Patent Grant
6958237
The present invention relates to the field of molecular virology and, more particularly, to construction of highly infectious rubella virus cDNA clones and to expression constructs based on rubella virus infectious clones.
Rubella virus is a major human pathogen. Infection with rubella virus can cause serious birth defects and chronic disease. There was a mini-epidemic of both rubella and congenital rubella syndrome in the United States between 1989 and 1991.
Rubella was first described in the eighteenth century in Germany. The symptoms of a rash and mild fever were similar to those of measles, so the disease was given the name German measles. The name “rubella” was coined in 1814 when physicians realized that the disease was unique and was not merely a variant of scarlatina (scarlet fever) or rubeola (measles).
Rubella is a relatively harmless disease in young children. However, during the first trimester of pregnancy, rubella virus infection can cause fetal death. If the fetus survives, it may be born deaf or have cataracts, cardiac abnormalities, microcephaly, motor deficits or other congenital anomalies. The infant may also be born with thrombocytopenic purpura, hepatosplenomegaly, icterus, anemia, and low birth weight. The presence of one or more of these defects has been termed “congenital rubella syndrome” or CRS.
The rubella virus was isolated in 1962 at the beginning of a worldwide rubella epidemic which lasted from 1962 to 1965. This epidemic peaked in the United States in 1964, resulting in the birth of approximately 20,000 infants exhibiting CRS.
Scientists began development of an effective vaccine against the rubella virus during the rubella epidemic. Effective attenuated vaccines became available in the late 1960's and are still used today. These attenuated vaccines are live viruses that have been passaged to reduce their virulence. Attenuated vaccines produce immunity, but can cause disease. Protection is believed to persist for at least 15 years after inoculation with the attenuated rubella vaccine.
Various vaccination schedules have been set up in different parts of the world to eliminate rubella infection, especially of the human fetus. The rubella immunization program established in Great Britain requires vaccination of all girls between the ages of 10 and 14. The United States immunization program vaccinates infants at approximately 15 months and requires a certificate of vaccination prior to attending school. The United States program is designed to eradicate the disease among the population that is most responsible for transmission of rubella, whereas the program of Great Britain seeks to achieve complete protection for those at risk for pregnancy. One disadvantage to the United States program is that protection against rubella may dissipate at the very time when immunity is most needed, namely, during the child-bearing years.
Vaccination of women of child-bearing age having undetectable antibody titers is recommended in both the United States and Great Britain. However, there are several risks to this procedure. First, there is a risk that these women may be pregnant and not be aware of their pregnancy, or they may become pregnant within a few months following immunization. Vaccination against rubella is contraindicated in pregnant women because the live virus in the vaccine can cross the placenta and infect the fetus. Pregnant women who have not previously been infected with the rubella virus or who have not been vaccinated prior to becoming pregnant are advised to refrain from becoming vaccinated during their pregnancy. These women are therefore at risk for contracting rubella by coming in contact with infectious persons, including those recently vaccinated with the attenuated vaccine.
Vaccination of older women has been associated with chronic arthritis and neurological symptoms. Scientists believe that these symptoms may be due to the persistent nature of the attenuated rubella virus in the currently available vaccines.
Rubella virus is a small, quasi-spherical, enveloped, nonsegmented, plus-strand RNA virus that is the the sole member of the rubivirus genus of the togavirus family (Togaviridae). Molecular biology of rubella virus is summarized by Frey, T. K. in Adv. Virus Res. 44:69-160 (1994). One other member of the togavirus family is alphaviruses (see Strauss, J. H., and E. G. Strauss, Microbiol. Rev. 58:491-562. (1994) for a detailed description), which include a number of viruses pathogenic for vertebrates, including humans. The rubella virion (virus particle) consists of single-stranded RNA encapsidated in an icosahedral nucleocapsid surrounded by a lipid envelope. Multiple copies of a viral protein, designated the C protein (MW (molecular weight)=32,000-38,000 daltons), make up the nucleocapsid. Two types of viral glycoprotein, designated E1 and E2 (MW=53,000-58,000 daltons and 42,000-48,000 daltons, respectively), are embedded in the envelope, as reported by Waxham, M. N. and Wolinsky, J. S., Virology 126:194-203 (1983). The E2 glycoprotein has been further subdivided into two subgroups, designated E2a and E2b, by their ability to migrate differently when resolved by polyacrylamide gel electrophoresis, as described by Oker-Blom, C., et al., J. Virol. 46:964-973 (1983). E1 is the viral hemagglutinin. Neutralizing epitopes have been found on both E1 and E2 by Waxham, M. N. and Wolinsky, J. S., Virology 143:153-165 (1985) and Green, K. Y., and Dorsett, P. H., J. Virol., 57:893-898 (1986).
The rubella genome consists of RNA of positive polarity that is roughly 10,000 nucleotides long and is capped and polyadenylated. In infected cells, three viral RNA species are synthesized: the genomic RNA, which also is the mRNA for translation of the nonstructural proteins (whose function is in viral RNA synthesis) from a long open reading frame (ORF) at the 5′ end of the genome; a complementary genome-length RNA of minus polarity which is the template for synthesis of plus-strand RNA species; and a subgenomic (SG) RNA which is initiated internally and contains the sequences of the 3′-terminal one-third of the genome (3327 nucleotides) and serves as the mRNA for the translation of the structural proteins. The structural proteins are proteolytically processed from a polyprotein precursor during translation. The order of these proteins in the polyprotein is NH2—C-E2-E1—COOH, as reported by Oker-Blom, C., et al. (1983); Oker-Blom, C., J. Virol. 51:354-358 (1984). In the other togavirus genus, the alphaviruses, synthesis of the SG RNA is directed by a short, approximately 25 nucleotide sequence located immediately upstream from the SG start site known as the SG promoter, as reported by Strauss, et al., Microbiol. Rev. 58:491-562 (1994). The exact location of the SG promoter in rubella virus genome is not known.
Recombinant vaccines are based on live microorganisms which have been genetically manipulated so that they are not pathogenic, but result in immunity against the virulent organism. Recombinant vaccines can only cause disease if a rare genetic mutation or recombinant event occurs which allows the microorganism to revert to wild type. A recombinant vaccine is generally safer and more effective than an attenuated vaccine because the engineered mutations remove or inactivate only specific portions of the genome, whereas attenuated vaccines contain random mutations. In order to develop a recombinant vaccine, one must first have the nucleic acid sequence of the entire viral genome, including both the information required for infection and at least limited replication of the virus, and for antigenicity. Once the entire sequence has been determined, a cDNA clone can be produced that is infectious and can be modified to be non-virulent.
