Rotavirus peptide compositions and methods of use

TECHNICAL FIELD
The invention relates to peptides which are useful as vaccines and immunogens capable of simulating neutralizing antibodies against rotavirus. In particular, the invention concerns the epitopic regions of rotavirus proteins VP7, VP6 and VP4 (VP3) which have been formulated into vaccines.
BACKGROUND ART
Rotaviruses are important causes of gastrointestinal disorders and diarrhea in avian and animal species, including man. There are at least eleven known serotypes of rotavirus, some of which are found in humans and others found in various animals and birds. There appears to be some cross-protection among strains, but this is not complete. A number of the important capsid proteins have been sequenced and show considerable homology among serotypes.
The rotavirus genome is thought to consist of eleven segments of double-stranded RNA regardless of the strain. A designation system for the proteins encoded by these segments and present in the intact virus has been proposed, but has not remained constant over the years. There appear to be three proteins associated with the inner shell (VP1, VP2, and VP6) and three associated with the outer capsid. Of interest herein are the inner capsid protein VP6 and two of the outer capsid proteins, VP7 and VP4 (designated VP3 in former nomenclature).
(In various rotaviruses, the absolute order of the genomic fragments does not always conform to the same genes; for example in rotavirus strains SA11, W, and Wa, gene 9 codes for VP7, while in rotavirus strains DS-1, and UK bovine rotavirus (BRV) gene 8 codes for VP7. Also, especially for bovine and human rotavirus, there are variations in the mobility of proteins derived from different isolates originating from the same species. However, the identity of the various virus proteins (VP) designated by the foregoing designations is not in doubt for any particular species.)
As the invention concerns vaccines comprised of epitopes from VP7, VP4 and VP6, further descriptions of these particular proteins are provided as follows:
The major glycoprotein of the outer shell, VP7, has an approximate apparent molecular weight of 38.2 kd in its unreduced form and 41.9 kd in its reduced form and has been shown to be the major antigen responsible for inducing neutralizing antibodies to the virus, and for attachment to cells. A 14 kd fragment of this protein from BRV was also shown to raise neutralizing antibodies against the virus. (Sabara, M., et al., J Virol (1985) 53:58-66). Regions of conservation among strains infecting human and animal species in this protein have been reviewed by Estes, M. K., et al., Microbiol Rev (1989) 53:410-449. The complete amino acid sequence of rotavirus VP7 glycoprotein for three strains of rotavirus, and a partial sequence for a fourth strain are shown in FIG. 1.
Gunn, P. R., et al., J Virol (1985) 54:791-797, investigated various putative antigenic determinants in VP7 of the SA11 serotype. These authors compared the amino acid sequences of the VP7 protein of SA11, NCDV, S2 and Wa serotypes. They investigated the immunogenicity of peptides corresponding to positions 66-76; 90-103; 174-183; 208-225; 247-259; and 275-295 conjugated to keyhole limpet hemacyanin (KLH) using 1-ethyl-(3,3-dimethylaminopropyl)carbodiimide (EDCI) with mixed results. All of the peptides were capable of generating antisera immunoreactive with the immunizing peptides themselves and the denatured form of VP7. However, high titer polyclonal neutralizing antiserum directed against the whole SA11 virus did not recognize any of the seven peptides when they were immobilized on microtiter dishes, pretreated with glutaraldehyde. Further, in a virus neutralization assay, where control polyclonal antiserum prepared against whole virus had a neutralization titer of 10.sup.6 U/ml, none of the peptide antisera showed significant neutralizing activity. Further, none of the sera recognized whole virus in solid phase RIA. The authors concluded that in the native virus the regions represented by these peptides were not properly exposed, and suggested the possibility of the antigenic sites being composed of discontinuous determinants.
The various serotypes of rotavirus are defined by the neutralizing activity stimulated by VP7; on this basis, eleven serotypes have been identified, six of which are found in humans.
VP4 (formerly called VP3) is also an outer capsid protein and has an approximate apparent molecular weight of 82 kd in unreduced form and 84 kd in reduced form. FIG. 3 shows the amino acid sequences of two strains of rotavirus--C486 which is a bovine strain and SA11 which is a simian-infecting strain.
The inner capsid protein of interest herein is VP6 which is a 45 kd molecular weight protein. Antibodies raised against VP6 appear to be the most cross-species reactive among those raised to viral proteins. The nucleotide sequence and deduced amino acid sequence of the SA11 VP6 protein, as disclosed by Estes et al., Nucleic Acids Res (1984) 12:1875-1887 is shown in FIG. 3. In addition to being itself immunogenic, VP6 has been shown, at least partially by virtue of its abilities to form aggregates of various shapes, to be a superior carrier for other haptens. This is disclosed EPO application 87/3077465.
The present invention provides subunit peptide vaccines corresponding to the epitopic regions of VP7, VP4, and VP6 which are effective as vaccines in that they show demonstrated protection against challenge and/or elicit the production of neutralizing antibodies. The use of these subunit vaccines confers a number of advantages, including safety, economy, and effectiveness.
DISCLOSURE OF THE INVENTION
The invention is directed to peptide subunits derived from VP7, VP4, and VP6 of various rotavirus strains which are capable of producing neutralizing antibodies and are effective as vaccines. Specifically, the invention is directed to peptide-based vaccines which include as an active ingredient a peptide having an amino acid sequence corresponding to positions 275-295 of VP7 from various strains and to similar compositions capable of raising neutralizing antibodies which contain, as active ingredient, a peptide derived from positions 247-259 of these proteins. Similar vaccines and antibody-producing compositions which contain as active ingredient the peptide representing positions 232-255 or 240-248 of the VP4 protein, and similar compositions of matter containing as active ingredient the peptide corresponding to positions 40-60 of VP6 are included in the invention. The peptide derived from the sequence at positions 232-255 or 240-248 of VP4 corresponds to the trypsin cleavage site and can compete with the virus for trypsin to interfere with infectivity. Compositions containing these peptides can thus also be used therapeutically and as prophylactics in preventing infection.
The invention is, therefore, directed to compositions of matter containing these peptides, including pharmaceutical and vaccine compositions, and to methods to immunize and treat (therapeutically and prophylactically) animal subjects with these materials.

BRIEF DESCRIPTION OF THE DRAWINGS
FIGS. 1(a-c) shows the amino acid sequences of several rotavirus VP7 glycoproteins (SEQ ID NO:12), (SEQ ID NO:13), (SEQ ID NO:14), (SEQ ID NO:15).
FIG. 2 shows the amino acid sequences of the VP4 proteins from the bovine C486 strain and the simian SA11 rotavirus strain (SEQ ID NO:16) and (SEQ ID NO:17).
FIG. 3(a-b) shows the nucleotide sequence and deduced amino acid sequence of the VP6 protein from SA11 (SEQ ID NO:18) and (SEQ ID NO:19)
FIG. 4 shows the production of antibodies by administration of VP7 glycoprotein or its 14 kd fragment.
FIG. 5 shows the ability of VP7 subunits 247-259 and 275-295 to block virus attachment to host cells.
FIG. 6 shows the ability of the VP7 subunits to elicit antiviral peptides by ELISA analysis.
FIG. 7 shows the ability of vaccines comprising the peptides 247-249 and 275-295 derived from VP7 to produce virus-neutralizing antibodies.
FIG. 8 shows the ability of the 232-235 peptide from VP4 to inhibit cleavage of VP4 by trypsin.

