers to oligonucleotide-directed mutagenesis of P-35 or HM-175 cDNA clones. A chimeric viral genome refers to the construction of a chimeric viral genome using portions of P-35 cDNA clone and PCR-generated fragments of the MRC-5 cell-adapted virus 4380. ND means that this study has not yet been performed. The + symbol refers to virus that has some growth in that cell type. The--symbol refers to virus that has little or no growth in that cell type. The two cell types employed to test the growth of the chimeric viruses are the human lung fibroblast-like cell line MRC-5 and fetal rhesus monkey kidney epithelial-like cell line, FRhK-4. Note that Virus #1 in the Table refers to MRC-5-adapted HAV 4380. Viruses #2 through 10 are chimeric viruses of this invention.
TABLE VI______________________________________Differences in Nucleotide Sequenceof MRC-5-Adapted Hepatitis A Virus:Comparison with P-35 HM-175 Virus Growth ofNucleotide Method Mutated VirusDifferences Mutation in Cell Culturesfrom P-35 HM-175 Introduced FRhKA MRC-5______________________________________Virus #1 (MRC-5-adapted) Cell Culture + +591 A to G646 G to A669 C to T687 T to G2750 C to T3027 T to A3196 G to A3934 A to G4418 A to T4563 A to G4643 A to T5145 A to G5745 A to T6908 T to C7032 C to T7255 A to TVirus #2 Chimera + +591 A to G646 G to A669 C to T687 T to GVirus #3 Chimera + +124 C to T131 d to T132 d to T133 d to T134 d to G152 G to A203-207 d to T591 A to G646 G to A669 C to T687 T to GVirus #4 Chimera + +591 A to G646 G to A669 C to T687 T to G4418 A to T4563 A to G4643 A to TVirus #5 Chimera + +124 C to T131 d to T132 d to T133 d to T134 d to T152 G to A203-207 d to T591 A to G646 G to A669 C to T687 T to G4418 A to T4563 A to G4643 A to TVirus #6 Chimera + -4418 A to T4563 A to G4643 A to TVirus #7 Chimera + ND Mutagenesis591 A to G4418 A to T4563 A to G4643 A to TVirus #8 Chimera + ND Mutagenesis646 G to A4418 A to T4563 A to G4643 A to TVirus #9 Chimera + ND Mutagenesis669 C to T4418 A to T4563 A to G4643 A to TVirus #10 Chimera + ND Mutagenesis687 T to G4418 A to T4563 A to G4643 A to T______________________________________ d = Base at this position deleted in P35 compared to wildtype
Introduction of four mutations found in the 5' noncoding region, at nucleotide positions 591, 646, 669, and 687 of the P-35 genome, appear to be important for HAV host range in cell culture. They allow some growth of the transfected virus in MRC-5 cells, but do not account entirely for MRC-5 cell culture adaptation.
Introduction of three mutations, at nucleotides 4418, 4563 and 4643 in the 2C region of the MRC-5-adapted virus, with the 5' mutations allows full growth in MRC-5 cells. Thus the four mutations in the 5' noncoding region and the three mutations in the 2C region of the genome of the MRC-5 cell-adapted virus appear to act synergistically in adaptation of this virus to efficient growth in MRC-5 cells. Introduction of only the three mutations in the 2C region into the P-35 AGMK genome does not permit discernible growth of the transfected virus in MRC-5 cells.
EXAMPLE 4
Comparison of End Point Dilution of Chimeric Viruses in FRhK-4 Versus MRC-5 Cells
Chimeric viruses with the composition described in Table VI were serially diluted in ten-fold increments, and an equal aliquot of each dilution was plated onto FRhK-4 and MRC-5 cells. After 21 days incubation at 34.5.degree. C. to permit virus growth, the cells were lysed by the addition of a buffer solution containing sodium dodecyl sulfate. The viral RNA was extracted with phenol and quantified by slot blot hybridization using a [32P]-labeled riboprobe specific for hepatitis A virus. A radioautograph of the slot blot obtained from the FRhK-4 cells and from the MRC-5 cells illustrates that the endpoint dilution of the MRC-5-adapted virus was the same in both cell lines, indicating that this virus can grow in either cell line. In contrast, the P35 HM-175 virus had an endpoint dilution of 10-5 on FRhK-4 cells and <10.sup.-1 on MRC-5 cells, demonstrating that this virus is unable to grow successfully on MRC-5 cells. As FIG. 5 illustrates, virus #6 was most like the pass 35 virus while virus #4 was most like the MRC-5 adapted virus and viruses #2, 3, and 5 were intermediate. These results show that certain mutations from the MRC-5-adapted virus can be introduced into the pHAV/7 cDNA clone to generate new viruses which also have acquired the ability to grow in MRC-5 cells.
EXAMPLE 5
Nucleotide Sequence of MRC-5/9 Virus Compared with the MR8 cDNA Clone
The full length cDNA clone of an HAV chimeric virus, called MR8, was constructed by sequential replacement of AGMK/35m restriction fragments with those generated by RT-PCR amplification of the HAV 4380 (MRC-5/9) virus genome. The nucleotide sequence of the MR8 cDNA and of a subcloned PCR product from the 3' end of the viral genome (base 7000 to polyA tail) were compared to that of a PCR consensus sequence previously determined for the MRC-5/9 virus. Based on these comparisons the original list of 12 mutations believed to be unique to MRC-5/9 virus has been changed by the addition of six more coding mutations (positions 2750, 3027, 3196, 4563, 7032 and 7255) and the deletion of two mutations (position 2864 and 6216) that originally were thought to have occurred during passage in MRC-5 cells but which were actually present in a subset of HM175 wild-type cDNA clones made from virus before passage in cell culture. The two new mutations were confirmed after reamplification of the MRC-5/9 RNA by RT-PCR.
The nucleotide sequence of the MR8 clone differed from the AGMK/35m clone at nucleotide numbers 591, 646, 669 and 687 in the 5' non-coding region (identical to those in Table I). It also contained the same changes in Table I at nucleotides 2750, 3027, 3196, 3934, 4418, 4563, 4643, 5145, 5745, and 6908. It also contained at nucleotide 6383 a U, at nucleotide 7255 an A, and at nucleotide 7430 an A. Thus it contained only 7 mutations resulting in amino acid changes from AGMK/35m: (two in VP1/2A, one in 2B, two in 2C, one in 3A, and one in 3C). Only a few mutations, therefore, are responsible for a marked difference in the ability of the AGMK/35 virus and the MRC-5/9 virus to grow in MRC-5 cells.
All publications identified above are incorporated by reference. The parent applications are incorporated by reference. Numerous modifications and variations of the present invention are included in the above-identified specification and are expected to be obvious to one of skill in the art. Such modifications and alterations to the compositions and processes of the present invention are believed to be encompassed in the scope of the claims appended hereto.
__________________________________________________________________________# SEQUENCE LISTING- <160> NUMBER OF SEQ ID NOS: 6- <210> SEQ ID NO 1<211> LENGTH: 7493<212> TYPE: DNA<213> ORGANISM: WILD-TYPE HUMAN HEPATITIS A VIRUS, - # STRAIN HM-175<220> FEATURE:<221> NAME/KEY: CDS<222> LOCATION: (735)..(7415)- <400> SEQUENCE: 1- ttcaagaggg gtctccggga atttccggag tccctcttgg aagtccatgg tg - #aggggact 60- tgatacctca ccgccgtttg cctaggctat aggctaaatt ttccctttcc ct - #tttccctt 120- tcctattccc tttgttttgc ttgtaaatat taattcctgc aggttcaggg tt - #cttaaatc 180- tgtttctcta taagaacact catttttcac gctttctgtc ttctttcttc ca - #gggctctc 240- cccttgccct aggctctggc cgttgcgccc ggcggggtca actccatgat ta - #gcatggag 300- ctgtaggagt ctaaattggg gacacagatg tttggaacgt caccttgcag tg - #ttaacttg 360- gctttcatga atctctttga tcttccacaa ggggtaggct acgggtgaaa cc - #tcttaggc 420- taatacttct atgaagagat gccttggata gggtaacagc ggcggatatt gg - #tgagttgt 480- taagacaaaa accattcaac gccggaggac tgactctcat ccagtggatg ca - #ttgagtgg 540- attgactgtc agggctgtct ttaggcttaa ttccagacct ctctgtgctt ag - #ggcaaaca 600- tcatttggcc ttaaatggga ttctgtgaga ggggatccct ccattgacag ct - #ggactgtt 660- ctttggggcc ttatgtggtg tttgcctctg aggtactcag gggcatttag gt - #ttttcctc 720- attcttaaat aata atg aac atg tct aga caa ggt a - #tt ttc cag act gtt 770 Met A - #sn Met Ser Arg Gln Gly Ile Phe Gln Thr Va - #l# 10- ggg agt ggt ctt gac cac atc ctg tct ttg gc - #a gac att gag gaa gag 818Gly Ser Gly Leu Asp His Ile Leu Ser Leu Al - #a Asp Ile Glu Glu Glu# 25- caa atg att caa tca gtt gat agg act gca gt - #g act ggt gct tct tat 866Gln Met Ile Gln Ser Val Asp Arg Thr Ala Va - #l Thr Gly Ala Ser Tyr# 40- ttt act tct gtg gat caa tct tca gtt cat ac - #a gct gag gtt gga tca 914Phe Thr Ser Val Asp Gln Ser Ser Val His Th - #r Ala Glu Val Gly Ser# 60- cac cag gtt gaa cct ttg aga acc tct gtt ga - #t aaa ccc ggt tca aag 962His Gln Val Glu Pro Leu Arg Thr Ser Val As - #p Lys Pro Gly Ser Lys# 75- aag act cag gga gag aaa ttt ttc ttg att ca - #t tct gca gat tgg ctt1010Lys Thr Gln Gly Glu Lys Phe Phe Leu Ile Hi - #s Ser Ala Asp Trp Leu# 90- act aca cat gct ctt ttc cat gaa gtt gca aa - #a ttg gat gtg gtg aaa1058Thr Thr His Ala Leu Phe His Glu Val Ala Ly - #s Leu Asp Val Val Lys# 105- tta tta tac aat gag cag ttt gct gtt caa gg - #g ttg ttg aga tac cat1106Leu Leu Tyr Asn Glu Gln Phe Ala Val Gln Gl - #y Leu Leu Arg Tyr His# 120- aca tat gca aga ttt ggc att gaa att caa gt - #t cag ata aac cct aca1154Thr Tyr Ala Arg Phe Gly Ile Glu Ile Gln Va - #l Gln Ile Asn Pro Thr125 1 - #30 1 - #35 1 -#40- cct ttc caa cag ggg gga ttg atc tgt gct at - #g gtt cct ggt gac cag1202Pro Phe Gln Gln Gly Gly Leu Ile Cys Ala Me - #t Val Pro Gly Asp Gln# 155- agc tat ggt tct ata gca tca ttg act gtt ta - #t cct cat ggt ttg tta1250Ser Tyr Gly Ser Ile Ala Ser Leu Thr Val Ty - #r Pro His Gly Leu Leu# 170- aat tgc aat att aac aat gtg gtt aga ata aa - #g gtt cca ttt att tac1298Asn Cys Asn Ile Asn Asn Val Val Arg Ile Ly - #s Val Pro Phe Ile Tyr# 185- aca aga ggt gct tac cac ttt aaa gat cca ca - #a tac cca gtt tgg gaa1346Thr Arg Gly Ala Tyr His Phe Lys Asp Pro Gl - #n Tyr Pro Val Trp Glu# 200- ttg aca att aga gtt tgg tca gaa tta aat at - #t ggg aca gga act tca1394Leu Thr Ile Arg Val Trp Ser Glu Leu Asn Il - #e Gly Thr Gly Thr Ser205 2 - #10 2 - #15 2 -#20- gct tat act tca ctc aat gtt tta gct aga tt - #t aca gat ttg gag ttg1442Ala Tyr Thr Ser Leu Asn Val Leu Ala Arg Ph - #e Thr Asp Leu Glu Leu# 235- cat gga tta act cct ctt tct aca caa atg at - #g aga aat gaa ttt agg1490His Gly Leu Thr Pro Leu Ser Thr Gln Met Me - #t Arg Asn Glu Phe Arg# 250- gtc agt act act gag aat gtg gtg aat ctg tc - #a aat tat gaa gat gca1538Val Ser Thr Thr Glu Asn Val Val Asn Leu Se - #r Asn Tyr Glu Asp Ala# 265- aga gca aag atg tct ttt gct ttg gat cag ga - #a gat tgg aaa tct gat1586Arg Ala Lys Met Ser Phe Ala Leu Asp Gln Gl - #u Asp Trp Lys Ser Asp# 280- ccg tcc cag ggt ggt ggg atc aaa att act ca - #t ttt act act tgg aca1634Pro Ser Gln Gly Gly Gly Ile Lys Ile Thr Hi - #s Phe Thr Thr Trp Thr285 2 - #90 2 - #95 3 -#00- tct att cca act ttg gct gct cag ttt cca tt - #t aat gct tca gac tca1682Ser Ile Pro Thr Leu Ala Ala Gln Phe Pro Ph - #e Asn Ala Ser Asp Ser# 315- gtt ggt caa caa att aaa gtt att cca gtt ga - #c cca tat ttt ttc caa1730Val Gly Gln Gln Ile Lys Val Ile Pro Val As - #p Pro Tyr Phe Phe Gln# 330- atg aca aat acg aat cct gac caa aaa tgt at - #a act gct ttg gct tct1778Met Thr Asn Thr Asn Pro Asp Gln Lys Cys Il - #e Thr Ala Leu Ala Ser# 345- att tgt cag atg ttt tgt ttt tgg aga gga ga - #t ctt gtc ttt gat ttt1826Ile Cys Gln Met Phe Cys Phe Trp Arg Gly As - #p Leu Val Phe Asp Phe# 360- caa gtt ttt ccc acc aaa tat cat tca ggt ag - #a tta ctg ttt tgt ttt1874Gln Val Phe Pro Thr Lys Tyr His Ser Gly Ar - #g Leu Leu Phe Cys Phe365 3 - #70 3 - #75 3 -#80- gtt cct ggc aat gag cta ata gat gtt tct gg - #a atc aca tta aag caa1922Val Pro Gly Asn Glu Leu Ile Asp Val Ser Gl - #y Ile Thr Leu Lys Gln# 395- gca act act gct cct tgt gca gta atg gat at - #t aca gga gtg cag tca1970Ala Thr Thr Ala Pro Cys Ala Val Met Asp Il - #e Thr Gly Val Gln Ser# 410- act ttg aga ttt cgt gtt ccc tgg att tct ga - #c act cct tac aga gtg2018Thr Leu Arg Phe Arg Val Pro Trp Ile Ser As - #p Thr Pro Tyr Arg Val# 425- aac agg tat aca aag tca gca cat cag aaa gg - #t gag tac act gcc att2066Asn Arg Tyr Thr Lys Ser Ala His Gln Lys Gl - #y Glu Tyr Thr Ala Ile# 440- ggg aag ctt att gtg tat tgt tat aac aga tt - #g acc tct cct tct aac2114Gly Lys Leu Ile Val Tyr Cys Tyr Asn Arg Le - #u Thr Ser Pro Ser Asn445 4 - #50 4 - #55 4 -#60- gtt gct tcc cat gtc aga gtg aat gtt tat ct - #t tca gca att aac ttg2162Val Ala Ser His Val Arg Val Asn Val Tyr Le - #u Ser Ala Ile Asn Leu# 475- gaa tgt ttt gct cct ctt tat cat gct atg ga - #t gtt act aca caa gtt2210Glu Cys Phe Ala Pro Leu Tyr His Ala Met As - #p Val Thr Thr Gln Val# 490- gga gat gat tct gga ggt ttt tca aca aca gt - #t tct aca gaa cag aat2258Gly Asp Asp Ser Gly Gly Phe Ser Thr Thr Va - #l Ser Thr Glu Gln Asn# 505- gtt cca gat ccc caa gtt ggt ata aca acc at - #g aaa gat ttg aaa gga2306Val Pro Asp Pro Gln Val Gly Ile Thr Thr Me - #t Lys Asp Leu Lys Gly# 520- aaa gct aac aga ggg aaa atg gat gtt tca gg - #a gta caa gca cct gtg2354Lys Ala Asn Arg Gly Lys Met Asp Val Ser Gl - #y Val Gln Ala Pro Val525 5 - #30 5 - #35 5 -#40- gga gct atc aca aca att gag gat cca gtt tt - #a gca aag aaa gta cct2402Gly Ala Ile Thr Thr Ile Glu Asp Pro Val Le - #u Ala Lys Lys Val Pro# 555- gag aca ttt cct gaa ttg aaa cct gga gaa tc - #c aga cat aca tca gat2450Glu Thr Phe Pro Glu Leu Lys Pro Gly Glu Se - #r Arg His Thr Ser Asp# 570- cat atg tcc atc tac aag ttt atg gga agg tc - #t cat ttc ttg tgc act2498His Met Ser Ile Tyr Lys Phe Met Gly Arg Se - #r His Phe Leu Cys Thr# 585- ttt aca ttc aat tca aat aat aaa gag tac ac - #a ttt cct ata acc ttg2546Phe Thr Phe Asn Ser Asn Asn Lys Glu Tyr Th - #r Phe Pro Ile Thr Leu# 600- tct tca acc tct aat cct cct cat ggt ttg cc - #a tca aca ctg agg tgg2594Ser Ser Thr Ser Asn Pro Pro His Gly Leu Pr - #o Ser Thr Leu Arg Trp605 6 - #10 6 - #15 6 -#20- ttt ttc aac ttg ttt cag ttg tat aga ggg cc - #t tta gat ctg aca att2642Phe Phe Asn Leu Phe Gln Leu Tyr Arg Gly Pr - #o Leu Asp Leu Thr Ile# 635- att att aca gga gca act gat gta gat ggc at - #g gcc tgg ttc act cca2690Ile Ile Thr Gly Ala Thr Asp Val Asp Gly Me - #t Ala Trp Phe Thr Pro# 650- gta ggt ctt gcc gtt gat act cct tgg gta ga - #g aag gag tca gct ttg2738Val Gly Leu Ala Val Asp Thr Pro Trp Val Gl - #u