An infectious cDNA clone is a complete DNA copy of an RNA virus genome contained in a vector, such as a plasmid, from which RNA transcripts of the genome can be synthesized in vitro. In the case of positive-polarity RNA viruses such as rubella, such transcripts are infectious when transfected into cells. The development of an infectious clone is a landmark event in the molecular biology of any RNA virus. Although an infectious clone for rubella virus has been described (Wang, et al., J. Virol. 68:3550-3557 (1994)), this cDNA clone displayed low infectivity (approximately 5 plaques/10 μg of transcripts). Increasing the infectivity of this clone would increase the efficiency of a recombinant attenuated rubella vaccine derived from the clone and would provide an improved molecular biology tool for studying rubella virus replication.
However, successful generation of highly infectious cDNA clones has often been problematic due to the presence of mutations in the virus RNA template population caused by the inherent mutability of RNA viruses, the relatively low fidelity of the DNA polymerases used in cDNA synthesis, instability and toxicity of viral sequences in bacterial hosts, and the infidelity of the RNA polymerases used for in vitro transcriptions (Boyer and Haenni, Virology 198:415-426 (1994)). It is clear that there remains a strong need for an infectious cDNA clone of the rubella virus genome having a higher infectivity than currently available rubella virus clones, and for a recombinant rubella virus vaccine. The isolation of a highly infectious cDNA clone will be useful for the development of a recombinant rubella vaccine vector. A recombinant vaccine vector based on live, attenuated rubella vaccines is also highly desirable in a pediatric setting, where immunization with a recombinant rubella vaccine expression vector can be used to induce immunity against rubella alone, or both rubella and another virus or viruses whose genes may be introduced into the vector. Such vaccine vector is also desirable in an adult patient setting, where a recombinant rubella vaccine is needed that can be safely administered to pregnant and older women without risk of birth defects, auto immune disease, or neurologic symptoms. Thus, rubella virus expression vectors that can be used to produce and develop recombinant vaccines against rubella and other viruses would be highly useful to combat rubella and other diseases in various populations. Also, the development of a method to improve the stability of togavirus expression vectors would be very useful for the development of the expression vectors and recombinant vaccines for rubella virus and other viruses of this family, such as alphaviruses. The instability of alphavirus expression vectors is well known, as reported by Pugachev, K. V., et al., Virology 209:155-166 (1995) and Pugachev, K. V., et al., Virology 212:587-594 (1995). Futhermore, rubella virus expression vectors would serve as valuable molecular biology tools to study rubella virus and other viruses of the togavirus family.
There has been a long-standing problem of an inability to produce highly infectious rubella virus clones. Applicants discovered that by replacing a portion of a low infectivity clone with a corresponding fragment that was synthesized by a method known to produce sequences with few mutations, Applicants obtained a chimera exhibiting high infectivity. Therefore, the present invention includes methods of producing highly infectious rubella virus clones by replacing segments of a low infectivity clone with corresponding segments produced by a protocol known to generate sequences having a minimal number of mutations.
Additionally, highly infectious cDNA clones of the rubella virus are provided herein. The clones are chimeric DNA molecule constructs containing portions of a rubella virus cDNA clone having a low specific infectivity and one or more portions of at least one rubella virus genome synthesized by a method known to produce sequences having a minimal number of mutations. The highly infectious rubella virus clones of the invention are useful as molecular biology tools for studying rubella virus and can be useful for developing recombinant vaccines against rubella.
The highly infectious cDNA clones have a specific infectivity greater than 0.5 plaques/μg of transcript. In several preferred embodiments of the invention, the specific infectivities of viral transcripts are approximately 104 plaques/μg of transcript.
In preferred embodiments the cDNA clones are prepared by replacing one or more fragments of a known w-Therien-derived infectious cDNA clone having low specific infectivity with corresponding fragments from an f-Therien rubella virus strain synthesized by a method known to produce sequences having a minimal number of mutations.
Togavirus expression vectors for the expression of live, attenuated togavirus and a foreign gene are also dherein. The expression vector constructs contain a togavirus non-structural protein open reading frame; a first expression element for expression of a heterologous virus; a gene encoding the foreign gene or a multiple cloning site into which the foreign gene may be inserted; a second expression element for the expression of the live, attenuated togavirus; and a togavirus structural protein open reading frame. The togavirus non-structural protein open reading frame and togavirus structural protein open reading frame are preferably from an infectious rubella virus clone. The preferred foreign gene is a heterologous virus. The expression element is either a subgenomic (SG) promoter or an internal ribosome entry site (IRES). Administration of the vector as an immunization agents is useful for the induction of immuity against the togavirus, the heterologous virus, or both. The incorporation of at least one IRES in the vector results in a recombinant virus of improved stability.
In a preferred embodiment, the expression elements for expression of both the foreign gene and the togavirus are SG promoters. A multiple cloning site (MCS) is located between the two SG promoters. The MCS is useful for the insertion of the foreign genes under the control of the upstream SG promoter, including but not limited to reporter genes or heterologous virus genes. Exemplary reporter genes include green fluorescent protein (GFP) or chloramphenicol acetyltransferase (CAT) genes. Exemplary heterologous virus genes include Japanese encephalitis virus genes.
In another preferred embodiment, the second expression element, which controls expression of the togavirus structural protein, is replaced by an internal ribosome entry site (IRES). The IRES is a sequence capable of promoting the entry of a ribosome into an RNA molecule at an internal site, independently of the polyadenylated cap.
This construct is prepared by replacing an indigenous SG promoter of an infectious rubella cDNA clone with the IRES, thus placing the expression of rubella virus structural genes under the control of IRES. Surprisingly, this construct gives rise to viable rubella virus. This recombinant construct is yet another embodiment of the present invention. A duplicate copy of the SG promoter region is then placed into the intermediate construct directly upstream of IRES. A MCS is placed downstream of the SG promoter to allow for the insertion of the foreign genes. Introduction of the IRES element results in improved stability of the recombinant virus, including improved expression of the foreign gene protein.
In the present embodiments, the vectors are prepared using a backbone of an infectious rubella cDNA clone containing portions of both a cDNA clone having a low specific infectivity and a second rubella virus genome Robo302, described herein, and Robo402 described in Pugachev, K. V., et al., (2000) Virology, 273, 189-197, incorporated herein by reference in its entirety.
The vectors are useful for the induction of immunity or to develop recombinant vaccines against rubella and/or a heterologous virus whose genes may be inserted into the expression vector. The vectors can also be used to study rubella, particularly rubella virus replication. The method of introduction of an IRES element into an expression vector based on rubella virus, which belongs to togavirus family (Togaviridae), can be used to develop other togavirus expression vectors of improved stability.
It is therefore an object of the present invention to provide a highly infectious cDNA clone of the rubella virus genomic RNA.
It is a further object of the present invention to provide a molecular biology tool for studying rubella, particularly rubella virus replication.
It is a further object of the present invention to provide cDNA clones for the development of a recombinant rubella virus vaccine.
It is another object of the present invention to provide an expression vector based on rubella virus.