MODES OF CARRYING OUT THE INVENTION
The invention provides short peptide subunit sequences which are effective active ingredients in vaccines. There are five subunits of the rotavirus peptides which are the subject of the present invention. These are the peptides represented by positions 232-255 or 240-248 of the VP4 protein; a subunit representing positions 40-60 of VP6; and peptides representing position 247-259 or positions 275-295 of VP7. These peptides are represented herein by the designations "232-255"; "240-248"; "40-60"; "247-259"; and "275-295"; respectively.
As is illustrated in the figures and examples below, and is generally known in the art, certain conservative amino acid substitutions can be made in these peptides without affecting their immunological activity. Specifically, for example, FIG. 1 shows that even in the highly conserved region of VP7 at positions 275-295, the four strains illustrated show some differences; at position 278, for example, Val, Ala, and Thr appear to be interchangeable; at position 281 Val and Thr; at position 284, Ile and Met. Thus, such conservative changes, especially with regard to relatively nonpolar amino acids Thr, Met, Val, Ile, Leu, and Ala, appear to be tolerated. This is also demonstrated in Examples 7 and 8 wherein the apparent immunogenicity and trypsin susceptibility of the VP4 subunit 232-255 is not altered by the substitution of alanine residues in the synthesized peptide for the valine residues in the native protein. Accordingly, the designations "232-256,""275-295, " etc., designate not only those sequences which occur natively in the various serotypes of rotavirus, but also include conservative amino acid substitutions of the type just mentioned, where the nonpolar residues set forth above are readily interchangeable.
Furthermore, these designations include both the discrete peptide referred to, and these peptides which are included within larger proteins wherein the remainder of the sequence is not derived from the corresponding rotavirus protein. Thus, for instance, the designation "275-295" includes proteins which contain this sequence, but wherein the additional sequence is nowhere found in the VP7 protein of any rotavirus.
A typical occurrence of such additional peptide lies in the synthesis of extended forms of the relevant antigenic portion by sequence intended to facilitate linkage to a carrier. Commonly a cysteine residue may be added to the N- or C-terminus or even inserted within the relevant sequence (see, for example, Silversides et al., J Reprod Immunol (1988) 13:249-261) to provide a sulfhydryl group for reactivity to commercially available linkers such as those available from Pierce Chemical Co., Rockford, Ill. As the Silversides article shows, even interruption of the antigenic sequence with the cysteine residue does not destroy the antigenic or immunogenic properties of the peptide. The cysteine residue linked to the N- or C-terminus may also be spaced from the antigenic region by one or more amino acid residues, usually those of, for example, alanine or glycine, which have relatively inconsequential sidechains. These extensions are also included in the illustrated peptides below.
Furthermore, these peptides include embodiments wherein the relevant antigenic region, denoted by the numbers, is present in a repeated motif, either a tandem repeat directly coupled through amide linkages or separated by additional nonrotavirus derived sequence. The repetition of the relevant antigenic sequence or the inclusion of additional nonrotaviral peptide as a fusion protein in many cases enhances the immunogenicity of the peptide.
Consistent with the foregoing, a peptide which consists essentially of an amino acid sequence "substantially equivalent" to positions 275-295 of rotavirus VP7 viral protein includes peptides which have the sequence of amino acids 275-295 of any naturally occurring rotavirus, as well as such peptides wherein one or more nonpolar amino acids has been replaced by a conservative substitute from among the group set forth above, and which retain the antigenic characteristics of the naturally occurring sequence. By "antigenic characteristics" is meant the ability to crossreact with antibodies raised against the naturally-occurring sequence. "Consists essentially of" refers to the possibility that the peptide contains 1-4 additional amino acids (e.g., cys) which facilitate conjugation to carrier as illustrated in the examples below.
Similar definitions apply with respect to the other four subunit peptides of the invention.
By the term "protein having as its sole antigenic determinant the amino acid sequence substantially equivalent to positions 275-295 of rotavirus VP7" is meant a protein wherein the sequence represented by positions 275-295, defined as set forth above, is the only rotavirus sequence of the parent protein (in this case VP7) included in the protein. Thus, such proteins would include longer chain moieties where additional, non-VP7 sequence is included along with either the sequence found in these positions in wild-type VP7, or the conservatively substituted, antigen characteristic retaining sequences described above. Such additional protein might include, for example, a binding protein as described in examples 5 and 6, an additional fusion protein derived from bacteria which might act as an immunogenic carrier, or additional sequence which would be useful in purification, etc. As above, similar definitions apply with respect to the other four subunit peptides of the invention.
The invention subunit peptides, as described above, are useful as vaccines for protection of animal and avian subjects against infection by rotavirus. As these invention peptides represent relatively short portions of the viral proteins from which they are derived, it is generally preferred, when the peptides per se are used, to enhance their immunogenicity by coupling them to carriers. Such coupling can be done using conventional protocols using covalent conjugation to traditional carriers such as BSA or keyhole limpet hemocyanin (KLH), the E. coli pilin protein K99 or preferably to the particulate form of VP6 from rotavirus. The conjugation can also be effected by creation of fusion proteins using recombinant techniques wherein the peptide which comprises the active portion is made a part of a larger recombinant peptide containing, other than the region represented as the epitope and described herein, only nonrotaviral sequences. Furthermore, the active epitopic regions can be prepared as tandem repeats. In addition, the peptide active ingredients can be fused to, or otherwise conjugated to a binding peptide for protein/protein binding to the VP6 carrier as described in the above-referenced copending applications and as wet forth hereinbelow.
In addition to the peptide active ingredient which may be conjugated to carrier, invention compositions may include an immunostimulant or adjuvant, such as complete Freund's adjuvant, aluminum hydroxide, and liposomes. The active ingredients can be formulated using generally known methods to prepare pharmaceutically useful compositions such as those described in Remington's Pharmaceutical Science, Mack Publishing Co., Easton, Pa. (latest edition). These compositions contain an effective amount of the active ingredient peptide together with a suitable amount of carrier vehicle. Other descriptions of preparation of vaccine formulations may be found in "New Trends and Developments in Vaccine," Voller, A., et al., University Park Press, Baltimore, Md. (1978).
The vaccines can be administered in generally recognized manner, generally systemically through injection; however, other effective means of administration are included within the scope of the invention. Dosage levels depend on the mode of administration, the nature of the subject, and the quality of the carrier/adjuvant formulation. Typical amounts are in the range of 1 .mu.g-1 mg/kg. Preferred amounts are in the range of 50-100 .mu.g/kg. Multiple administration to immunize the subject is preferred, and protocols are those standard in the art adapted to the subject in question.
The invention peptides are also useful as diagnostic tools to detect the presence or absence of rotaviral infection. For use in such protocols, standard immunoassay procedures can be used to detect the presence of antirotaviral antibodies in a fluid sample from the subject to be tested. In these procedures, the sample is contacted with the peptide in order to form an immunocomplex, and the formation of the complex is then detected as a measure of the presence of antibodies. A wide variety of protocols including immuno-precipitation, agglutination, and solid support assays can be adapted to this utility.
For all of the foregoing utilities, varying amounts of cross-reactivity among strains and serotypes has been found, as will be clear from the examples below.
Therefore, the peptide subunits and proteins containing them may have variable efficacy depending upon the level of cross-reactivity with strains other than those from which they are specifically derived. It may be desirable in some instances to supply cocktails of specific sequences derived from more than one strain in order to provide cross-reactivity if desired.
The peptide subunits of the VP4, 232-255 and 240-248, also can be used for prophylactic protection or for therapy with respect to rotaviral infection. As illustrated in Examples 8 and 9 below, the peptide subunit represents the trypsin cleavage region of the VP4 and can compete with intact VP4 for the enzyme; the peptides are also demonstrated to be capable of plaque reduction and prophylactic protection of suitable subjects. Thus, prophylactic and therapeutic compositions containing peptides with these regions as the sole antigenic determinant or peptides consisting essentially of these sequences can be formulated according to standard art-recognized procedures for prophylaxis and therapy.
In general, administration of such therapeutic and prophylactic compositions is systemic, including administration by injection and transmucosal or transdermal administration, or the compositions can be administered orally. For oral administration, delivery in a formulation protective against the low pH of the stomach and/or the proteolytic action of the small intestine is desirable. Such formulations, such as enteric or capsular formulations may be found for example, in Remington's Pharmaceutical Sciences, (supra). Typical dosage ranges for prophylactic or therapeutic use of these subunits is in the range of 500 .mu.g/kg-500 mg/kg, preferably 500 .mu.g/kg-200 mg/kg, more preferably 50 .mu.g/kg-20 mg/kg. These are dosage estimates, and the actual range is determined by the nature of the subject, the level of the challenge, the mode of administration, and the judgment of the practitioner. Thus, dosage values outside the suggested range are also included within the scope of the invention.
The following examples are intended to illustrate but not to limit the invention.
EXAMPLE 1
Immunogenicity of the "14K" Fragment of VP7
The ability of the 14K subunit VP7 effectively to mimic the total protein effect when injected into mice was illustrated as follows:
A bovine rotavirus (isolate C486, subclone 13) was propagated in MA-104 cells and purified by centrifugation. The 14 kd polypeptide fragment was prepared by in situ enzyme digestion of the 38.2 kd glycoprotein as described by Cleveland, D. W., et al., J Biol Chem (1977) 25:1102-1106. A gel strip containing the 38.2 kd VP7 glycoprotein was placed into the well of a 5% stacking/20% resolving polyacrylamide gel. A 13 cm.times.1 cm gel strip was treated with papain (Calbiochem-Boehring, San Diego, Calif.) at a concentration of 130 .mu.g/cm of gel since this gave the best yield of the 14 kd polypeptide.