Lys Glu Ser Ala Leu# 665- tct att gac tac aaa act gct ctt gga gct gt - #c aga ttt aac aca agg2786Ser Ile Asp Tyr Lys Thr Ala Leu Gly Ala Va - #l Arg Phe Asn Thr Arg# 680- aga aca ggg aac att cag att aga tta cca tg - #g tat tct tat tta tat2834Arg Thr Gly Asn Ile Gln Ile Arg Leu Pro Tr - #p Tyr Ser Tyr Leu Tyr685 6 - #90 6 - #95 7 -#00- gct gtg tct gga gca ctg gat ggt ttg ggt ga - #c aag aca gat tct aca2882Ala Val Ser Gly Ala Leu Asp Gly Leu Gly As - #p Lys Thr Asp Ser Thr# 715- ttt gga ttg gtt tct att cag att gca aat ta - #c aat cat tct gat gaa2930Phe Gly Leu Val Ser Ile Gln Ile Ala Asn Ty - #r Asn His Ser Asp Glu# 730- tac ttg tct ttt agt tgt tat ttg tct gtc ac - #a gaa caa tca gag ttt2978Tyr Leu Ser Phe Ser Cys Tyr Leu Ser Val Th - #r Glu Gln Ser Glu Phe# 745- tat ttt ccc aga gct cca ttg aac tca aat gc - #c atg tta tcc act gaa3026Tyr Phe Pro Arg Ala Pro Leu Asn Ser Asn Al - #a Met Leu Ser Thr Glu# 760- tca atg atg agc aga att gca gct gga gac tt - #g gag tca tca gtg gat3074Ser Met Met Ser Arg Ile Ala Ala Gly Asp Le - #u Glu Ser Ser Val Asp765 7 - #70 7 - #75 7 -#80- gat cct aga tca gag gaa gat aaa aga ttt ga - #g agt cat ata gaa tgc3122Asp Pro Arg Ser Glu Glu Asp Lys Arg Phe Gl - #u Ser His Ile Glu Cys# 795- agg aag cca tat aaa gaa ctg aga tta gaa gt - #t ggg aaa caa aga ctc3170Arg Lys Pro Tyr Lys Glu Leu Arg Leu Glu Va - #l Gly Lys Gln Arg Leu# 810- aag tat gct cag gaa gaa ttg tca aat gaa gt - #a ctt cca ccc cct agg3218Lys Tyr Ala Gln Glu Glu Leu Ser Asn Glu Va - #l Leu Pro Pro Pro Arg# 825- aaa atg aag gga ctg ttt tca caa gcc aaa at - #t tct ctt ttt tat act3266Lys Met Lys Gly Leu Phe Ser Gln Ala Lys Il - #e Ser Leu Phe Tyr Thr# 840- gag gag cat gaa ata atg aag ttt tcc tgg ag - #a ggt gtg act gct gat3314Glu Glu His Glu Ile Met Lys Phe Ser Trp Ar - #g Gly Val Thr Ala Asp845 8 - #50 8 - #55 8 -#60- act aga gct tta agg agg ttt gga ttc tct tt - #g gcc gca ggc aga agt3362Thr Arg Ala Leu Arg Arg Phe Gly Phe Ser Le - #u Ala Ala Gly Arg Ser# 875- gtg tgg act ctt gaa atg gat gct ggg gtt ct - #t act ggg aga ctg att3410Val Trp Thr Leu Glu Met Asp Ala Gly Val Le - #u Thr Gly Arg Leu Ile# 890- aga ttg aat gat gag aaa tgg aca gaa atg aa - #g gat gac aag att gtt3458Arg Leu Asn Asp Glu Lys Trp Thr Glu Met Ly - #s Asp Asp Lys Ile Val# 905- tca ttg att gaa aag ttt aca agt aac aaa ta - #t tgg tcc aaa gtg aat3506Ser Leu Ile Glu Lys Phe Thr Ser Asn Lys Ty - #r Trp Ser Lys Val Asn# 920- ttc cca cat ggg atg ttg gat ctt gaa gaa at - #t gct gcc aat tct aag3554Phe Pro His Gly Met Leu Asp Leu Glu Glu Il - #e Ala Ala Asn Ser Lys925 9 - #30 9 - #35 9 -#40- gat ttt cct aac atg tct gaa acg gat ttg tg - #t ttc ttg ctg cat tgg3602Asp Phe Pro Asn Met Ser Glu Thr Asp Leu Cy - #s Phe Leu Leu His Trp# 955- tta aat cca aag aaa att aat tta gca gat ag - #a atg ctt gga ttg tct3650Leu Asn Pro Lys Lys Ile Asn Leu Ala Asp Ar - #g Met Leu Gly Leu Ser# 970- gga gtt cag gaa att aaa gaa caa ggt gtt gg - #a tta ata gca gag tgt3698Gly Val Gln Glu Ile Lys Glu Gln Gly Val Gl - #y Leu Ile Ala Glu Cys# 985- aga act ttc tta gat tct att gct gga act tt - #a aaa tct atg atg ttt3746Arg Thr Phe Leu Asp Ser Ile Ala Gly Thr Le - #u Lys Ser Met Met Phe# 1000- gga ttt cat cat tct gtg act gtt gaa att at - #a aac act gtg ctc tgt3794Gly Phe His His Ser Val Thr Val Glu Ile Il - #e Asn Thr Val Leu Cys# 10205 0- ttt gtt aag agt gga att ttg ctt tat gta at - #a caa caa ttg aat cag3842Phe Val Lys Ser Gly Ile Leu Leu Tyr Val Il - #e Gln Gln Leu Asn Gln# 10350- gat gaa cat tct cac ata att ggt ttg ttg ag - #a gtc atg aat tat gca3890Asp Glu His Ser His Ile Ile Gly Leu Leu Ar - #g Val Met Asn Tyr Ala# 10505- gat att ggt tgt tca gtt att tca tgt ggc aa - #a gtt ttt tcc aaa atg3938Asp Ile Gly Cys Ser Val Ile Ser Cys Gly Ly - #s Val Phe Ser Lys Met# 10650- ctg gaa aca gtc ttt aat tgg caa atg gac tc - #c aga atg atg gag tta3986Leu Glu Thr Val Phe Asn Trp Gln Met Asp Se - #r Arg Met Met Glu Leu# 10805- agg act cag agt ttt tcc aac tgg tta aga ga - #t att tgt tct ggg atc4034Arg Thr Gln Ser Phe Ser Asn Trp Leu Arg As - #p Ile Cys Ser Gly Ile# 11005 0- acc att ttt aaa aac ttc aag gat gca att ta - #t tgg ctt tat aca aaa4082Thr Ile Phe Lys Asn Phe Lys Asp Ala Ile Ty - #r Trp Leu Tyr Thr Lys# 11150- tta aag gac ttt tat gaa gtg aat tat ggc aa - #g aag aag gac att tta4130Leu Lys Asp Phe Tyr Glu Val Asn Tyr Gly Ly - #s Lys Lys Asp Ile Leu# 11305- aat att ctt aaa gat aac caa caa aaa ata ga - #g aaa gcc att gag gaa4178Asn Ile Leu Lys Asp Asn Gln Gln Lys Ile Gl - #u Lys Ala Ile Glu Glu# 11450- gcc gat gaa ttt tgc att ttg caa atc caa ga - #t gtg gaa aaa ttt gaa4226Ala Asp Glu Phe Cys Ile Leu Gln Ile Gln As - #p Val Glu Lys Phe Glu# 11605- cag tat cag aaa ggg gtt gac ttg ata caa aa - #a ttg aga act gtt cat4274Gln Tyr Gln Lys Gly Val Asp Leu Ile Gln Ly - #s Leu Arg Thr Val His# 11805 0- tca atg gct cag gtt gat cca aat tta atg gt - #t cat ttg tca cct ttg4322Ser Met Ala Gln Val Asp Pro Asn Leu Met Va - #l His Leu Ser Pro Leu# 11950- aga gat tgt ata gca aga gtt cat cag aaa ct - #t aaa aac ctt gga tct4370Arg Asp Cys Ile Ala Arg Val His Gln Lys Le - #u Lys Asn Leu Gly Ser# 12105- ata aat cag gca atg gta acg aga tgt gag cc - #a gtt gtt tgt tat tta4418Ile Asn Gln Ala Met Val Thr Arg Cys Glu Pr - #o Val Val Cys Tyr Leu# 12250- tat ggc aaa aga ggg gga gga aag agc tta ac - #a tca att gca ttg gca4466Tyr Gly Lys Arg Gly Gly Gly Lys Ser Leu Th - #r Ser Ile Ala Leu Ala# 12405- acc aaa att tgt aaa cat tat ggt gtt gag cc - #t gaa aag aat atc tat4514Thr Lys Ile Cys Lys His Tyr Gly Val Glu Pr - #o Glu Lys Asn Ile Tyr# 12605 0- act aaa cct gtg gct tca gat tac tgg gat gg - #a tat agt gga caa tta4562Thr Lys Pro Val Ala Ser Asp Tyr Trp Asp Gl - #y Tyr Ser Gly Gln Leu# 12750- gtt tgc atc att gat gat att ggc caa aac ac - #a aca gat gag gat tgg4610Val Cys Ile Ile Asp Asp Ile Gly Gln Asn Th - #r Thr Asp Glu Asp Trp# 12905- tca gat ttt tgt cag tta gtg tca gga tgt cc - #a atg aga tta aac atg4658Ser Asp Phe Cys Gln Leu Val Ser Gly Cys Pr - #o Met Arg Leu Asn Met# 13050- gcc tct ctt gag gag aag ggt agg cat ttt tc - #t tct cct ttt ata ata4706Ala Ser Leu Glu Glu Lys Gly Arg His Phe Se - #r Ser Pro Phe Ile Ile# 13205- gca act tca aat tgg tca aat cca agt cca aa - #a aca gtt tat gtt aag4754Ala Thr Ser Asn Trp Ser Asn Pro Ser Pro Ly - #s Thr Val Tyr Val Lys# 13405 0- gaa gca att gac cgc aga ctc cat ttc aag gt - #t gaa gtt aaa cct gct4802Glu Ala Ile Asp Arg Arg Leu His Phe Lys Va - #l Glu Val Lys Pro Ala# 13550- tca ttt ttc aaa aat cct cac aat gat atg tt - #g aat gtt aat tta gct4850Ser Phe Phe Lys Asn Pro His Asn Asp Met Le - #u Asn Val Asn Leu Ala# 13705- aaa aca aat gat gca atc aaa gat atg tct tg - #t gtt gat ttg ata atg4898Lys Thr Asn Asp Ala Ile Lys Asp Met Ser Cy - #s Val Asp Leu Ile Met# 13850- gat gga cat aat gtt tca ttg atg gat ttg ct - #c agt tct tta gtc atg4946Asp Gly His Asn Val Ser Leu Met Asp Leu Le - #u Ser Ser Leu Val Met# 14005- aca gtt gaa att aga aaa caa aac atg act ga - #a ttc atg gag ttg tgg4994Thr Val Glu Ile Arg Lys Gln Asn Met Thr Gl - #u Phe Met Glu Leu Trp# 14205 0- tct cag gga att tca gat gat gat aat gat ag - #t gca gta gct gag ttt5042Ser Gln Gly Ile Ser Asp Asp Asp Asn Asp Se - #r Ala Val Ala Glu Phe# 14350- ttc cag tct ttt cca tct ggt gaa cca tcg aa - #c tct aaa tta tct ggc5090Phe Gln Ser Phe Pro Ser Gly Glu Pro Ser As - #n Ser Lys Leu Ser Gly# 14505- ttt ttc caa tct gtt act aat cac aag tgg gt - #t gct gtg gga gct gca5138Phe Phe Gln Ser Val Thr Asn His Lys Trp Va - #l Ala Val Gly Ala Ala# 14650- gtt ggc att ctt gga gtg ctc gtt gga gga tg - #g ttt gtg tat aag cat5186Val Gly Ile Leu Gly Val Leu Val Gly Gly Tr - #p Phe Val Tyr Lys His# 14805- ttc tcc cgc aaa gag gag gaa cca atc cca gc - #t gaa ggg gta tat cat5234Phe Ser Arg Lys Glu Glu Glu Pro Ile Pro Al - #a Glu Gly Val Tyr His# 15005 0- ggt gta act aag ccc aag caa gtg att aaa tt - #a gat gca gat cca gta5282Gly Val Thr Lys Pro Lys Gln Val Ile Lys Le - #u Asp Ala Asp Pro Val# 15150- gaa tct cag tca act ttg gaa ata gca gga ct - #g gtt agg aag aac ttg5330Glu Ser Gln Ser Thr Leu Glu Ile Ala Gly Le - #u Val Arg Lys Asn Leu# 15305- gtt cag ttt gga gtt gga gag aag aat gga tg - #t gtg aga tgg gtt atg5378Val Gln Phe Gly Val Gly Glu Lys Asn Gly Cy - #s Val Arg Trp Val Met# 15450- aat gcc ttg gga gtg aaa gat gat tgg ctg ct - #t gtg cct tcc cat gct5426Asn Ala Leu Gly Val Lys Asp Asp Trp Leu Le - #u Val Pro Ser His Ala# 15605- tat aaa ttt gag aaa gat tat gaa atg atg ga - #g ttt tat ttt aat aga5474Tyr Lys Phe Glu Lys Asp Tyr Glu Met Met Gl - #u Phe Tyr Phe Asn Arg# 15805 0- ggt gga act tac tat tca att tca gct ggt aa - #t gtt gtt att caa tct5522Gly Gly Thr Tyr Tyr Ser Ile Ser Ala Gly As - #n Val Val Ile Gln Ser# 15950- ttg gat gtg gga ttc cag gat gtt gtt ctg at - #g aag gtt cct aca att5570Leu Asp Val Gly Phe Gln Asp Val Val Leu Me - #t Lys Val Pro Thr Ile# 16105- cct aag ttt aga gat att act cag cat ttt at - #t aag aaa ggg gat gtg5618Pro Lys Phe Arg Asp Ile Thr Gln His Phe Il - #e Lys Lys Gly Asp Val# 16250- cct aga gct ttg aat cgc ctg gca aca tta gt - #g aca act gta aat gga5666Pro Arg Ala Leu Asn Arg Leu Ala Thr Leu Va - #l Thr Thr Val Asn Gly# 16405- acc cct atg tta att tct gag ggc cca cta aa - #g atg gaa gag aaa gct5714Thr Pro Met Leu Ile Ser Glu Gly Pro Leu Ly - #s Met Glu Glu Lys Ala# 16605 0- act tat gtt cat aag aaa aat gat ggt aca ac - #a gtt gat tta act gtg5762Thr Tyr Val His Lys Lys Asn Asp Gly Thr Th - #r Val Asp Leu Thr Val# 16750- gat cag gca tgg aga gga aaa ggc gaa ggt ct - #t cct gga atg tgt ggt5810Asp Gln Ala Trp Arg Gly Lys Gly Glu Gly Le - #u Pro Gly Met Cys Gly# 16905- ggg gcc ttg gtt tca tcg aat caa tct ata ca - #g aat gca atc ttg ggc5858Gly Ala Leu Val Ser Ser Asn Gln Ser Ile Gl - #n Asn Ala Ile Leu Gly# 17050- atc cat gtt gct gga gga aat tca att ctt gt - #t gca aaa ttg gtt act5906Ile His Val Ala Gly Gly Asn Ser Ile Leu Va - #l Ala Lys Leu Val Thr# 17205- caa gaa atg ttc caa aat att gat aag aaa at - #t gaa agt cag aga att5954Gln Glu Met Phe Gln Asn Ile Asp Lys Lys Il - #e Glu Ser Gln Arg Ile# 17405 0- atg aaa gtg gag ttt act cag tgt tca atg aa - #t gtg gtc tcc aaa acg6002Met Lys Val Glu Phe Thr Gln Cys Ser Met As - #n Val Val Ser Lys Thr# 17550- ctt ttt aga aag agt ccc att tat cat cac at - #t gat aaa acc atg att6050Leu Phe Arg Lys Ser Pro Ile Tyr His His Il - #e Asp Lys Thr Met Ile# 17705- aat ttt cct gca gct atg ccc ttt tct aaa gc - #t gaa att gat cca atg6098Asn Phe Pro Ala Ala Met Pro Phe Ser Lys Al - #a Glu Ile Asp Pro Met# 17850- gct gtg atg tta tct aag tat tca tta cct at - #t gta gaa gaa cca gag6146Ala Val Met Leu Ser Lys Tyr Ser Leu Pro Il - #e Val Glu Glu Pro Glu# 18005- gat tat aaa gag gct tca att ttt tat caa aa - #t aaa ata gtg ggt aag6194Asp Tyr Lys Glu Ala Ser Ile Phe Tyr Gln As - #n Lys Ile Val Gly Lys# 18205 0- act cag tta gtt gat gat ttt tta gat ctt ga - #t atg gcc att aca ggg6242Thr Gln Leu Val Asp Asp Phe Leu Asp Leu As - #p Met Ala Ile Thr Gly# 18350- gcc cca gga att gat gct atc aac atg gat tc - #a tct cct gga ttt cct6290Ala Pro Gly Ile Asp Ala Ile Asn Met Asp Se - #r Ser Pro Gly Phe Pro# 18505- tat gtc cag gag aag ttg acc aaa aga gat tt - #a att tgg ttg gat gaa6338Tyr Val Gln Glu Lys Leu Thr Lys Arg Asp Le - #u Ile Trp Leu Asp Glu# 18650- aat ggt tta ttg ctg gga gtt cat cca aga tt - #g gct cag aga atc tta6386Asn Gly Leu Leu Leu Gly Val His Pro Arg Le - #u Ala Gln Arg Ile Leu# 18805- ttc aat act gtc atg atg gaa aat tgt tct ga - #t ttg gat gtt gtt ttt6434Phe Asn Thr Val Met Met Glu Asn Cys Ser As - #p Leu Asp Val Val Phe# 19005 0- aca acc tgt cca aaa gat gaa ttg aga cca tt - #a gag aaa gtg ttg gaa6482Thr Thr Cys Pro Lys Asp Glu Leu Arg Pro Le - #u Glu Lys Val Leu Glu# 19150- tca aaa aca aga gct att gat gct tgt cct ct - #g gat tac tca att ttg6530Ser Lys Thr Arg Ala Ile Asp Ala Cys Pro Le - #u Asp Tyr Ser Ile Leu# 19305- tgc cga atg tat tgg ggt cca gct att agt ta - #t ttt cat ttg aat cca6578Cys Arg Met Tyr Trp Gly Pro Ala Ile Ser Ty - #r Phe His Leu Asn Pro# 19450- ggt ttc cat aca ggt gtt gct att ggc ata ga - #t cct gat aga cag tgg6626Gly Phe His Thr Gly Val Ala Ile Gly Ile As - #p Pro Asp Arg Gln Trp# 19605- gat gaa tta ttt aaa aca atg ata aga ttc gg - #a gat gtt ggt ctt gat6674Asp Glu Leu Phe Lys Thr Met Ile Arg Phe Gl - #y Asp Val Gly Leu Asp# 19801970 - # 1975- tta gat ttc tct gct ttt gat gct agt ctt ag - #t cca ttt atg att aga6722Leu Asp Phe Ser Ala Phe Asp Ala Ser Leu Se - #r Pro Phe Met Ile Arg# 19950- gaa gca ggt aga atc atg agt gaa cta tct gg - #a act cca tcc cat ttt6770Glu Ala Gly Arg Ile Met Ser Glu Leu Ser Gl - #y Thr Pro Ser His Phe# 20105- ggc aca gct ctt atc aat act atc att tat tc - #c aag cat ttg ctg tat6818Gly Thr Ala Leu Ile Asn Thr Ile Ile Tyr Se - #r Lys His Leu Leu Tyr# 20250- aac tgt tgt tac cat gtc tgt ggt tca atg cc - #c tct ggg tct cct tgt6866Asn Cys Cys Tyr His Val Cys Gly Ser Met Pr - #o Ser Gly Ser Pro Cys# 20405- aca gct ttg cta aat tca att att aat aat gt - #c aat ttg tat tat gtg6914Thr Ala Leu Leu Asn Ser Ile Ile Asn Asn Va - #l Asn Leu Tyr Tyr Val# 20602050 - # 2055- ttt tcc aag ata ttt gga aag tct cca gtt tt - #c ttt tgt cag gct ttg6962Phe Ser Lys Ile Phe Gly Lys Ser Pro Val Ph - #e Phe Cys Gln Ala Leu# 20750- aag att ctc tgt tat gga gat gat gtt tta at - #a gtt ttc tct cga gat7010Lys Ile Leu Cys Tyr Gly Asp Asp Val Leu Il - #e Val Phe Ser Arg Asp# 20905- gtt cag att gat aat ctt gat ttg att gga ca - #a aaa att gta gat gag7058Val Gln Ile Asp Asn Leu Asp Leu Ile Gly Gl - #n Lys Ile Val Asp Glu# 21050- ttt aag aaa ctt ggc atg aca gct act tct gc - #t gac aag aat gta cct7106Phe Lys Lys Leu Gly Met Thr Ala Thr Ser Al - #a Asp Lys Asn Val Pro# 21205- cag ctg aaa cca gtt tcg gaa ttg act ttt ct - #c aaa aga tct ttc aat7154Gln Leu Lys Pro Val Ser Glu Leu Thr Phe Le - #u Lys Arg Ser Phe Asn# 21405 0- ttg gta gag gat aga att aga cct gca att tc - #g gaa aaa aca att tgg7202Leu Val Glu Asp Arg Ile Arg Pro Ala Ile Se - #r Glu Lys Thr Ile Trp# 21550- tct tta ata gca tgg cag aga agt aac gct ga - #g ttt gag cag aat tta7250Ser Leu Ile Ala Trp Gln Arg Ser Asn Ala Gl - #u Phe Glu Gln Asn Leu# 21705- gaa aat gct cag tgg ttt gct ttt atg cat gg - #c tat gag ttt tat cag7298Glu Asn Ala Gln Trp Phe Ala Phe Met His Gl - #y Tyr Glu Phe Tyr Gln# 21850- aaa ttt tat tat ttt gtt cag tcc tgt ttg ga - #g