It is a further object of the present invention to provide an expression vector based on rubella virus for the expression of protein or proteins whose genes are inserted into the vector.
It is a further object of the present invention to provide an expression vector based on rubella virus for the expression of protein or proteins in eukaryotic cells, including animal cells.
It is a further object of the present invention to provide an expression vector based on rubella virus for the induction of immunity against rubella and/or a different virus or viruses whose genes are inserted into the vector.
It is a further object of the present invention to provide an expression vector based on rubella virus for the development of recombinant vaccines against rubella virus and/or a different virus or viruses whose genes are inserted into the vector.
It is a further object of the present invention to provide an expression vector based on highly infectious cDNA clones of the rubella virus.
It is yet another object of the present invention to provide a viable cDNA rubella clone that contains IRES as one of its promoters.
It is a further object of the present invention to provide an expression vector based on rubella virus having enhanced stability.
It is yet another object of the present invention to provide a molecular biology tool to study rubella, including but not limited to rubella virus replication and protein expression.
It is yet another object of the present invention to provide a molecular biology tool to study the function of IRES elements in the context of a togavirus genome.
It is yet another object of the present invention to provide a molecular biology tool to study togaviruses other than rubella, in particular their replication and protein expression, by means of introducing IRES elements into their genome.
There has been a long-standing problem of an inability to produce highly infectious rubella virus clones. Applicants discovered that, by replacing a portion of a low infectivity clone with a corresponding fragment that was synthesized by a method known to produce fragments with few mutations, Applicants obtained a chimera exhibiting high infectivity. Therefore, the present invention includes methods of producing highly infectious rubella virus clones by replacing segments of a low infectivity clone with corresponding segments produced by a protocol known to generate sequences having a minimal number of mutations.
Also disclosed are highly infectious, isolated cDNA clones of rubella virus. The infectious rubella virus clones are useful as molecular biology tools for studying rubella virus and for developing recombinant vaccines against rubella.
The term “highly infectious cDNA clone” is defined herein as a cDNA clone having a high specific infectivity, which is defined as a specific infectivity of greater than 0.5 plaques/μg of transcript. The term “low infectivity” or “low specific infectivity” is defined herein as a specific infectivity of less than or equal to 0.5 plaques/μg of transcript.
The highly infectious, isolated cDNA molecules are inserted into a vector that enables replication of the nucleotide sequence of the molecules. A preferred vector is a bacterial plasmid such as pUC 19, pGEM, or PBR-322 (all available from Promega Biotec, Madison, Wis.) or pC11921 adjacent to a bacteriophage RNA polymerase promoter sequence such as the SP6 RNA polymerase (Promega Biotec) such that RNA copies of the rubella virus DNA can be synthesized in vitro. The vector is chemically introduced into susceptible culture cells, for example, E. coli, for amplification and production of large amounts of the cDNA clone. For use, the purified infectious clone is restricted with a restriction endonuclease such as Nsi 1 (New England Biolabs, Beverly, Mass.) for linearization at the termination of the rubella virus cDNA sequences. The linearized plasmid is then transcribed with an RNA polymerase such as SP6 RNA polymerase, which results in production of RNA transcripts templated from the rubella virus cDNA sequence in the non-pathogenic infectious clone.
In preferred embodiments of the present invention, the rubella virus clones have specific infectivities of approximately 104 plaques/μg of transcript. In these preferred embodiments, the rubella virus cDNA clones contain portions of a cDNA clone having a low specific infectivity of approximately 0.5 plaques/ug of transcript or less. In the preferred embodiment, the cDNA clone having a low specific infectivity is the clone described by Wang, et al., J. Virol. 68:3550-3557 (1994), having the sequence shown in SEQ ID NO:1.
The chimeric constructs also contain portions, or fragments, of cDNA from a rubella virus genome in which the cDNA fragments have been produced in a manner known to generate sequences having a minimal number of mutations. The highly infectious constructs are prepared by replacing one or more portions of the cDNA clone having low infectivity with corresponding DNA fragments having fewer mutations. The corresponding DNA fragments may be derived from any rubella virus strain. The specific infectivities of the cDNA clones of the present invention exhibit an increase of at least 104 fold over infectivity of a cDNA clone derived solely from a strain known to have a low specific infectivity.
Rubella Genome Fragments Conferring High Infectivity
Rubella genome fragments that confer the highly infectious property upon the chimera are those produced in a manner known to generate sequences having a minimal number of mutations. The fragments that confer the highly infectious property are obtained as follows. w-Therien, f-Therien and other rubella virus genomes are available from laboratories specializing in rubella virus research. Rubella virus genomes may also be obtained by drawing blood from a person or animal infected with the rubella virus and isolating the genomes by methods that are standard in the art. Such methods can be found in standard lab manuals.
Any rubella virus strains that are or may become available can be used to produce a fragment using a protocol known to generate sequences having a minimal number of mutations. No specific rubella virus genome need be used as a template for the DNA fragments because any rubella virus genome will achieve the desired result. Possible DNA fragments include those derived from the original genome from which the low infectivity clone was produced, as long as the DNA fragments have been produced by a protocol known to generate sequences having a minimal number of mutations.
The fragments can then used for replacing a corresponding fragment of rubella virus clones having a specific infectivity of less than or equal to 0.5 plaques/μg of transcript. Materials and protocols for replacing regions of a cDNA clone with a replacement region are standard in the art. No special materials or protocols are required. Protocols can be found in standard laboratory manuals, such as Sambrook et al., Molecular Cloning: A Laboratory Manual, second edition, Cold Spring Harbor Laboratory Press, New York (1989). Materials can be purchased from widely used and well-known companies, such as, Sigma Chemical, Inc., Promega, and New England Biolabs.
In the most preferred embodiments of the present invention, the cDNA clone having a low specific infectivity is derived from the w-Therien rubella virus strain and the cDNA fragments used to replace portions of the cDNA clone are derived from the f-Therien rubella virus strain. Most preferably, the chimeric constructs contain one or more portions of the infectious cDNA clone Robo102, derived from the w-Therien rubella virus strain, as described in Wang, et al., J. Virol. 68:3550-3557 (1994), and in U.S. patent application Ser. No. 08/459,041, now U.S. Pat. No. 5,663,065, which is incorporated by reference herein (and shown in SEQ ID NO:1), and one or more fragments of synthesized cDNA having few mutations and derived from the f-Therien rubella virus strains.
Any method for producing corresponding DNA fragments having a minimal number of mutations may be used to make the clones of the present invention. Three preferred fragments derived from f-Therien are fragment III (SEQ ID NO:10), fragment I (SEQ ID NO:2), and fragment II (SEQ ID NO:3).
