WO2007143442A2 - A novel virulence determinant within the e2 structural glycoprotein of classical swine fever virus - Google Patents
A novel virulence determinant within the e2 structural glycoprotein of classical swine fever virus Download PDFInfo
- Publication number
- WO2007143442A2 WO2007143442A2 PCT/US2007/069852 US2007069852W WO2007143442A2 WO 2007143442 A2 WO2007143442 A2 WO 2007143442A2 US 2007069852 W US2007069852 W US 2007069852W WO 2007143442 A2 WO2007143442 A2 WO 2007143442A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- csfv
- virus
- glycoprotein
- swine fever
- fever virus
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/12—Viral antigens
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/005—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from viruses
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N7/00—Viruses; Bacteriophages; Compositions thereof; Preparation or purification thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/51—Medicinal preparations containing antigens or antibodies comprising whole cells, viruses or DNA/RNA
- A61K2039/525—Virus
- A61K2039/5254—Virus avirulent or attenuated
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2770/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA ssRNA viruses positive-sense
- C12N2770/00011—Details
- C12N2770/24011—Flaviviridae
- C12N2770/24311—Pestivirus, e.g. bovine viral diarrhea virus
- C12N2770/24322—New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2770/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA ssRNA viruses positive-sense
- C12N2770/00011—Details
- C12N2770/24011—Flaviviridae
- C12N2770/24311—Pestivirus, e.g. bovine viral diarrhea virus
- C12N2770/24334—Use of virus or viral component as vaccine, e.g. live-attenuated or inactivated virus, VLP, viral protein
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2770/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA ssRNA viruses positive-sense
- C12N2770/00011—Details
- C12N2770/24011—Flaviviridae
- C12N2770/24311—Pestivirus, e.g. bovine viral diarrhea virus
- C12N2770/24361—Methods of inactivation or attenuation
Definitions
- This invention relates to the isolation and characterization of novel Classical Swine Fever Virus (CSFV) virulence determinants within the E2 structural glycoprotein and utilization of these novel virulence determinants to design live attenuated CSF vaccines.
- CSFV Classical Swine Fever Virus
- CSF Classical swine fever
- BVDV bovine viral diarrhea virus
- BDV border disease virus
- the 12.5 kb CSFV genome contains a single open reading frame which encodes a 4000 amino acid polyprotein and ultimately yields 11 to 12 final cleavage products (NH2-Npro-C-Ems-E1-E2-p7-NS2- NS3-NS4A-NS4B-NS5A-NS5B-COOH) through co- and posttranslational processing of the polyprotein by cellular and viral proteases (Rice, C. M. 1996. In: Fundamental
- Virulence and host range phenotypes vary among CSFV isolates and between pestiviruses. Infection with highly virulent CSFV strains leads to death in infected animals, whereas isolates of moderate to low virulence induce a prolonged chronic disease (van Oirschot, supra). In addition, BVDV and BDV, while etiologic agents of diseases in bovine and ovine species, respectively, can also infect swine without inducing clinical disease (van Oirschot, supra).
- the capsid protein, and glycoproteins Ems, E1 , and E2 are the structural components of the CSFV virion with E1 and E2 anchored to the envelope by their carboxyl termini and Ems loosely associated with the viral envelope (Thiel et al. 1991. J. Virol. 65: 4705-4712; Weiland et al. 1990. J. Virol. 64: 3563-3569; Weiland et al. 1999. J. Gen. Virol. 80: 1157-1165). All three glycoproteins have been associated with CSFV virulence (Meyers, supra; Risatti et al. 2005 a, b, supra).
- E2 glycoprotein is considered essential for CSFV replication, as virus mutants containing partial or complete deletions of the E2 gene have proven non-viable (van Gennip et al. 2002. Vaccine 20: 1544-1556).
- E2 has been implicated, along with Ems (Mayer et al., supra) and E1 (Wang et al. 2004. Virology 330: 332-341 ), in viral adsorption to host ceils; indeed, chimeric pestiviruses exhibit infectivity and cell tropism phenotypes consistent with those of the E2 gene donor (van Gennip et al. 2000, 2002, supra).
- CSFV E2 is the most immunogenic of the CSFV glycoproteins (Konig et al. 1995. J. Virol. 69: 6479-6486; Weiland et al. 1990, supra), inducing neutralizing antibodies and protection against lethal challenge.
- CSFV E2 also contains, between residues 829 and 837, an epitope recognized by monoclonal antibody (mAb) WH303 (Lin et al. 2000. J. Virol. 74:11619-11625), a reagent which fails to react with BVDV or BDV E2 and is routinely used for CSF diagnostics.
- mAb monoclonal antibody
- CSFV classical swine fever virus
- An added object of the invention is to provide immunogenic compositions comprising a viable recombinant classical swine fever virus comprising a modified CSFV E2 glycoprotein.
- An additional object of the invention is to provide a rationally designed live attenuated CSFV vaccine which lessens severity of CSF.
- Another object of the invention is to provide a rationally designed live attenuated CSFV vaccine effective to protect an animal from clinical CSF disease when challenged with virulent Brescia CSFV.
- a further object of the invention is to provide a marker vaccine which allows a serological distinction between vaccinated animals and animals infected with CSFV.
- a still further object of the invention is to provide a method for protecting an animal against CSF by administering an effective amount of rationally designed live attenuated CSFV vaccine.