aaa gag atg ata gaa7346Lys Phe Tyr Tyr Phe Val Gln Ser Cys Leu Gl - #u Lys Glu Met Ile Glu# 22005- tac aga ctt aaa tct tat gat tgg tgg aga at - #g aga ttt tat gac cag7394Tyr Arg Leu Lys Ser Tyr Asp Trp Trp Arg Me - #t Arg Phe Tyr Asp Gln# 2220 2210 - # 2215- tgt ttc att tgt gac ctt tca tgatttgttt aaacaaatt - #t tcttaaaatt7445Cys Phe Ile Cys Asp Leu Ser 2225# 7493ttct tttatcagta aataaaaaaa aaaaaaaa- <210> SEQ ID NO 2<211> LENGTH: 2227<212> TYPE: PRT<213> ORGANISM: WILD-TYPE HUMAN HEPATITIS A VIRUS, - # STRAIN HM-175- <400> SEQUENCE: 2- Met Asn Met Ser Arg Gln Gly Ile Phe Gln Th - #r Val Gly Ser Gly Leu# 15- Asp His Ile Leu Ser Leu Ala Asp Ile Glu Gl - #u Glu Gln Met Ile Gln# 30- Ser Val Asp Arg Thr Ala Val Thr Gly Ala Se - #r Tyr Phe Thr Ser Val# 45- Asp Gln Ser Ser Val His Thr Ala Glu Val Gl - #y Ser His Gln Val Glu# 60- Pro Leu Arg Thr Ser Val Asp Lys Pro Gly Se - #r Lys Lys Thr Gln Gly# 80- Glu Lys Phe Phe Leu Ile His Ser Ala Asp Tr - #p Leu Thr Thr His Ala# 95- Leu Phe His Glu Val Ala Lys Leu Asp Val Va - #l Lys Leu Leu Tyr Asn# 110- Glu Gln Phe Ala Val Gln Gly Leu Leu Arg Ty - #r His Thr Tyr Ala Arg# 125- Phe Gly Ile Glu Ile Gln Val Gln Ile Asn Pr - #o Thr Pro Phe Gln Gln# 140- Gly Gly Leu Ile Cys Ala Met Val Pro Gly As - #p Gln Ser Tyr Gly Ser145 1 - #50 1 - #55 1 -#60- Ile Ala Ser Leu Thr Val Tyr Pro His Gly Le - #u Leu Asn Cys Asn Ile# 175- Asn Asn Val Val Arg Ile Lys Val Pro Phe Il - #e Tyr Thr Arg Gly Ala# 190- Tyr His Phe Lys Asp Pro Gln Tyr Pro Val Tr - #p Glu Leu Thr Ile Arg# 205- Val Trp Ser Glu Leu Asn Ile Gly Thr Gly Th - #r Ser Ala Tyr Thr Ser# 220- Leu Asn Val Leu Ala Arg Phe Thr Asp Leu Gl - #u Leu His Gly Leu Thr225 2 - #30 2 - #35 2 -#40- Pro Leu Ser Thr Gln Met Met Arg Asn Glu Ph - #e Arg Val Ser Thr Thr# 255- Glu Asn Val Val Asn Leu Ser Asn Tyr Glu As - #p Ala Arg Ala Lys Met# 270- Ser Phe Ala Leu Asp Gln Glu Asp Trp Lys Se - #r Asp Pro Ser Gln Gly# 285- Gly Gly Ile Lys Ile Thr His Phe Thr Thr Tr - #p Thr Ser Ile Pro Thr# 300- Leu Ala Ala Gln Phe Pro Phe Asn Ala Ser As - #p Ser Val Gly Gln Gln305 3 - #10 3 - #15 3 -#20- Ile Lys Val Ile Pro Val Asp Pro Tyr Phe Ph - #e Gln Met Thr Asn Thr# 335- Asn Pro Asp Gln Lys Cys Ile Thr Ala Leu Al - #a Ser Ile Cys Gln Met# 350- Phe Cys Phe Trp Arg Gly Asp Leu Val Phe As - #p Phe Gln Val Phe Pro# 365- Thr Lys Tyr His Ser Gly Arg Leu Leu Phe Cy - #s Phe Val Pro Gly Asn# 380- Glu Leu Ile Asp Val Ser Gly Ile Thr Leu Ly - #s Gln Ala Thr Thr Ala385 3 - #90 3 - #95 4 -#00- Pro Cys Ala Val Met Asp Ile Thr Gly Val Gl - #n Ser Thr Leu Arg Phe# 415- Arg Val Pro Trp Ile Ser Asp Thr Pro Tyr Ar - #g Val Asn Arg Tyr Thr# 430- Lys Ser Ala His Gln Lys Gly Glu Tyr Thr Al - #a Ile Gly Lys Leu Ile# 445- Val Tyr Cys Tyr Asn Arg Leu Thr Ser Pro Se - #r Asn Val Ala Ser His# 460- Val Arg Val Asn Val Tyr Leu Ser Ala Ile As - #n Leu Glu Cys Phe Ala465 4 - #70 4 - #75 4 -#80- Pro Leu Tyr His Ala Met Asp Val Thr Thr Gl - #n Val Gly Asp Asp Ser# 495- Gly Gly Phe Ser Thr Thr Val Ser Thr Glu Gl - #n Asn Val Pro Asp Pro# 510- Gln Val Gly Ile Thr Thr Met Lys Asp Leu Ly - #s Gly Lys Ala Asn Arg# 525- Gly Lys Met Asp Val Ser Gly Val Gln Ala Pr - #o Val Gly Ala Ile Thr# 540- Thr Ile Glu Asp Pro Val Leu Ala Lys Lys Va - #l Pro Glu Thr Phe Pro545 5 - #50 5 - #55 5 -#60- Glu Leu Lys Pro Gly Glu Ser Arg His Thr Se - #r Asp His Met Ser Ile# 575- Tyr Lys Phe Met Gly Arg Ser His Phe Leu Cy - #s Thr Phe Thr Phe Asn# 590- Ser Asn Asn Lys Glu Tyr Thr Phe Pro Ile Th - #r Leu Ser Ser Thr Ser# 605- Asn Pro Pro His Gly Leu Pro Ser Thr Leu Ar - #g Trp Phe Phe Asn Leu# 620- Phe Gln Leu Tyr Arg Gly Pro Leu Asp Leu Th - #r Ile Ile Ile Thr Gly625 6 - #30 6 - #35 6 -#40- Ala Thr Asp Val Asp Gly Met Ala Trp Phe Th - #r Pro Val Gly Leu Ala# 655- Val Asp Thr Pro Trp Val Glu Lys Glu Ser Al - #a Leu Ser Ile Asp Tyr# 670- Lys Thr Ala Leu Gly Ala Val Arg Phe Asn Th - #r Arg Arg Thr Gly Asn# 685- Ile Gln Ile Arg Leu Pro Trp Tyr Ser Tyr Le - #u Tyr Ala Val Ser Gly# 700- Ala Leu Asp Gly Leu Gly Asp Lys Thr Asp Se - #r Thr Phe Gly Leu Val705 7 - #10 7 - #15 7 -#20- Ser Ile Gln Ile Ala Asn Tyr Asn His Ser As - #p Glu Tyr Leu Ser Phe# 735- Ser Cys Tyr Leu Ser Val Thr Glu Gln Ser Gl - #u Phe Tyr Phe Pro Arg# 750- Ala Pro Leu Asn Ser Asn Ala Met Leu Ser Th - #r Glu Ser Met Met Ser# 765- Arg Ile Ala Ala Gly Asp Leu Glu Ser Ser Va - #l Asp Asp Pro Arg Ser# 780- Glu Glu Asp Lys Arg Phe Glu Ser His Ile Gl - #u Cys Arg Lys Pro Tyr785 7 - #90 7 - #95 8 -#00- Lys Glu Leu Arg Leu Glu Val Gly Lys Gln Ar - #g Leu Lys Tyr Ala Gln# 815- Glu Glu Leu Ser Asn Glu Val Leu Pro Pro Pr - #o Arg Lys Met Lys Gly# 830- Leu Phe Ser Gln Ala Lys Ile Ser Leu Phe Ty - #r Thr Glu Glu His Glu# 845- Ile Met Lys Phe Ser Trp Arg Gly Val Thr Al - #a Asp Thr Arg Ala Leu# 860- Arg Arg Phe Gly Phe Ser Leu Ala Ala Gly Ar - #g Ser Val Trp Thr Leu865 8 - #70 8 - #75 8 -#80- Glu Met Asp Ala Gly Val Leu Thr Gly Arg Le - #u Ile Arg Leu Asn Asp# 895- Glu Lys Trp Thr Glu Met Lys Asp Asp Lys Il - #e Val Ser Leu Ile Glu# 910- Lys Phe Thr Ser Asn Lys Tyr Trp Ser Lys Va - #l Asn Phe Pro His Gly# 925- Met Leu Asp Leu Glu Glu Ile Ala Ala Asn Se - #r Lys Asp Phe Pro Asn# 940- Met Ser Glu Thr Asp Leu Cys Phe Leu Leu Hi - #s Trp Leu Asn Pro Lys945 9 - #50 9 - #55 9 -#60- Lys Ile Asn Leu Ala Asp Arg Met Leu Gly Le - #u Ser Gly Val Gln Glu# 975- Ile Lys Glu Gln Gly Val Gly Leu Ile Ala Gl - #u Cys Arg Thr Phe Leu# 990- Asp Ser Ile Ala Gly Thr Leu Lys Ser Met Me - #t Phe Gly Phe His His# 10050- Ser Val Thr Val Glu Ile Ile Asn Thr Val Le - #u Cys Phe Val Lys Ser# 10205- Gly Ile Leu Leu Tyr Val Ile Gln Gln Leu As - #n Gln Asp Glu His Ser# 10401030 - # 1035- His Ile Ile Gly Leu Leu Arg Val Met Asn Ty - #r Ala Asp Ile Gly Cys# 10550- Ser Val Ile Ser Cys Gly Lys Val Phe Ser Ly - #s Met Leu Glu Thr Val# 10705- Phe Asn Trp Gln Met Asp Ser Arg Met Met Gl - #u Leu Arg Thr Gln Ser# 10850- Phe Ser Asn Trp Leu Arg Asp Ile Cys Ser Gl - #y Ile Thr Ile Phe Lys# 11005- Asn Phe Lys Asp Ala Ile Tyr Trp Leu Tyr Th - #r Lys Leu Lys Asp Phe# 11201110 - # 1115- Tyr Glu Val Asn Tyr Gly Lys Lys Lys Asp Il - #e Leu Asn Ile Leu Lys# 11350- Asp Asn Gln Gln Lys Ile Glu Lys Ala Ile Gl - #u Glu Ala Asp Glu Phe# 11505- Cys Ile Leu Gln Ile Gln Asp Val Glu Lys Ph - #e Glu Gln Tyr Gln Lys# 11650- Gly Val Asp Leu Ile Gln Lys Leu Arg Thr Va - #l His Ser Met Ala Gln# 11805- Val Asp Pro Asn Leu Met Val His Leu Ser Pr - #o Leu Arg Asp Cys Ile# 12001190 - # 1195- Ala Arg Val His Gln Lys Leu Lys Asn Leu Gl - #y Ser Ile Asn Gln Ala# 12150- Met Val Thr Arg Cys Glu Pro Val Val Cys Ty - #r Leu Tyr Gly Lys Arg# 12305- Gly Gly Gly Lys Ser Leu Thr Ser Ile Ala Le - #u Ala Thr Lys Ile Cys# 12450- Lys His Tyr Gly Val Glu Pro Glu Lys Asn Il - #e Tyr Thr Lys Pro Val# 12605- Ala Ser Asp Tyr Trp Asp Gly Tyr Ser Gly Gl - #n Leu Val Cys Ile Ile# 12801270 - # 1275- Asp Asp Ile Gly Gln Asn Thr Thr Asp Glu As - #p Trp Ser Asp Phe Cys# 12950- Gln Leu Val Ser Gly Cys Pro Met Arg Leu As - #n Met Ala Ser Leu Glu# 13105- Glu Lys Gly Arg His Phe Ser Ser Pro Phe Il - #e Ile Ala Thr Ser Asn# 13250- Trp Ser Asn Pro Ser Pro Lys Thr Val Tyr Va - #l Lys Glu Ala Ile Asp# 13405- Arg Arg Leu His Phe Lys Val Glu Val Lys Pr - #o Ala Ser Phe Phe Lys# 13601350 - # 1355- Asn Pro His Asn Asp Met Leu Asn Val Asn Le - #u Ala Lys Thr Asn Asp# 13750- Ala Ile Lys Asp Met Ser Cys Val Asp Leu Il - #e Met Asp Gly His Asn# 13905- Val Ser Leu Met Asp Leu Leu Ser Ser Leu Va - #l Met Thr Val Glu Ile# 14050- Arg Lys Gln Asn Met Thr Glu Phe Met Glu Le - #u Trp Ser Gln Gly Ile# 14205- Ser Asp Asp Asp Asn Asp Ser Ala Val Ala Gl - #u Phe Phe Gln Ser Phe# 14401430 - # 1435- Pro Ser Gly Glu Pro Ser Asn Ser Lys Leu Se - #r Gly Phe Phe Gln Ser# 14550- Val Thr Asn His Lys Trp Val Ala Val Gly Al - #a Ala Val Gly Ile Leu# 14705- Gly Val Leu Val Gly Gly Trp Phe Val Tyr Ly - #s His Phe Ser Arg Lys# 14850- Glu Glu Glu Pro Ile Pro Ala Glu Gly Val Ty - #r His Gly Val Thr Lys# 15005- Pro Lys Gln Val Ile Lys Leu Asp Ala Asp Pr - #o Val Glu Ser Gln Ser# 15201510 - # 1515- Thr Leu Glu Ile Ala Gly Leu Val Arg Lys As - #n Leu Val Gln Phe Gly# 15350- Val Gly Glu Lys Asn Gly Cys Val Arg Trp Va - #l Met Asn Ala Leu Gly# 15505- Val Lys Asp Asp Trp Leu Leu Val Pro Ser Hi - #s Ala Tyr Lys Phe Glu# 15650- Lys Asp Tyr Glu Met Met Glu Phe Tyr Phe As - #n Arg Gly Gly Thr Tyr# 15805- Tyr Ser Ile Ser Ala Gly Asn Val Val Ile Gl - #n Ser Leu Asp Val Gly# 16001590 - # 1595- Phe Gln Asp Val Val Leu Met Lys Val Pro Th - #r Ile Pro Lys Phe Arg# 16150- Asp Ile Thr Gln His Phe Ile Lys Lys Gly As - #p Val Pro Arg Ala Leu# 16305- Asn Arg Leu Ala Thr Leu Val Thr Thr Val As - #n Gly Thr Pro Met Leu# 16450- Ile Ser Glu Gly Pro Leu Lys Met Glu Glu Ly - #s Ala Thr Tyr Val His# 16605- Lys Lys Asn Asp Gly Thr Thr Val Asp Leu Th - #r Val Asp Gln Ala Trp# 16801670 - # 1675- Arg Gly Lys Gly Glu Gly Leu Pro Gly Met Cy - #s Gly Gly Ala Leu Val# 16950- Ser Ser Asn Gln Ser Ile Gln Asn Ala Ile Le - #u Gly Ile His Val Ala# 17105- Gly Gly Asn Ser Ile Leu Val Ala Lys Leu Va - #l Thr Gln Glu Met Phe# 17250- Gln Asn Ile Asp Lys Lys Ile Glu Ser Gln Ar - #g Ile Met Lys Val Glu# 17405- Phe Thr Gln Cys Ser Met Asn Val Val Ser Ly - #s Thr Leu Phe Arg Lys# 17601750 - # 1755- Ser Pro Ile Tyr His His Ile Asp Lys Thr Me - #t Ile Asn Phe Pro Ala# 17750- Ala Met Pro Phe Ser Lys Ala Glu Ile Asp Pr - #o Met Ala Val Met Leu# 17905- Ser Lys Tyr Ser Leu Pro Ile Val Glu Glu Pr - #o Glu Asp Tyr Lys Glu# 18050- Ala Ser Ile Phe Tyr Gln Asn Lys Ile Val Gl - #y Lys Thr Gln Leu Val# 18205- Asp Asp Phe Leu Asp Leu Asp Met Ala Ile Th - #r Gly Ala Pro Gly Ile# 18401830 - # 1835- Asp Ala Ile Asn Met Asp Ser Ser Pro Gly Ph - #e Pro Tyr Val Gln Glu# 18550- Lys Leu Thr Lys Arg Asp Leu Ile Trp Leu As - #p Glu Asn Gly Leu Leu# 18705- Leu Gly Val His Pro Arg Leu Ala Gln Arg Il - #e Leu Phe Asn Thr Val# 18850- Met Met Glu Asn Cys Ser Asp Leu Asp Val Va - #l Phe Thr Thr Cys Pro# 19005- Lys Asp Glu Leu Arg Pro Leu Glu Lys Val Le - #u Glu Ser Lys Thr Arg# 19201910 - # 1915- Ala Ile Asp Ala Cys Pro Leu Asp Tyr Ser Il - #e Leu Cys Arg Met Tyr# 19350- Trp Gly Pro Ala Ile Ser Tyr Phe His Leu As - #n Pro Gly Phe His Thr# 19505- Gly Val Ala Ile Gly Ile Asp Pro Asp Arg Gl - #n Trp Asp Glu Leu Phe# 19650- Lys Thr Met Ile Arg Phe Gly Asp Val Gly Le - #u Asp Leu Asp Phe Ser# 19805- Ala Phe Asp Ala Ser Leu Ser Pro Phe Met Il - #e Arg Glu Ala Gly Arg# 20001990 - # 1995- Ile Met Ser Glu Leu Ser Gly Thr Pro Ser Hi - #s Phe Gly Thr Ala Leu# 20150- Ile Asn Thr Ile Ile Tyr Ser Lys His Leu Le - #u Tyr Asn Cys Cys Tyr# 20305- His Val Cys Gly Ser Met Pro Ser Gly Ser Pr - #o Cys Thr Ala Leu Leu# 20450- Asn Ser Ile Ile Asn Asn Val Asn Leu Tyr Ty - #r Val Phe Ser Lys Ile# 20605- Phe Gly Lys Ser Pro Val Phe Phe Cys Gln Al - #a Leu Lys Ile Leu Cys# 20802070 - # 2075- Tyr Gly Asp Asp Val Leu Ile Val Phe Ser Ar - #g Asp Val Gln Ile Asp# 20950- Asn Leu Asp Leu Ile Gly Gln Lys Ile Val As - #p Glu Phe Lys Lys Leu# 21105- Gly Met Thr Ala Thr Ser Ala Asp Lys Asn Va - #l Pro Gln Leu Lys Pro# 21250- Val Ser Glu Leu Thr Phe Leu Lys Arg Ser Ph - #e Asn Leu Val Glu Asp# 21405- Arg Ile Arg Pro Ala Ile Ser Glu Lys Thr Il - #e Trp Ser Leu Ile Ala# 21602150 - # 2155- Trp Gln Arg Ser Asn Ala Glu Phe Glu Gln As - #n Leu Glu Asn Ala Gln# 21750- Trp Phe Ala Phe Met His Gly Tyr Glu Phe Ty - #r Gln Lys Phe Tyr Tyr# 21905- Phe Val Gln Ser Cys Leu Glu Lys Glu Met Il - #e Glu Tyr Arg Leu Lys# 22050- Ser Tyr Asp Trp Trp Arg Met Arg Phe Tyr As - #p Gln Cys Phe Ile Cys# 22205- Asp Leu Ser2225- <210> SEQ ID NO 3<211> LENGTH: 7488<212> TYPE: DNA#HM-175RGANISM: Attenuated (Pass 35) HAV, strain<220> FEATURE:<221> NAME/KEY: CDS<222> LOCATION: (730)..(7410)- <400> SEQUENCE: 3- ttcaagaggg gtctccggga atttccggag tccctcttgg aagtccatgg tg - #aggggact 60- tgatacctca ccgccgtttg cctaggctat aggctaaatt ttccctttcc ct - #tttccctt 120- tcccattccc ttttgcttgt aaatattgat tcctgcaggt tcagggttct ta - #aatctgtt 180- tctctataag aacactcatt ttcacgcttt ctgtcttctt tcttccaggg ct - #ctcccctt 240- gccctaggct ctggccgttg cgcccggcgg ggtcaactcc atgattagca tg - #gagctgta 300- ggagtctaaa ttggggacac agatgtttgg aacgtcacct tgcagtgtta ac - #ttggcttt 360- catgaatctc tttgatcttc cacaaggggt aggctacggg tgaaacctct ta - #ggctaata 420- cttctatgaa gagatgcctt ggatagggta acagcggcgg atattggtga gt - #tgttaaga 480- caaaaaccat tcaacgccgg aggactgact ctcatccagt ggatgcattg ag - #tggattga 540- ctgtcagggc tgtctttagg cttaattcca gacctctctg tgcttagggc aa - #acatcatt 600- tggccttaaa tgggattctg tgagagggga tccctccatt gacagctgga ct - #gttctttg 660- gggccttatg tggtgtttgc ctctgaggta ctcaggggca tttaggtttt tc - #ctcattct 720- taaataata atg aac atg tct aga caa ggt att ttc - # cag act gtt ggg agt 771#Gln Gly Ile Phe Gln Thr Val Gly Ser# 10- ggt ctt gac cac atc ctg tct ttg gca gac at - #t gag gaa gag caa atg 819Gly Leu Asp His Ile Leu Ser Leu Ala Asp Il - #e Glu Glu Glu Gln Met# 30- att caa tca gtt gat agg act gca gtg act gg - #t gct tct tat ttt act 867Ile Gln Ser Val Asp Arg Thr Ala Val Thr Gl - #y Ala Ser Tyr Phe Thr# 45- tct gtg gat caa tct tca gtt cat aca gct ga - #g gtt gga tca cac cag 915Ser Val Asp Gln Ser Ser Val His Thr Ala Gl - #u Val Gly Ser His Gln# 60- gtt gaa cct ttg aga acc tct gtt gat aaa cc - #c ggt tca aag agg act 963Val Glu Pro Leu Arg Thr Ser Val Asp Lys Pr - #o Gly Ser Lys Arg Thr# 75- cag gga gag aaa ttt ttc ttg att cat tct gc - #a gat tgg ctt act aca1011Gln Gly Glu Lys Phe Phe Leu Ile His Ser Al - #a Asp Trp Leu Thr Thr# 90- cat gct ctt ttc cat gaa gtt gca aaa ttg ga - #t gtg gtg aaa tta tta1059His Ala Leu Phe His Glu Val Ala Lys Leu As - #p Val Val Lys Leu Leu#110- tac aat gag cag ttt gct gtt caa ggg ttg tt - #g aga tac cat aca tat1107Tyr Asn Glu Gln Phe Ala Val Gln Gly Leu Le - #u Arg Tyr His Thr Tyr# 125- gca aga ttt ggc att gaa att caa gtt cag at - #a aac cct aca cct ttc1155Ala Arg Phe Gly Ile Glu Ile Gln Val Gln Il - #e Asn Pro Thr Pro Phe# 140- caa cag ggg gga ttg atc tgt gct atg gtt cc - #t ggt gac cag agc tat1203Gln Gln Gly Gly Leu Ile Cys Ala Met Val Pr - #o Gly Asp Gln Ser Tyr# 155- ggt tct ata gca tca ttg act gtt tat cct ca - #t ggt ttg tta aat tgc1251Gly Ser Ile Ala Ser Leu Thr Val Tyr Pro Hi - #s Gly Leu Leu Asn Cys# 170- aat att aac aat gtg gtt aga ata aag gtt cc - #a ttt att tac aca aga1299Asn Ile Asn Asn Val