Preferably, the cDNA fragments are created using the technique known by those skilled in the art as reverse transcriptase-long polymerase chain reaction (RT-long PCR) or high-fidelity long PCR, which allows for the amplification of long nucleic acid sequences. This use of this technique results in a reduction of the number of mutations in the genomic cDNA. High-fidelity long PCR amplification of rubella virus cDNA fragments is achieved with first strand cDNA synthesis, using currently available nucleic acid synthesis kits such as the RiboClone cDNA Synthesis System kit (Promega Corporation, Madison, Wis.) according to the protocol of the manufacturer, followed by PCR amplification. In a preferred embodiment, a high-fidelity DNA polymerase, such as ExTaq polymeraserom PanVera Corp., which has a proofreading capacity, is employed for PCR amplification. Exemplary oligonucleotide primers for the generation of nucleic acid fragments, with which to replace the portions of the cDNA clone having low infectivity, are set forth in the Examples below.
Other methods of producing fragments that generate sequences having a minimal number of mutations may become available in the future.
By employing the method of the present invention on a low infectivity rubella virus clone, Applicants discovered that some type of error or mutations in a particular region may cause low infectivity of a rubella virus clone. As discussed in more detail in Example 2, Applicants discovered the deleterious regions in Robo 102 by inserting three different fragment DNAs into three corresponding regions of Robo 102. Insertion of fragment I or fragment II, individually, did not increase the infectivity of subsequently produced viral transcripts. However, the replacement of fragment III into Robo102 did result in increased infectivity. This method may be used on other low infectivity clones to determine if specific locations are the cause of low infectivity.
The following steps may be followed to prepare a highly infectious rubella virus clone of the invention from a low infectivity clone. A low infectivity DNA molecule clone may be obtained by the method described in Wang, et al., J. Virol. 68:3550-3557 (1994). A copy of a rubella virus genome may be obtained from a laboratory specializing in this area, or from the American Type Culture Collection, or isolated from a person infected with the disease. DNA fragments of the genome may be synthesized by a method known to produce sequences having a minimal number of mutations for substitution into the DNA molecule encoding an infectious rubella virus having low infectivity. Portions of the low infectivity clone are then replaced with the newly synthesized corresponding fragments to obtain a chimeric construct exhibiting high infectivity.
As shown in
In another preferred embodiment of the present invention, three fragments from a second rubella virus genome (the f-Therien rubella virus genome), are used to replace the corresponding fragments of the infectious rubella virus cDNA clone having low specific infectivity (Robo102) to create a chimeric construct having high specific infectivity (Robo302). As shown in
In another preferred embodiment of the present invention, fragments I (SEQ ID NO:2) and III replace the corresponding portions of the infectious cDNA clone having low infectivity (Robo102) to produce a highly infectious cDNA clone (Robo202/I). As shown in
In another preferred embodiment of the present invention, fragments II (SEQ ID NO:3) and III as described above, replace the corresponding portions of the infectious cDNA clone having low infectivity (Robo102) to produce a highly infectious cDNA clone (Robo202/II). As shown in
The specific infectivity of highly infectious clones Robo 202, Robo 302, Robo 202/I, and Robo 202/II is approximately 104 plaques per μg. As a comparison, the specific infectivity of the rubella virus RNA is 105 plaques per μg.
Recombinant togavirus expression vector constructs are described herein. The vectors are useful for protein expression in vitro or in vivo, induction of immunity, or for development recombinant vaccines against rubella and/or a heterologous virus whose genes may be inserted into the expression vector. The expression vectors can also be used as molecular biology tools to study togaviruses, particulary rubella viruses, more particularly rubella virus replication and protein expression. The vectors can also be used to study the function of IRES elements in the context of a togavirus genome. The method of incorporating IRES elements into the rubella virus expression vectors can be used to study togaviruses other than rubella, particularly their replication and protein expression.
The expression vector constructs contain a togavirus non-structural protein open reading frame; a first expression element for expression of a heterologous virus; a gene encoding the foreign gene or a multiple cloning site into which the foreign gene may be inserted; a second expression element for the expression of the live, attenuated togavirus; and a togavirus structural protein open reading frame. The togavirus non-structural protein open reading frame and togavirus structural protein open reading frame are preferably from an infectious rubella virus clone. The preferred foreign gene is a heterologous virus gene. The expression element is either a subgenomic (SG) promoter or an internal ribosome entry site (IRES). The incorporation into the vector of at least one IRES results in a recombinant virus of improved stability. Administration of the vector as an immunization agent is useful for the induction of immunity against the togavirus, the heterologous virus, or both.
The term “improved stability” is defined herein as the ability to maintain the expression of foreign genes by the recombinant virus for longer than three passages through the cell culture, wherein the recombinant virus results from the infection of cells by the virus expression vector.
The term “foreign gene” as used herein means a heterologous gene whose expression by the expression vector described herein is desirable.
In a preferred embodiment, the expression elements for expression of both the foreign gene and the togavirus are SG promoters. A multiple cloning site (MCS) is located between the two SG promoters. The MCS is useful for the insertion of the foreign genes under the control of the upstream SG promoter, including but not limited to reporter genes or heterologous virus genes. Exemplary reporter genes include green fluorescent protein (GFP) or chloramphenicol acetyltransferase (CAT) genes. Exemplary heterologous virus genes include encephalitis virus, hepatitis and Dengue virus genes.
In another preferred embodiment, the second expression element, which controls expression of the togavirus structural protein, is replaced by an internal ribosome entry site (IRES). The IRES is a sequence capable of promoting the entry of a ribosome into an RNA molecule at an internal site, independently of the polyadenylated cap
This construct is prepared by replacing an indigenous SG promoter of an infectious rubella cDNA clone with the IRES, thus placing the expression of rubella virus structural genes under the control of IRES. Surprisingly, this construct gives rise to viable rubella virus. This recombinant construct is yet another embodiment of the present invention. A duplicate copy of the SG promoter region is then placed into the intermediate construct directly upstream of IRES. A MCS is placed downstream of the SG promoter to allow for the insertion of the foreign genes. Introduction of the IRES element results in improved stability of the recombinant virus, including improved expression of the foreign gene protein.
In the present embodiments, the vectors are prepared using a backbone of an infectious rubella cDNA clone containing portions of both a cDNA clone having a low specific infectivity and a second rubella virus genome, such as Robo302, described herein, or Robo402 described in Pugachev, K. V., et al., (2000) Virology, 273, 189-197, incorporated herein by reference in its entirety, or a combination of the two clones.
The expression vector is constructed using an infectious rubella cDNA clone and modifying its subgenomic promoter-containing site. The molecular biology techniques employed to perform such modifications are well-known to the one skilled in the art and are detailed in such common in the art manuals as Sambrook, J., Fritsch, E. F., and Maniatis, T. Molecular Cloning: A Laboratory Manual, 2nd ed. Cold Spring Harbor Laboratory Press, Plainview, N.Y. (1989). A preferred starting cDNA clone is a chimeric DNA construct based on a bacterial plasmid such as pUC 19, pGEM, or PBR-322 (all available from Promega Biotec, Madison, Wis.) containing a cDNA copy of a viral genome positioned adjacent to an RNA polymerase promoter, such as an the SP6 RNA Polymerase (Promega Biotec) such that infectious in vitro transcripts can be synthesized. The most preferred cDNA clone is a highly infectious cDNA clone such as wild-type Therien strain rubella infectious clone Robo302 described herein, or Robo402 described in Pugachev, K. V., et al., (2000) Virology, 273, 189-197, incorporated herein by reference in its entirety.