Prestained molecular weight markers were used in order to visualize the time of maximum resolution between the 14.3 kd and 18.4 kd markers. The 14 kd peptide fragment was then electroeluted from gel slices, and a protein determination performed. Confirmation of the authenticity and purity of the peptide was by examination of its profile on polyacrylamide gels and by its reaction with monoclonal antibody from hybridoma 11D12-6.
The electroeluted 14 kd polypeptide was then lyophilized and a portion of the preparation was conjugated to bovine serum albumin (BSA) as follows. One mg of peptide was dissolved in 125 .mu.l of 0.1 M PBS pH 7.4. The BSA solution was prepared by dissolving 1.25 mg BSA in 600 .mu.l 0.1 M PBS pH 7.4 and to this were added dropwise 250 .mu.l of a 2.5 M glutaraldehyde solution and the peptide solution consecutively over 15 minutes. The reaction mixture was gently agitated for 24 hours at room temperature and then dialyzed extensively against sterile distilled water. Lyophilization of the conjugated peptide yielded a pinkish powder which was stored in desiccant at -20.degree. C.
Groups of ten mice (Charles River, Wilmington, Mass.) were immunized with either the unconjugated 14 kd peptide, BSA-conjugated 14 kd peptide, infectious double-shelled virus, or purified VP7 according to the protocol outlined in Table 1.
TABLE 1__________________________________________________________________________Schedule for Mice Immunized with 14K Peptide, VP7 and Infectious VirusGroups/Immunogen 1 DAYS51 61.sup.2 68 8 31 37 44__________________________________________________________________________A. Unconjugated 14 kd Prebleed 13.6 .mu.g; 13.6 .mu.g; Bleed 13.6 .mu.g; Bleed 0.675 .mu.g Bleed I.P.; F.I. I.P.; F.C..sup.1 I.P.; F.I I.P.; F.I.B. Conjugated 14 kd " 13.6 .mu.g 13.6 .mu.g " 13.6 .mu.g " 0.675 .mu.g " I.P.; F.I. I.P.; F.C. I.P.; F.C. I.P.; F.I.C. Glycoprotein VP7 " 4.5 .mu.g 4.5 .mu.g " 4.5 .mu.g " 0.675 .mu.g " I.P.; F.I. I.P.; F.C. I.P.; F.C. I.P.; F.I.D. Infectious virus " 0.675 .mu.g 0.675 .mu.g " 0.675 .mu.g " 0.675 .mu.g " I.P.; F.I. I.P.; F.C. I.P.; F.I. I.P.; F.I.E. Negative Control " saline; saline; "saline;" E.sub.1 -0.675 .mu.g " I.P.; F.I. I.P.; F.C. I.P.; F.I. I.P.; F.I. E.sub.1 -saline; " I.P.; F.I.__________________________________________________________________________ .sup.1 The quantities given are per mouse (10 mice per group); I.P. = intraperitoneal; F.C. = Freund's Complete Adjuvant. .sup.2 All mice, except 5 mice in group E.sub.2 were boosted with infectious virus.
The quantities of antigen to be administered were determined on an equimolar basis. Antibody responses to the different antigens were characterized by ELISA and immunoblot ELISA using bovine rotavirus (isolate C486 subclones 12 and 13) as the antigen and by serum neutralization assays.
As illustrated in FIG. 4 (upper panel), there was a significant antibody response to all the antigens used. Noteworthy is the similarity in response between the total 38.2 kd VP7 glycoprotein and the 14 kd peptide fragment. It also appears that conjugation of the 14 kd polypeptide to a carrier was not necessary to induce a good antibody response. This may be due to the large size of the polypeptide fragment thereby increasing the probability of its containing both B-cell and T-cell determinants.
To investigate the possibility of the 14 kd fragments priming an immune response, animals which had been immunized with the 14K fragments were boosted at 61 days with infectious, double-shelled virus. These animals showed an additional, but minor, response after the infectious virus was administered (68 days).
The antibodies produced in the foregoing protocol had neutralizing ability. Sera from all groups administered 14 kd peptide, VP7, or virus possessed neutralizing antibodies (FIG. 4, lower panel). The best response was produced by animals immunized with infectious virus (Group D). Total antibody titers are measured by ELISA and neutralizing antibody titers were similar for both the conjugated and unconjugated form of the 14 kd peptide.
At 68 days, after all the groups had been exposed to infectious virus, the neutralizing antibody titer increased slightly over that seen at 51 days, suggesting that each subsequent exposure further stimulates the immune response, or alternatively, there may abe other antigens in the infectious virus that are capable of inducing a neutralizing response. The presence of antibodies to the 45 kd protein VP6 was shown by immuno-blot ELISA reactions at 68 days; however, antibodies to the 84 kd VP4 protein could not be detected.
Immunoblot ELISA reactions of sera from selected animals in each group at 37, 51 and 68 days showed that all the sera, except those obtained prior to immunization and the negative control group (E), possessed antibodies to VP7. Antipeptide antibodies produced to 14 kd peptide from clone 13 were also immunoreactive with VP7 from clone 12 although the mRNA encoding VP7 from these species is not identical. The similar intensity displayed by the reaction of the glycoprotein species with antipeptide antibodies suggests that the 14 kd polypeptide may represent an immunodominant region of the glycoprotein.
EXAMPLE 2
Localization of the 14 kd Peptide
The 14 kd peptide is characterized in that it has i) a carbohydrate moiety, ii) extensive disulfide bridging, iii) relatively conserved region(s) among different rotavirus serotypes, iv) hydrophilic areas, and v) potential immunogenic regions. In addition, the cleav-age patterns obtained by partial proteolysis of the glycoprotein using chymotrypsin, S. aureus V8 protease, papain and cyanogen bromide permitted the localization of the fragment from the known amino acid sequences shown in FIG. 1. The amino acid sequence of Nebraska calf diarrhea virus (NCDV bovine rotavirus), which exhibits high nucleic acid homology with the C486 bovine rotavirus and is of the same serotype, was used to map the 14K polypeptide fragment to the region spanning amino acids 165-295. The position of this fragment is shown boxed in this figure.
EXAMPLE 3
Subunit Immunogens of VP7
A hydrophilicity plot of the corresponding NCDV glycoprotein identified several hydrophilic regions within this area. Based on this, four peptides, corresponding to amino acid residues 175-183; 179-183 and 251-259 spliced together; 247-259; and 275-295 of bovine rotavirus VP7 were synthesized by the solid-phase peptide synthesis method of Merrifield.
The specific amino acid sequence of each peptide is as follows:
__________________________________________________________________________Peptide 175-183: Tyr-Gln-Gln-Thr-Asp-Glu-Ala-Asn-Lys (SEQ ID NO: 1)Peptide (179-183)-(251-259): Asp-Glu-Ala-Asn-Lys-Lys-Leu-Gly-Pro-Arg-Glu-Asn-Val-Ala (SEQ ID NO: 2)Peptide 247-259: Arg-Asn-Cys-Lys-Lys-Leu-Gly-Pro-Arg-Glu-Asn-Val-Ala (SEQ ID NO: 3)Peptide 275-295: Pro-Thr-Thr-Ala-Pro-Gln-Thr-Glu-Arg-Met-Met-Arg-Ile-Asn-Trp-Lys-Lys-Trp-Trp-Gln-Val. (SEQ ID NO:__________________________________________________________________________4)
The purity of each peptide was assessed using thin-layer chromatography and reverse-phase high-performance liquid chromatography. Fast atom bombardment mass spectrometry was used to confirm molecular weights.
In addition, the foregoing were coupled to an N-terminal Cys residue to facilitate coupling to carrier.
The reactivity and specificity of the synthetic peptides were determined by ELISA using either anti-VP7 monospecific VP7 serum or monoclonal antibodies specific for the various regions of VP7 and by adsorption blocking assays. Table 2 shows the results of the ELISAS. As shown in the table, while all of the peptides were immunoreactive with the antiserum, only the peptides representing positions 247-259 and 275-295 were specifically immunoreactive with monoclonals directed to particular determinants.
TABLE 2__________________________________________________________________________Reactivity.sup.a of Monoclonal Antibodies and Monospecific SerumWith Synthetic Peptides of the 14K Fragment of VP7 SYNTHETIC PEPTIDES p174-183 p(179-183)-(252-259) p247-259 p275-295__________________________________________________________________________Monospecific anti- 2,500.sup.a 5,000 1,000 1,250glycoprotein (VP7)serumMonoclonal antibodies4B5-5 50 50 5,000 5011D10-4 10 250 4,000 10011D12-6 10 50 100 8,50010D207 10 50 20 10,000__________________________________________________________________________ .sup.a Antibody titers were determined by ELISA and are expressed as the reciprocal of the dilution giving a 50% end point.
FIG. 5 shows the results of the assay for ability of the peptides to inhibit attachment of virus to MA104 cells; again, only peptides representing positions 247-259 and 275-295 were able to block virus attachment to these cells.
For testing immunogenicity, the peptides were conjugated to carrier. Peptide 175-183 was conjugated to keyhole limpet hemocyanin (KLH) via a bis-diazotized toluidine linkage that produces N-terminally bound peptides. The other three peptides were conjugated to KLH via N-maleimidobenzoyl-N'-hydroxysuccinimide ester through the N-terminal Cys residue producing N-terminally bound peptide conjugates. Each of the conjugates was administered to groups of 10 CD-1 mice according to the schedule outlined in Table 3.
TABLE 3______________________________________Immunization Schedule for Mice Injectedwith Synthetic Peptides Within 14K of VP7GroupDesignation 0 1 2 3______________________________________1 Pre- -100 .mu.g; -- --p175-183 bleed FC.sup.a2 Pre- -100 .mu.g; -- --p(179-183)- bleed FC(251-259)3 Pre- -100 .mu.g; -- --p247-259 bleed FC4 Pre- -100 .mu.g; -- --p275-295 bleed FC5 Pre- -25 .mu.g; FC -- --p175-183 bleed -25 .mu.g; FCp(175-183)-(251-259) -25 .mu.g; FCp247-259 -25 .mu.g; FCp275-2956 Pre- -1.6 .mu.g; FC -- --Infectious bleedVirus7 Pre-saline; FC -- --Controls bleed______________________________________GroupDesignation 4 5 6 7______________________________________bleed --bleedbleedp175-183 -100 .mu.g; -100 .mu.g; FI.sup.a FI2bleed --bleedbleedp(179-183)-(251-259) -100 .mu.g -100 .mu.g; FI FI3bleed --bleedbleedp247-259 -100 .mu.g; -100 .mu.g; FI FI4bleed --bleedbleedp275-295 -100 .mu.g; -- -100 .mu.g; FI FI5bleed --bleedbleedp175-183 -25 .mu.g; FI -25 .mu.g; FI -25 .mu.g; FIp(175-183)-(251-259) -25 .mu.g; FI -25 .mu.g; FI -25 .mu.g; FIp247-259 -25 .mu.g; FI -25 .mu.g; FI -25 .mu.g; FIp275-295 -25 .mu.g; FI -25 .mu.g; FI -25 .mu.g; FI6bleed --bleedbleedInfectious -1.6 .mu.g; FI -1.6 .mu.g; FI -1.6 .mu.g; FIVirus7bleed --bleedbleedControlssaline; FIsaline; FIsaline; FI______________________________________ .sup.a FC = Freund's Complete Adjuvant; FI = Freund's Incomplete Adjuvant.
Each mouse in Groups 1 to 4 of Table 3 was given 100 .mu.g of each KLH-conjugated peptide in Freund's adjuvant. Group 5 was given 25 .mu.g of each of the four KLH-conjugated peptides in Freund's Adjuvant. Group 6 received 1.6 .mu.g of infectious double-shelled rotavirus and Group 7 represented the negative control group which received saline plus Freund's Adjuvant. The antigen preparations were administered three times over a six-week period and mice were bled prior to each immunization.
The sera were titrated using ELISA with either double-shelled rotavirus or to the individual peptides which had been used for immunization. In FIG. 6, all of the peptides were capable of eliciting an antibody response which was antigenic to the virus (upper panel) or to the peptide itself (lower panels).
EXAMPLE 4
Production of Neutralizing Antibodies by VP7 Subunits