Val Arg Ile Lys Val Pr - #o Phe Ile Tyr Thr Arg175 1 - #80 1 - #85 1 -#90- ggt gct tac cac ttt aaa gat cca caa tac cc - #a gtt tgg gaa ttg aca1347Gly Ala Tyr His Phe Lys Asp Pro Gln Tyr Pr - #o Val Trp Glu Leu Thr# 205- att aga gtt tgg tca gaa tta aat att ggg ac - #a gga act tca gct tat1395Ile Arg Val Trp Ser Glu Leu Asn Ile Gly Th - #r Gly Thr Ser Ala Tyr# 220- act tca ctc aat gtt tta gct aga ttt aca ga - #t ttg gag ttg cat gga1443Thr Ser Leu Asn Val Leu Ala Arg Phe Thr As - #p Leu Glu Leu His Gly# 235- tta act cct ctt tct aca caa atg atg aga aa - #t gaa ttt agg gtc agt1491Leu Thr Pro Leu Ser Thr Gln Met Met Arg As - #n Glu Phe Arg Val Ser# 250- act act gag aat gtg gtg aat ctg tca aat ta - #t gaa gat gca aga gca1539Thr Thr Glu Asn Val Val Asn Leu Ser Asn Ty - #r Glu Asp Ala Arg Ala255 2 - #60 2 - #65 2 -#70- aag atg tct ttt gct ttg gat cag gaa gat tg - #g aaa tct gat ccg tcc1587Lys Met Ser Phe Ala Leu Asp Gln Glu Asp Tr - #p Lys Ser Asp Pro Ser# 285- cag ggt ggt ggg atc aaa att act cat ttt ac - #t act tgg aca tct att1635Gln Gly Gly Gly Ile Lys Ile Thr His Phe Th - #r Thr Trp Thr Ser Ile# 300- cca act ttg gct gct cag ttt cca ttt aat gc - #t tca gac tca gtt ggt1683Pro Thr Leu Ala Ala Gln Phe Pro Phe Asn Al - #a Ser Asp Ser Val Gly# 315- caa caa att aaa gtt att cca gtt gac cca ta - #t ttt ttc caa atg aca1731Gln Gln Ile Lys Val Ile Pro Val Asp Pro Ty - #r Phe Phe Gln Met Thr# 330- aat aca aat cct gac caa aaa tgt ata act gc - #t ttg gct tct att tgt1779Asn Thr Asn Pro Asp Gln Lys Cys Ile Thr Al - #a Leu Ala Ser Ile Cys335 3 - #40 3 - #45 3 -#50- cag atg ttt tgt ttt tgg aga gga gat ctt gt - #c ttt gat ttt caa gtt1827Gln Met Phe Cys Phe Trp Arg Gly Asp Leu Va - #l Phe Asp Phe Gln Val# 365- ttt ccc acc aaa tat cat tca ggt aga tta ct - #g ttt tgt ttt gtt cct1875Phe Pro Thr Lys Tyr His Ser Gly Arg Leu Le - #u Phe Cys Phe Val Pro# 380- ggc aat gag cta ata gat gtt tct gga atc ac - #a tta aag caa gca act1923Gly Asn Glu Leu Ile Asp Val Ser Gly Ile Th - #r Leu Lys Gln Ala Thr# 395- act gct cct tgt gca gta atg gat att aca gg - #a gtg cag tca act ttg1971Thr Ala Pro Cys Ala Val Met Asp Ile Thr Gl - #y Val Gln Ser Thr Leu# 410- aga ttt cgt gtt ccc tgg att tct gac act cc - #t tac aga gtg aac agg2019Arg Phe Arg Val Pro Trp Ile Ser Asp Thr Pr - #o Tyr Arg Val Asn Arg415 4 - #20 4 - #25 4 -#30- tat aca aag tca gca cat cag aaa ggt gag ta - #c act gcc att ggg aag2067Tyr Thr Lys Ser Ala His Gln Lys Gly Glu Ty - #r Thr Ala Ile Gly Lys# 445- ctt att gtg tat tgt tat aac aga ttg acc tc - #t cct tct aac gtt gct2115Leu Ile Val Tyr Cys Tyr Asn Arg Leu Thr Se - #r Pro Ser Asn Val Ala# 460- tcc cat gtc aga gtg aat gtt tat ctt tca gc - #a att aac ttg gaa tgt2163Ser His Val Arg Val Asn Val Tyr Leu Ser Al - #a Ile Asn Leu Glu Cys# 475- ttt gct cct ctt tat cat gct atg gat gtt ac - #t aca caa gtt gga gat2211Phe Ala Pro Leu Tyr His Ala Met Asp Val Th - #r Thr Gln Val Gly Asp# 490- gat tct gga ggt ttt tca aca aca gtt tct ac - #a gaa cag aat gtt cca2259Asp Ser Gly Gly Phe Ser Thr Thr Val Ser Th - #r Glu Gln Asn Val Pro495 5 - #00 5 - #05 5 -#10- gat ccc caa gtt ggt ata aca acc atg aaa ga - #t ttg aaa gga aaa gct2307Asp Pro Gln Val Gly Ile Thr Thr Met Lys As - #p Leu Lys Gly Lys Ala# 525- aac aga ggg aaa atg gat gtt tca gga gta ca - #a gca cct gtg gga gct2355Asn Arg Gly Lys Met Asp Val Ser Gly Val Gl - #n Ala Pro Val Gly Ala# 540- atc aca aca att gag gat cca gtt tta gca aa - #g aaa gta cct gag aca2403Ile Thr Thr Ile Glu Asp Pro Val Leu Ala Ly - #s Lys Val Pro Glu Thr# 555- ttt cct gaa ttg aaa cct gga gaa tcc aga ca - #t aca tca gat cat atg2451Phe Pro Glu Leu Lys Pro Gly Glu Ser Arg Hi - #s Thr Ser Asp His Met# 570- tcc atc tac aag ttt atg gga agg tct cat tt - #c ttg tgc act ttt aca2499Ser Ile Tyr Lys Phe Met Gly Arg Ser His Ph - #e Leu Cys Thr Phe Thr575 5 - #80 5 - #85 5 -#90- ttc aat tca aat aat aaa gag tac aca ttt cc - #t ata acc ttg tct tca2547Phe Asn Ser Asn Asn Lys Glu Tyr Thr Phe Pr - #o Ile Thr Leu Ser Ser# 605- acc tct aat cct cct cat ggt ttg cca tca ac - #a ctg agg tgg ttt ttc2595Thr Ser Asn Pro Pro His Gly Leu Pro Ser Th - #r Leu Arg Trp Phe Phe# 620- aac ttg ttt cag ttg tat aga ggg cct tta ga - #t ctg aca att att att2643Asn Leu Phe Gln Leu Tyr Arg Gly Pro Leu As - #p Leu Thr Ile Ile Ile# 635- aca gga gca act gat gta gat ggc atg gcc tg - #g ttc act cca gta ggt2691Thr Gly Ala Thr Asp Val Asp Gly Met Ala Tr - #p Phe Thr Pro Val Gly# 650- ctt gcc gtt gat act cct tgg gta gag aag ga - #g tca gct ttg tct att2739Leu Ala Val Asp Thr Pro Trp Val Glu Lys Gl - #u Ser Ala Leu Ser Ile655 6 - #60 6 - #65 6 -#70- gac tac aaa act gct ctt gga gct gtc aga tt - #t aac aca agg aga aca2787Asp Tyr Lys Thr Ala Leu Gly Ala Val Arg Ph - #e Asn Thr Arg Arg Thr# 685- ggg aac att cag att aga tta cca tgg tat tc - #t tat tta tat gct gtg2835Gly Asn Ile Gln Ile Arg Leu Pro Trp Tyr Se - #r Tyr Leu Tyr Ala Val# 700- tct gga gca ctg gat ggt ttg gga gac aag ac - #a gat tct aca ttt gga2883Ser Gly Ala Leu Asp Gly Leu Gly Asp Lys Th - #r Asp Ser Thr Phe Gly# 715- ttg gtt tct att cag att gca aat tac aat ca - #t tct gat gaa tac ttg2931Leu Val Ser Ile Gln Ile Ala Asn Tyr Asn Hi - #s Ser Asp Glu Tyr Leu# 730- tct ttt agt tgt tat ttg tct gtc aca gaa ca - #a tca gag ttt tat ttt2979Ser Phe Ser Cys Tyr Leu Ser Val Thr Glu Gl - #n Ser Glu Phe Tyr Phe735 7 - #40 7 - #45 7 -#50- ccc aga gct cca ttg aac tca aat gcc atg tt - #a tcc act gta tca atg3027Pro Arg Ala Pro Leu Asn Ser Asn Ala Met Le - #u Ser Thr Val Ser Met# 765- atg agc aga att gca gct gga gac ttg gag tc - #a tca gtg gat gat cct3075Met Ser Arg Ile Ala Ala Gly Asp Leu Glu Se - #r Ser Val Asp Asp Pro# 780- aga tca gag gaa gat aaa aga ttt gag agt ca - #t ata gaa tgc agg aag3123Arg Ser Glu Glu Asp Lys Arg Phe Glu Ser Hi - #s Ile Glu Cys Arg Lys# 795- cca tat aaa gaa ctg aga tta gaa gtt ggg aa - #a caa aga ctc aag tat3171Pro Tyr Lys Glu Leu Arg Leu Glu Val Gly Ly - #s Gln Arg Leu Lys Tyr# 810- gct cag gaa gaa ttg tca agt gaa gta ctt cc - #a ccc cct agg aaa atg3219Ala Gln Glu Glu Leu Ser Ser Glu Val Leu Pr - #o Pro Pro Arg Lys Met815 8 - #20 8 - #25 8 -#30- aag gga ctg ttt tca caa gcc aaa att tct ct - #t ttt tat act gag gag3267Lys Gly Leu Phe Ser Gln Ala Lys Ile Ser Le - #u Phe Tyr Thr Glu Glu# 845- cat gaa ata atg aag ttt tcc tgg aga ggt gt - #g act gct gat act aga3315His Glu Ile Met Lys Phe Ser Trp Arg Gly Va - #l Thr Ala Asp Thr Arg# 860- gct tta agg agg ttt gga ttc tct ttg gcc gc - #a ggc aga agt gtg tgg3363Ala Leu Arg Arg Phe Gly Phe Ser Leu Ala Al - #a Gly Arg Ser Val Trp# 875- act ctt gaa atg gat gct ggg gtt ctt act gg - #g aga ctg att aga ttg3411Thr Leu Glu Met Asp Ala Gly Val Leu Thr Gl - #y Arg Leu Ile Arg Leu# 890- aat gat gag aaa tgg aca gaa atg aag gat ga - #c aag att gtt tca ttg3459Asn Asp Glu Lys Trp Thr Glu Met Lys Asp As - #p Lys Ile Val Ser Leu895 9 - #00 9 - #05 9 -#10- att gaa aag ttt aca agt aac aaa tat tgg tc - #c aaa gtg aat ttc cca3507Ile Glu Lys Phe Thr Ser Asn Lys Tyr Trp Se - #r Lys Val Asn Phe Pro# 925- cat ggg atg ttg gat ctt gaa gaa att gct gc - #c aat tct aag gat ttt3555His Gly Met Leu Asp Leu Glu Glu Ile Ala Al - #a Asn Ser Lys Asp Phe# 940- cct aac atg tct gaa acg gat ttg tgt ttc tt - #g ctg cat tgg tta aat3603Pro Asn Met Ser Glu Thr Asp Leu Cys Phe Le - #u Leu His Trp Leu Asn# 955- cca aag aaa att aat tta gca gat aga atg ct - #t gga ttg tct gga gtt3651Pro Lys Lys Ile Asn Leu Ala Asp Arg Met Le - #u Gly Leu Ser Gly Val# 970- cag gaa att aaa gaa caa ggt gtt gga tta at - #a gca gag tgt aga act3699Gln Glu Ile Lys Glu Gln Gly Val Gly Leu Il - #e Ala Glu Cys Arg Thr975 9 - #80 9 - #85 9 -#90- ttc tta gat tct att gct gga act tta aaa tc - #t atg atg ttt gga ttt3747Phe Leu Asp Ser Ile Ala Gly Thr Leu Lys Se - #r Met Met Phe Gly Phe# 10050- cat cat tct gtg act gtt gaa att ata aac ac - #t gtg ctc tgt ttt gtt3795His His Ser Val Thr Val Glu Ile Ile Asn Th - #r Val Leu Cys Phe Val# 10205- aag agt gga att ttg ctt tat gta ata caa ca - #a ttg aat cag gat gaa3843Lys Ser Gly Ile Leu Leu Tyr Val Ile Gln Gl - #n Leu Asn Gln Asp Glu# 10350- cat tct cac ata att ggt ttg ttg aga gtc at - #g aat tat gta gat att3891His Ser His Ile Ile Gly Leu Leu Arg Val Me - #t Asn Tyr Val Asp Ile# 10505- ggt tgt tca gtt att tca tgt gcc aaa gtt tt - #t tcc aaa atg ctg gaa3939Gly Cys Ser Val Ile Ser Cys Ala Lys Val Ph - #e Ser Lys Met Leu Glu# 10701060 - # 1065- aca gtc ttt aat tgg caa atg gac tcc aga at - #g atg gag tta agg act3987Thr Val Phe Asn Trp Gln Met Asp Ser Arg Me - #t Met Glu Leu Arg Thr# 10850- cag agt ttt tcc aac tgg tta aga gat att tg - #t tct ggg atc acc att4035Gln Ser Phe Ser Asn Trp Leu Arg Asp Ile Cy - #s Ser Gly Ile Thr Ile# 11005- ttc aaa aac ttc aag gat gca att tat tgg ct - #t tat aca aaa tta atg4083Phe Lys Asn Phe Lys Asp Ala Ile Tyr Trp Le - #u Tyr Thr Lys Leu Met# 11150- gac ttt tat gaa gtg aat tat ggc aag aag aa - #g gac att tta aat att4131Asp Phe Tyr Glu Val Asn Tyr Gly Lys Lys Ly - #s Asp Ile Leu Asn Ile# 11305- ctt aaa gat aac caa caa aaa ata gag aaa gc - #c att gag gaa gcc gat4179Leu Lys Asp Asn Gln Gln Lys Ile Glu Lys Al - #a Ile Glu Glu Ala Asp# 11505 0- aaa ttt tgc att ttg caa atc caa gat gtg ga - #a aaa tct gaa cag tat4227Lys Phe Cys Ile Leu Gln Ile Gln Asp Val Gl - #u Lys Ser Glu Gln Tyr# 11650- cag aaa ggg gtt gac ttg ata caa aaa ttg ag - #a act gtt cat tca atg4275Gln Lys Gly Val Asp Leu Ile Gln Lys Leu Ar - #g Thr Val His Ser Met# 11805- gct cag gtt gat cca aat tta atg gtt cat tt - #g tca cct ttg aga gat4323Ala Gln Val Asp Pro Asn Leu Met Val His Le - #u Ser Pro Leu Arg Asp# 11950- tgt ata gca aga gtt cat cag aaa ctt aaa aa - #c ctt gga tct ata aat4371Cys Ile Ala Arg Val His Gln Lys Leu Lys As - #n Leu Gly Ser Ile Asn# 12105- cag gca atg gta acg aga tgt gag cca gtt gt - #t tgt tat tta tat ggc4419Gln Ala Met Val Thr Arg Cys Glu Pro Val Va - #l Cys Tyr Leu Tyr Gly# 12301220 - # 1225- aaa aga ggg gga gga aag agc tta aca tca at - #t gca ttg gca acc aaa4467Lys Arg Gly Gly Gly Lys Ser Leu Thr Ser Il - #e Ala Leu Ala Thr Lys# 12450- att tgt aaa cat tat ggt gtt gag cct gaa aa - #g aat atc tat act aaa4515Ile Cys Lys His Tyr Gly Val Glu Pro Glu Ly - #s Asn Ile Tyr Thr Lys# 12605- cct gtg gct tca gat tac tgg gat gga tat ag - #t gga caa tta att tgc4563Pro Val Ala Ser Asp Tyr Trp Asp Gly Tyr Se - #r Gly Gln Leu Ile Cys# 12750- atc att gat gat att ggc caa aac aca aca ga - #t gag gat tgg tca gat4611Ile Ile Asp Asp Ile Gly Gln Asn Thr Thr As - #p Glu Asp Trp Ser Asp# 12905- ttt tgt cag tta gtg tca gga tgt cca atg ag - #a tta aac atg gcc tct4659Phe Cys Gln Leu Val Ser Gly Cys Pro Met Ar - #g Leu Asn Met Ala Ser# 13101300 - # 1305- ctt gag gag aag ggt agg cat ttt tct tct cc - #t ttt ata ata gca act4707Leu Glu Glu Lys Gly Arg His Phe Ser Ser Pr - #o Phe Ile Ile Ala Thr# 13250- tca aat tgg tca aat cca agt cca aaa aca gt - #t tat gtt aag gaa gca4755Ser Asn Trp Ser Asn Pro Ser Pro Lys Thr Va - #l Tyr Val Lys Glu Ala# 13405- att gac cgc aga ctc cat ttc aag gtt gaa gt - #t aaa cct gct tca ttt4803Ile Asp Arg Arg Leu His Phe Lys Val Glu Va - #l Lys Pro Ala Ser Phe# 13550- ttc aaa aat cct cac aat gat atg ttg aat gt - #t aat tta gct aaa aca4851Phe Lys Asn Pro His Asn Asp Met Leu Asn Va - #l Asn Leu Ala Lys Thr# 13705- aat gat gca atc aaa gat atg tct tgt gtt ga - #t ttg ata atg gat gga4899Asn Asp Ala Ile Lys Asp Met Ser Cys Val As - #p Leu Ile Met Asp Gly# 13901380 - # 1385- cat aat gtt tca ttg atg gat ttg ctc agt tc - #t tta gtc atg aca gtt4947His Asn Val Ser Leu Met Asp Leu Leu Ser Se - #r Leu Val Met Thr Val# 14050- gaa att aga aaa caa aac atg act gaa ttc at - #g gag ttg tgg tct cag4995Glu Ile Arg Lys Gln Asn Met Thr Glu Phe Me - #t Glu Leu Trp Ser Gln# 14205- gga att tca gat gat gat aat gat agt gca gt - #a gct gag ttt ttc cag5043Gly Ile Ser Asp Asp Asp Asn Asp Ser Ala Va - #l Ala Glu Phe Phe Gln# 14350- tct ttt cca tct ggt gaa cca tcg aac tct aa - #a tta tct ggc ttt ttc5091Ser Phe Pro Ser Gly Glu Pro Ser Asn Ser Ly - #s Leu Ser Gly Phe Phe# 14505- caa tct gtt act aat cac aag tgg gtt gct gt - #g gga gct gca gtt ggc5139Gln Ser Val Thr Asn His Lys Trp Val Ala Va - #l Gly Ala Ala Val Gly# 14701460 - # 1465- att ctt gga gtg ctc gtt gga gga tgg ttt gt - #g tat aag cat ttc tcc5187Ile Leu Gly Val Leu Val Gly Gly Trp Phe Va - #l Tyr Lys His Phe Ser# 14850- cgc aaa gag gaa gaa cca atc cca gct gaa gg - #g gta tat tat ggt gta5235Arg Lys Glu Glu Glu Pro Ile Pro Ala Glu Gl - #y Val Tyr Tyr Gly Val# 15005- act aag ccc aag caa gtg att aaa tta gat gc - #a gat cca gta gaa tct5283Thr Lys Pro Lys Gln Val Ile Lys Leu Asp Al - #a Asp Pro Val Glu Ser# 15150- cag tca act ttg gaa ata gca gga ctg gtt ag - #g aag aac ttg gtt cag5331Gln Ser Thr Leu Glu Ile Ala Gly Leu Val Ar - #g Lys Asn Leu Val Gln# 15305- ttt gga gtt gga gag aag aat gga tgt gtg ag - #a tgg gtt atg aat gcc5379Phe Gly Val Gly Glu Lys Asn Gly Cys Val Ar - #g Trp Val Met Asn Ala# 15505 0- ttg gga gtg aaa gat gat tgg ctg ctt gtg cc - #t tcc cat gct tat aaa5427Leu Gly Val Lys Asp Asp Trp Leu Leu Val Pr - #o Ser His Ala Tyr Lys# 15650- ttt gag aaa gat tat gaa atg atg gag ttt ta - #t ttt aat aga ggt gga5475Phe Glu Lys Asp Tyr Glu Met Met Glu Phe Ty - #r Phe Asn Arg Gly Gly# 15805- act tac tat tca att tca gct ggt aat gtt gt - #t att caa tct ttg gat5523Thr Tyr Tyr Ser Ile Ser Ala Gly Asn Val Va - #l Ile Gln Ser Leu Asp# 15950- gtg gga ttc cag gat gtt gtt ctg atg aag gt - #t cct aca att cct aag5571Val Gly Phe Gln Asp Val Val Leu Met Lys Va - #l Pro Thr Ile Pro Lys# 16105- ttt aga gat att act cag cat ttt att aag aa - #a ggg gat gtg cct aga5619Phe Arg Asp Ile Thr Gln His Phe Ile Lys Ly - #s Gly Asp Val Pro Arg# 16301620 - # 1625- gct ttg aat cgc ctg gca aca tta gtg aca ac - #t gta aat gga acc cct5667Ala Leu Asn Arg Leu Ala Thr Leu Val Thr Th - #r Val Asn Gly Thr Pro# 16450- atg tta att tct gag ggc cca cta aag atg ga - #a gag aaa gct act tat5715Met Leu Ile Ser Glu Gly Pro Leu Lys Met Gl - #u Glu Lys Ala Thr Tyr# 16605- gtt cat aag aaa aat gat ggt aca aca gtt ga - #t tta act gtg gat cag5763Val His Lys Lys Asn Asp Gly Thr Thr Val As - #p Leu Thr Val Asp Gln# 16750- gca tgg aga gga aaa ggc gaa ggt ctt cct gg - #a atg tgt ggt ggg gcc5811Ala Trp Arg Gly Lys Gly Glu Gly Leu Pro Gl - #y Met Cys Gly Gly Ala# 16905- ttg gtt tca tcg aat caa tct ata cag aat gc - #a atc