In the preferred embodiments of the present invention, the subgenomic (SG) promoter containing site of a cDNA rubella virus clone is modified to contain, between a non-structural-protein open reading frame (ORF) and structural protein ORF, a promoter followed by restriction nuclease recognition (cloning) site or sites that may be used to introduce a foreign gene, including but not limited to reporter genes, such as green fluorescent protein or chloramphenicol acetyltransferase, and heterologous virus, such as Japanese encephalitis virus, genes. The subgenomic structural protein genes of rubella virus either remain under the control of another promoter, such as the indigenous subgenomic promoter, or an internal ribosome entry site. For use, the vector is chemically introduced into susceptible culture cells, for example, E. coli, for amplification and production of large amounts of the cDNA clone. For use, the purified infectious clone is restricted with a restriction endonuclease such as EcoRI (New England Biolabs, Beverly, Mass.) for linearization at the termination of the rubella virus cDNA sequences. The linearized plasmid is then transcribed in vitro with an RNA polymerase such as SP6 RNA polymerase, which results in production of RNA transcripts. The resulting RNA transcripts are used to transfect the cells by transfection procedures known to those skilled in the art. The cells, in turn, will produce both the native structural proteins of the rubella virus and the protein encoded by the foreign gene. The replication of the RNA sequences and the expression of the encoded protein by the cells may be monitored by various means known to the ones skilled in the art. The cells will further produce recombinant virus particles which, in turn, may be used to infect cells or organisms.
When an appropriate amount of the infectious clone RNA transcript is transfected into susceptible cells by transfection procedures known to those skilled in the art, less virulent togavirus is recovered from the culture fluid within several days incubation. The identity of the virus recovered from the transfected cells can be confirmed by sequencing a specific region of the infectious clone in which a mutation exists which distinguishes it from the wild-type virus.
The less virulent togavirus is then combined with a pharmaceutically acceptable carrier to provide a safe, effective vaccine, such as a rubella virus vaccine. The carrier can be oil, water, saline, phosphate buffer, polyethylene glycol, glycerine, propylene glycol, and combinations thereof, or other vehicles routinely used by the pharmaceutical industry for these purposes. The vaccine is usually provided in lyophilized form and therefore is free of preservatives.
It will be understood by those skilled in the art that modified cDNA for other DNA or RNA viruses could be inserted into the vector in combination with the rubella virus cDNA to make a vaccine effective in immunizing a patient against more than one virus. For example, the modified cDNA of RNA viruses such as encephalitis, hepatitis or Dengue fever virus, is inserted into the vector to produce a combined recombinant vaccine, particularly Japanese encephalitis or hepatitis C virus.
The vaccine can be administered by any appropriate route, for example, orally, parenterally, intravenously, intradermally, intramuscularly, subcutaneously, or topically, in liquid or solid form, in a single dose or a dose repeated after a certain time interval. Preferably, the administration of the vaccine will result in in vivo protein expression of the proteins encoded by the open reading frames contained in the expression vector construct. Most preferably, the administration of the vaccine will result in the induction of immunity against the viruses whose proteins are encoded by the open reading frames. The vaccine is preferably administered subcutaneously at a concentration range from 102 to 104 TCID50/person. (TCID is an abbreviation for tissue culture infectious doses). Preferably, the vaccine is provided to the physician in a lyophilized form, reconstituted in an appropriate solvent such as deionized water or saline, and administered as a single injection.
Expression Vector Construction
In a preferred embodiment of the present invention, a rubella expression vector is constructed using the wild-type Therien strain rubella infections clone Robo302 described herein. As shown in
In the alphavirus-based vectors, the second SG promoter is placed both between the ORFs and downstream of the SP-ORF within the 3′ untranslated region, which is 400 to 500 nucleotides long in these viruses. In the vectors described herein, the region between the structural and non-structural protein ORFs, rather than the region downstream of the structural protein ORF (3′ untranslated region), was chosen for the location of the additional SG promoter because the rubella virus 3′ untranslated region is relatively short (60 nucleotides) and the 3′ 300 nucleotides (including the 3′ end of the structural protein ORF) appear to be necessary for efficient virus replication, as reported by Chen, et al., J. Virol. 73:3386-3403 (1999).
As the rubella SG promoter has not been mapped, a region consisting of the 3′-terminal 126 nucleotides of the nonstructural protein ORF (NSP-ORF) and the entire 120-nt noncoding region between the NSP-ORF and the SP-ORF is duplicated. A multiple cloning site (MCS) containing convenient restriction sites (including unique sites for restriction endonucleases XbaI, BstBI, HpaI, and NsiI, all available from New England Biolabs, Beverly, Mass.) is located between the SG promoters for insertion of foreign genes. Thus, in this construct the SG RNA transcribed from the upstream SG promoter is translated to produce the foreign gene that may be placed in MCS, while the SG RNA transcribed from the downstream SG promoter is equivalent to the standard SG RNA and is translated to produce the virus structural proteins. The plasmid is termed dsRobo302.
In another preferred embodiment, an IRES element is incorporated into the rubella expression vector in place of the second SG promoter. Construction of this vector is initiated by replacing the SG promoter with the IRES in Robo402. Surprisingly, transcripts from this construct, Robo402/IRES, shown in
In another preferred embodiment, the non-structural protein ORF is followed by a SG promoter followed, in turn, by the MCS for the introduction of foreign genes, such as the gene for the green fluorescent protein gene (GFP), followed by an IRES element, followed by the structural protein ORF. In this particular embodiment, the construct is developed from the intermediate construct Robo402/IRES. This expression vector results in a virus of improved stability when passaged multiple times through the Vero cells compared to dsRobo302.
Modifications and variations of the DNA encoding an infectious rubella virus and rubella virus expression vectors, methods of making and use thereof, methods of making a less virulent rubella virus and use thereof, an improved rubella virus vaccine and methods making and use thereof are intended to come within the scope of the present invention.
The foregoing invention will be further understood with reference to the following non-limiting examples.
Vero cells (ATCC, Rockville, Md.) were infected with f-Therien rubella virus (multiplicity of infection (m.o.i.)=0.5). Four days post infection, culture medium was harvested and PEG-precipitated virion RNA was isolated using either TRI-Reagent LS (Molecular Research Center, Cincinnati, Ohio), according to the protocol provided by the manufacturer, or by using the method described by Wang, C. Y. et al., J. Virol. 68:3550-3557 (1994). The extracted RNA was further purified by oligo-(dT)-cellulose chromatography, redissolved in 50 μl of water, and stored at −70° C.