The sera obtained in Example 3 were tested for their ability to neutralize the infectivity of the bovine rotavirus isolate C486 using a standard 50% plaque reduction assay. In this assay, virus dilutions representing 30-50 PFU were mixed 1:1 with various dilutions of antibody and incubated for 1 hour at 37.degree. C. Virus attachment to MA104 monolayers was allowed to proceed at 37.degree. C. for 2 hours before the virus inoculum was removed; the cells were washed with MEM and then overlaid with 1.6% Bacto-agar (Difco) diluted in MEM and supple-mented with 5 .mu.g of pancreatin per ml, 0.7% of a 1:1000 neutral red stock solution, and 0.1% DEAE-dextran. Plaques appeared after 5 to 6 days of incubation at 37.degree. C.
As shown in FIG. 7, peptide 247-259, peptide 275-295 and the mixture of the four peptides induced virus-neutralizing antibodies which increased after each immunization.
A passive antibody transfer experiment was also used to predict ability to raise protective responses. Monoclonal antibody 10D2-7, which specifically recognizes synthetic peptide 275-295 (Table 2) was used to provide passive protection. The protocol and results of this study are outlined in Table 4.
TABLE 4______________________________________Passive Antibody Transfer of Monoclonal Antibody 10D2-7GroupDesig- Time 0.sup.a Time 1.sup.a Titer.sup.b Diar-nation Preparations Preparations (PFU/mL) rhea.sup.c______________________________________I 1:50 dilution 5 .times. 10.sup.6 3.5 .times. 10.sup.2 .+-. of Mab 10D2-7 PFU/ml mouse PFU/ml rotavirusII 1:50 dilution of MAB MEM 5 .times. 10.sup.1 - 10D2-7 mixed with PFU/ml 5 .times. 10.sup.6 PFU/ml of mouse rotavirus 1 hour prior to administrationIII MEM 5 .times. 10.sup.6 PFU/mL 4 .times. 10.sup.5 + mouse rotavirus PFU/ml +IV MEM MEM 0 -______________________________________ .sup.a Time 0 and Time 1 preparations were made as described above. 100 .mu.l of the preparations were administered by tubing to the stomach of each neonate. .sup.b PFU/ml = plaqueforming units of rotavirus per ml of intestinal homogenate. .sup.c Diarrhea was assessed by the color and consistency of the fecal material compared to the control groups (III and IV).
Four groups each consisting of ten 7-day-old mice were first separated from their mothers for 2 hours and then given the indicated Time 0 preparations by tubing to the stomach. Approximately 1 hour later they were given the Time 1 preparation. The mice were kept at 33.degree. C. for 8 hours with constant monitoring of fecal consistency. After 8 hours, the mice were sacrificed and their intestines removed and pulverized. The amount of infectious virus in the intestine was determined by 50% plaque-reduction assay.
Mice in Group III which did not receive mono-clonal antibody were not protected. They became diarrhetic and had 5 logs of rotavirus in intestinal homogenates prepared 8 hours after challenge. There was a significant reduction in the amount of diarrhea and in the level of virus in intestinal homogenates of mice in Group I (given monoclonal antibody orally before challenge with virus) and Group II (challenged with a mixture of monoclonal antibody and virus).
EXAMPLE 5
Preparation of Conjugates with 275-295 VP7 Subunit
Additional peptides representing positions 275-295 of the VP7 protein were synthesized, which had minor modifications to facilitate conjugation to carrier. To facilitate incorporation with KLH, the 275-295 peptide set forth above in Example 3 was also prepared with a cysteine residue at its carboxy terminus. This peptide is designated 275-295C.
A second 275-295 peptide contains additional sequence at its amino terminus which permits protein-protein interaction with VP6 carrier. This additional peptide has the sequence: Cys-Gly-Ala-Ser-Arg-Asn-Ile-Val-Tyr-Thr-Arg-Ala-Gly-(275-295) (SEQ ID NO:6). The resulting peptide is designated herein BP-(275-295) (SEQ ID NO:6).
The 275-295C peptide was coupled to KLH using the procedure of Green, N., et al., Cell (1982) 28:477-487. Briefly, KLH (20 mg) in 1 ml of 0.01 M sodium phosphate buffer, pH 7.2, was stirred with m-maleimidobenzoyl-N-hydroxysuccinimide ester (MBS) (5.1 mg, 25.5 .mu.M dissolved in 500 .mu.l dimethylformamide) at room temperature for one hour. Unreacted MBS was removed by HPLC on Synchropak the GPC-100 gel filtration column (500.times.10 mm ID), equilibrated with 0.1 M potassium phosphate buffer, pH 6.0, and the conjugate was eluted with the same buffer. The maleimido group bound to KLH was estimated graphically by adding aliquots of L-cysteine to the conjugate and reacting excess cysteine with Ellman's reagent. The 275-295C peptide in 200 .mu.l of 0.1 M PBS, 0.72, was added to a solution of the KLH-MBS conjugate (1 ml) containing approximately 0.5 .mu.M of the maleimido group, and the pH was adjusted to 7.8 with 0.1 N NaOH. The mixture was stirred at room temperature for 12 hours and dialyzed against 0.1 M PBS buffer, pH 7.2. The resulting conjugate is designated 275-295C-KLH as the carrier is bound to the carboxy terminus of the peptide.
Conjugation to the VP6 carrier was achieved in several protocols. Recombinant VP6 used as carrier was prepared as follows:
The construction of recombinant Autographa californica nuclear polyhedrosis virus (AcNPV) containing gene 6 from BRV and the assembly of VP6 particles following infection of spodoptera frugiperda (SF9) cells is described by Redmond, M. J., et al., Mol Immunol (1990, in press). Briefly, genomic RNA extracted from purified bovine rotavirus strain C486 was used to produce cDNA, which was ligated into the PstI site of pBR322 and used to transform E. coli strain DH1. The resulting colonies were probed with radiolabeled cDNA prepared from purified genomic RNA segment 6 as template. The gene 6 cDNA was tailored and ligated into the baculovirus transfer vector pAc373. Rotavirus gene was integrated into the genome of A. californica by homologous recombination in S. frugidperda (SF9) cells as outlined by Summers, M. D., et al., Texas Agr Exptl Sta Bull (1987) 1555:26-27. Recombinants were identified by plaque hybridization using radiolabeled VP6 cDNA described above, plaque purified and analyzed for expression of recombinant gene 6 produced proteins by SDS-PAGE analysis and Western blot.
The recovered virus containing gene 6 was used to infect SF9 cells. Following incubation for 72 hours at 27, the cells were lysed in a 2 ml bicarbonate buffer, pH 7.5, containing 0.05% triton X-100 and 0.2 trypsin inhibitor units per ml, and cellular debris was removed by centrifugation at 1500 g. The supernatant was dialyzed against 0.1 M glycine buffer, pH 2.4, for 24 hours. The dialysis solution was exchanged for 0.01 M citrate buffer, pH 4.0, for 24 hours, and then for 0.01 M tris-HCl, pH 7.4. Dialysis was continued until the protein suspension became clear. The quality of the VP6 spheres produced by this method was determined by electronmicroscopy and purity confirmed by SDS-PAGE.
In one approach, the BP-(275-295) was conjugated to VP6 through protein-protein interaction. In this protocol, the BP-(275-295) and the VP6 carrier were mixed at a 10:1 (w/w) peptide:carrier ratio in 0.1M PBS, pH 6.5 and incubated for 30 minutes at 37.degree. C. The binding peptide and VP6 automatically associate to provide the conjugate, designated VP6-(BP-275-295).
The 275-295 peptide per se was also coupled to VP6 using the routine carbodiimide (EDCI) coupling procedure using a coupling ratio of 10:1 (w/w). This conjugate is designated herein VP6-(275-295).
In all cases, coupling to VP6 was analyzed using SDS-PAGE under nonreducing conditions, indicating an increase in the molecular weight of carrier protein VP6 corresponding to the molecular weight of the coupled peptide. In Western blot assay, the bands reacted with anti-VP6 and anti-rotavirus sera.
In addition to the foregoing, conjugates were prepared using the K99E. coil pilin peptide and the 275-295 VP7 subunit. This conjugate was prepared by first isolating the K99 from E. coli pilin by urea extraction and ammonium sulfate precipitation. The conjugation was conducted using the carbodiimide method to yield a conjugate with a peptide:carrier ratio of 3.5:1 as determined by UV spectroscopy, amino acid analysis and gel electrophoresis.
EXAMPLE 6
Protection of Neonates
In initial experiments, the K99-(C275-295) conjugate was used to immunize cows prior to parturition-using 100 .mu.g of the conjugate in DDA-aluminum hydroxide gel. (C275-295) represents the peptide having a Cys residue at its N-terminus and conjugated to carrier through this residue. After one immunization, anti-rotavirus titers determined by ELISA increased from 8-10,000 in two tested cows, to 100,000. No effect on the anti-rotavirus titers was obtained by injection of the carrier alone.
In further experiments, these conjugates as well as the conjugates prepared as set forth in Example 5 were used in an immunization protocol to show their ability to protect mice against challenge. The protocol is as follows: In a primary immunizing dose, the conjugate was emulsified with Freund's Complete Adjuvant;
in the second and third immunizations, emulsification was with Freund's Incomplete Adjuvant, using equal volumes of conjugate and adjuvant in every case. All doses were 50 .mu.g of conjugate. Groups of mice were immunized intramuscularly three times before and after breeding.
The first immunization was given at 7 weeks of age, and the second and third at two-week intervals. Litters were born when the mice were 12-14 weeks old. The mice used were Harlan Sprague-Dawley CD-1 rotavirus-free mice purchased at six weeks of age and weighing 25-30 g. The mice were verified to be seronegative for rotavirus antibodies.
Following birth, the mouse pups were allowed to suckle their dams and were challenged at 7 days of age with one of four rotavirus isolates: Bovine rotavirus strain C-486 (serotype 6), simian rotavirus SA11 (serotype 3), human rotavirus DS-1 (serotype 1), and Wa (serotype 2). All except C-486 were obtained from Dr.
Marta Sabara (Praxis Biologics, New York). C-486 was adapted to grow in MA104 cells (Babiuk, L. A., et al., J Clin Microbiol (1977) 6:610-617).
The virus used for challenge was grown in MA104 cells, harvested and concentrated by the method described by Ijaz, M. K., et al. (Antiviral Res (1987) 8:283-298). The challenge dose was approximately 10.sup.4 pfu/mouse, unless otherwise noted, suspended in 100 .mu.l MEM and administered by intubation of the stomach with a soft, flexible plastic feeding tube. Trypan dye was used to assess accuracy of intubation.
The administration of 100 .mu.g of the K99-(C275-295) or KLH-(C275-295) peptide in the presence of either FCA or DDA was evaluated using this protocol. The K99-(C275-295) vaccine gave partial protection against challenge in neonatal mice following three immunizations of their dams resulting in diarrhea scores of ++ (diarrhea scores of ++++ resulted where there was no immunization). Complete protection, comparable to administration of whole virus, was given when KLH-(C275-295) was used. In this experiment, a very high challenge dose (10.sup.6 -10.sup.7 pfu) was used; thus the level of protection afforded is quite significant.
In a second set of determinations, the protective effect of the vaccines prepared from the conjugates described in Example 5 was evaluated using two criteria--the prevention of diarrhea in the pups, and the prevention of decreased xylose adsorption from the intestine.
The appearance of diarrhea was scored clinically up to 72 hours postchallenge using clinical scores as follows:
(0) no sign of diarrhea in live mice, or on necropsy;
(+) no external signs of diarrhea but semi-liquid colon contents at autopsy;
(++) fluid was apparent on palpation of the abdomen and the colon was filled with liquid feces and gas;
(+++) the external anal region was soiled with feces and intestinal fluid was present on palpation;
(++++) liquid feces were present around the anal region and on palpation of the abdomen intestinal fluid was present and oozed from the anus; severe dehydration, internal liquid content in colon and caecum and distention due to accumulation of gas.