ttg ggc atc cat5859Leu Val Ser Ser Asn Gln Ser Ile Gln Asn Al - #a Ile Leu Gly Ile His# 17101700 - # 1705- gtt gct gga gga aat tca att ctt gtt gca aa - #a ttg gtt act caa gaa5907Val Ala Gly Gly Asn Ser Ile Leu Val Ala Ly - #s Leu Val Thr Gln Glu# 17250- atg ttc caa aat att gat aag aaa att gaa ag - #t cag aga att atg aaa5955Met Phe Gln Asn Ile Asp Lys Lys Ile Glu Se - #r Gln Arg Ile Met Lys# 17405- gtg gag ttt act cag tgt tca atg aat gtg gt - #c tcc aaa acg ctt ttt6003Val Glu Phe Thr Gln Cys Ser Met Asn Val Va - #l Ser Lys Thr Leu Phe# 17550- aga aag agt ccc att tat cat cac att gat aa - #a acc atg att aat ttt6051Arg Lys Ser Pro Ile Tyr His His Ile Asp Ly - #s Thr Met Ile Asn Phe# 17705- cct gca gct atg ccc ttt tct aaa gct gaa at - #t gat cca atg gct gtg6099Pro Ala Ala Met Pro Phe Ser Lys Ala Glu Il - #e Asp Pro Met Ala Val# 17901780 - # 1785- atg tta tct aag tat tca tta cct att gta ga - #a gaa cca gag aat tat6147Met Leu Ser Lys Tyr Ser Leu Pro Ile Val Gl - #u Glu Pro Glu Asn Tyr# 18050- aaa gag gct tca att ttt tat caa aat aaa at - #a gtg ggt aag act cag6195Lys Glu Ala Ser Ile Phe Tyr Gln Asn Lys Il - #e Val Gly Lys Thr Gln# 18205- tta gtt gat gat ttt tta gat ctt gat atg gc - #c att aca ggg gcc cca6243Leu Val Asp Asp Phe Leu Asp Leu Asp Met Al - #a Ile Thr Gly Ala Pro# 18350- gga att gat gct atc aac atg gat tca tct cc - #t gga ttt cct tat gtc6291Gly Ile Asp Ala Ile Asn Met Asp Ser Ser Pr - #o Gly Phe Pro Tyr Val# 18505- cag gag aag ttg acc aaa aga gat tta att tg - #g ttg gat gaa aat ggt6339Gln Glu Lys Leu Thr Lys Arg Asp Leu Ile Tr - #p Leu Asp Glu Asn Gly# 18701860 - # 1865- tta ttg ctg gga gtt cat cca aga ttg gct ca - #g aga atc tta ttc aat6387Leu Leu Leu Gly Val His Pro Arg Leu Ala Gl - #n Arg Ile Leu Phe Asn# 18850- act gtc atg atg gaa aat tgt tct gat ttg ga - #t gtt gtt ttt aca acc6435Thr Val Met Met Glu Asn Cys Ser Asp Leu As - #p Val Val Phe Thr Thr# 19005- tgt cca aaa gat gaa ttg aga cca tta gag aa - #a gtg ttg gaa tca aaa6483Cys Pro Lys Asp Glu Leu Arg Pro Leu Glu Ly - #s Val Leu Glu Ser Lys# 19150- aca aga gct att gat gct tgt cct ctg gat ta - #c aca att ttg tgc cga6531Thr Arg Ala Ile Asp Ala Cys Pro Leu Asp Ty - #r Thr Ile Leu Cys Arg# 19305- atg tat tgg ggt cca gct att agt tat ttt ca - #t ttg aat cca ggt ttc6579Met Tyr Trp Gly Pro Ala Ile Ser Tyr Phe Hi - #s Leu Asn Pro Gly Phe# 19501940 - # 1945- cat aca ggt gtt gct att ggc ata gat cct ga - #t aga cag tgg gat gaa6627His Thr Gly Val Ala Ile Gly Ile Asp Pro As - #p Arg Gln Trp Asp Glu# 19650- tta ttt aaa aca atg ata aga ttc gga gat gt - #t ggt ctt gat tta gat6675Leu Phe Lys Thr Met Ile Arg Phe Gly Asp Va - #l Gly Leu Asp Leu Asp# 19805- ttc tct gct ttt gat gct agt ctt agt cca tt - #t atg att aga gaa gca6723Phe Ser Ala Phe Asp Ala Ser Leu Ser Pro Ph - #e Met Ile Arg Glu Ala# 19950- ggt aga atc atg agt gaa cta tct gga act cc - #a tcc cat ttt ggc aca6771Gly Arg Ile Met Ser Glu Leu Ser Gly Thr Pr - #o Ser His Phe Gly Thr# 20105- gct ctt atc aat act atc att tat tcc aag ca - #t ttg ctg tat aac tgt6819Ala Leu Ile Asn Thr Ile Ile Tyr Ser Lys Hi - #s Leu Leu Tyr Asn Cys# 20302020 - # 2025- tgt tac cat gtc tgt ggt tca atg ccc tct gg - #g tct cct tgt aca gct6867Cys Tyr His Val Cys Gly Ser Met Pro Ser Gl - #y Ser Pro Cys Thr Ala# 20450- ttg cta aat tca att att aat aat gtc aat tt - #g tat tat gtg ttt tcc6915Leu Leu Asn Ser Ile Ile Asn Asn Val Asn Le - #u Tyr Tyr Val Phe Ser# 20605- aag ata ttt gga aag tct cca gtt ttc ttt tg - #t cag gct ttg aag att6963Lys Ile Phe Gly Lys Ser Pro Val Phe Phe Cy - #s Gln Ala Leu Lys Ile# 20750- ctc tgt tat gga gat gat gtt tta ata gtt tt - #c tct cga gat gtt cag7011Leu Cys Tyr Gly Asp Asp Val Leu Ile Val Ph - #e Ser Arg Asp Val Gln# 20905- att gat aat ctt gat ctg att gga caa aaa at - #t gta gat gag ttt aag7059Ile Asp Asn Leu Asp Leu Ile Gly Gln Lys Il - #e Val Asp Glu Phe Lys# 21102100 - # 2105- aaa ctt ggc atg aca gct act tct gct gac aa - #g aat gta cct cag ctg7107Lys Leu Gly Met Thr Ala Thr Ser Ala Asp Ly - #s Asn Val Pro Gln Leu# 21250- aaa cca gtt tcg gaa ttg act ttt ctc aaa ag - #a tct ttc aat ttg gta7155Lys Pro Val Ser Glu Leu Thr Phe Leu Lys Ar - #g Ser Phe Asn Leu Val# 21405- gag gat aga att aga cct gca att tcg gaa aa - #a aca att tgg tct tta7203Glu Asp Arg Ile Arg Pro Ala Ile Ser Glu Ly - #s Thr Ile Trp Ser Leu# 21550- ata gca tgg cag aga agt aac gct gag ttt ga - #g cag aat tta gaa aat7251Ile Ala Trp Gln Arg Ser Asn Ala Glu Phe Gl - #u Gln Asn Leu Glu Asn# 21705- gct cag tgg ttt gct ttt atg cat ggc tat ga - #g ttt tat cag aaa ttt7299Ala Gln Trp Phe Ala Phe Met His Gly Tyr Gl - #u Phe Tyr Gln Lys Phe# 21902180 - # 2185- tat tat ttt gtt cag tcc tgt ttg gag aaa ga - #g atg ata gaa tac aga7347Tyr Tyr Phe Val Gln Ser Cys Leu Glu Lys Gl - #u Met Ile Glu Tyr Arg# 22050- ctt aaa tct tat gat tgg tgg aga atg aga tt - #t tat gac cag tgt ttc7395Leu Lys Ser Tyr Asp Trp Trp Arg Met Arg Ph - #e Tyr Asp Gln Cys Phe# 22205- att tgt gac ctt tca tgatttgttt aaacgaattt tcttaaaat - #t tctgaggttt7450Ile Cys Asp Leu Ser 2225# 7488 agta aataaaaaaa aaaaaaaa- <210> SEQ ID NO 4<211> LENGTH: 2227<212> TYPE: PRT#HM-175RGANISM: Attenuated HAV (Pass 35), strain- <400> SEQUENCE: 4- Met Asn Met Ser Arg Gln Gly Ile Phe Gln Th - #r Val Gly Ser Gly Leu# 15- Asp His Ile Leu Ser Leu Ala Asp Ile Glu Gl - #u Glu Gln Met Ile Gln# 30- Ser Val Asp Arg Thr Ala Val Thr Gly Ala Se - #r Tyr Phe Thr Ser Val# 45- Asp Gln Ser Ser Val His Thr Ala Glu Val Gl - #y Ser His Gln Val Glu# 60- Pro Leu Arg Thr Ser Val Asp Lys Pro Gly Se - #r Lys Arg Thr Gln Gly# 80- Glu Lys Phe Phe Leu Ile His Ser Ala Asp Tr - #p Leu Thr Thr His Ala# 95- Leu Phe His Glu Val Ala Lys Leu Asp Val Va - #l Lys Leu Leu Tyr Asn# 110- Glu Gln Phe Ala Val Gln Gly Leu Leu Arg Ty - #r His Thr Tyr Ala Arg# 125- Phe Gly Ile Glu Ile Gln Val Gln Ile Asn Pr - #o Thr Pro Phe Gln Gln# 140- Gly Gly Leu Ile Cys Ala Met Val Pro Gly As - #p Gln Ser Tyr Gly Ser145 1 - #50 1 - #55 1 -#60- Ile Ala Ser Leu Thr Val Tyr Pro His Gly Le - #u Leu Asn Cys Asn Ile# 175- Asn Asn Val Val Arg Ile Lys Val Pro Phe Il - #e Tyr Thr Arg Gly Ala# 190- Tyr His Phe Lys Asp Pro Gln Tyr Pro Val Tr - #p Glu Leu Thr Ile Arg# 205- Val Trp Ser Glu Leu Asn Ile Gly Thr Gly Th - #r Ser Ala Tyr Thr Ser# 220- Leu Asn Val Leu Ala Arg Phe Thr Asp Leu Gl - #u Leu His Gly Leu Thr225 2 - #30 2 - #35 2 -#40- Pro Leu Ser Thr Gln Met Met Arg Asn Glu Ph - #e Arg Val Ser Thr Thr# 255- Glu Asn Val Val Asn Leu Ser Asn Tyr Glu As - #p Ala Arg Ala Lys Met# 270- Ser Phe Ala Leu Asp Gln Glu Asp Trp Lys Se - #r Asp Pro Ser Gln Gly# 285- Gly Gly Ile Lys Ile Thr His Phe Thr Thr Tr - #p Thr Ser Ile Pro Thr# 300- Leu Ala Ala Gln Phe Pro Phe Asn Ala Ser As - #p Ser Val Gly Gln Gln305 3 - #10 3 - #15 3 -#20- Ile Lys Val Ile Pro Val Asp Pro Tyr Phe Ph - #e Gln Met Thr Asn Thr# 335- Asn Pro Asp Gln Lys Cys Ile Thr Ala Leu Al - #a Ser Ile Cys Gln Met# 350- Phe Cys Phe Trp Arg Gly Asp Leu Val Phe As - #p Phe Gln Val Phe Pro# 365- Thr Lys Tyr His Ser Gly Arg Leu Leu Phe Cy - #s Phe Val Pro Gly Asn# 380- Glu Leu Ile Asp Val Ser Gly Ile Thr Leu Ly - #s Gln Ala Thr Thr Ala385 3 - #90 3 - #95 4 -#00- Pro Cys Ala Val Met Asp Ile Thr Gly Val Gl - #n Ser Thr Leu Arg Phe# 415- Arg Val Pro Trp Ile Ser Asp Thr Pro Tyr Ar - #g Val Asn Arg Tyr Thr# 430- Lys Ser Ala His Gln Lys Gly Glu Tyr Thr Al - #a Ile Gly Lys Leu Ile# 445- Val Tyr Cys Tyr Asn Arg Leu Thr Ser Pro Se - #r Asn Val Ala Ser His# 460- Val Arg Val Asn Val Tyr Leu Ser Ala Ile As - #n Leu Glu Cys Phe Ala465 4 - #70 4 - #75 4 -#80- Pro Leu Tyr His Ala Met Asp Val Thr Thr Gl - #n Val Gly Asp Asp Ser# 495- Gly Gly Phe Ser Thr Thr Val Ser Thr Glu Gl - #n Asn Val Pro Asp Pro# 510- Gln Val Gly Ile Thr Thr Met Lys Asp Leu Ly - #s Gly Lys Ala Asn Arg# 525- Gly Lys Met Asp Val Ser Gly Val Gln Ala Pr - #o Val Gly Ala Ile Thr# 540- Thr Ile Glu Asp Pro Val Leu Ala Lys Lys Va - #l Pro Glu Thr Phe Pro545 5 - #50 5 - #55 5 -#60- Glu Leu Lys Pro Gly Glu Ser Arg His Thr Se - #r Asp His Met Ser Ile# 575- Tyr Lys Phe Met Gly Arg Ser His Phe Leu Cy - #s Thr Phe Thr Phe Asn# 590- Ser Asn Asn Lys Glu Tyr Thr Phe Pro Ile Th - #r Leu Ser Ser Thr Ser# 605- Asn Pro Pro His Gly Leu Pro Ser Thr Leu Ar - #g Trp Phe Phe Asn Leu# 620- Phe Gln Leu Tyr Arg Gly Pro Leu Asp Leu Th - #r Ile Ile Ile Thr Gly625 6 - #30 6 - #35 6 -#40- Ala Thr Asp Val Asp Gly Met Ala Trp Phe Th - #r Pro Val Gly Leu Ala# 655- Val Asp Thr Pro Trp Val Glu Lys Glu Ser Al - #a Leu Ser Ile Asp Tyr# 670- Lys Thr Ala Leu Gly Ala Val Arg Phe Asn Th - #r Arg Arg Thr Gly Asn# 685- Ile Gln Ile Arg Leu Pro Trp Tyr Ser Tyr Le - #u Tyr Ala Val Ser Gly# 700- Ala Leu Asp Gly Leu Gly Asp Lys Thr Asp Se - #r Thr Phe Gly Leu Val705 7 - #10 7 - #15 7 -#20- Ser Ile Gln Ile Ala Asn Tyr Asn His Ser As - #p Glu Tyr Leu Ser Phe# 735- Ser Cys Tyr Leu Ser Val Thr Glu Gln Ser Gl - #u Phe Tyr Phe Pro Arg# 750- Ala Pro Leu Asn Ser Asn Ala Met Leu Ser Th - #r Val Ser Met Met Ser# 765- Arg Ile Ala Ala Gly Asp Leu Glu Ser Ser Va - #l Asp Asp Pro Arg Ser# 780- Glu Glu Asp Lys Arg Phe Glu Ser His Ile Gl - #u Cys Arg Lys Pro Tyr785 7 - #90 7 - #95 8 -#00- Lys Glu Leu Arg Leu Glu Val Gly Lys Gln Ar - #g Leu Lys Tyr Ala Gln# 815- Glu Glu Leu Ser Ser Glu Val Leu Pro Pro Pr - #o Arg Lys Met Lys Gly# 830- Leu Phe Ser Gln Ala Lys Ile Ser Leu Phe Ty - #r Thr Glu Glu His Glu# 845- Ile Met Lys Phe Ser Trp Arg Gly Val Thr Al - #a Asp Thr Arg Ala Leu# 860- Arg Arg Phe Gly Phe Ser Leu Ala Ala Gly Ar - #g Ser Val Trp Thr Leu865 8 - #70 8 - #75 8 -#80- Glu Met Asp Ala Gly Val Leu Thr Gly Arg Le - #u Ile Arg Leu Asn Asp# 895- Glu Lys Trp Thr Glu Met Lys Asp Asp Lys Il - #e Val Ser Leu Ile Glu# 910- Lys Phe Thr Ser Asn Lys Tyr Trp Ser Lys Va - #l Asn Phe Pro His Gly# 925- Met Leu Asp Leu Glu Glu Ile Ala Ala Asn Se - #r Lys Asp Phe Pro Asn# 940- Met Ser Glu Thr Asp Leu Cys Phe Leu Leu Hi - #s Trp Leu Asn Pro Lys945 9 - #50 9 - #55 9 -#60- Lys Ile Asn Leu Ala Asp Arg Met Leu Gly Le - #u Ser Gly Val Gln Glu# 975- Ile Lys Glu Gln Gly Val Gly Leu Ile Ala Gl - #u Cys Arg Thr Phe Leu# 990- Asp Ser Ile Ala Gly Thr Leu Lys Ser Met Me - #t Phe Gly Phe His His# 10050- Ser Val Thr Val Glu Ile Ile Asn Thr Val Le - #u Cys Phe Val Lys Ser# 10205- Gly Ile Leu Leu Tyr Val Ile Gln Gln Leu As - #n Gln Asp Glu His Ser# 10401030 - # 1035- His Ile Ile Gly Leu Leu Arg Val Met Asn Ty - #r Val Asp Ile Gly Cys# 10550- Ser Val Ile Ser Cys Ala Lys Val Phe Ser Ly - #s Met Leu Glu Thr Val# 10705- Phe Asn Trp Gln Met Asp Ser Arg Met Met Gl - #u Leu Arg Thr Gln Ser# 10850- Phe Ser Asn Trp Leu Arg Asp Ile Cys Ser Gl - #y Ile Thr Ile Phe Lys# 11005- Asn Phe Lys Asp Ala Ile Tyr Trp Leu Tyr Th - #r Lys Leu Met Asp Phe# 11201110 - # 1115- Tyr Glu Val Asn Tyr Gly Lys Lys Lys Asp Il - #e Leu Asn Ile Leu Lys# 11350- Asp Asn Gln Gln Lys Ile Glu Lys Ala Ile Gl - #u Glu Ala Asp Lys Phe# 11505- Cys Ile Leu Gln Ile Gln Asp Val Glu Lys Se - #r Glu Gln Tyr Gln Lys# 11650- Gly Val Asp Leu Ile Gln Lys Leu Arg Thr Va - #l His Ser Met Ala Gln# 11805- Val Asp Pro Asn Leu Met Val His Leu Ser Pr - #o Leu Arg Asp Cys Ile# 12001190 - # 1195- Ala Arg Val His Gln Lys Leu Lys Asn Leu Gl - #y Ser Ile Asn Gln Ala# 12150- Met Val Thr Arg Cys Glu Pro Val Val Cys Ty - #r Leu Tyr Gly Lys Arg# 12305- Gly Gly Gly Lys Ser Leu Thr Ser Ile Ala Le - #u Ala Thr Lys Ile Cys# 12450- Lys His Tyr Gly Val Glu Pro Glu Lys Asn Il - #e Tyr Thr Lys Pro Val# 12605- Ala Ser Asp Tyr Trp Asp Gly Tyr Ser Gly Gl - #n Leu Ile Cys Ile Ile# 12801270 - # 1275- Asp Asp Ile Gly Gln Asn Thr Thr Asp Glu As - #p Trp Ser Asp Phe Cys# 12950- Gln Leu Val Ser Gly Cys Pro Met Arg Leu As - #n Met Ala Ser Leu Glu# 13105- Glu Lys Gly Arg His Phe Ser Ser Pro Phe Il - #e Ile Ala Thr Ser Asn# 13250- Trp Ser Asn Pro Ser Pro Lys Thr Val Tyr Va - #l Lys Glu Ala Ile Asp# 13405- Arg Arg Leu His Phe Lys Val Glu Val Lys Pr - #o Ala Ser Phe Phe Lys# 13601350 - # 1355- Asn Pro His Asn Asp Met Leu Asn Val Asn Le - #u Ala Lys Thr Asn Asp# 13750- Ala Ile Lys Asp Met Ser Cys Val Asp Leu Il - #e Met Asp Gly His Asn# 13905- Val Ser Leu Met Asp Leu Leu Ser Ser Leu Va - #l Met Thr Val Glu Ile# 14050- Arg Lys Gln Asn Met Thr Glu Phe Met Glu Le - #u Trp Ser Gln Gly Ile# 14205- Ser Asp Asp Asp Asn Asp Ser Ala Val Ala Gl - #u Phe Phe Gln Ser Phe# 14401430 - # 1435- Pro Ser Gly Glu Pro Ser Asn Ser Lys Leu Se - #r Gly Phe Phe Gln Ser# 14550- Val Thr Asn His Lys Trp Val Ala Val Gly Al - #a Ala Val Gly Ile Leu# 14705- Gly Val Leu Val Gly Gly Trp Phe Val Tyr Ly - #s His Phe Ser Arg Lys# 14850- Glu Glu Glu Pro Ile Pro Ala Glu Gly Val Ty - #r Tyr Gly Val Thr Lys# 15005- Pro Lys Gln Val Ile Lys Leu Asp Ala Asp Pr - #o Val Glu Ser Gln Ser# 15201510 - # 1515- Thr Leu Glu Ile Ala Gly Leu Val Arg Lys As - #n Leu Val Gln Phe Gly# 15350- Val Gly Glu Lys Asn Gly Cys Val Arg Trp Va - #l Met Asn Ala Leu Gly# 15505- Val Lys Asp Asp Trp Leu Leu Val Pro Ser Hi - #s Ala Tyr Lys Phe Glu# 15650- Lys Asp Tyr Glu Met Met Glu Phe Tyr Phe As - #n Arg Gly Gly Thr Tyr# 15805- Tyr Ser Ile Ser Ala Gly Asn Val Val Ile Gl - #n Ser Leu Asp Val Gly# 16001590 - # 1595- Phe Gln Asp Val Val Leu Met Lys Val Pro Th - #r Ile Pro Lys Phe Arg# 16150- Asp Ile Thr Gln His Phe Ile Lys Lys Gly As - #p Val Pro Arg Ala Leu# 16305- Asn Arg Leu Ala Thr Leu Val Thr Thr Val As - #n Gly Thr Pro Met Leu# 16450- Ile Ser Glu Gly Pro Leu Lys Met Glu Glu Ly - #s Ala Thr Tyr Val His# 16605- Lys Lys Asn Asp Gly Thr Thr Val Asp Leu Th - #r Val Asp Gln Ala Trp# 16801670 - # 1675- Arg Gly Lys Gly Glu Gly Leu Pro Gly Met Cy - #s Gly Gly Ala Leu Val# 16950- Ser Ser Asn Gln Ser Ile Gln Asn Ala Ile Le - #u Gly Ile His Val Ala# 17105- Gly Gly Asn Ser Ile Leu Val Ala Lys Leu Va - #l Thr Gln Glu Met Phe# 17250- Gln Asn Ile Asp Lys Lys Ile Glu Ser Gln Ar - #g Ile Met Lys Val Glu# 17405- Phe Thr Gln Cys Ser Met Asn Val Val Ser Ly - #s Thr Leu Phe Arg Lys# 17601750 - # 1755- Ser Pro Ile Tyr His His Ile Asp Lys Thr Me - #t Ile Asn Phe Pro Ala# 17750- Ala Met Pro Phe Ser Lys Ala Glu Ile Asp Pr - #o Met Ala Val Met Leu# 17905- Ser Lys Tyr Ser Leu Pro Ile Val Glu Glu Pr - #o Glu Asn Tyr Lys Glu# 18050- Ala Ser Ile Phe Tyr Gln Asn Lys Ile Val Gl - #y Lys Thr Gln Leu Val# 18205- Asp Asp Phe Leu Asp Leu Asp Met Ala Ile Th - #r Gly Ala Pro Gly Ile# 18401830 - # 1835- Asp Ala Ile Asn Met Asp Ser Ser Pro Gly Ph - #e Pro Tyr Val Gln Glu# 18550- Lys Leu Thr Lys Arg Asp Leu Ile Trp Leu As - #p Glu Asn Gly Leu Leu# 18705- Leu Gly Val His Pro Arg Leu Ala Gln Arg Il - #e Leu Phe Asn Thr Val# 18850- Met Met Glu Asn Cys Ser Asp Leu Asp Val Va - #l Phe Thr Thr Cys Pro# 19005- Lys Asp Glu Leu Arg Pro Leu Glu Lys Val Le - #u Glu Ser Lys Thr Arg# 19201910 - # 1915- Ala Ile Asp Ala Cys Pro Leu Asp Tyr Thr Il - #e Leu Cys Arg Met Tyr# 19350- Trp Gly Pro Ala Ile Ser Tyr Phe His Leu As - #n Pro Gly Phe His Thr# 19505- Gly Val Ala Ile Gly Ile Asp Pro Asp Arg Gl - #n Trp Asp Glu Leu Phe# 19650- Lys Thr Met Ile Arg Phe Gly Asp Val Gly Le - #u Asp Leu Asp Phe Ser# 19805- Ala Phe Asp Ala Ser Leu Ser Pro Phe Met Il - #e Arg Glu Ala Gly Arg# 20001990 - # 1995- Ile Met Ser Glu Leu Ser Gly Thr Pro Ser Hi - #s Phe Gly Thr Ala Leu# 20150- Ile Asn Thr Ile Ile Tyr Ser Lys His Leu Le - #u Tyr Asn Cys Cys Tyr# 20305- His Val Cys Gly Ser Met Pro Ser Gly Ser Pr - #o Cys Thr Ala Leu Leu# 20450- Asn Ser Ile Ile Asn Asn Val Asn Leu Tyr Ty - #r Val Phe Ser Lys Ile# 20605- Phe Gly Lys Ser Pro Val Phe Phe Cys Gln Al - #a Leu Lys Ile Leu Cys# 20802070 - # 2075- Tyr Gly Asp Asp Val Leu Ile Val Phe Ser Ar - #g Asp Val Gln Ile Asp# 20950- Asn Leu Asp Leu Ile Gly Gln Lys Ile Val As - #p Glu Phe Lys Lys Leu# 21105- Gly Met Thr Ala Thr Ser Ala Asp Lys Asn Va - #l Pro Gln Leu Lys Pro# 21250- Val Ser Glu Leu Thr Phe Leu Lys Arg Ser Ph - #e Asn Leu Val Glu Asp# 21405- Arg Ile Arg Pro Ala Ile Ser Glu Lys Thr Il - #e Trp Ser Leu Ile Ala# 21602150 - # 2155- Trp Gln Arg Ser Asn Ala Glu Phe Glu Gln As - #n Leu Glu Asn Ala Gln# 21750- Trp Phe Ala Phe Met His Gly Tyr Glu Phe Ty - #r Gln Lys Phe Tyr Tyr# 21905- Phe Val Gln Ser Cys Leu Glu Lys Glu Met Il - #e Glu Tyr Arg Leu Lys# 22050- Ser Tyr Asp Trp Trp Arg Met Arg Phe Tyr As - #p Gln Cys Phe Ile Cys# 22205- Asp Leu Ser2225- <210> SEQ ID NO 5<211> LENGTH: 7486<212> TYPE: DNA<213> ORGANISM: Attenuated HAV (4380), strain HM-1 - #75<220> FEATURE:<221> NAME/KEY: CDS<222> LOCATION: (730)..