First strand cDNA synthesis was performed with AMV reverse transcriptase (RiboClone™ cDNA Synthesis Kit; Promega, Madison, Wis.), according to the protocol provided by the manufacturer, in the presence of sodium pyrophosphate with one of the following three primers:
Three large cDNA clones were then generated using the PCR techniques described by Barnes, W. M., et al., Proc. Natl. Acad. Sci. USA 91:2216-2220 (1994) and Cheng, S., et al., Proc. Natl. Acad. Sci. USA 91:5695-5699 (1994), the teachings of which are incorporated by reference herein. The single-stranded products, Fragments I (SEQ ID NO:2), II (SEQ ID NO:3), and III were phenol-chloroform extracted and precipitated twice with ethanol, first in the presence of 2M ammonium acetate and second in the presence of 0.3 M sodium acetate. The precipitates were redissolved in 10 μg of water and 2 to 5 μl were used in 50 μl PCR reactions that contained 2.5 units of ExTaq temperature stable DNA polymerase (TaKaRa LA PCR kit, Pan Vera Corp., Madison, Wis.), and the following three primers:
(contains a HindII site (double underlined), the SP6 RNA polymerase promoter (dot underlined), and nucleotides 1-28 of the rubella virus genome (single underlined));
The following primers and amplification protocols were utilized: for fragment I, the primer set forth in SEQ ID NO:7 served as a primer for 30 cycles of 20 seconds at 98° C., one second at 55° C. and three minutes at 70° C.; for fragment II, the primer set forth in SEQ ID NO:8 served as a primer for 30 cycles of 20 seconds at 98° C., one second at 50° C., and five minutes at 70° C.; and for fragment III, the primer set forth in SEQ ID NO:9 served as a primer for 30 cycles of 20 seconds at 98° C., one second at 52° C., and seven minutes at 68° C. These techniques were slightly modified by the addition of 10% DMSO to the PCR amplifications due to the high G+C content of the rubella genome. Roughly ten percent of the rubella virus genome between fragments I (SEQ ID NO:2) and II (SEQ ID NO:3) could not be amplified from the virion RNA, presumably due to peculiarities of secondary and or tertiary structure in this region.
Using standard recombinant DNA techniques, fragments I (SEQ ID NO:2), II (SEQ ID NO:3), and III were digested with the restriction enzymes HindIII and KpnI, NheI and BglII, or BglII and EcoRI, respectively, as described below, and individually ligated with Robo102 from which the corresponding fragment had been removed. Phenol-chloroform extracted and linearized constructs were transcribed in vitro as described in Pugachev, K. V., P. W. Mason, and T. K. Frey Virology 209:155-166 (1995), using SP6 RNA polymerase (Epicentre Technologies, Madison, Wis.) in the presence of a cap structure analog, and transfected into Vero cells using lipofectin-mediated techniques described by Rice et al., New Biol. 1:285-296 (1989).
Freshly linearized Robo plasmids in the presence of the m7G(5′)ppp(5′)G cap structure analog (New England Biolabs, Beverly, Mass.) were used in the transcription reactions in accordance with the method of Rice et al., New Biol. 1:285-296 (1989), with the modification that Opti-MEMI-reduced serum medium replaced phosphate buffered saline (PBS) during transfection. Transfected cells were incubated and tested for rubella induced cytopathic effects.
As shown in
The specific infectivity of the rubella virus cDNA clone designated Robo202, as described above in Example 1, was determined as follows. After PCR amplification of fragment III (SEQ ID NO:10), as described above, the fragment was digested with restriction enzymes BglII and EcoRI and ligated with a similarly digested Robo102 clone, as shown in FIG. 1. In vitro transcription of the newly constructed clone, Robo202, and subsequent transfection into Vero cells resulted a 104-fold increase in infectivity. While the slightly infectious Robo102 clone did not induce cytopathic effects within eight days after transfection into Vero cells, insertion of fragment III into the Robo102 clone resulted in cytopathic effects within five days of transfection into Vero cells. However, insertion of either fragment I (SEQ ID NO:2) or fragment II (SEQ ID NO:3) produced viral transcripts, and therefore the mutation that caused low infectivity of Robo102 is believed to be located in the region replaced by fragment III.
Following PCR amplification of fragments I (SEQ ID NO:2) and II (SEQ ID NO:3), the fragments were digested with restriction enzymes HindIII and KpnI, and NheI and BglII, respectively. The fragments were simultaneously inserted into a Robo202 clone wherein the corresponding fragments had been removed, resulting in the Robo302 construct, as shown in FIG. 1. The addition of fragments I (SEQ ID NO:2) and II (SEQ ID NO:3) to the Robo202 construct, produced viral transcripts with an increased specific infectivity.
Vero cells grown in 24-well plates were infected with the indicated viruses at an m.o.i. of 2 pfu/cell. At indicated times post infection, cells were trypsinized, washed with PBS and stained with trypan blue. Three aliquots of each trypsinized cell suspension were counted. As shown in
Fragments I (SEQ ID NO:2) and II (SEQ ID NO:3) were excised from the Robo302 construct with the appropriate restriction enzymes, and introduced individually to produce the Robo202/I and Robo202/II constructs, respectively. Introduction of either fragment resulted in decreased plaque opacity, with Robo202/II producing the most clear plaques, slightly smaller than the plaques produced by Robo302.
To elucidate the basis of the difference in plaque phenotype between the Robo constructs, growth curves of the resulting viruses and their ability to kill infected cells were investigated. Because of the limited titer to which one of the viruses, Robo202/I, replicated, an m.o.i. of 2 pfu/cell was used in these experiments. As shown in
To analyze molecular differences between these viruses that could account for the difference in plaque morphology/cell killing, virus macromolecular synthesis was characterized. Production of the rubella virus-specific RNAs (of both positive and negative polarity) was examined by northern hybridization of total intracellular RNAs extracted from infected cells with the result that all of these viruses produced equivalent amounts of all the virus RNA species (data not shown). Non-structural and structural protein synthesis was analyzed by immunoprecipitation of the proteins from lysates of infected cells radiolabeled for 1.5 hours. As shown in
As shown in
Following digestion of amplicon 1 with BglII and XbaI and amplicon 2 with XbaI and AscI, the fragments were inserted simultaneously by means of three-fragment ligation, into Robo302 digested with BglII and AscI (which removed the corresponding fragment from Robo302). This resulted in a rubella virus construct which containes a subgenomic promoter directly downstream of the non-structural gene ORF, followed by multiple cloning site introduced by primer K3, followed by the second subgenomic promoter and structural protein ORF. When in vitro transcripts from dsRobo302 were used to transfect Vero cells (ATCC, Rockville, Md.), virus was recovered. Production of in vitro transcripts from the plasmids and subsequent transfection of Vero cells were done according to standart procedures as described in Pugachev, K. V., et al., J. Virol. 71:562-568 (1997).
aThe sequences of oligonucleotide primers used in two manipulations, duplication of the SG promoter in Robo302, and substitution of the SG promoter in Robo402/NsiI with an IRES from EMCV are given. In both manipulations, two PCR amplicons were generated and the manipulation was done via a three-fragment ligation. The upstream primer (U) sequence is at the 5′ end of the amplicon
bNucleotides in the primers containing RUB sequences are underlined; those in the genome (numbered from the 5′ end) to which the nucleotides in the primer are colinear or complementary are given in parentheses. NA, not applicable.
cRestriction site sequences in the primer used for cloning and the corresponding name are in bold. In the case of primer K3, used to create the MCS in dsRobo302, several restriction sites are present; they are alternately shown in bold and all italics.