Small intestinal infection was measured by a xylose adsorption test 72 hours postchallenge. Mice were given 100 .mu.l of 5% w/v solution of xylose by intubation orally as described above. Two hours later, they were sacrificed by decapitation and blood collected in heparinized Hematocrit tubes. Plasma was collected and assayed for D-xylose as described by Ijaz, M. K., et al., J Virol Meth (1987) 18:153-157. Decreased xylose absorption is an indication of intestinal damage due to virus infection.
The results of the immunization are shown in Tables 5 and 6. Table 5 shows the protective effect as measured by clinical criteria; Table 6 shows the results as judged by the xylose absorption test.
TABLE 5______________________________________Protection Against Infection (Diarrhea) Diarrheal Score Following Challenge with Rotavirus IsolateGroups Immunogen Wa DS-1 SA-11 BRV______________________________________1 Placebo +++ +++ ++++ ++++2 VP6 ++ ++ +++ ++3 BRV 0 0 ++ 04 275-295C ND ND ++++ +++5 275-295C-KLH 0 + ++++ ++6 VP6-(C275-295) 0 0 ++++ +7 VP6-(BP-275-295) ++ 0 +++ ++______________________________________ ND = Not done; baby mice were cannibalized by mother.
As shown in Table 5, protection was not achieved with respect to the SA11 serotype, even with whole BRV virus. However, in strains Wa and DS-1, where whole BRV virus was protective, excellent protection was achieved using the 275-295 peptide, especially when conjugated to the VP6 or KLH carrier. Protection was also shown, though to a less complete extent, against challenge by BRV.
TABLE 6______________________________________Protection Against Infection (Xylose Absorption)Groups Immunogen Wa DS-1 SA-11 BRV______________________________________1 Placebo 65 63 54 602 VP6 68.6 67.2 58 63.73 BRV 110 112 69 1184 275-295C ND 60 53 595 (275-295C)-KLH ND 80 55 656 VP6 (275-295) 119 114 56 787 VP6-(BP-275-295) 89 102 59 65 Non-challenged 118 119 119 120 Control______________________________________
These results were confirmed using the xylose absorption assay as shown in Table 6. The levels of plasma xylose shown after challenge with the various viral strains for the VP6/BP-photo-275-295 conjugate are essentially identical to those achieved by vaccination with whole BRV. Again, the simian strain SA11 does not show cross-reactivity.
EXAMPLE 7
Subunit Vaccines Derived from VP4
The trypsin cleavage site of VP4 was identified at the location shown boxed in FIG. 2 by taking advantage of the known amino acid sequence of the protein, the nature of trypsin specificity, and the size of the fragments resulting from trypsin cleavage. According to these criteria, positions 232-255 inclusive were identified as comprising the trypsin cleavage site.
As shown in the figure, the sequence shown at the location of positions 232-235 in both the bovine C486 strain and the simian SA11 strain are identical; the position notations reflect those shown in the figure as the sequences are there disposed.
As seen in FIG. 2, the amino acid sequence in these positions of C486 strain and simian SA11 strain is Asn-Ile-Val-Pro-Val-Ser-Ile-Val-Ser-Arg-Asn-Ile-Val-Tyr-Thr-Arg-Ala-Gln-Pro-Asn-Gln-Asp-Ile-Val (position 229-252 of SEQ ID NO:16). If a synthetic peptide is constructed wherein Ala is substituted for all of the Val residues, the sequence of this peptide would be Asn-Ile-Ala-Pro-Ala-Ser-Ile-Ala-Ser-Arg-Asn-Ile-Ala-Tyr-Thr-Arg-Ala-Gln-Pro-Asn-Gln-Asp-Ile-Ala (SEQ ID NO:21).
A synthetic peptide designed to mimic this sequence but having some substitutions for ease of synthesis was constructed as follows:
______________________________________Asn-Ile-Ala-Pro-Ala-Ser-Ile-Val-Ser-Arg-Asn-Ile-Val-Tyr-Thr-Arg-Ala-Gln-Pro-Asn-Asp-Ile-Ala (positions 2-25 ofSED ID NO. 7).______________________________________
The synthesized protein also was extended with N-terminal cysteine not present in the native protein for ease in conjugation to carrier (SEQ ID No. 7). These peptides have substitutions of alanine for valines at positions 234, 236 and 255 of the native VP4 in FIG. 2 as shown. It is believed that valine and alanine are interchangeable at these positions with respect to the behavior of the peptide biologically.
For use as an immunogen, the synthetic peptide described was coupled to KLH and to VP6. The conjugation to KLH is conducted through the cysteine at the N-terminus under the protocol described for VP7 peptide in Example 5 above. The conjugate is designated KLH-(232-255).
The coupling of the 232-255 peptide to VP6 was conducted by protein-protein interaction. The VP4 subunit peptide has the properties of a binding peptide intrinsically, shown as follows.
When 100 .mu.g of the peptide was reacted with 2 .mu.g purified virus for 30 minutes at 37.degree. C., the VP6 45 kd capsid protein from the virus showed a laddering effect upon polyacrylamide gel electrophoresis; at 25 .mu.g of the peptide, the laddering was not apparent. Laddering occurred both at the VP6 monomeric molecular weight of 45 kd and at the aggregate molecular weights of 90 kd and 135 kd regions. The increment in the ladder steps matched the MW of the 232-255 peptide. Trypsin treatment of the virus/peptide complex reduced the ladder to a virus profile identical with that of the trypsin-treated virus. The ladder could be detected with antisera produced against the synthetic peptide.
The 232-255 VP4 synthetic peptide maintained its reactivity with VP6 under conditions where samples were treated with urea sample buffer for 30 minutes at 37.degree. C., and when samples were treated with Laemmli buffer without .beta.-mercaptoethanol (BME) but with boiling. However, when BME was included in the sample buffer and the sample was boiled prior to electrophoresis, the ladders in both the 45 kd and 90 kd regions disappeared. Thus, secondary structure specified by disulfide bridging is apparently necessary to maintain the complex.
The 232-255 VP4 peptide was mixed with the VP6 carrier prepared as described above in 0.1 M PBS, pH 6.5, for 30 minutes at 37.degree. C. The weight ratio of peptide to carrier was 10:1 (w/w). The resulting conjugates were designated VP6-(232-255).
The KLH conjugate, prepared as described above, was initially used in standard immunization protocols in mice and the 50% plaque reduction assay described above was used to determine the neutralizing ability of the resulting antiserum. A 50% reduction in plaques occurred at a 5000-fold dilution of the resultant antiserum. A 10,000-fold dilution of monoclonal antibody immunoreactive with the synthetic peptide also showed 50% plaque reduction.
In addition to testing for neutralization, the ability of the VP4 subunit peptide to protect against infection was assessed as described for the VP7 subunit peptides in Example 6. The conjugates were administered at 50 .mu.g dosages emulsified with Freund's Complete Adjuvant in the primary immunization and with Freund's Incomplete Adjuvant in the second and third immunizations conducted at 2-week intervals. The antisera produced reacted specifically both with reduced and nonreduced VP4. Both VP6-(232-255) and KLH-(232-255) showed complete protection against infection as measured by clinical (diarrhea) data with respect to the Wa and DS-1 strains. The VP6 conjugate also showed complete protection against BRV and SA11 infection. Partial protection was shown in these strains by the KLH conjugate. Furthermore, when mixed with VP6-(BP275-295), VP6-(232-255) gave complete protection with respect to all strains. These data were confirmed by the D-xylose adsorption assay, as shown by the results in Table 7.
TABLE 7______________________________________Protection Against Infection (Xylose Adsorption) Plasma D-Xylose Concentration (.mu.g/100 ml) Following Challenge with Rotavirus Isolate*Groups Immunogen Wa DS-1 SA11 BRV______________________________________10 KLH-(232-255) 110 114 70 7711 VP6-(232-255) 112.5 110 108 11312 VP6(232-255) + 117 111 109 119 VP6 BP (275-295) Non-challenged 118 119 119 120 Control______________________________________
As shown in Table 7, the VP6-(232-255) conjugate gave complete protection against infection by all strains.
EXAMPLE 8
Therapeutic Activity of the VP4 Subunit (232-255)
Susceptibility of the synthetic peptide to trypsin was confirmed by reaction with trypsin followed by electrophoresis. The peptide was shown to be cleaved by trypsin in a dose-dependent manner. It was also established that the peptide could compete with intact VP4 for the enzyme. This was determined by measuring the ability of increasing concentrations of the synthetic peptide to reduce the amount of VP4 cleaved into the two products of molecular weight 60 kd and 28 kd. As shown in FIG. 8, increasing amounts of synthetic peptide provided protection against VP4 cleavage. Initially, trypsin was used in a quantity which resulted in complete cleavage of VP4 (25 .mu.g (232-255)/25 .mu.g VP4); when the synthetic peptide was increased to 200 .mu.g, intact VP4 is evident.
The 232-255 VP4 peptide was also capable of plaque reduction in a dose-dependent manner when mixed with infectious virus. In a protocol similar to a standard plaque reduction assay, MA104 cells were treated with 100 pfu of the virus in the absence of and in the presence of 100 .mu.g, 200 .mu.g and 300 .mu.g of the 232-255 peptide. At high concentrations of the peptide, plaques were seen in the test wells only 5-6 days after plaques in the control wells were seen, and were very small and diffuse.
EXAMPLE 9
Prophylactic Activity of the VP4 Subunit (232-255)
The 232-255 peptide synthesized in Example 7 was diluted serially in Eagle's Minimal Essential Medium. The peptide solutions of various dilutions were administered in 100 .mu.l dosages to neonatal mice by oral administration. The pups were born of rotavirus-free strain CD-1 dams and administration was at 7 days of age (when the pups weigh about 4 g). Approximately one hour later the mice were challenged with 10.sup.4 pfu of BRV strain C486. Clinical protection was scored as described in Example 6. Diarrhea was scored clinically as well as on necropsy, and plasma D-xylose was determined by administering 100 .mu.l of 5% w/v D-xylose solution, sacrificing the mice two hours later, collecting the blood and determining plasma D-xylose concentration as described above. Virus titers were determined in the mouse intestines by suspending in MEM and homogenizing for virus titration. Mice which received no challenge had plasma D-xylose levels of 119 .mu.g/100 .mu.l and zero viral titers. The results are shown in Table 8.
TABLE 8______________________________________Passive Protection by 232-255 of VP4Peptide Plasma VirusAdministered Diarrheal D-Xylose Titre(.mu.g) Score (.mu.g/100 .mu.l) (PFU/ml)______________________________________100 +++ 92 1.2 .times. 10.sup.3250 ++ 70 4.0 .times. 10.sup.2500 0 101 01000 0 112 00 ++++ 57 5 .times. 10.sup.3______________________________________
As shown in Table 8, administered peptides in the amount of 500-1000 .mu.g completely protected the mice against viral infection.
EXAMPLE 10
VP4 Subunit Vaccine 240-248
A contracted subunit of the VP4 peptide 232-255 of the foregoing examples was synthesized using solid phase synthesis. This peptide corresponds to amino acids 240-248 of BRV strain C486 with an N-terminal extension to facilitate conjugation to carrier. Thus, the peptide has the amino acid sequence: Cys-Gly-Ala-Ser-Arg-Asn-Ile-Val-Tyr-Thr-Arg-Ala. (SEQ ID NO:8)
The Cys-Gly-Ala at the N-terminus contains a Gly-Ala spacer and an N-terminal cysteine. This peptide was purified using reverse-phase HPLC before conjugation to carrier.
VP6 carrier was prepared and induced to form spheres as described hereinabove in Example 5. Conjugation to carrier was effected by protein-protein interaction wherein the VP6 carrier protein and the peptide were mixed at 1:10 (w/w) carrier:peptide ratio in 0.1 M PBS, pH 7.4 and incubated for 30 min. at 37.degree. C. The resulting conjugate was verified by SDS-PAGE.