(7410)- <400> SEQUENCE: 5- ttcaagaggg gtctccggga atttccggag tccctcttgg aagtccatgg tg - #aggggact 60- tgatacctca ccgccgtttg cctaggctat aggctaaatt ttccctttcc ct - #tttccctt 120- tcccattccc ttttgcttgt aaatattgat tcctgcaggt tcagggttct ta - #aatctgtt 180- tctctataag aacactcatt ttcacgcttt ctgtcttctt tcttccaggg ct - #ctcccctt 240- gccctaggct ctggccgttg cgcccggcgg ggtcaactcc atgattagca tg - #gagctgta 300- ggagtctaaa ttggggacac agatgtttgg aacgtcacct tgcagtgtta ac - #ttggcttt 360- catgaatctc tttgatcttc cacaaggggt aggctacggg tgaaacctct ta - #ggctaata 420- cttctatgaa gagatgcctt ggatagggta acagcggcgg atattggtga gt - #tgttaaga 480- caaaaaccat tcaacgccgg aggactgact ctcatccagt ggatgcattg ag - #tggattga 540- ctgtcagggc tgtctttagg cttaattcca gacctctctg tgcttggggc aa - #acatcatt 600- tggccttaaa tgggattctg tgagagggga tccctccatt aacagctgga ct - #gttctttg 660- gggtcttatg tggtgtttgc cgctgaggta ctcaggggca tttaggtttt tc - #ctcattct 720- taaataata atg aac atg tct aga caa ggt att ttc - # cag act gtt ggg agt 771#Gln Gly Ile Phe Gln Thr Val Gly Ser# 10- ggt ctt gac cac atc ctg tct ttg gca gac at - #t gag gaa gag caa atg 819Gly Leu Asp His Ile Leu Ser Leu Ala Asp Il - #e Glu Glu Glu Gln Met# 30- att caa tca gtt gat agg act gca gtg act gg - #t gct tct tat ttt act 867Ile Gln Ser Val Asp Arg Thr Ala Val Thr Gl - #y Ala Ser Tyr Phe Thr# 45- tct gtg gat caa tct tca gtt cat aca gct ga - #g gtt gga tca cac cag 915Ser Val Asp Gln Ser Ser Val His Thr Ala Gl - #u Val Gly Ser His Gln# 60- gtt gaa cct ttg aga acc tct gtt gat aaa cc - #c ggt tca aag agg act 963Val Glu Pro Leu Arg Thr Ser Val Asp Lys Pr - #o Gly Ser Lys Arg Thr# 75- cag gga gag aaa ttt ttc ttg att cat tct gc - #a gat tgg ctt act aca1011Gln Gly Glu Lys Phe Phe Leu Ile His Ser Al - #a Asp Trp Leu Thr Thr# 90- cat gct ctt ttc cat gaa gtt gca aaa ttg ga - #t gtg gtg aaa tta tta1059His Ala Leu Phe His Glu Val Ala Lys Leu As - #p Val Val Lys Leu Leu#110- tac aat gag cag ttt gct gtt caa ggg ttg tt - #g aga tac cat aca tat1107Tyr Asn Glu Gln Phe Ala Val Gln Gly Leu Le - #u Arg Tyr His Thr Tyr# 125- gca aga ttt ggc att gaa att caa gtt cag at - #a aac cct aca cct ttc1155Ala Arg Phe Gly Ile Glu Ile Gln Val Gln Il - #e Asn Pro Thr Pro Phe# 140- caa cag ggg gga ttg atc tgt gct atg gtt cc - #t ggt gac cag agc tat1203Gln Gln Gly Gly Leu Ile Cys Ala Met Val Pr - #o Gly Asp Gln Ser Tyr# 155- ggt tct ata gca tca ttg act gtt tat cct ca - #t ggt ttg tta aat tgc1251Gly Ser Ile Ala Ser Leu Thr Val Tyr Pro Hi - #s Gly Leu Leu Asn Cys# 170- aat att aac aat gtg gtt aga ata aag gtt cc - #a ttt att tac aca aga1299Asn Ile Asn Asn Val Val Arg Ile Lys Val Pr - #o Phe Ile Tyr Thr Arg175 1 - #80 1 - #85 1 -#90- ggt gct tac cac ttt aaa gat cca caa tac cc - #a gtt tgg gaa ttg aca1347Gly Ala Tyr His Phe Lys Asp Pro Gln Tyr Pr - #o Val Trp Glu Leu Thr# 205- att aga gtt tgg tca gaa tta aat att ggg ac - #a gga act tca gct tat1395Ile Arg Val Trp Ser Glu Leu Asn Ile Gly Th - #r Gly Thr Ser Ala Tyr# 220- act tca ctc aat gtt tta gct aga ttt aca ga - #t ttg gag ttg cat gga1443Thr Ser Leu Asn Val Leu Ala Arg Phe Thr As - #p Leu Glu Leu His Gly# 235- tta act cct ctt tct aca caa atg atg aga aa - #t gaa ttt agg gtc agt1491Leu Thr Pro Leu Ser Thr Gln Met Met Arg As - #n Glu Phe Arg Val Ser# 250- act act gag aat gtg gtg aat ctg tca aat ta - #t gaa gat gca aga gca1539Thr Thr Glu Asn Val Val Asn Leu Ser Asn Ty - #r Glu Asp Ala Arg Ala255 2 - #60 2 - #65 2 -#70- aag atg tct ttt gct ttg gat cag gaa gat tg - #g aaa tct gat ccg tcc1587Lys Met Ser Phe Ala Leu Asp Gln Glu Asp Tr - #p Lys Ser Asp Pro Ser# 285- cag ggt ggt ggg atc aaa att act cat ttt ac - #t act tgg aca tct att1635Gln Gly Gly Gly Ile Lys Ile Thr His Phe Th - #r Thr Trp Thr Ser Ile# 300- cca act ttg gct gct cag ttt cca ttt aat gc - #t tca gac tca gtt ggt1683Pro Thr Leu Ala Ala Gln Phe Pro Phe Asn Al - #a Ser Asp Ser Val Gly# 315- caa caa att aaa gtt att cca gtt gac cca ta - #t ttt ttc caa atg aca1731Gln Gln Ile Lys Val Ile Pro Val Asp Pro Ty - #r Phe Phe Gln Met Thr# 330- aat aca aat cct gac caa aaa tgt ata act gc - #t ttg gct tct att tgt1779Asn Thr Asn Pro Asp Gln Lys Cys Ile Thr Al - #a Leu Ala Ser Ile Cys335 3 - #40 3 - #45 3 -#50- cag atg ttt tgt ttt tgg aga gga gat ctt gt - #c ttt gat ttt caa gtt1827Gln Met Phe Cys Phe Trp Arg Gly Asp Leu Va - #l Phe Asp Phe Gln Val# 365- ttt ccc acc aaa tat cat tca ggt aga tta ct - #g ttt tgt ttt gtt cct1875Phe Pro Thr Lys Tyr His Ser Gly Arg Leu Le - #u Phe Cys Phe Val Pro# 380- ggc aat gag cta ata gat gtt tct gga atc ac - #a tta aag caa gca act1923Gly Asn Glu Leu Ile Asp Val Ser Gly Ile Th - #r Leu Lys Gln Ala Thr# 395- act gct cct tgt gca gta atg gat att aca gg - #a gtg cag tca act ttg1971Thr Ala Pro Cys Ala Val Met Asp Ile Thr Gl - #y Val Gln Ser Thr Leu# 410- aga ttt cgt gtt ccc tgg att tct gac act cc - #t tac aga gtg aac agg2019Arg Phe Arg Val Pro Trp Ile Ser Asp Thr Pr - #o Tyr Arg Val Asn Arg415 4 - #20 4 - #25 4 -#30- tat aca aag tca gca cat cag aaa ggt gag ta - #c act gcc att ggg aag2067Tyr Thr Lys Ser Ala His Gln Lys Gly Glu Ty - #r Thr Ala Ile Gly Lys# 445- ctt att gtg tat tgt tat aac aga ttg acc tc - #t cct tct aac gtt gct2115Leu Ile Val Tyr Cys Tyr Asn Arg Leu Thr Se - #r Pro Ser Asn Val Ala# 460- tcc cat gtc aga gtg aat gtt tat ctt tca gc - #a att aac ttg gaa tgt2163Ser His Val Arg Val Asn Val Tyr Leu Ser Al - #a Ile Asn Leu Glu Cys# 475- ttt gct cct ctt tat cat gct atg gat gtt ac - #t aca caa gtt gga gat2211Phe Ala Pro Leu Tyr His Ala Met Asp Val Th - #r Thr Gln Val Gly Asp# 490- gat tct gga ggt ttt tca aca aca gtt tct ac - #a gaa cag aat gtt cca2259Asp Ser Gly Gly Phe Ser Thr Thr Val Ser Th - #r Glu Gln Asn Val Pro495 5 - #00 5 - #05 5 -#10- gat ccc caa gtt ggt ata aca acc atg aaa ga - #t ttg aaa gga aaa gct2307Asp Pro Gln Val Gly Ile Thr Thr Met Lys As - #p Leu Lys Gly Lys Ala# 525- aac aga ggg aaa atg gat gtt tca gga gta ca - #a gca cct gtg gga gct2355Asn Arg Gly Lys Met Asp Val Ser Gly Val Gl - #n Ala Pro Val Gly Ala# 540- atc aca aca att gag gat cca gtt tta gca aa - #g aaa gta cct gag aca2403Ile Thr Thr Ile Glu Asp Pro Val Leu Ala Ly - #s Lys Val Pro Glu Thr# 555- ttt cct gaa ttg aaa cct gga gaa tcc aga ca - #t aca tca gat cat atg2451Phe Pro Glu Leu Lys Pro Gly Glu Ser Arg Hi - #s Thr Ser Asp His Met# 570- tcc atc tac aag ttt atg gga agg tct cat tt - #c ttg tgc act ttt aca2499Ser Ile Tyr Lys Phe Met Gly Arg Ser His Ph - #e Leu Cys Thr Phe Thr575 5 - #80 5 - #85 5 -#90- ttc aat tca aat aat aaa gag tac aca ttt cc - #t ata acc ttg tct tca2547Phe Asn Ser Asn Asn Lys Glu Tyr Thr Phe Pr - #o Ile Thr Leu Ser Ser# 605- acc tct aat cct cct cat ggt ttg cca tca ac - #a ctg agg tgg ttt ttc2595Thr Ser Asn Pro Pro His Gly Leu Pro Ser Th - #r Leu Arg Trp Phe Phe# 620- aac ttg ttt cag ttg tat aga ggg cct tta ga - #t ctg aca att att att2643Asn Leu Phe Gln Leu Tyr Arg Gly Pro Leu As - #p Leu Thr Ile Ile Ile# 635- aca gga gca act gat gta gat ggc atg gcc tg - #g ttc act cca gta ggt2691Thr Gly Ala Thr Asp Val Asp Gly Met Ala Tr - #p Phe Thr Pro Val Gly# 650- ctt gcc gtt gat act cct tgg gta gag aag ga - #g tca gct ttg tct att2739Leu Ala Val Asp Thr Pro Trp Val Glu Lys Gl - #u Ser Ala Leu Ser Ile655 6 - #60 6 - #65 6 -#70- gac tat aaa act gct ctt gga gct gtc aga tt - #t aac aca agg aga aca2787Asp Tyr Lys Thr Ala Leu Gly Ala Val Arg Ph - #e Asn Thr Arg Arg Thr# 685- ggg aac att cag att aga tta cca tgg tat tc - #t tat tta tat gct gtg2835Gly Asn Ile Gln Ile Arg Leu Pro Trp Tyr Se - #r Tyr Leu Tyr Ala Val# 700- tct gga gca ctg gat ggt ttg gga gac aag ac - #a gat tct aca ttt gga2883Ser Gly Ala Leu Asp Gly Leu Gly Asp Lys Th - #r Asp Ser Thr Phe Gly# 715- ttg gtt tct att cag att gca aat tac aat ca - #t tct gat gaa tac ttg2931Leu Val Ser Ile Gln Ile Ala Asn Tyr Asn Hi - #s Ser Asp Glu Tyr Leu# 730- tct ttt agt tgt tat ttg tct gtc aca gaa ca - #a tca gag ttt tat ttt2979Ser Phe Ser Cys Tyr Leu Ser Val Thr Glu Gl - #n Ser Glu Phe Tyr Phe735 7 - #40 7 - #45 7 -#50- ccc aga gct cca ttg aac tca aat gcc atg tt - #a tcc act gta aca atg3027Pro Arg Ala Pro Leu Asn Ser Asn Ala Met Le - #u Ser Thr Val Thr Met# 765- atg agc aga att gca gct gga gac ttg gag tc - #a tca gtg gat gat cct3075Met Ser Arg Ile Ala Ala Gly Asp Leu Glu Se - #r Ser Val Asp Asp Pro# 780- aga tca gag gaa gat aaa aga ttt gag agt ca - #t ata gaa tgc agg aag3123Arg Ser Glu Glu Asp Lys Arg Phe Glu Ser Hi - #s Ile Glu Cys Arg Lys# 795- cca tat aaa gaa ctg aga tta gaa gtt ggg aa - #a caa aga ctc aag tat3171Pro Tyr Lys Glu Leu Arg Leu Glu Val Gly Ly - #s Gln Arg Leu Lys Tyr# 810- gct cag gaa gaa ttg tca aat gaa gta ctt cc - #a ccc cct agg aaa atg3219Ala Gln Glu Glu Leu Ser Asn Glu Val Leu Pr - #o Pro Pro Arg Lys Met815 8 - #20 8 - #25 8 -#30- aag gga ctg ttt tca caa gcc aaa att tct ct - #t ttt tat act gag gag3267Lys Gly Leu Phe Ser Gln Ala Lys Ile Ser Le - #u Phe Tyr Thr Glu Glu# 845- cat gaa ata atg aag ttt tcc tgg aga ggt gt - #g act gct gat act aga3315His Glu Ile Met Lys Phe Ser Trp Arg Gly Va - #l Thr Ala Asp Thr Arg# 860- gct tta agg agg ttt gga ttc tct ttg gcc gc - #a ggc aga agt gtg tgg3363Ala Leu Arg Arg Phe Gly Phe Ser Leu Ala Al - #a Gly Arg Ser Val Trp# 875- act ctt gaa atg gat gct ggg gtt ctt act gg - #g aga ctg att aga ttg3411Thr Leu Glu Met Asp Ala Gly Val Leu Thr Gl - #y Arg Leu Ile Arg Leu# 890- aat gat gag aaa tgg aca gaa atg aag gat ga - #c aag att gtt tca ttg3459Asn Asp Glu Lys Trp Thr Glu Met Lys Asp As - #p Lys Ile Val Ser Leu895 9 - #00 9 - #05 9 -#10- att gaa aag ttt aca agt aac aaa tat tgg tc - #c aaa gtg aat ttc cca3507Ile Glu Lys Phe Thr Ser Asn Lys Tyr Trp Se - #r Lys Val Asn Phe Pro# 925- cat ggg atg ttg gat ctt gaa gaa att gct gc - #c aat tct aag gat ttt3555His Gly Met Leu Asp Leu Glu Glu Ile Ala Al - #a Asn Ser Lys Asp Phe# 940- cct aac atg tct gaa acg gat ttg tgt ttc tt - #g ctg cat tgg tta aat3603Pro Asn Met Ser Glu Thr Asp Leu Cys Phe Le - #u Leu His Trp Leu Asn# 955- cca aag aaa att aat tta gca gat aga atg ct - #t gga ttg tct gga gtt3651Pro Lys Lys Ile Asn Leu Ala Asp Arg Met Le - #u Gly Leu Ser Gly Val# 970- cag gaa att aaa gaa caa ggt gtt gga tta at - #a gca gag tgt aga act3699Gln Glu Ile Lys Glu Gln Gly Val Gly Leu Il - #e Ala Glu Cys Arg Thr975 9 - #80 9 - #85 9 -#90- ttc tta gat tct att gct gga act tta aaa tc - #t atg atg ttt gga ttt3747Phe Leu Asp Ser Ile Ala Gly Thr Leu Lys Se - #r Met Met Phe Gly Phe# 10050- cat cat tct gtg act gtt gaa att ata aac ac - #t gtg ctc tgt ttt gtt3795His His Ser Val Thr Val Glu Ile Ile Asn Th - #r Val Leu Cys Phe Val# 10205- aag agt gga att ttg ctt tat gta ata caa ca - #a ttg aat cag gat gaa3843Lys Ser Gly Ile Leu Leu Tyr Val Ile Gln Gl - #n Leu Asn Gln Asp Glu# 10350- cat tct cac ata att ggt ttg ttg aga gtc at - #g aat tat gta gat att3891His Ser His Ile Ile Gly Leu Leu Arg Val Me - #t Asn Tyr Val Asp Ile# 10505- ggt tgt tca gtt att tca tgt gcc aaa gtt tt - #t tcc aga atg ctg gaa3939Gly Cys Ser Val Ile Ser Cys Ala Lys Val Ph - #e Ser Arg Met Leu Glu# 10701060 - # 1065- aca gtc ttt aat tgg caa atg gac tcc aga at - #g atg gag tta agg act3987Thr Val Phe Asn Trp Gln Met Asp Ser Arg Me - #t Met Glu Leu Arg Thr# 10850- cag agt ttt tcc aac tgg tta aga gat att tg - #t tct ggg atc acc att4035Gln Ser Phe Ser Asn Trp Leu Arg Asp Ile Cy - #s Ser Gly Ile Thr Ile# 11005- ttc aaa aac ttc aag gat gca att tat tgg ct - #t tat aca aaa tta atg4083Phe Lys Asn Phe Lys Asp Ala Ile Tyr Trp Le - #u Tyr Thr Lys Leu Met# 11150- gac ttt tat gaa gtg aat tat ggc aag aag aa - #g gac att tta aat att4131Asp Phe Tyr Glu Val Asn Tyr Gly Lys Lys Ly - #s Asp Ile Leu Asn Ile# 11305- ctt aaa gat aac caa caa aaa ata gag aaa gc - #c att gag gaa gcc gat4179Leu Lys Asp Asn Gln Gln Lys Ile Glu Lys Al - #a Ile Glu Glu Ala Asp# 11501140 - # 1145- aaa ttt tgc att ttg caa atc caa gat gtg ga - #a aaa tct gaa cag tat4227Lys Phe Cys Ile Leu Gln Ile Gln Asp Val Gl - #u Lys Ser Glu Gln Tyr# 11650- cag aaa ggg gtt gac ttg ata caa aaa ttg ag - #a act gtt cat tca atg4275Gln Lys Gly Val Asp Leu Ile Gln Lys Leu Ar - #g Thr Val His Ser Met# 11805- gct cag gtt gat cca aat tta atg gtt cat tt - #g tca cct ttg aga gat4323Ala Gln Val Asp Pro Asn Leu Met Val His Le - #u Ser Pro Leu Arg Asp# 11950- tgt ata gca aga gtt cat cag aaa ctt aaa aa - #c ctt gga tct ata