To test expression from dsRobo302, the reporter genes chloramphenicol acetyltransferase (CAT) was introduced into the multiple cloning site of dsRobo302. The resulting construct was termed dsRobo302/CAT. When in vitro transcripts from dsRobo302/CAT were used to transfect Vero cells, virus was recovered. As shown in
GFP was PCR amplified from SINrep/GFP plasmid (obtained from I. Frolov, currently and University of Texas Medical Center, Galveston, Tex.) with the primers that retained the initiation and termination codons of the GFP gene but added flanking XbaI and NsiI sites and cloned into the MCS of the dsRobo302 plasmid using these two enzymes. When in vitro transcripts from dsRobo302/GFP were used to transfect Vero cells, virus was recovered. GFP expression by the dsRobo vector was detected by examining living Vero cell cultures infected with dsRobo/GFP virus under a microscope with epifluorescence capability and by immunoprecipitation, as shown in FIG. 6. Vero cells were mock infected (Mock), or infected with Robo402 virus (R402) or a passaged stock of dsRobo/GFP virus. In these multiple passages, P0 is virus recovered from transfection which was subsequently passaged at a low MOI (˜0.1 PFU/cell) to produce P1, P2, etc. For this experiment, the MOI for each virus stock was adjusted to ˜1 PFU/cell. Three days postinfection, cells were metabolically radiolabeled with [35S]methionine (1,000 Ci/mmol; Amersham) for 1.5 h followed by lysis with radioimmunoprecipitation buffer, immunoprecipitation using an anti-GFP polyclonal immunoglobulin G (Clontech), and SDS-PAGE, as described by Forng, R.-Y, et al., Virology 206:843-854 (1995). The percentage of cells in an infected culture expressing GFP was determined by flow cytometry, as shown in FIG. 4. Vero cells were infected at an MOI of 1 PFU/cell with dsRobo/GFP stocks produced by multiple low-MOI passages (virus recovered from transfected cells, designated P0, was passaged in Vero cells to produce P1, P2, etc.). Three to four days postinfection, when 100% of the cells are infected with Robo302 virus under these conditions, to determine the percentage of cells expressing GFP, the infected cultures were trypsinized, and the cells were resuspended in medium and subjected to fluorescence-activated cell sorting analysis using a Becton Dickinson FACS Calibur flow cytometer (equipped with a 388-nm, 16-mW argon laser) with CellQuest software (Becton Dickinson); 20,000 events were used to determine each percentage.
The majority of plaques formed by P0 (passage 0, initial round of infection of cells by viruses) dsRobo and dsRobo/GFP virus (virus produced by transfected cultures) were smaller than Robo302 virus plaques; however, ˜1% were similar in size to Robo302 virus plaques. P0 dsRobo and dsRobo/GFP virus titers were roughly 5×105 PFU/ml, in comparison to average P0 Robo302 virus titers of 5×106 PFU/ml. The analysis of intracellular RNA from infected cells is shown in FIG. 8.
When P0 dsRobo/GFP virus was passaged (multiplicity of infection [MOI] of 0.1 PFU/cell, with harvest at 5 to 6 days postinfection), the level of GFP expression diminished and was undetectable by radioimmunoprecipitation by P3, as shown in FIG. 6A. For this experiment, Vero cells were mock infected (Mock), or infected with Robo402 virus (R402)or a passaged stock of dsRobo/GFP virus. In these multiple passages, P0 is virus recovered from transfection which was subsequently passaged at a low MOI (˜0.1 PFU/cell) to produce P1, P2, etc. For this experiment, the MOI for each virus stock was adjusted to ˜1 PFU/cell. Three days postinfection, cells were metabolically radiolabeled with [35S]methionine (1,000 Ci/mmol; Amersham) for 1.5 h followed by lysis with radioimmunoprecipitation buffer, immunoprecipitation using an anti-GFP polyclonal immunoglobulin G (Clontech), and SDS-PAGE (4). The percentage of cells in infected cultures expressing GFP declined precipitously through P3, and GFP-positive cells were not detectable in the fourth and subsequent passages, as shown in FIG. 7. Thus, GFP expression was unstable.
To eliminate the possibility of homologous recombination in the rubella vector, it was investigated whether an IRES element could be incorporated into our rubella expression vector in place of the second SG promoter. Schematic map of the resulting Robo402/IRES vector is shown FIG. 4. First, Robo402 construct described in 12 was modified by the addition of an NsiI site immediately following the NSP-ORF to produce Robo402/NsiI. Then, a ˜600-nucleotide amplicon containing the complete encephalomyocarditis virus internal ribosome entry site (IRES) was PCR amplified from pCEN plasmid (obtained from I. Frolov, currently at University of Texas Medical Center, Galveston, Tex.) using primers IR-5 and IR-3 (Table 1). This amplicon was rendered blunt ended with T4 DNA polymerase and then digested with NsiI. A second amplicon containing rubella sequence between the second codon of the SP-ORF and AscI (nucleotide 7313) was PCR amplified using primers IRES-R and 1 (Table 1). This amplicon was digested with Eco47III and AscI. The two amplicons were then combined in a three-fragment ligation with NsiI-AscI-digested Robo402/NsiI. Surprisingly, transcripts from this construct, Robo402/IRES, gave rise to viable virus which formed plaques on Vero cells. The average P0 titer of Robo402/IRES virus was 8.5×105 PFU/ml; the titer rose to 2.4×106 PFU/ml at P3 and 6.0×107 PFU/ml at P5.
A schematic map of a siRobo402 vector is shown in FIG. 4. To construct the siRobo402/GFP vector, the SG promoter followed by the GFP gene was introduced into Robo402/IRES. The BglII-NsiI fragment of dsRobo302/GFP was ligated into Robo402/IRES that had been restricted with these two enzymes. Virus produced from this construct should synthesize a single SG RNA; in this SG RNA, the GFP gene is 5′ proximal and is followed by the IRES and the SP-ORF. A siRobo402 vector containing the dsRobo302 multiple cloning site between the SG promoter and the IRES element was created by similar introduction of the BglII-NsiI fragment from dsRobo402 into Robo402/IRES.