The conjugates were used in an immunization protocol in mouse dams as described in the mouse immunization portion of Example 6. Suckling seven-day-old mice from the immunized dams were challenged with rotavirus isolates at 10.sup.4 pfu per mouse and the morbidity and mortality were scored clinically as described; the intestinal dysfunction induced post-rotavirus infection was assessed by D-xylose absorption and the protection scores are based on both clinical scores and plasma D-xylose concentration.
C, or complete protection, corresponds to zero clinical score and xylose greater than 100 .mu.g/100 .mu.l;
P, or partial protection, corresponds to less than ++ clinical score and xylose greater than 10 .mu.g/100 .mu.l; and
N, or no protection, corresponds to greater than ++ clinical score and xylose concentration less than 60 .mu.g/100 .mu.l plasma.
The results of this protocol with respect to several rotavirus strains are shown in Table 9.
TABLE 9______________________________________Protection by VP4 240-248 Conjugate Wa DS-1 SA-11 BRV______________________________________Placebo N N N NVP6 P P N PBRV C C P CVP6-(240-248) C C P C______________________________________
As seen in Table 9, complete protection was obtained with respect to strains Wa, DS-1 and BRV. The subunit provides comparable protection to that provided by the whole virus and better than that provided by carrier VP6 alone.
EXAMPLE 11
Therapeutic Activity of VP4 240-248
The peptide synthesized in Example 10 representing positions 240-248 of VP4 was shown to be effective in preventing plaque formation by rotavirus in permissive cells. The plaque assay was that described by Aha and Sabara, J Virol Methods (1990) 28:25-32, modified as follows. Replicate cultures of MA-104 cells were incubated with dilutions of peptide ranging from 30-600 .mu.g/ml for 1 hr at 37.degree. C. A peptide control consisting of the sequence 469-492 of bovine herpes virus type I glycoprotein gI was included with the range of dilutions. The cultures were washed with minimal essential medium (MEM). The cells were then incubated with 63 pfu of rotavirus strain C486 for 1 hr at 37.degree. C. and the remainder of the assay was conducted as described in the reference. The results showed that the VP4 240-248 peptide was effective in preventing plaque formation.
Furthermore, the 240-248 peptide blocks the attachment of rotavirus to susceptible cells. Bovine rotavirus strain C486 was produced in tissue culture by infection of MA-104 cells. The infected cells were pulsed for 1 hr with 25 .mu.Ci of .sup.35 S-labeled methionine and infection was allowed to proceed. The virus was then purified and concentrated by centrifugation in a sucrose gradient as described by Sabara et al., J Virol (1985) 56:1037-1040.
Replicate cultures of MA-104 cells were incubated with dilutions of peptides ranging from 30-600 .mu.g/ml for 1 hr at 37.degree. C. As above, the peptide control derived from gp gI was included with the dilution range. Cells were then washed with MEN and a total of 0.045 .mu.Ci (10.sup.4 cpm) of .sup.35 S-labeled virus was added to each culture. After incubation for 1 hr at 37.degree. C. in a humidified atmosphere containing 5% CO.sub.2, the cells were washed thoroughly and solubilized in 0.1 M PBS, pH 7.4 containing 0.1% SDS, 0.5% Nonidet P40, and 0.5% sodium deoxycholate. The samples were prepared for scintillation counting and incorporation of a radiolabel into the cultures was determined.
The results showed that samples incubated with at least 30 .mu.g (total) (300 .mu.g/ml dilution) of the peptide showed essentially no uptake of labeled virus.
Finally, hemagglutinating activity was measured using a modification of the method described by Kalica et al., J Clin Microbiol (1978) 7:314-315. (VP4 is believed to be the rotavirus hemagglutinating protein required for attachment.) Two-fold dilutions of the peptide were prepared with the starting concentration of 500 .mu.g/ml and human group O Rhesus-positive erythrocytes were added to each sample to produce a final concentration equivalent to 0.4% packed cell volume. After incubation for 2 hr, the tests were scored for agglutination. Peptide 240-248 was found to produce hemagglutination at 500 .mu.g/ml. Thus, the peptide may be an effective diluent of VP4 activity in situ.
EXAMPLE 12
VP6-Derived Subunit Vaccine
A subunit of the VP6 rotavirus protein was designed based on amino acid positions 40-60 inclusive. FIG. 3 shows the amino acid sequence of the VP6 protein of the strain SA11. The peptide corresponding to this subunit, modified to facilitate coupling was synthesized using standard solid phase techniques and has the structure:
__________________________________________________________________________ Thr-Met-Asn-Gly-Asn-Glu-Phe-Gln-Thr-Gly-Gly-Ile-Gly-Asn-Leu-Pro-Ile-Arg-Asn-Trp-Asn-Gly-Cys. (SEQ ID NO:__________________________________________________________________________9)
The Gly-Cys at the C-terminus is added to provide a linkage site.
The synthesized peptide itself was reactive in an ELISA with anti-VP6 monospecific serum and with several monoclonal antibodies known to be immunoreactive with the VP6 protein. These monoclonals, designated 1D7, 1B4 , 1B9 and 1D10 were mildly neutralizing in a plaque reduction assay and were immunoreactive with the 40-60 peptide at reciprocal dilutions of 5,000-8,000.
To test the immunogenicity and protective effect of the 40-60 VP6 peptide, the peptide was conjugated to KLH and E. coli pilin protein K99 using the procedures set forth above with respect to the VP7 subunit. Both conjugates were capable of raising significant anti-rotavirus ELISA titers after several immunizations. In addition, these conjugates were shown to be protective in mice. Female mice were immunized three times during a schedule of breeding and pregnancy wherein the last immunization was given two weeks prior to whelping, as described above. Immunizations were conducted using 100 .mu.g immunogen in the presence of either Freund's Complete Adjuvant, or dimethyl dioctadecyl ammonium bromide (DDA) adjuvant. The mouse pups were allowed to suckle and challenged at 7 days with bovine rotavirus. Morbidity, mortality and severity of diarrhea were scored over a 48 hour period following challenge; most diarrhea and morbidity was apparent within 3-5 hours following challenge.
Using the scoring system set forth above, (40-60)-KLH using FCA as adjuvant gave some protection as did K99-(40-60) in the presence of FCA (diarrhea score +, as compared to ++++ in KLH controls). K99-(40-60) in the presence of DDA gave almost complete protection by these criteria.
Finally, the VP6 40-60 subunit was tested for its ability to protect neonates against challenge in the same protocols described above with respect to the VP7 and VP4 subunits. The KLH-(40-60) conjugate was used in the same experiments for which the results are reported in Tables 5 and 6 above. The KLH-(40-60) results are shown in Table 10.
TABLE 10______________________________________ Wa DS-1 SA11 BRV______________________________________Diarrhea ScoreKLH-(40-60) + + ++++ ++Negative Control +++ +++ ++++ ++++BRV 0 0 ++ 0Xylose AbsorptionKLH-(40-60) 74 81 53 64Negative Control 65 63 54 60BRV 110 112 69 118Nonchallenged 118 119 119 120Control______________________________________
As shown in Table 10, the KLH conjugated 40-60 peptide gives partial protection to challenge by Wa and DS-1 strains, but little or no protection with respect to SA11 and BRV, as judged by clinical criteria. These results are consistent with those obtained using xylose absorption.
EXAMPLE 13
Effect of Carrier and Adjuvant
The KLH carrier (approximately 3500 kd) and K99 (approximately 19 kd) were compared using the VP7 275-295 subunit and the VP6 40-60 subunit. The conjugates were prepared through an N-terminal cysteine in each case. Mice were immunized with 100 .mu.g of the KLH and K99 conjugates of these peptides in an immunization protocol involving three immunizations. Table 11 shows the antibody titers against rotavirus of mice which were seronegative at the time of immunization. As shown in the table, the use of either KLH or K99 as a carrier gave comparable results, although K99 appeared to be slightly more immunogenic with respect to 40-60.
TABLE 11______________________________________Anti-Rotavirus ELISA Titers Following Immunization 2 Weeks Post 2 Weeks Post 2 Weeks Post Car- 1st 2nd 3rdPeptide rier Immunization Immunization Immunization______________________________________VP6-40-60 KLH 1,333 13,335 42,170 K99 13,335 31,623 74,990VP7-275-295 KLH 4,870 42,170 56,234 K99 7,500 23,713 56,234______________________________________
The effect of adjuvant was also tested, in comparing Freund's Complete Adjuvant (FCA) and dimethyl dioctadecyl ammonium bromide (DDA). The K99 conjugate with the VP7 275-295 subunit was tested on seronegative mice using 100 .mu.g of conjugate with either 0.1 ml FCA or 100 .mu.g DDA. The results are shown in Table 12; both adjuvants resulted in obtaining significant antirotaviral titers two weeks after the second immunization. These levels are comparable to those obtained using immunization with virus per se, without carrier which gave an ELISA rotavirus titer of 15,850 two weeks post-second immunization. The ability of the peptide to raise anti-rotavirus titers was dose-dependent; 1 .mu.g and 10 .mu.g immunizations did not provide significant anti-rotavirus titers.
TABLE 12______________________________________ELISA Titers Following Immunization Two Weeks Post Two Weeks Post First SecondAdjuvant Immunization Immunization______________________________________Freund's Complete Anti-rota 9 6,310Adjuvant Anti-K99 31,600 50,120Dimethyl dioctadecyl Anti-rota 89 7,495Ammonium Bromide Anti-K99 251,200 10,000,000______________________________________
__________________________________________________________________________# SEQUENCE LISTING- (1) GENERAL INFORMATION:- (iii) NUMBER OF SEQUENCES: 24- (2) INFORMATION FOR SEQ ID NO:1:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 9 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:1:- Tyr Gln Gln Thr Asp Glu Ala Asn Lys1 5- (2) INFORMATION FOR SEQ ID NO:2:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 14 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:2:- Asp Glu Ala Asn Lys Lys Leu Gly Pro Arg Gl - #u Asn Val Ala# 10- (2) INFORMATION FOR SEQ ID NO:3:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 13 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:3:- Arg Asn Cys Lys Lys Leu Gly Pro Arg Glu As - #n Val Ala# 10- (2) INFORMATION FOR SEQ ID NO:4:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 21 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:4:- Pro Thr Thr Ala Pro Gln Thr Glu Arg Met Me - #t Arg Ile Asn Trp Lys# 15- Lys Trp Trp Gln Val 20- (2) INFORMATION FOR SEQ ID NO:5:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 13 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:5:- Cys Gly Ala Ser Arg Gln Ile Val Tyr Thr Ar - #g Ala Gly# 10- (2) INFORMATION FOR SEQ ID NO:6:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 34 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:6:- Cys Gly Ala Ser Arg Asn Ile Val Tyr Thr Ar - #g Ala Gly Pro Thr Thr# 15- Ala Pro Gln Thr Glu Arg Met Met Arg Ile As - #n Trp Lys Lys Trp Trp# 30- Gln Val- (2) INFORMATION FOR SEQ ID NO:7:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 25 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:7:- Cys Asn Ile Ala Pro Ala Ser Ile Val Ser Ar - #g Asn Ile Val Tyr Thr# 15- Arg Ala Gln Pro Asn Gln Asp Ile Ala# 25- (2) INFORMATION FOR SEQ ID NO:8:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 12 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:8:- Cys Gly Ala Ser Arg Asn Ile