aat4371Cys Ile Ala Arg Val His Gln Lys Leu Lys As - #n Leu Gly Ser Ile Asn# 12105- cag gca atg gta acg aga tgt gag cca gtt gt - #t tgt tat ttt tat ggc4419Gln Ala Met Val Thr Arg Cys Glu Pro Val Va - #l Cys Tyr Phe Tyr Gly# 12301220 - # 1225- aaa aga ggg gga gga aag agc tta aca tca at - #t gca ttg gca acc aaa4467Lys Arg Gly Gly Gly Lys Ser Leu Thr Ser Il - #e Ala Leu Ala Thr Lys# 12450- att tgt aaa cat tat ggt gtt gag cct gaa aa - #g aat atc tat act aaa4515Ile Cys Lys His Tyr Gly Val Glu Pro Glu Ly - #s Asn Ile Tyr Thr Lys# 12605- cct gtg gct tca gat tac tgg gat gga tat ag - #t gga caa tta gtt tgc4563Pro Val Ala Ser Asp Tyr Trp Asp Gly Tyr Se - #r Gly Gln Leu Val Cys# 12750- atc att gat gat att ggc caa aac aca aca ga - #t gag gat tgg tca gat4611Ile Ile Asp Asp Ile Gly Gln Asn Thr Thr As - #p Glu Asp Trp Ser Asp# 12905- ttt tgt cag tta gtg tca gga tgt cct atg ag - #a tta aac atg gcc tct4659Phe Cys Gln Leu Val Ser Gly Cys Pro Met Ar - #g Leu Asn Met Ala Ser# 13101300 - # 1305- ctt gag gag aag ggt agg cat ttt tct tct cc - #t ttt ata ata gca act4707Leu Glu Glu Lys Gly Arg His Phe Ser Ser Pr - #o Phe Ile Ile Ala Thr# 13250- tca aat tgg tca aat cca agt cca aaa aca gt - #t tat gtt aag gaa gca4755Ser Asn Trp Ser Asn Pro Ser Pro Lys Thr Va - #l Tyr Val Lys Glu Ala# 13405- att gac cgc aga ctc cat ttc aag gtt gaa gt - #t aaa cct gct tca ttt4803Ile Asp Arg Arg Leu His Phe Lys Val Glu Va - #l Lys Pro Ala Ser Phe# 13550- ttc aaa aat cct cac aat gat atg ttg aat gt - #t aat tta gct aaa aca4851Phe Lys Asn Pro His Asn Asp Met Leu Asn Va - #l Asn Leu Ala Lys Thr# 13705- aat gat gca atc aaa gat atg tct tgt gtt ga - #t ttg ata atg gat gga4899Asn Asp Ala Ile Lys Asp Met Ser Cys Val As - #p Leu Ile Met Asp Gly# 13901380 - # 1385- cat aat gtt tca ttg atg gat ttg ctc agt tc - #t tta gtc atg aca gtt4947His Asn Val Ser Leu Met Asp Leu Leu Ser Se - #r Leu Val Met Thr Val# 14050- gaa att aga aaa caa aac atg act gaa ttc at - #g gag ttg tgg tct cag4995Glu Ile Arg Lys Gln Asn Met Thr Glu Phe Me - #t Glu Leu Trp Ser Gln# 14205- gga att tca gat gat gat aat gat agt gca gt - #a gct gag ttt ttc cag5043Gly Ile Ser Asp Asp Asp Asn Asp Ser Ala Va - #l Ala Glu Phe Phe Gln# 14350- tct ttt cca tct ggt gaa cca tcg aac tct aa - #a tta tct ggc ttt ttc5091Ser Phe Pro Ser Gly Glu Pro Ser Asn Ser Ly - #s Leu Ser Gly Phe Phe# 14505- caa tct gtt act aat cac aag tgg gtt gct gt - #g gga gct gca gtt ggc5139Gln Ser Val Thr Asn His Lys Trp Val Ala Va - #l Gly Ala Ala Val Gly# 14701460 - # 1465- gtt ctt gga gtg ctc gtt gga gga tgg ttt gt - #g tat aag cat ttc tcc5187Val Leu Gly Val Leu Val Gly Gly Trp Phe Va - #l Tyr Lys His Phe Ser# 14850- cgc aaa gag gaa gaa cca atc cca gct gaa gg - #g gta tat tat ggt gta5235Arg Lys Glu Glu Glu Pro Ile Pro Ala Glu Gl - #y Val Tyr Tyr Gly Val# 15005- act aag ccc aag caa gtg att aaa tta gat gc - #a gat cca gta gaa tct5283Thr Lys Pro Lys Gln Val Ile Lys Leu Asp Al - #a Asp Pro Val Glu Ser# 15150- cag tca act ttg gaa ata gca gga ctg gtt ag - #g aag aac ttg gtt cag5331Gln Ser Thr Leu Glu Ile Ala Gly Leu Val Ar - #g Lys Asn Leu Val Gln# 15305- ttt gga gtt gga gag aag aat gga tgt gtg ag - #a tgg gtt atg aat gcc5379Phe Gly Val Gly Glu Lys Asn Gly Cys Val Ar - #g Trp Val Met Asn Ala# 15501540 - # 1545- ttg gga gtg aaa gat gat tgg ctg ctt gtg cc - #t tcc cat gct tat aaa5427Leu Gly Val Lys Asp Asp Trp Leu Leu Val Pr - #o Ser His Ala Tyr Lys# 15650- ttt gag aaa gat tat gaa atg atg gag ttt ta - #t ttt aat aga ggt gga5475Phe Glu Lys Asp Tyr Glu Met Met Glu Phe Ty - #r Phe Asn Arg Gly Gly# 15805- act tac tat tca att tca gct ggt aat gtt gt - #t att caa tct ttg gat5523Thr Tyr Tyr Ser Ile Ser Ala Gly Asn Val Va - #l Ile Gln Ser Leu Asp# 15950- gtg gga ttc cag gat gtt gtt ctg atg aag gt - #t cct aca att cct aag5571Val Gly Phe Gln Asp Val Val Leu Met Lys Va - #l Pro Thr Ile Pro Lys# 16105- ttt aga gat att act cag cat ttt att aag aa - #a ggg gat gtg cct aga5619Phe Arg Asp Ile Thr Gln His Phe Ile Lys Ly - #s Gly Asp Val Pro Arg# 16301620 - # 1625- gct ttg aat cgc ctg gca aca tta gtg aca ac - #t gta aat gga acc cct5667Ala Leu Asn Arg Leu Ala Thr Leu Val Thr Th - #r Val Asn Gly Thr Pro# 16450- atg tta att tct gag ggc cca cta aag atg ga - #a gag aaa gct act tat5715Met Leu Ile Ser Glu Gly Pro Leu Lys Met Gl - #u Glu Lys Ala Thr Tyr# 16605- gtt cat aag aaa aat gat ggt aca tca gtt ga - #t tta act gtg gat cag5763Val His Lys Lys Asn Asp Gly Thr Ser Val As - #p Leu Thr Val Asp Gln# 16750- gca tgg aga gga aaa ggc gaa ggt ctt cct gg - #a atg tgt ggt ggg gcc5811Ala Trp Arg Gly Lys Gly Glu Gly Leu Pro Gl - #y Met Cys Gly Gly Ala# 16905- ttg gtt tca tcg aat caa tct ata cag aat gc - #a atc ttg ggc atc cat5859Leu Val Ser Ser Asn Gln Ser Ile Gln Asn Al - #a Ile Leu Gly Ile His# 17101700 - # 1705- gtt gct gga gga aat tca att ctt gtt gca aa - #a ttg gtt act caa gaa5907Val Ala Gly Gly Asn Ser Ile Leu Val Ala Ly - #s Leu Val Thr Gln Glu# 17250- atg ttc caa aat att gat aag aaa att gaa ag - #t cag aga att atg aaa5955Met Phe Gln Asn Ile Asp Lys Lys Ile Glu Se - #r Gln Arg Ile Met Lys# 17405- gtg gag ttt act cag tgt tca atg aat gtg gt - #c tcc aaa acg ctt ttt6003Val Glu Phe Thr Gln Cys Ser Met Asn Val Va - #l Ser Lys Thr Leu Phe# 17550- aga aag agt ccc att tat cat cac att gat aa - #a acc atg att aat ttt6051Arg Lys Ser Pro Ile Tyr His His Ile Asp Ly - #s Thr Met Ile Asn Phe# 17705- cct gca gct atg ccc ttt tct aaa gct gaa at - #t gat cca atg gct gtg6099Pro Ala Ala Met Pro Phe Ser Lys Ala Glu Il - #e Asp Pro Met Ala Val# 17901780 - # 1785- atg tta tct aag tat tca tta cct att gta ga - #a gaa cca gag aat tat6147Met Leu Ser Lys Tyr Ser Leu Pro Ile Val Gl - #u Glu Pro Glu Asn Tyr# 18050- aaa gag gct tca att ttt tat caa aat aaa at - #a gtg ggt aag act cag6195Lys Glu Ala Ser Ile Phe Tyr Gln Asn Lys Il - #e Val Gly Lys Thr Gln# 18205- tta gtt gat gat ttt cta gat ctt gat atg gc - #c att aca ggg gcc cca6243Leu Val Asp Asp Phe Leu Asp Leu Asp Met Al - #a Ile Thr Gly Ala Pro# 18350- gga att gat gct atc aac atg gat tca tct cc - #t gga ttt cct tat gtc6291Gly Ile Asp Ala Ile Asn Met Asp Ser Ser Pr - #o Gly Phe Pro Tyr Val# 18505- cag gag aag ttg acc aaa aga gat tta att tg - #g ttg gat gaa aat ggt6339Gln Glu Lys Leu Thr Lys Arg Asp Leu Ile Tr - #p Leu Asp Glu Asn Gly# 18701860 - # 1865- tta ttg ctg gga gtt cat cca aga ttg gct ca - #g aga atc tta ttc aat6387Leu Leu Leu Gly Val His Pro Arg Leu Ala Gl - #n Arg Ile Leu Phe Asn# 18850- act gtc atg atg gaa aat tgt tct gat ttg ga - #t gtt gtt ttt aca acc6435Thr Val Met Met Glu Asn Cys Ser Asp Leu As - #p Val Val Phe Thr Thr# 19005- tgt cca aaa gat gaa ttg aga cca tta gag aa - #a gtg ttg gaa tca aaa6483Cys Pro Lys Asp Glu Leu Arg Pro Leu Glu Ly - #s Val Leu Glu Ser Lys# 19150- aca aga gct att gat gct tgt cct ctg gat ta - #c aca att ttg tgc cga6531Thr Arg Ala Ile Asp Ala Cys Pro Leu Asp Ty - #r Thr Ile Leu Cys Arg# 19305- atg tat tgg ggt cca gct att agt tat ttt ca - #t ttg aat cca ggt ttc6579Met Tyr Trp Gly Pro Ala Ile Ser Tyr Phe Hi - #s Leu Asn Pro Gly Phe# 19501940 - # 1945- cat aca ggt gtt gct att ggc ata gat cct ga - #t aga cag tgg gat gaa6627His Thr Gly Val Ala Ile Gly Ile Asp Pro As - #p Arg Gln Trp Asp Glu# 19650- tta ttt aaa aca atg ata aga ttc gga gat gt - #t ggt ctt gat tta gat6675Leu Phe Lys Thr Met Ile Arg Phe Gly Asp Va - #l Gly Leu Asp Leu Asp# 19805- ttc tct gct ttt gat gct agt ctt agt cca tt - #t atg att aga gaa gca6723Phe Ser Ala Phe Asp Ala Ser Leu Ser Pro Ph - #e Met Ile Arg Glu Ala# 19950- ggt aga atc atg agt gaa cta tct gga act cc - #a tcc cat ttt ggc aca6771Gly Arg Ile Met Ser Glu Leu Ser Gly Thr Pr - #o Ser His Phe Gly Thr# 20105- gct ctt atc aat act atc att tat tcc aag ca - #t ttg ctg tat aac tgt6819Ala Leu Ile Asn Thr Ile Ile Tyr Ser Lys Hi - #s Leu Leu Tyr Asn Cys# 20302020 - # 2025- tgt tac cat gtc tgt ggt tca atg ccc tct gg - #g tct cct tgt aca gct6867Cys Tyr His Val Cys Gly Ser Met Pro Ser Gl - #y Ser Pro Cys Thr Ala# 20450- ttg cta aat tca att att aat aat gtc aat tt - #g tac tat gtg ttt tcc6915Leu Leu Asn Ser Ile Ile Asn Asn Val Asn Le - #u Tyr Tyr Val Phe Ser# 20605- aag ata ttt gga aag tct cca gtt ttc ttt tg - #t cag gct ttg aag att6963Lys Ile Phe Gly Lys Ser Pro Val Phe Phe Cy - #s Gln Ala Leu Lys Ile# 20750- ctc tgt tat gga gat gat gtt tta ata gtt tt - #c tct cga gat gtt cag7011Leu Cys Tyr Gly Asp Asp Val Leu Ile Val Ph - #e Ser Arg Asp Val Gln# 20905- att gat aat ctt gat ttg att gga caa aaa at - #t gta gat gag ttt aag7059Ile Asp Asn Leu Asp Leu Ile Gly Gln Lys Il - #e Val Asp Glu Phe Lys# 21102100 - # 2105- aaa ctt ggc atg aca gct act tct gct gac aa - #g aat gta cct cag ctg7107Lys Leu Gly Met Thr Ala Thr Ser Ala Asp Ly - #s Asn Val Pro Gln Leu# 21250- aaa cca gtt tcg gaa ttg act ttt ctc aaa ag - #a tct ttc aat ttg gta7155Lys Pro Val Ser Glu Leu Thr Phe Leu Lys Ar - #g Ser Phe Asn Leu Val# 21405- gag gat aga att aga cct gca att tcg gaa aa - #a aca att tgg tct tta7203Glu Asp Arg Ile Arg Pro Ala Ile Ser Glu Ly - #s Thr Ile Trp Ser Leu# 21550- ata gca tgg cag aga agt aac gct gag ttt ga - #g cag aat tta gaa att7251Ile Ala Trp Gln Arg Ser Asn Ala Glu Phe Gl - #u Gln Asn Leu Glu Ile# 21705- gct cag tgg ttt gct ttt atg cat ggc tat ga - #g ttt tat cag aaa ttt7299Ala Gln Trp Phe Ala Phe Met His Gly Tyr Gl - #u Phe Tyr Gln Lys Phe# 21902180 - # 2185- tat tat ttt gtt cag tcc tgt ttg gag aaa ga - #g atg ata gaa tac aga7347Tyr Tyr Phe Val Gln Ser Cys Leu Glu Lys Gl - #u Met Ile Glu Tyr Arg# 22050- ctt aaa tct tat gat tgg tgg aga atg aga tt - #t tat gac cag tgt ttc7395Leu Lys Ser Tyr Asp Trp Trp Arg Met Arg Ph - #e Tyr Asp Gln Cys Phe# 22205- att tgt gac ctt tca tgatttgttt aaacgaattt tcttaaaat - #t tctgaggttt7450Ile Cys Asp Leu Ser 2225# 7486 agta aataaaaaaa aaaaaa- <210> SEQ ID NO 6<211> LENGTH: 2227<212> TYPE: PRT<213> ORGANISM: Attenuated (4380) HAV, strain HM-1 - #75- <400> SEQUENCE: 6- Met Asn Met Ser Arg Gln Gly Ile Phe Gln Th - #r Val Gly Ser Gly Leu# 15- Asp His Ile Leu Ser Leu Ala Asp Ile Glu Gl - #u Glu Gln Met Ile Gln# 30- Ser Val Asp Arg Thr Ala Val Thr Gly Ala Se - #r Tyr Phe Thr Ser Val# 45- Asp Gln Ser Ser Val His Thr Ala Glu Val Gl - #y Ser His Gln Val Glu# 60- Pro Leu Arg Thr Ser Val Asp Lys Pro Gly Se - #r Lys Arg Thr Gln Gly# 80- Glu Lys Phe Phe Leu Ile His Ser Ala Asp Tr - #p Leu Thr Thr His Ala# 95- Leu Phe His Glu Val Ala Lys Leu Asp Val Va - #l Lys Leu Leu Tyr Asn# 110- Glu Gln Phe Ala Val Gln Gly Leu Leu Arg Ty - #r His Thr Tyr Ala Arg# 125- Phe Gly Ile Glu Ile Gln Val Gln Ile Asn Pr - #o Thr Pro Phe Gln Gln# 140- Gly Gly Leu Ile Cys Ala Met Val Pro Gly As - #p Gln Ser Tyr Gly Ser145 1 - #50 1 - #55 1 -#60- Ile Ala Ser Leu Thr Val Tyr Pro His Gly Le - #u Leu Asn Cys Asn Ile# 175- Asn Asn Val Val Arg Ile Lys Val Pro Phe Il - #e Tyr Thr Arg Gly Ala# 190- Tyr His Phe Lys Asp Pro Gln Tyr Pro Val Tr - #p Glu Leu Thr Ile Arg# 205- Val Trp Ser Glu Leu Asn Ile Gly Thr Gly Th - #r Ser Ala Tyr Thr Ser# 220- Leu Asn Val Leu Ala Arg Phe Thr Asp Leu Gl - #u Leu His Gly Leu Thr225 2 - #30 2 - #35 2 -#40- Pro Leu Ser Thr Gln Met Met Arg Asn Glu Ph - #e Arg Val Ser Thr Thr# 255- Glu Asn Val Val Asn Leu Ser Asn Tyr Glu As - #p Ala Arg Ala Lys Met# 270- Ser Phe Ala Leu Asp Gln Glu Asp Trp Lys Se - #r Asp Pro Ser Gln Gly# 285- Gly Gly Ile Lys Ile Thr His Phe Thr Thr Tr - #p Thr Ser Ile Pro Thr# 300- Leu Ala Ala Gln Phe Pro Phe Asn Ala Ser As - #p Ser Val Gly Gln Gln305 3 - #10 3 - #15 3 -#20- Ile Lys Val Ile Pro Val Asp Pro Tyr Phe Ph - #e Gln Met Thr Asn Thr# 335- Asn Pro Asp Gln Lys Cys Ile Thr Ala Leu Al - #a Ser Ile Cys Gln Met# 350- Phe Cys Phe Trp Arg Gly Asp Leu Val Phe As - #p Phe Gln Val Phe Pro# 365- Thr Lys Tyr His Ser Gly Arg Leu Leu Phe Cy - #s Phe Val Pro Gly Asn# 380- Glu Leu Ile Asp Val Ser Gly Ile Thr Leu Ly - #s Gln Ala Thr Thr Ala385 3 - #90 3 - #95 4 -#00- Pro Cys Ala Val Met Asp Ile Thr Gly Val Gl - #n Ser Thr Leu Arg Phe# 415- Arg Val Pro Trp Ile Ser Asp Thr Pro Tyr Ar - #g Val Asn Arg Tyr Thr# 430- Lys Ser Ala His Gln Lys Gly Glu Tyr Thr Al - #a Ile Gly Lys Leu Ile# 445- Val Tyr Cys Tyr Asn Arg Leu Thr Ser Pro Se - #r Asn Val Ala Ser His# 460- Val Arg Val Asn Val Tyr Leu Ser Ala Ile As - #n Leu Glu Cys Phe Ala465 4 - #70 4 - #75 4 -#80- Pro Leu Tyr His Ala Met Asp Val Thr Thr Gl - #n Val Gly Asp Asp Ser# 495- Gly Gly Phe Ser Thr Thr Val Ser Thr Glu Gl - #n Asn Val Pro Asp Pro# 510- Gln Val Gly Ile Thr Thr Met Lys Asp Leu Ly - #s Gly Lys Ala Asn Arg# 525- Gly Lys Met Asp Val Ser Gly Val Gln Ala Pr - #o Val Gly Ala Ile Thr# 540- Thr Ile Glu Asp Pro Val Leu Ala Lys Lys Va - #l Pro Glu Thr Phe Pro545 5 - #50 5 - #55 5 -#60- Glu Leu Lys Pro Gly Glu Ser Arg His Thr Se - #r Asp His Met Ser Ile# 575- Tyr Lys Phe Met Gly Arg Ser His Phe Leu Cy - #s Thr Phe Thr Phe Asn# 590- Ser Asn Asn Lys Glu Tyr Thr Phe Pro Ile Th - #r Leu Ser Ser Thr Ser# 605- Asn Pro Pro His Gly Leu Pro Ser Thr Leu Ar - #g Trp Phe Phe Asn Leu# 620- Phe Gln Leu Tyr Arg Gly Pro Leu Asp Leu Th - #r Ile Ile Ile Thr Gly625 6 - #30 6 - #35 6 -#40- Ala Thr Asp Val Asp Gly Met Ala Trp Phe Th - #r Pro Val Gly Leu Ala# 655- Val Asp Thr Pro Trp Val Glu Lys Glu Ser Al - #a Leu Ser Ile Asp Tyr# 670- Lys Thr Ala Leu Gly Ala Val Arg Phe Asn Th - #r Arg Arg Thr Gly Asn# 685- Ile Gln Ile Arg Leu Pro Trp Tyr Ser Tyr Le - #u Tyr Ala Val Ser Gly# 700- Ala Leu Asp Gly Leu Gly Asp Lys Thr Asp Se - #r Thr Phe Gly Leu Val705 7 - #10 7 - #15 7 -#20- Ser Ile Gln Ile Ala Asn Tyr Asn His Ser As - #p Glu Tyr Leu Ser Phe# 735- Ser Cys Tyr Leu Ser Val Thr Glu Gln Ser Gl - #u Phe Tyr Phe Pro Arg# 750- Ala Pro Leu Asn Ser Asn Ala Met Leu Ser Th - #r Val Thr Met Met Ser# 765- Arg Ile Ala Ala Gly Asp Leu Glu Ser Ser Va - #l Asp Asp Pro Arg Ser# 780- Glu Glu Asp Lys Arg Phe Glu Ser His Ile Gl - #u Cys Arg Lys Pro Tyr785 7 - #90 7 - #95 8 -#00- Lys Glu Leu Arg Leu Glu Val Gly Lys Gln Ar - #g Leu Lys Tyr Ala Gln# 815- Glu Glu Leu Ser Asn Glu Val Leu Pro Pro Pr - #o Arg Lys Met Lys Gly# 830- Leu Phe Ser Gln Ala Lys Ile Ser Leu Phe Ty - #r Thr Glu Glu His Glu# 845- Ile Met Lys Phe Ser Trp Arg Gly Val Thr Al - #a Asp Thr Arg Ala Leu# 860- Arg Arg Phe Gly Phe Ser Leu Ala Ala Gly Ar - #g Ser Val Trp Thr Leu865 8 - #70 8 - #75 8 -#80- Glu Met Asp Ala Gly Val Leu Thr Gly Arg Le - #u Ile Arg Leu Asn Asp# 895- Glu Lys Trp Thr Glu Met Lys Asp