Transcripts from siRobo402/GFP gave rise to virus following transfection of Vero cells. P0 titers of siRobo/GFP virus were 3×104 PFU/ml but rose to 4×106 PFU/ml at P3 and 1.2×107 PFU/ml at P5. GFP expression by siRobo/GFP virus assayed by immunoprecitpitation, as shown in FIG. 6B. Vero cells were mock infected (Mock), infected with Robo402 virus (R402), Robo402/IRES virus (402/IRES), or a passaged stock of dsRobo/GFP (ds/GFP) or siRobo/GFP virus. In these multiple passages, P0 is virus recovered from transfection which was subsequently passaged at a low MOI (˜0.1 PFU/cell) to produce P1, P2, etc. For this experiment, the MOI for each virus stock was adjusted to ˜1 PFU/cell. Three days postinfection, cells were metabolically radiolabeled with [35S]methionine (1,000 Ci/mmol; Amersham) for 1.5 h followed by lysis with radioimmunoprecipitation buffer, immunoprecipitation using an anti-GFP polyclonal immunoglobulin G (Clontech), and SDS-PAGE (4). GFP expression by siRobo/GFP virus also analyzed by flow cytometry of infected cultures as shown in FIG. 4. Vero cells were infected at an MOI of 1 PFU/cell with siRobo/GFP stocks produced by multiple low-MOI passages (virus recovered from transfected cells, designated P0, was passaged in Vero cells to produce P1, P2, etc.). Three to four days postinfection, when 100% of the cells are infected with Robo302 virus under these conditions, to determine the percentage of cells expressing GFP, the infected cultures were trypsinized, and the cells were resuspended in medium and subjected to fluorescence-activated cell sorting analysis using a Becton Dickinson FACS Calibur flow cytometer (equipped with a 388-nm, 16-mW argon laser) with CellQuest software (Becton Dickinson); 20,000 events were used to determine each percentage. GFP expression by siRobo/GFP virus was relatively stable through P5 as assayed by both methods. P0 siRobo/GFP virus formed small opaque plaques, and this was the majority plaque morphology through P5, when ˜10% of the plaques had Robo402 virus morphology. Analysis of intracellular virus-specific RNA produced by siRobo viruses is shown in FIG. 5B. Vero cells were mock infected (Mock) or infected at an MOI of ˜1 PFU/cell with Therien strain rubella (WT [wild type]), Robo402 virus (R402), or stocks of dsRobo/GFP (dsGFP), Robo402/IRES (402/IRES), or siRobo/GFP viruses passaged one (P1), three (P3), or five (P5) times in Vero cells (MOI of ˜0.1 PFU/cell at each passage). Except for dsRobo/GFP virus [ds/GFP], for which only P1 stock was tested. Three days postinfection, total cell RNA was extracted and subjected to agarose gel electrophoresis and virus-specific RNA species were detected by Northern hybridization using a probe complementary to the rubella SP-ORF ([32P]CTP-labeled negative-polarity RNA transcripts synthesized from pRUB-SP-ORF, as described in Marr, et al., Virology 180:400-405 (1991). The amount of radioactivity present in RNA bands on autoradiographs was quantitated by densitometry with a Fujix BAS1000 Bio Imaging analyzer (Fuji Photo Film, Tokyo, Japan), using software provided by the manufacturer. This analysis revealed that the presence of the genomic RNA and an SG RNA larger than the standard SG RNA in P1 siRobo/GFP-infected cells, as expected. However, by P3, a band of intermediate size between the siRobo/GFP SG RNA and the standard SG RNA was present, and by P5 a band of similar in size to the standard SG RNA appeared. Concomitantly, a shorter genomic RNA band appeared with a size similar to the size of the standard genomic RNA. Thus, deletion events occurred during passage of siRobo/GFP virus, but at a much lower rate compared to dsRobo viruses. In
A truncated form of the immunogenic E proteins of Japanese encephalitis virus was expressed in both dsRobo and siRobo as prototype vaccine candidates. As rubella virus replicates in a variety of vertebrate cell types and in most of these replication is to low titers and without accompanying cytopathogenicity (unlike the Vero cells used in this study), one of the possible advantages of a rubella expression vector would be for low-level expression without a drastic effect on the cell, which has been a problem for the highly cytopathic alphavirus vectors described in prior art as described in Schlesinger, S., et al., Curr. Opin. Biotechnol. 10:434-439 (1999). A rubella-based vaccine would be useful in many settings, including but not limited to a pediatric setting to target systemic pathogens against which universal immunization was desired, such as human immunodeficiency virus, respiratory syncytial virus, or one of the hepatitis agents; a cocktail of rubella-based vaccines targeting different pathogens could be used to induce immunity simultaneously against each pathogen targeted in the cocktail.
All patents and publications mentioned herein are hereby incorporated by reference.
This is a continuation-in-part of U.S. patent application Ser. No. 09/557,232, filed Apr. 24, 2000, now abandoned which is a continuation of U.S. patent application Ser. No. 08/999,733 filed Sep. 2, 1997, now U.S. Pat. No. 6,054,573, which is a continuation-in-part of U.S. patent application Ser. No. 08/459,041 filed Jun. 2, 1995, now U.S. Pat. No. 5,663,065, which is a continuation-in-part of U.S. patent application Ser. No. 08/093,453, filed Jul. 19, 1993, now U.S. Pat. No. 5,439,814, which is a continuation of U.S. patent application Ser. No. 07/722,334, filed on Jun. 28, 1991, now abandoned. This application claims the benefit of U.S. Provisional Patent Application Ser. No. 60/329,686, filed Oct. 15, 2001.
The U.S. Government has rights in this invention arising out of National Institutes of Health (NIAID) grant number AI-21389.
| Number | Name | Date | Kind |
|---|---|---|---|
| 5439814 | Frey et al. | Aug 1995 | A |
| 5663065 | Frey et al. | Sep 1997 | A |
| 5925565 | Berlioz et al. | Jul 1999 | A |
| 6054573 | Frey et al. | Apr 2000 | A |
| Number | Date | Country | |
|---|---|---|---|
| 20030130498 A1 | Jul 2003 | US |
| Number | Date | Country | |
|---|---|---|---|
| 60329686 | Oct 2001 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 08999733 | Sep 1997 | US |
| Child | 09557232 | US | |
| Parent | 07722334 | Jun 1991 | US |
| Child | 08093453 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 09557232 | Apr 2000 | US |
| Child | 10271311 | US | |
| Parent | 08459041 | Jun 1995 | US |
| Child | 08999733 | US | |
| Parent | 08093453 | Jul 1993 | US |
| Child | 08459041 | US |