Val Tyr Thr Ar - #g Ala# 10- (2) INFORMATION FOR SEQ ID NO:9:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 23 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:9:- Thr Met Asn Gly Asn Glu Phe Gln Thr Gly Gl - #y Ile Gly Asn Leu Pro# 15- Ile Arg Asn Trp Asn Gly Cys 20- (2) INFORMATION FOR SEQ ID NO:10:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 25 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:10:- Cys Asn Ile Val Pro Val Ser Ile Val Ser Ar - #g Asn Ile Ala Tyr Thr# 15- Arg Ala Gln Pro Asn Gln Asp Ile Ala# 25- (2) INFORMATION FOR SEQ ID NO:11:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 326 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:11:- Met Tyr Gly Ile Glu Tyr Thr Thr Ile Leu Th - #r Ile Leu Ile Ser Ile# 15- Ile Leu Leu Asn Tyr Ile Leu Lys Thr Ile Th - #r Asn Thr Met Asp Tyr# 30- Ile Ile Phe Arg Phe Leu Leu Leu Ile Ala Le - #u Ile Ser Pro Phe Val# 45- Arg Thr Gln Asn Tyr Gly Met Tyr Leu Pro Il - #e Thr Gly Ser Leu Asp# 60- Ala Val Tyr Thr Asn Ser Thr Ser Gly Glu Pr - #o Phe Leu Thr Ser Thr#80- Leu Cys Leu Tyr Tyr Pro Ala Glu Ala Lys As - #n Glu Ile Ser Asp Asp# 95- Glu Trp Glu Asn Thr Leu Ser Gln Leu Phe Le - #u Thr Lys Gly Trp Pro# 110- Ile Gly Ser Val Tyr Phe Lys Asp Tyr Asn As - #p Ile Asn Thr Phe Ser# 125- Val Asn Pro Gln Leu Tyr Cys Asp Tyr Asn Va - #l Val Leu Met Arg Tyr# 140- Asp Asn Thr Ser Glu Leu Asp Ala Ser Glu Le - #u Ala Asp Leu Ile Leu145 1 - #50 1 - #55 1 -#60- Asn Glu Trp Leu Cys Asn Pro Met Asp Ile Se - #r Leu Tyr Tyr Tyr Gln# 175- Gln Ser Ser Glu Ser Asn Lys Trp Ile Ser Me - #t Gly Thr Asp Cys Thr# 190- Val Lys Val Cys Pro Leu Asn Thr Gln Thr Le - #u Gly Ile Gly Cys Lys# 205- Thr Thr Asp Val Asn Thr Phe Glu Ile Val Al - #a Ser Ser Glu Lys Leu# 220- Val Ile Thr Asp Val Val Asn Gly Val Asn Hi - #s Asn Ile Asn Ile Ser225 2 - #30 2 - #35 2 -#40- Ile Asn Thr Cys Thr Ile Arg Asn Cys Asn Ly - #s Leu Gly Pro Arg Glu# 255- Asn Val Ala Ile Ile Gln Val Gly Gly Pro As - #n Ala Leu Asp Ile Thr# 270- Ala Asp Pro Thr Thr Val Pro Gln Val Gln Ar - #g Ile Met Arg Ile Asn# 285- Trp Lys Lys Trp Trp Gln Val Phe Tyr Thr Va - #l Val Asp Tyr Ile Asn# 300- Gln Val Ile Gln Val Met Ser Lys Arg Ser Ar - #g Ser Leu Asp Ala Ala305 3 - #10 3 - #15 3 -#20- Ala Phe Tyr Tyr Arg Ile 325- (2) INFORMATION FOR SEQ ID NO:12:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 326 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:12:- Met Tyr Gly Ile Glu Tyr Thr Thr Val Leu Th - #r Phe Leu Ile Ser Thr# 15- Ile Leu Leu Asn Tyr Ile Leu Lys Ser Leu Th - #r Arg Ile Met Asp Phe# 30- Ile Ile Tyr Arg Phe Leu Phe Ile Ile Val Il - #e Leu Ser Pro Phe Leu# 45- Arg Ala Gln Asn Tyr Gly Ile Asn Leu Pro Il - #e Ala Gly Ser Met Asp# 60- Thr Ala Tyr Ala Asn Ser Thr Gln Glu Glu Pr - #o Phe Leu Thr Ser Thr#80- Leu Cys Leu Tyr Tyr Pro Thr Glu Ala Ala Th - #r Glu Ile Asn Asp Asn# 95- Ser Trp Lys Asp Thr Leu Ser Gln Leu Phe Le - #u Thr Lys Gly Trp Pro# 110- Thr Glu Ser Val Tyr Phe Lys Glu Tyr Thr As - #n Ile Ala Ser Phe Ser# 125- Val Asp Pro Gln Leu Tyr Cys Asp Tyr Asn Va - #l Val Leu Met Lys Tyr# 140- Asp Ala Thr Leu Gln Leu Asp Met Ser Glu Le - #u Ala Asp Leu Ile Leu145 1 - #50 1 - #55 1 -#60- Asn Glu Trp Leu Cys Asn Pro Met Asp Ile Th - #r Leu Tyr Tyr Tyr Gln# 175- Gln Thr Asp Glu Ala Asn Lys Trp Ile Ser Me - #t Gly Ser Ser Cys Thr# 190- Ile Lys Val Cys Pro Leu Asn Thr Gln Thr Le - #u Gly Ile Gly Cys Leu# 205- Thr Thr Asp Ala Thr Thr Phe Glu Glu Val Pr - #o Thr Ala Glu Lys Leu# 220- Val Ile Thr Asp Val Val Asp Gly Val Asn Hi - #s Lys Leu Asp Val Thr225 2 - #30 2 - #35 2 -#40- Thr Ala Thr Cys Thr Ile Arg Asn Cys Lys Ly - #s Leu Gly Pro Arg Glu# 255- Asn Val Ala Val Ile Gln Val Gly Gly Ser As - #p Ile Leu Asp Ile Thr# 270- Ala Asp Pro Thr Thr Ala Pro Gln Thr Glu Ar - #g Met Met Arg Ile Asn# 285- Trp Lys Lys Trp Trp Gln Val Phe Tyr Thr Va - #l Val Asp Tyr Val Asp# 300- Gln Ile Ile Gln Val Met Ser Lys Arg Ser Ar - #g Ser Leu Asn Ser Ala305 3 - #10 3 - #15 3 -#20- Ala Phe Tyr Tyr Arg Val 325- (2) INFORMATION FOR SEQ ID NO:13:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 326 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:13:- Met Tyr Gly Ile Glu Tyr Thr Thr Ile Leu Il - #e Phe Leu Thr Ser Ile# 15- Thr Leu Leu Asn Tyr Ile Leu Lys Ser Ile Th - #r Arg Ile Met Asp Tyr# 30- Ile Ile Tyr Arg Phe Leu Leu Ile Val Val Va - #l Leu Ala Thr Met Ile# 45- Arg Ala Gln Asn Tyr Gly Val Asn Leu Pro Il - #e Thr Gly Ser Met Asp# 60- Thr Ala Tyr Ala Asp Ser Thr Gln Ser Glu Pr - #o Phe Leu Thr Ser Thr#80- Leu Cys Leu Tyr Tyr Pro Val Glu Ala Ser As - #n Glu Ile Ala Asp Thr# 95- Glu Trp Lys Asp Thr Leu Ser Gln Leu Phe Le - #u Thr Lys Gly Trp Pro# 110- Thr Gly Ser Val Tyr Leu Lys Glu Tyr Ala As - #p Ile Ala Ala Phe Ser# 125- Val Glu Pro Gln Leu Tyr Cys Asp Tyr Asn Le - #u Val Leu Met Lys Tyr# 140- Asp Ser Thr Gln Glu Leu Asp Met Ser Glu Le - #u Ala Asp Leu Ile Leu145 1 - #50 1 - #55 1 -#60- Asn Glu Trp Leu Cys Asn Pro Met Asp Ile Th - #r Leu Tyr Tyr Tyr Gln# 175- Gln Thr Asp Glu Ala Asn Lys Trp Ile Ser Th - #r Gly Ser Ser Cys Thr# 190- Val Lys Val Cys Pro Leu Asn Thr Gln Thr Le - #u Gly Ile Gly Cys Leu# 205- Ile Thr Asn Pro Asp Thr Phe Glu Thr Val Al - #a Thr Met Glu Lys Leu# 220- Val Ile Thr Asp Val Val Asp Gly Val Asn Hi - #s Lys Leu Asn Val Thr225 2 - #30 2 - #35 2 -#40- Thr Ala Thr Cys Thr Ile Arg Asn Cys Lys Ly - #s Leu Gly Pro Arg Glu# 255- Asn Val Ala Val Ile Gln Val Gly Gly Ala As - #n Val Leu Asp Ile Thr# 270- Ala Asp Pro Thr Thr Ala Pro Gln Thr Glu Ar - #g Met Met Arg Ile Asn# 285- Trp Lys Lys Trp Trp Gln Val Phe Tyr Thr Va - #l Val Asp Tyr Val Asn# 300- Gln Ile Ile Gln Thr Met Ser Lys Arg Ser Ar - #g Ser Leu Asn Ser Ser305 3 - #10 3 - #15 3 -#20- Ala Phe Tyr Tyr Arg Val 325- (2) INFORMATION FOR SEQ ID NO:14:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 326 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:14:- Met Tyr Gly Ile Glu Tyr Thr Thr Ile Leu Il - #e Phe Leu Thr Ser Ile# 15- Thr Leu Leu Asn Tyr Ile Leu Lys Ser Ile Th - #r Arg Met Met Asp Tyr# 30- Ile Ile Tyr Arg Phe Leu Leu Ile Val Val Il - #e Leu Ala Thr Ile Ile# 45- Asn Ala Gln Asn Tyr Gly Val Asn Leu Pro Il - #e Thr Gly Ser Met Asp# 60- Thr Ala Tyr Ala Asp Ser Thr Gln Ser Glu Pr - #o Phe Leu Thr Ser Thr#80- Leu Cys Leu Tyr Tyr Pro Val Glu Ala Ser As - #n Glu Ile Ala Asp Thr# 95- Glu Trp Lys Asp Thr Leu Ser Gln Leu Phe Le - #u Thr Lys Gly Trp Pro# 110- Thr Gly Ser Val Tyr Leu Lys Glu Tyr Ala As - #p Ile Ala Ala Phe Ser# 125- Val Glu Pro Gln Leu Tyr Cys Asp Tyr Asn Le - #u Val Leu Met Lys Tyr# 140- Asp Ser Thr Gln Glu Leu Asp Met Ser Glu Le - #u Ala Asp Leu Ile Leu145 1 - #50 1 - #55 1 -#60- Asn Glu Trp Leu Cys Asn Pro Met Asp Ile Th - #r Leu Tyr Tyr Tyr Gln# 175- Gln Thr Asp Glu Ala Asn Lys Trp Ile Ser Th - #r Gly Ser Ser Cys Thr# 190- Val Lys Val Cys Pro Leu Asn Thr Gln Thr Le - #u Gly Ile Gly Cys Leu# 205- Ile Thr Asn Pro Asp Thr Phe Glu Thr Val Al - #a Thr Met Glu Lys Leu# 220- Val Ile Thr Asp Val Val Asp Gly Val Asn Hi - #s Lys Leu Asn Val Thr225 2 - #30 2 - #35 2 -#40- Thr Ala Thr Cys Thr Ile Arg Asn Cys Lys Ly - #s Leu Gly Pro Arg Glu# 255- Asn Val Ala Val Ile Gln Val Gly Gly Ala As - #n Val Leu Asp Ile Thr# 270- Ala Asp Pro Thr Thr Thr Pro Gln Thr Glu Ar - #g Met Met Arg Ile Asn# 285- Trp Lys Lys Trp Trp Gln Val Phe Tyr Thr Va - #l Val Asp Tyr Val Asn# 300- Gln Ile Ile Gln Thr Met Ser Lys Arg Ser Ar - #g Ser Leu Asn Ser Ser305 3 - #10 3 - #15 3 -#20- Ala Phe Tyr Tyr Arg Val 325- (2) INFORMATION FOR SEQ ID NO:15:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 776 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:15:- Met Ala Ser Leu Ile Tyr Arg Gln Leu Leu Th - #r Asn Ser Tyr Thr Val# 15- Glu Leu Ser Asp Glu Ile Gln Glu Ile Gly Se - #r Thr Lys Thr Gln Asn# 30- Val Thr Val Asn Pro Gly Pro Phe Ala Gln Th - #r Asn Tyr Ala Ser Val# 45- Asn Trp Gly Pro Gly Glu Thr Asn Asp Ser Th - #r Thr Val Glu Pro Val# 60- Leu Asp Gly Pro Tyr Gln Pro Thr Thr Phe As - #n Pro Pro Val Ser Tyr#80- Trp Met Leu Leu Ala Pro Thr Asn Ala Gly Va - #l Val Asp Gln Gly Thr# 95- Asn Asn Thr Asn Arg Trp Leu Ala Thr Ile Le - #u Ile Lys Pro Asn Val# 110- Gln Gln Val Glu Arg Thr Tyr Thr Leu Phe Gl - #y Gln Gln Val Gln Val# 125- Thr Val Ser Asn Asp Ser Gln Thr Lys Trp Ly - #s Phe Val Asp Leu Ser# 140- Lys Gln Thr Gln Asp Gly Asn Tyr Ser Gln Hi - #s Gly Pro Leu Leu Ser145 1 - #50 1 - #55 1 -#60- Thr Pro Lys Leu Tyr Gly Val Met Lys His Gl - #y Gly Lys Ile Tyr Thr# 175- Tyr Asn Gly Glu Thr Pro Asn Ala Thr Thr Gl - #y Tyr Tyr Ser Thr Thr# 190- Asn Phe Asp Thr Val Asn Met Thr Ala Tyr Cy - #s Asp Phe Tyr Ile Ile# 205- Pro Leu Ala Gln Glu Ala Lys Cys Thr Glu Ty - #r Ile Asn Asn Gly Leu# 220- Pro Pro Ile Gln Asn Thr Arg Asn Ile Val Pr - #o Val Ser Ile Val Ser225 2 - #30 2 - #35 2 -#40- Arg Asn Ile Val Tyr Thr Arg Ala Gln Pro As - #n Gln Asp Ile Val Val# 255- Ser Lys Thr Ser Leu Trp Lys Glu Met Gln Ty - #r Asn Arg Asp Ile Val# 270- Ile Arg Phe Lys Phe Ala Asn Ser Ile Ile Ly - #s Ser Gly Gly Leu Gly# 285- Tyr Lys Trp Ser Glu Val Ser Phe Lys Pro Al - #a Asn Tyr Gln Tyr Thr# 300- Tyr Thr Arg Asp Gly Glu Glu Val Thr Ala Hi - #s Thr Thr Cys Ser Val305 3 - #10 3 - #15 3 -#20- Asn Gly Ile Asn Asp Phe Asn Tyr Asn Gly Gl - #y Ser Leu Pro Thr Asp# 335- Phe Val Ile Ser Lys Tyr Glu Val Ile Lys Gl - #u Asn Ser Phe Val Tyr# 350- Ile Asp Tyr Trp Asp Asp Ser Gln Ala Phe Ar - #g Asn Met Val Tyr Val# 365- Arg Ser Leu Ala Ala Asp Leu Asn Ser Val Me - #t Cys Thr Gly Gly Asp# 380- Tyr Ser Phe Ala Ile Pro Val Gly Asn Tyr Pr - #o Val Met Thr Gly Gly385 3 - #90 3 - #95 4 -#00- Ala Val Ser Leu His Ser Ala Gly Val Thr Le - #u Ser Thr Gln Phe Thr# 415- Asp Phe Val Ser Leu Asn Ser Leu Arg Phe Ar - #g Phe Arg Leu Ser Val# 430- Glu Glu Pro Pro Phe Ser Ile Leu Arg Thr Ar - #g Val Ser Gly Leu Tyr# 445- Gly Leu Pro Ala Ala Lys Pro Asn Asn Ser Gl - #n Glu Tyr Tyr Glu Ile# 460- Ala Gly Arg Phe Ser Leu Ile Ser Leu Val Pr - #o Ser Asn Asp Asp Tyr465 4 - #70 4 - #75 4 -#80- Gln Thr Pro Ile Ile Asn Ser Val Thr Val Ar - #g Gln Asp Leu Glu Arg# 495- Gln Leu Gly Glu Leu Arg Asp Glu Phe Asn As - #n Leu Ser Gln Gln Ile# 510- Ala Met Ser Gln Leu Ile Asp Leu Ala Leu Le - #u Pro Leu Asp Met Phe# 525- Ser Met Phe Ser Gly Ile Lys Ser Thr Ile As - #p Ala Ala Lys Ser Met# 540- Ala Thr Asn Val Met Lys Arg Phe Lys Lys Se - #r Ser Leu Ala Asn Ser545 5 - #50 5 - #55 5 -#60- Val Ser Thr Leu Thr Asp Ser Leu Ser Asp Al - #a Ala Ser Ser Ile Ser# 575- Arg Ser Ala Ser Val Arg Ser Val Ser Ser Th - #r Ala Ser Ala Trp Thr# 590- Glu Val Ser Asn Ile Thr Ser Asp Ile Asn Va - #l Thr Thr Ser Ser Ile# 605- Ser Thr Gln Thr Ser Thr Ile Ser Arg Arg Le - #u Arg Leu Lys Glu Met# 620- Ala Thr Gln Thr Asp Gly Met Asn Phe Asp As - #p Ile Ser Ala Ala Val625 6 - #30 6 - #35 6 -#40- Leu Lys Thr Lys Ile Asp Lys Ser Thr Gln Le - #u Asn Thr Asn Thr Leu# 655- Pro Glu Ile Val Thr Glu Ala Ser Glu Lys Ph - #e Ile Pro Asn Arg Ala# 670- Tyr Arg Val Ile Lys Asp Asp Glu Val Leu Gl - #u Ala Ser Thr Asp Gly# 685- Lys Tyr Phe Ala Tyr Lys Val Glu Thr Ile Le - #u Lys Arg Phe His Ser# 700- Met Tyr Lys Phe Ala Asp Leu Val Thr Asp Se - #r Pro Val Ile Ser Ala705 7 - #10 7 - #15 7 -#20- Ile Ile Asp Phe Lys Thr Leu Lys Asn Leu As - #n Asp Asn Tyr Gly Ile# 735- Ser Arg Gln Gln Ala Leu Asn Leu Leu Arg Se - #r Asp Pro Arg Val Leu# 750- Arg Glu Phe Ile Asn Gln Asp Asn Pro Ile Il - #e Arg Asn Arg Ile Glu# 765- Ser Leu Ile Met Gln Cys Arg Leu# 775- (2) INFORMATION FOR SEQ ID NO:16:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 747 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:16:- Leu Ile Tyr Arg Gln Leu Leu Thr Asn Ser Ty - #r Thr Val Glu Leu Ser# 15- Asp Glu Ile Gln Glu Ile Gly Ser Thr Lys Th - #r Gln Asn Val Thr Val# 30- Asn Pro Gly Pro Phe Ala Gln Thr Asn Tyr Al - #a Pro Val Asn Trp Gly# 45- Pro Gly Glu Thr Asn Asp Ser Thr Thr Val Gl - #u Pro Val Leu Asp Gly# 60- Pro Tyr Gln Pro Thr Thr Phe Asn Pro Pro Va - #l Ser Tyr Trp Met Leu#80- Leu Ala Pro Thr Asn Ala Gly Val Val Val Gl - #u Gly Thr Asn Asn Thr# 95- Asn Arg Trp Leu Ala