Asp Lys Il - #e Val Ser Leu Ile Glu# 910- Lys Phe Thr Ser Asn Lys Tyr Trp Ser Lys Va - #l Asn Phe Pro His Gly# 925- Met Leu Asp Leu Glu Glu Ile Ala Ala Asn Se - #r Lys Asp Phe Pro Asn# 940- Met Ser Glu Thr Asp Leu Cys Phe Leu Leu Hi - #s Trp Leu Asn Pro Lys945 9 - #50 9 - #55 9 -#60- Lys Ile Asn Leu Ala Asp Arg Met Leu Gly Le - #u Ser Gly Val Gln Glu# 975- Ile Lys Glu Gln Gly Val Gly Leu Ile Ala Gl - #u Cys Arg Thr Phe Leu# 990- Asp Ser Ile Ala Gly Thr Leu Lys Ser Met Me - #t Phe Gly Phe His His# 10050- Ser Val Thr Val Glu Ile Ile Asn Thr Val Le - #u Cys Phe Val Lys Ser# 10205- Gly Ile Leu Leu Tyr Val Ile Gln Gln Leu As - #n Gln Asp Glu His Ser# 10401030 - # 1035- His Ile Ile Gly Leu Leu Arg Val Met Asn Ty - #r Val Asp Ile Gly Cys# 10550- Ser Val Ile Ser Cys Ala Lys Val Phe Ser Ar - #g Met Leu Glu Thr Val# 10705- Phe Asn Trp Gln Met Asp Ser Arg Met Met Gl - #u Leu Arg Thr Gln Ser# 10850- Phe Ser Asn Trp Leu Arg Asp Ile Cys Ser Gl - #y Ile Thr Ile Phe Lys# 11005- Asn Phe Lys Asp Ala Ile Tyr Trp Leu Tyr Th - #r Lys Leu Met Asp Phe# 11201110 - # 1115- Tyr Glu Val Asn Tyr Gly Lys Lys Lys Asp Il - #e Leu Asn Ile Leu Lys# 11350- Asp Asn Gln Gln Lys Ile Glu Lys Ala Ile Gl - #u Glu Ala Asp Lys Phe# 11505- Cys Ile Leu Gln Ile Gln Asp Val Glu Lys Se - #r Glu Gln Tyr Gln Lys# 11650- Gly Val Asp Leu Ile Gln Lys Leu Arg Thr Va - #l His Ser Met Ala Gln# 11805- Val Asp Pro Asn Leu Met Val His Leu Ser Pr - #o Leu Arg Asp Cys Ile# 12001190 - # 1195- Ala Arg Val His Gln Lys Leu Lys Asn Leu Gl - #y Ser Ile Asn Gln Ala# 12150- Met Val Thr Arg Cys Glu Pro Val Val Cys Ty - #r Phe Tyr Gly Lys Arg# 12305- Gly Gly Gly Lys Ser Leu Thr Ser Ile Ala Le - #u Ala Thr Lys Ile Cys# 12450- Lys His Tyr Gly Val Glu Pro Glu Lys Asn Il - #e Tyr Thr Lys Pro Val# 12605- Ala Ser Asp Tyr Trp Asp Gly Tyr Ser Gly Gl - #n Leu Val Cys Ile Ile# 12801270 - # 1275- Asp Asp Ile Gly Gln Asn Thr Thr Asp Glu As - #p Trp Ser Asp Phe Cys# 12950- Gln Leu Val Ser Gly Cys Pro Met Arg Leu As - #n Met Ala Ser Leu Glu# 13105- Glu Lys Gly Arg His Phe Ser Ser Pro Phe Il - #e Ile Ala Thr Ser Asn# 13250- Trp Ser Asn Pro Ser Pro Lys Thr Val Tyr Va - #l Lys Glu Ala Ile Asp# 13405- Arg Arg Leu His Phe Lys Val Glu Val Lys Pr - #o Ala Ser Phe Phe Lys# 13601350 - # 1355- Asn Pro His Asn Asp Met Leu Asn Val Asn Le - #u Ala Lys Thr Asn Asp# 13750- Ala Ile Lys Asp Met Ser Cys Val Asp Leu Il - #e Met Asp Gly His Asn# 13905- Val Ser Leu Met Asp Leu Leu Ser Ser Leu Va - #l Met Thr Val Glu Ile# 14050- Arg Lys Gln Asn Met Thr Glu Phe Met Glu Le - #u Trp Ser Gln Gly Ile# 14205- Ser Asp Asp Asp Asn Asp Ser Ala Val Ala Gl - #u Phe Phe Gln Ser Phe# 14401430 - # 1435- Pro Ser Gly Glu Pro Ser Asn Ser Lys Leu Se - #r Gly Phe Phe Gln Ser# 14550- Val Thr Asn His Lys Trp Val Ala Val Gly Al - #a Ala Val Gly Val Leu# 14705- Gly Val Leu Val Gly Gly Trp Phe Val Tyr Ly - #s His Phe Ser Arg Lys# 14850- Glu Glu Glu Pro Ile Pro Ala Glu Gly Val Ty - #r Tyr Gly Val Thr Lys# 15005- Pro Lys Gln Val Ile Lys Leu Asp Ala Asp Pr - #o Val Glu Ser Gln Ser# 15201510 - # 1515- Thr Leu Glu Ile Ala Gly Leu Val Arg Lys As - #n Leu Val Gln Phe Gly# 15350- Val Gly Glu Lys Asn Gly Cys Val Arg Trp Va - #l Met Asn Ala Leu Gly# 15505- Val Lys Asp Asp Trp Leu Leu Val Pro Ser Hi - #s Ala Tyr Lys Phe Glu# 15650- Lys Asp Tyr Glu Met Met Glu Phe Tyr Phe As - #n Arg Gly Gly Thr Tyr# 15805- Tyr Ser Ile Ser Ala Gly Asn Val Val Ile Gl - #n Ser Leu Asp Val Gly# 16001590 - # 1595- Phe Gln Asp Val Val Leu Met Lys Val Pro Th - #r Ile Pro Lys Phe Arg# 16150- Asp Ile Thr Gln His Phe Ile Lys Lys Gly As - #p Val Pro Arg Ala Leu# 16305- Asn Arg Leu Ala Thr Leu Val Thr Thr Val As - #n Gly Thr Pro Met Leu# 16450- Ile Ser Glu Gly Pro Leu Lys Met Glu Glu Ly - #s Ala Thr Tyr Val His# 16605- Lys Lys Asn Asp Gly Thr Ser Val Asp Leu Th - #r Val Asp Gln Ala Trp# 16801670 - # 1675- Arg Gly Lys Gly Glu Gly Leu Pro Gly Met Cy - #s Gly Gly Ala Leu Val# 16950- Ser Ser Asn Gln Ser Ile Gln Asn Ala Ile Le - #u Gly Ile His Val Ala# 17105- Gly Gly Asn Ser Ile Leu Val Ala Lys Leu Va - #l Thr Gln Glu Met Phe# 17250- Gln Asn Ile Asp Lys Lys Ile Glu Ser Gln Ar - #g Ile Met Lys Val Glu# 17405- Phe Thr Gln Cys Ser Met Asn Val Val Ser Ly - #s Thr Leu Phe Arg Lys# 17601750 - # 1755- Ser Pro Ile Tyr His His Ile Asp Lys Thr Me - #t Ile Asn Phe Pro Ala# 17750- Ala Met Pro Phe Ser Lys Ala Glu Ile Asp Pr - #o Met Ala Val Met Leu# 17905- Ser Lys Tyr Ser Leu Pro Ile Val Glu Glu Pr - #o Glu Asn Tyr Lys Glu# 18050- Ala Ser Ile Phe Tyr Gln Asn Lys Ile Val Gl - #y Lys Thr Gln Leu Val# 18205- Asp Asp Phe Leu Asp Leu Asp Met Ala Ile Th - #r Gly Ala Pro Gly Ile# 18401830 - # 1835- Asp Ala Ile Asn Met Asp Ser Ser Pro Gly Ph - #e Pro Tyr Val Gln Glu# 18550- Lys Leu Thr Lys Arg Asp Leu Ile Trp Leu As - #p Glu Asn Gly Leu Leu# 18705- Leu Gly Val His Pro Arg Leu Ala Gln Arg Il - #e Leu Phe Asn Thr Val# 18850- Met Met Glu Asn Cys Ser Asp Leu Asp Val Va - #l Phe Thr Thr Cys Pro# 19005- Lys Asp Glu Leu Arg Pro Leu Glu Lys Val Le - #u Glu Ser Lys Thr Arg# 19201910 - # 1915- Ala Ile Asp Ala Cys Pro Leu Asp Tyr Thr Il - #e Leu Cys Arg Met Tyr# 19350- Trp Gly Pro Ala Ile Ser Tyr Phe His Leu As - #n Pro Gly Phe His Thr# 19505- Gly Val Ala Ile Gly Ile Asp Pro Asp Arg Gl - #n Trp Asp Glu Leu Phe# 19650- Lys Thr Met Ile Arg Phe Gly Asp Val Gly Le - #u Asp Leu Asp Phe Ser# 19805- Ala Phe Asp Ala Ser Leu Ser Pro Phe Met Il - #e Arg Glu Ala Gly Arg# 20001990 - # 1995- Ile Met Ser Glu Leu Ser Gly Thr Pro Ser Hi - #s Phe Gly Thr Ala Leu# 20150- Ile Asn Thr Ile Ile Tyr Ser Lys His Leu Le - #u Tyr Asn Cys Cys Tyr# 20305- His Val Cys Gly Ser Met Pro Ser Gly Ser Pr - #o Cys Thr Ala Leu Leu# 20450- Asn Ser Ile Ile Asn Asn Val Asn Leu Tyr Ty - #r Val Phe Ser Lys Ile# 20605- Phe Gly Lys Ser Pro Val Phe Phe Cys Gln Al - #a Leu Lys Ile Leu Cys# 20802070 - # 2075- Tyr Gly Asp Asp Val Leu Ile Val Phe Ser Ar - #g Asp Val Gln Ile Asp# 20950- Asn Leu Asp Leu Ile Gly Gln Lys Ile Val As - #p Glu Phe Lys Lys Leu# 21105- Gly Met Thr Ala Thr Ser Ala Asp Lys Asn Va - #l Pro Gln Leu Lys Pro# 21250- Val Ser Glu Leu Thr Phe Leu Lys Arg Ser Ph - #e Asn Leu Val Glu Asp# 21405- Arg Ile Arg Pro Ala Ile Ser Glu Lys Thr Il - #e Trp Ser Leu Ile Ala# 21602150 - # 2155- Trp Gln Arg Ser Asn Ala Glu Phe Glu Gln As - #n Leu Glu Ile Ala Gln# 21750- Trp Phe Ala Phe Met His Gly Tyr Glu Phe Ty - #r Gln Lys Phe Tyr Tyr# 21905- Phe Val Gln Ser Cys Leu Glu Lys Glu Met Il - #e Glu Tyr Arg Leu Lys# 22050- Ser Tyr Asp Trp Trp Arg Met Arg Phe Tyr As - #p Gln Cys Phe Ile Cys# 22205- Asp Leu Ser2225__________________________________________________________________________
Claims
  • 1. A hepatitis A virus adapted to growth in MRC-5 cells, said virus having a genome whose cDNA sequence corresponds to the cDNA sequence of HAV HM-175, Pass 35 except for nucleotide positions 591 and 687 which have guanines as bases, nucleotide position 646 which has an adenine as a base and nucleotide position 669 which has a thymine as a base; and optionally, at least one additional nucleotide selected from the group consisting of:
  • (a) T at position 2750;
  • (b) A at position 3027;
  • (c) A at position 3196
  • (d) G at position 3934;
  • (e) T at position 4418;
  • (f) G at position 4563;
  • (g) T at position 4643;
  • (h) G at position 5145;
  • (i) T at position 5745;
  • (j) C at position 6908;
  • (k) T at position 7032;
  • (l) T at position 7255;
  • wherein the nucleotide numbers shown above are those assigned to positions of the wild-type HM-175 sequence.
  • 2. The virus according to claim 1 wherein the additional nucleotide is a G at position 5145.
  • 3. The virus according to claim 1, wherein the additional nucleotide is at least one of the nucleotides (e) through (g).
  • 4. The virus according to claim 1, wherein the additional nuclcotides are (e) through (g).
  • 5. The virus, according to claim 1, wherein no additional nucleotides are selected.
CROSS-REFERENCE TO RELATED PATENT APPLICATIONS

This is a continuation-in-part of U.S. patent application Ser. No. 08/397,232, filed on Mar. 10, 1995, which is the national phase filing of International Patent Application No. PCT/US93/08610, filed on Sep. 17, 1993, which is a continuation-in-part of U.S. patent application Ser. No. 07/947,338, filed on Sep. 18, 1992, now abandoned.

Government Interests

This invention was made with government support under certain Collaborative Research and Development Agreements awarded by the Department of Health and Human Services. The government has certain rights in this invention.

US Referenced Citations (5)
Number Name Date Kind
4532215 Daemer et al. Jul 1985
4620978 Daemer et al. Nov 1986
4636469 Daemer et al. Jan 1987
4783407 Provost et al. Nov 1988
4894228 Purcell et al. Jan 1990
Foreign Referenced Citations (4)
Number Date Country
0323900 Jul 1989 EPX
2398504 Mar 1979 FRX
WOA9219268 Nov 1992 WOX
WO9309139 May 1993 WOX
Non-Patent Literature Citations (37)
Entry
Emerson et al., J. Virol. 66(2):650-654, Feb. 1992.
Provost et al. J. Med. Virol. 34(4):227-231, 1991.
Fineschi et al. J. Hepatol. 13(4):S146-S151, Apr. 1991.
Karron et al. J. Infect. Dis. 157(2):338-345, Feb. 1988.
Day et al., "A Single Base Mutation in the 5' Noncoding Region of HAV Enhances Replication of Virus In Vitro", Vaccines 90. Modern Approaches to New Vaccines Including Prevention of Aids, pp. 175-178 (1990).
Ross et al., "Molecular Cloning of cDNA From Hepatitis A Virus Strain HM-175 After Multiple Passages In Vivo and In Vitro", J. Med. Virol., vol. 67, pp. 1741-1744 (1986).
Najarian et al., "Primary Structure and Gene Organization Of Human Hepatitis A Virus", Proc. Nat'l. Acad. Sci. USA, vol. 82 pp. 2627-2631 (1985).
B. Ross et al, "Nucleotide Sequence of High-Passage Hepatitis A Virus Strain HM175: Comparison with Wild-type and Cell Culture-adapted Strains", J. Gen. Virol., 70:2805-2810 (Oct., 1989).
R. Jansen et al, "Complete Nucleotide Sequence of a Cell Culture-Adapted Variant of Hepatitis A Virus: Comparison with Wild-Type Virus with Restricted Capacity for in Vitro Replication", Virol., 163:299-307 (1988).
V. Tedeschi et al, "Partial Characterzation of Hepatitis A Viruses from Three Intermediate Passage Levels of a Series Resulting in Adaptation to Growth in Cell Culture and Attenuation of Virulence", J. Med., Virol., 39(1):16-21 (Jan. 1993).
N. Fineschi et al, "Characterization of a Hepatitis A Virus Strain Suitable for Vaccine Production", J. Hepatol., 13(4):S146-S151 (Apr., 1991).
P. Provost et al, "New Findings in Live, Attenuated Hepatitis A Vaccine Development", J. Med. Virol., 20:165-175 (1986) [Provost].
K. Midthun et al, "Safety and Immunogenicity of a Live Attenuated Hepatitis A Virus Vaccine in Seronegative Volunteers", J. Infect. Dis., 163:735-739 (Apr., 1991).
J. Mao et al, "Primary Study of Attenuated Live Hepatitis A Vaccine (H2 Strain) in Humans", J. Infect. Dis., 159(4):621-624 (Apr., 1989).
I. Gust et al, "The Origin of the HM175 Strain of Hepatitis A Virus", J. Infect. Dis., 151(2):365-366 (Feb., 1985).
F. Andre et al, "Inactivated Candidate Vaccines for Hepatitis A", Prog. Med. Virol. Basel, Karger, 37:72-95 (1990).
R. Daemer et al, "Propagation of Human Hepatitis A Virus in African Green Monkey Kidney Cell Culture: Primary Isolation and Serial Passage", Infect. Immun., 32:388-393 (Apr., 1981).
J. Melnick, "New Picornavirus Vaccines for Hepatitis A, and Lessons from the Control of Poliomyelitis by the Prototype Picornavirus Vaccines", Prog. Med. Virol. Basel, Karger, 37:47-55 (1990).
R. Karron et al, "Studies of Prototype Live Hepatitis A Virus Vaccines in Primate Models", J. Infect. Dis., 157(2):338-345 (Feb., 1988).
S. Emerson et al, "Mutations Responsible for Adaptation of Hepatitis A Virus to Efficient Growth in Cell Culture", J. Virol., 65(9):4882-4886 (Sep., 1991).
J. Cohen et al, "Complete Nucleotide Sequence of Wild-Type Hepatitis A Virus: Comparison with Different Strains of Hepatitis A Virus and Other Picornaviruses", J. Virol., 61(1):50-59 (Jan., 1987) [Cohen I].
J. Cohen et al, "Complete Nucleotide Sequence of an Attenuated Hepatitis A Virus: Comparison with Wild-Type Virus", Proc. Natl. Acad. Sci. USA, 84(8):2497-2501 (Apr., 1987) [Cohen II].
S. Lemon et al, "Serum Neutralizing Antibody Response to Hepatitis A Virus", J. Infect. Dis., 148(6):1033-1039 (Dec., 1983).
R. Purcelle et al, "A Microtiter Solid-Phase Radioimmunoassay for Hepatitis A Antigen and Antibody", J. Immunol., 116(2):349-356 (Feb., 1976).
J. Ticehurst et al, "Detection of Hepatitis A Virus by Extraction of Viral RNA and Molecular Hybridization", J. Clin. Microbiol., 25(10):1822-1829 (Oct., 1987).
J. Cohen et al, "Hepatitis A Virus cDNA and its RNA Transcripts are Infectious in Cell Culture", J. Virol., 61(10):3035-3039 (Oct., 1987) [Cohen III].
P. Provost et al, "Further Evaluation of a Live Hepatitis A Vaccine in Marmosets", J. Med. Virol., 34(4):227-231 (Aug., 1991) [Provost II].
B. Robertson et al, "Genetic Relatedness of Hepatitis A Virus Strains Recovered from Different Geographical Regions", J. Gen. Virol., 73:1365-1377 (May, 1992).
J. Graff et al, "Nucleotide Sequence of Wild-Type Hepatitis A Virus GBM in Comparison with Two Cell Culture-Adapted Variants", J. Virol., 68(1):548-554 (Jan., 1994).
F. Andre, "Approaches to a Vaccine Against Hepatitis A: Development and Manufacture of an Inactivated Vaccine", J. Infect. Dis., 171(Suppl 1):S33-S39 (Mar., 1995).
J. Peetermans, "Production, Quality Control and Characterization of an Inactivated Hepatitis A Vaccine", Vaccine, 10(Suppl 1):S99-S101 (Nov., 1992).
F. Andre, "Hepatitis A in Travellers: Development of a Safe, Immunogenic and Efficacious Inactivated Vaccine", Travel Medicine International, 13(1):10-14 (Jan., 1995).
Product Insert, "HA:L3A Prescribing Information, Hepatitis A Vaccine, Inactivated Havrix", distributed by SmithKline Beecham Pharmaceuticals (Feb., 1995).
Emerson et al., J. Virol., 66(2):650-654, Feb. 1992.
Provost et al., J. Med. Virol., 34(4):227-231, 1991 (Ref. B.S.).
Kineschi et al., J. Hepatol., 13(4):S146-S151, Apr. 1991 (Ref A.U.).
Karron et al., J. Infect. Dis., 157(2):338-345, Feb. 1988, (Ref. AAT).
Continuation in Parts (1)
Number Date Country
Parent 397232