Thr Ile Leu Ile Glu Pr - #o Asn Val Gln Gln Val# 110- Glu Arg Thr Tyr Thr Leu Phe Gly Gln Gln Va - #l Gln Val Thr Val Ser# 125- Asn Asp Ser Gln Thr Lys Trp Lys Phe Val As - #p Leu Ser Lys Gln Thr# 140- Gln Asp Gly Asn Tyr Ser Gln His Gly Ser Le - #u Leu Ser Thr Pro Lys145 1 - #50 1 - #55 1 -#60- Leu Tyr Gly Val Met Lys His Gly Gly Lys Il - #e Tyr Thr Tyr Asn Gly# 175- Glu Thr Pro Asn Ala Asn Thr Gly Tyr Tyr Se - #r Thr Thr Asn Phe Asp# 190- Thr Val Asn Met Thr Ala Tyr Cys Asp Phe Ty - #r Ile Ile Pro Leu Ala# 205- Gln Glu Ala Lys Cys Thr Glu Tyr Ile Asn As - #n Gly Leu Pro Pro Ile# 220- Gln Asn Thr Arg Asn Ile Val Pro Val Ser Il - #e Val Ser Arg Asn Ile225 2 - #30 2 - #35 2 -#40- Val Tyr Thr Arg Ala Gln Pro Asn Gln Asp Il - #e Val Val Ser Lys Thr# 255- Ser Leu Trp Lys Glu Met Gln Tyr Asn Arg As - #p Ile Val Ile Arg Phe# 270- Lys Phe Ala Asn Ser Ile Ile Lys Ser Gly Gl - #y Leu Gly Tyr Lys Trp# 285- Ser Glu Val Ser Phe Lys Pro Ala Phe Tyr Gl - #n Tyr Thr Tyr Thr Arg# 300- Asp Gly Glu Glu Val Thr Ala His Thr Thr Cy - #s Ser Val Asn Gly Val305 3 - #10 3 - #15 3 -#20- Asn Asp Phe Asn Tyr Asn Gly Gly Ser Leu Pr - #o Thr Asp Phe Val Ile# 335- Ser Lys Tyr Glu Val Ile Lys Glu Asn Ser Ph - #e Val Tyr Ile Asp Tyr# 350- Trp Asp Asp Ser Gln Ala Phe Arg Asn Met Va - #l Tyr Val Arg Ser Leu# 365- Ala Ala Asp Leu Asn Ser Val Met Cys Thr Gl - #y Gly Asp Tyr Ser Phe# 380- Ala Leu Pro Val Gly Asn Tyr Pro Val Met Th - #r Gly Gly Ala Val Ser385 3 - #90 3 - #95 4 -#00- Leu His Ser Ala Gly Val Thr Leu Ser Thr Gl - #n Phe Thr Asp Phe Val# 415- Ser Leu Asn Ser Leu Arg Phe Arg Phe Arg Le - #u Ser Val Glu Glu Pro# 430- Pro Phe Ser Ile Leu Arg Thr Arg Val Ser Gl - #y Leu Tyr Gly Leu Pro# 445- Ala Ala Lys Pro Asn Asn Ser Gln Glu Tyr Ty - #r Glu Ile Ala Gly Arg# 460- Phe Ser Leu Ile Ser Leu Val Pro Leu Asn As - #p Asp Tyr Gln Thr Pro465 4 - #70 4 - #75 4 -#80- Ile Met Asn Ser Val Thr Val Arg Gln Asp Le - #u Glu Arg Gln Leu Gly# 495- Glu Leu Arg Asp Glu Phe Asn Asn Leu Ser Gl - #n Gln Ile Ala Met Ser# 510- Gln Leu Ile Asp Leu Ala Leu Leu Pro Leu As - #p Met Phe Ser Met Phe# 525- Ser Gly Ile Lys Ser Thr Ile Asp Ala Ala Ly - #s Ser Met Ala Thr Asn# 540- Val Met Lys Arg Phe Lys Lys Ser Ser Leu Al - #a Asn Ser Val Ser Thr545 5 - #50 5 - #55 5 -#60- Leu Thr Asp Ser Leu Ser Asp Ala Ala Ser Se - #r Ile Ser Arg Ser Ala# 575- Ser Val Arg Ser Val Ser Ser Thr Ala Ser Al - #a Trp Thr Glu Val Ser# 590- Asn Ile Ala Ser Asp Ile Asn Val Thr Thr Se - #r Ser Ile Ser Thr Gln# 605- Thr Ser Thr Ile Ser Arg Arg Leu Arg Leu Ly - #s Glu Met Ala Thr Gln# 620- Thr Asp Gly Met Asn Phe Asp Asp Ile Ser Al - #a Ala Val Leu Lys Thr625 6 - #30 6 - #35 6 -#40- Lys Ile Asp Lys Ser Thr Gln Leu Asn Thr As - #n Thr Leu Pro Glu Ile# 655- Val Thr Glu Ala Ser Glu Lys Phe Ile Pro As - #n Arg Ala Tyr Arg Val# 670- Ile Lys Asp Asp Glu Val Leu Glu Ala Ser Il - #e Asp Gly Lys Tyr Phe# 685- Ala Tyr Lys Val Glu Thr Phe Glu Glu Ile Pr - #o Phe Asp Val Gln Lys# 700- Phe Ala Asp Leu Val Thr Asp Ser Pro Val Il - #e Ser Ala Ile Ile Asp705 7 - #10 7 - #15 7 -#20- Phe Lys Thr Leu Lys Asn Leu Asn Asp Asn Ty - #r Gly Ile Ser Arg Gln# 735- Gln Ala Leu Asn Leu Leu Arg Ser Asp Pro Ar - #g# 745- (2) INFORMATION FOR SEQ ID NO:17:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 1357 base (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: cDNA- (ix) FEATURE: (A) NAME/KEY: CDS (B) LOCATION: 24..1214- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:17:- GGCTTTTAAA CGAAGTCTTC AAC ATG GAT GTC CTA TAC TC - #T TTG TCA AAG 50#Leu Ser Lys Asp Val Leu Tyr Ser# 5 1- ACT CTT AAA GAC GCT AGA GAC AAA ATT GTC GA - #A GGC ACA TTG TAT TCT 98Thr Leu Lys Asp Ala Arg Asp Lys Ile Val Gl - #u Gly Thr Leu Tyr Ser# 25- AAC GTG AGT GAT CTA ATT CAA CAA TTT AAT CA - #A ATG ATA ATT ACT ATG 146Asn Val Ser Asp Leu Ile Gln Gln Phe Asn Gl - #n Met Ile Ile Thr Met# 40- AAT GGA AAT GAA TTT CAA ACT GGA GGA ATC GG - #T AAT TTG CCA ATT AGA 194Asn Gly Asn Glu Phe Gln Thr Gly Gly Ile Gl - #y Asn Leu Pro Ile Arg# 55- AAC TGG AAT TTT AAT TTC GGG TTA CTT GGA AC - #A ACT TTG CTG AAC TTA 242Asn Trp Asn Phe Asn Phe Gly Leu Leu Gly Th - #r Thr Leu Leu Asn Leu# 70- GAC GCT AAT TAT GTT GAA ACG GCA AGA AAT AC - #A ATT GAT TAT TTC GTG 290Asp Ala Asn Tyr Val Glu Thr Ala Arg Asn Th - #r Ile Asp Tyr Phe Val# 85- GAT TTT GTA GAC AAT GTA TGC ATG GAT GAG AT - #G GTT AGA GAA TCA CAA 338Asp Phe Val Asp Asn Val Cys Met Asp Glu Me - #t Val Arg Glu Ser Gln#105- AGG AAC GGA ATT GCA CCT CAA TCA GAC TCG CT - #A AGA AAG CTG TCA GCC 386Arg Asn Gly Ile Ala Pro Gln Ser Asp Ser Le - #u Arg Lys Leu Ser Ala# 120- ATT AAA TTC AAA AGA ATA AAT TTT GAT AAT TC - #G TCG GAA TAC ATA GAA 434Ile Lys Phe Lys Arg Ile Asn Phe Asp Asn Se - #r Ser Glu Tyr Ile Glu# 135- AAC TGG AAT TTG CAA AAT AGA AGA CAG AGG AC - #A GGT TTC ACT TTT CAT 482Asn Trp Asn Leu Gln Asn Arg Arg Gln Arg Th - #r Gly Phe Thr Phe His# 150- AAA CCA AAC ATT TTT CCT TAT TCA GCA TCA TT - #T ACA CTA AAT AGA TCA 530Lys Pro Asn Ile Phe Pro Tyr Ser Ala Ser Ph - #e Thr Leu Asn Arg Ser# 165- CAA CCC GCT CAT GAT AAT TTG ATG GGC ACA AT - #G TGG TTA AAC GCA GGA 578Gln Pro Ala His Asp Asn Leu Met Gly Thr Me - #t Trp Leu Asn Ala Gly170 1 - #75 1 - #80 1 -#85- TCG GAA ATT CAA GTC GCT GGA TTT GAC TAC TC - #A TGT GCT ATT AAC GCA 626Ser Glu Ile Gln Val Ala Gly Phe Asp Tyr Se - #r Cys Ala Ile Asn Ala# 200- CCA GCC AAT ATA CAA CAA TTT GAG CAT ATT GT - #G CCA CTC CGA AGA GTG 674Pro Ala Asn Ile Gln Gln Phe Glu His Ile Va - #l Pro Leu Arg Arg Val# 215- TTA ACT ACA GCT ACG ATA ACT CTT CTA CCA GA - #C GCG GAA AGG TTT AGT 722Leu Thr Thr Ala Thr Ile Thr Leu Leu Pro As - #p Ala Glu Arg Phe Ser# 230- TTT CCA AGA GTG ATC AAT TCA GCT GAC GGG GC - #A ACT ACA TGG TTT TTC 770Phe Pro Arg Val Ile Asn Ser Ala Asp Gly Al - #a Thr Thr Trp Phe Phe# 245- AAC CCA GTG ATT CTC AGG CCG AAT AAC GTT GA - #A GTG GAG TTT CTA TTG 818Asn Pro Val Ile Leu Arg Pro Asn Asn Val Gl - #u Val Glu Phe Leu Leu250 2 - #55 2 - #60 2 -#65- AAT GGA CAG ATA ATA AAC ACT TAT CAA GCA AG - #A TTT GGA ACT ATC GTA 866Asn Gly Gln Ile Ile Asn Thr Tyr Gln Ala Ar - #g Phe Gly Thr Ile Val# 280- GCT AGA AAT TTT GAT ACT ATT AGA CTA TCA TT - #C CAG TTA ATG AGA CCA 914Ala Arg Asn Phe Asp Thr Ile Arg Leu Ser Ph - #e Gln Leu Met Arg Pro# 295- CCA AAC ATG ACA CCA GCA GTA GCA GTA CTA TT - #C CCG AAT GCA CAG CCA 962Pro Asn Met Thr Pro Ala Val Ala Val Leu Ph - #e Pro Asn Ala Gln Pro# 310- TTC GAA CAT CAT GCA ACA GTG GGA TTG ACA CT - #T AGA ATT GAG TCT GCA1010Phe Glu His His Ala Thr Val Gly Leu Thr Le - #u Arg Ile Glu Ser Ala# 325- GTT TGT GAG TCT GTA CTC GCC GAT GCA AGT GA - #A ACT CTA TTA GCA AAT1058Val Cys Glu Ser Val Leu Ala Asp Ala Ser Gl - #u Thr Leu Leu Ala Asn330 3 - #35 3 - #40 3 -#45- GTA ACA TCC GTT AGG CAA GAG TAC GCA ATA CC - #A GTT GGA CCA GTC TTT1106Val Thr Ser Val Arg Gln Glu Tyr Ala Ile Pr - #o Val Gly Pro Val Phe# 360- CCA CCA GGT ATG AAC TGG ACT GAT TTA ATC AC - #C AAT TAT TCA CCG TCT1154Pro Pro Gly Met Asn Trp Thr Asp Leu Ile Th - #r Asn Tyr Ser Pro Ser# 375- AGG GAG GAC AAT TTG CAA CGC GTA TTT ACA GT - #G GCT TCC ATT AGA AGC1202Arg Glu Asp Asn Leu Gln Arg Val Phe Thr Va - #l Ala Ser Ile Arg Ser# 390- ATG CTC ATT AAA TGAGGACCAA GCTAACAACT TGGTATCCAA CT - #TTGGTGAG1254Met Leu Ile Lys 395- TATGTAGCTA TATCAAGCTG TTTGAACTCT GTAAGTAAGG ATGCGTATAC GC - #ATTCGCTA1314# 135 - #7GTATAGTG AGAGGATGTG ACC- (2) INFORMATION FOR SEQ ID NO:18:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 397 amino (B) TYPE: amino acid (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:18:- Met Asp Val Leu Tyr Ser Leu Ser Lys Thr Le - #u Lys Asp Ala Arg Asp# 15- Lys Ile Val Glu Gly Thr Leu Tyr Ser Asn Va - #l Ser Asp Leu Ile Gln# 30- Gln Phe Asn Gln Met Ile Ile Thr Met Asn Gl - #y Asn Glu Phe Gln Thr# 45- Gly Gly Ile Gly Asn Leu Pro Ile Arg Asn Tr - #p Asn Phe Asn Phe Gly# 60- Leu Leu Gly Thr Thr Leu Leu Asn Leu Asp Al - #a Asn Tyr Val Glu Thr# 80- Ala Arg Asn Thr Ile Asp Tyr Phe Val Asp Ph - #e Val Asp Asn Val Cys# 95- Met Asp Glu Met Val Arg Glu Ser Gln Arg As - #n Gly Ile Ala Pro Gln# 110- Ser Asp Ser Leu Arg Lys Leu Ser Ala Ile Ly - #s Phe Lys Arg Ile Asn# 125- Phe Asp Asn Ser Ser Glu Tyr Ile Glu Asn Tr - #p Asn Leu Gln Asn Arg# 140- Arg Gln Arg Thr Gly Phe Thr Phe His Lys Pr - #o Asn Ile Phe Pro Tyr145 1 - #50 1 - #55 1 -#60- Ser Ala Ser Phe Thr Leu Asn Arg Ser Gln Pr - #o Ala His Asp Asn Leu# 175- Met Gly Thr Met Trp Leu Asn Ala Gly Ser Gl - #u Ile Gln Val Ala Gly# 190- Phe Asp Tyr Ser Cys Ala Ile Asn Ala Pro Al - #a Asn Ile Gln Gln Phe# 205- Glu His Ile Val Pro Leu Arg Arg Val Leu Th - #r Thr Ala Thr Ile Thr# 220- Leu Leu Pro Asp Ala Glu Arg Phe Ser Phe Pr - #o Arg Val Ile Asn Ser225 2 - #30 2 - #35 2 -#40- Ala Asp Gly Ala Thr Thr Trp Phe Phe Asn Pr - #o Val Ile Leu Arg Pro# 255- Asn Asn Val Glu Val Glu Phe Leu Leu Asn Gl - #y Gln Ile Ile Asn Thr# 270- Tyr Gln Ala Arg Phe Gly Thr Ile Val Ala Ar - #g Asn Phe Asp Thr Ile# 285- Arg Leu Ser Phe Gln Leu Met Arg Pro Pro As - #n Met Thr Pro Ala Val# 300- Ala Val Leu Phe Pro Asn Ala Gln Pro Phe Gl - #u His His Ala Thr Val305 3 - #10 3 - #15 3 -#20- Gly Leu Thr Leu Arg Ile Glu Ser Ala Val Cy - #s Glu Ser Val Leu Ala# 335- Asp Ala Ser Glu Thr Leu Leu Ala Asn Val Th - #r Ser Val Arg Gln Glu# 350- Tyr Ala Ile Pro Val Gly Pro Val Phe Pro Pr - #o Gly Met Asn Trp Thr# 365- Asp Leu Ile Thr Asn Tyr Ser Pro Ser Arg Gl - #u Asp Asn Leu Gln Arg# 380- Val Phe Thr Val Ala Ser Ile Arg Ser Met Le - #u Ile Lys385 3 - #90 3 - #95- (2) INFORMATION FOR SEQ ID NO:19:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 23 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:19:- Thr Met Asn Gly Asn Glu Phe Gln Thr Gly Gl - #y Ile Gly Asn Leu Pro# 15- Ile Arg Asn Trp Asn Gly Cys 20- (2) INFORMATION FOR SEQ ID NO:20:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 9 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:20:- Ser Arg Asn Ile Val Tyr Thr Arg Ala1 5- (2) INFORMATION FOR SEQ ID NO:21:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 24 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:21:- Asn Ile Ala Pro Ala Ser Ile Ala Ser Arg As - #n Ile Ala Tyr Thr Arg# 15- Ala Cys Pro Asn Gln Asp Ile Ala 20- (2) INFORMATION FOR SEQ ID NO:22:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 24 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:22:- Asn Ile Val Pro Val Ser Ile Val Ser Arg As - #n Ile Val Tyr Thr Arg# 15- Ala Gln Pro Asn Gln Asp Ile Val 20- (2) INFORMATION FOR SEQ ID NO:23:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 24 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:23:- Asn Ile Ala Pro Ala Ser Ile Val Ser Arg As - #n Ile Val Tyr Thr Arg# 15- Ala Gln Pro Asn Gln Asp Ile Ala 20- (2) INFORMATION FOR SEQ ID NO:24:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 21 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:24:- Thr Met Asn Gly Asn Glu Phe Gln Thr Gly Gl - #y Ile Gly Asn Leu Pro# 15- Ile Arg Asn Trp Asn 20__________________________________________________________________________

Number	Name	Date
4190645	Almeida	Feb 1980
4474757	Arnon et al.	Oct 1984
4591552	Neurath	May 1986
4629783	Cosand	Dec 1986
4704275	Wyatt et al.	Nov 1987
4737487	Watts et al.	Apr 1988
5071651	Sabara et al.	Dec 1991

Number	Date	Country
0114759	Aug 1984	EPX
0117657	Sep 1984	EPX
10235391	Sep 1987	EPX
0259149	Mar 1988	EPX
WO8505122	Nov 1985	WOX

	Number	Date
Parent	661859	Feb 1991
Parent	241761	Sep 1988
Parent	903325	Sep 1986

	Number	Date
Parent	626041	Dec 1990
Parent	552350	Jul 1990
Parent	813661	Dec 1985

Rotavirus peptide compositions and methods of use

Information

Patent Number

Date Filed

Date Issued

Inventors

Original Assignees

Examiners

Agents

CPC

US Classifications

Field of Search

US

International Classifications

Abstract

Description

Claims

CROSS-REFERENCE TO RELATED APPLICATIONS

US Referenced Citations (7)

Foreign Referenced Citations (5)

Non-Patent Literature Citations (27)

Continuations (3)

Continuation in Parts (3)

Entry
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