- Figure 1 depicts a comparison of CSFV Brescia, BVDV strain NADL and CSFV T1-5 mutant viruses in the mAb WH303 epitope area of E2 glycoprotein. Amino acid residue positions in the CSFV polyprotein are indicated. Italics indicate residues different from those in Brescia EZ, both in BVDV strain NADL and CSFV T1v to T5v.
- Figures 2A and 2B compare characteristics of T1v-T5v mutants and BICv.
- Figure 2A shows in vitro growth characteristics of T1v-T5v mutants and BICv.
- Figure 2B shows plaque formation and mAb reactivity of mutants T1v-T5v and BICV.
- SK6 monolayers were infected with 50 to 100 TCID 50 , overlaid with 0.5% agarose and incubated at 37 0 C for 3 days. Plates were fixed with 50% (vol/vol) ethanol-acetone and differentially stained by immunohistochemistry with mAb WH303 and mAb WH308.
- Figure 3 shows clinical scores recorded from pigs infected with recombinant viruses T1v-T5v and BICv. Clinical Scores were calculated as previously described with modifications and were based on observations of two (T1v, T2v, T3v and T4v) or six (T5v and BICv) animals.
- Figures 4A-B show peripheral white blood cell ( Figure 4A) and platelet counts ( Figure 4B) in pigs infected with recombinant viruses T1v-T5v and BICv. Counts are expressed as numbers/ml and each point represents the mean and standard errors for two (T1v, T2v, T3v and T4v) or six (T5v and BICv) animals.
- Figures 5A-C depict virus titers in blood (Figure 5A), nasal swabs (Figure 5B), and tonsil scrapings (Figure 5C) from pigs infected with T1v-T5v mutants or BICv. Each point represents the mean TCIDso/mL and standard deviation for two (T1v, T2v, T3v and T4v) or six (T5v and BICv) animals.
- Figures 6A-B show peripheral white blood cell (Figure 6A) and platelet counts (Figure 6B) in pigs mock vaccinated or vaccinated with T5v and challenged at 3 or 21 DPI with BICv. Values for control, mock vaccinated, and challenged animals are represented with filled squares. Counts are expressed as numbers/ml and represent the mean of four individuals with error bars indicating standard error.
- WH 303 as a major immunodominant epitope have been recently observed during characterization of neutralizing monoclonal antibodies to CSFV E2 and Ems using phage-displayed random peptide library (Zhang et al. 2006. Archives of Virology 151 (1): 37-54). Those monoclonal antibodies were found to bind a common motif SPTxL that also map to WH 303 epitope (SPTTL). Furthermore, multi peptide-vaccines, containing the WH 303 epitope, consisting of six overlapping peptides ranging between 20 to 25 amino acids length induced immunity against CSFV (Dong et al. 2005. Vaccine 23:3630-3633).
- Ems, EI and E2 are structural glycoproteins in the CSFV virion envelope (Thiel et al., supra). Anchored to the envelope, E2 appears as both homo and heterodimers linked by disulfide bridges (Thiel et al., supra; Weiland et al. 1990, 1999, supra) and, along with Ems (Hulst et al. 1997. J. Gen. Virol. 78: 2779-2787) and E1 (Wang et al., supra) have been shown to be important for virus reception.
- Engineered Pestiviruses containing chimeric E2 proteins have altered host range.
- MDBK cells were still permissive to the chimera although the difference in viral progeny yield, 24 hours after infection, was 100 fold less than wild type BVDV.
- SK6 cells were similarly permissive for the chimera and BVDV E2 donor; however, the chimera did not gain BVDV ability to infect fetal bovine epithelial cells (van Gennip et al. 2000, supra).
- T4v and T5v presented a 10 fold viral progeny yield reduction in SK6 cells in comparison with BICv, T1v, T2v and T3v (Fig. 2A), and lack the ability to replicate efficiently in bovine kidney cells (MDBK) (data not shown).
- T4v and T5v exhibited an approximately 70% plaque size reduction compared with parental BICv in SK6 cells (Fig. 2B).
- a similar small plaque phenotype was observed with BVDV strain NADL on SK6 cells (data not shown), suggesting that these viruses have an in vitro altered capability of attachment and/or spreading.
- Hulst et al. J. Virol 74:9553-9561; Hulst et al.
- CSFV Brescia heparin sulfate binding dependent variants obtained after serial passages in cultured swine kidney cells have a reduced plaque size. These variants, containing a single amino acid mutation in the Ems protein, were virulent in pigs (Hulst et al. 2000, 2001. supra). However, two different CSFV strain Brescia derived recombinant viruses containing mutations in E1 (Risatti et a/. 2005b, supra) and E2 (Risatti et a/. 2005a, supra) showed reduced plaque size phenotype in cultured swine kidney cells and were attenuated in swine.
- Swine kidney cells (SK6) (29), free of BVDV, were cultured in Dulbecco' minimal essential medium (DMEM) (Gibco, Grand Island, NY) with 10% fetal calf serum (FCS) (Atlas Biologicals, Fort Collins, CO).
- DMEM Dulbecco' minimal essential medium
- FCS fetal calf serum
- CSFV Brescia strain was propagated in SK6 cells and used for the construction of an infectious cDNA clone (17). Titration of CSFV from clinical samples was performed using SK6 cells in 96 well plates (Costar, Cambridge, MA).
- Viral infectivity was detected, after 4 days in culture, by immunoperoxidase assay using the CSFV monoclonal antibodies WH303 or WH308 (1) and the Vectastain ABC kit (Vector Laboratories, Buringames, CA) (25). Titers were calculated using the method of Reed and Muench (14) and expressed as TCID50/ml. As performed, test sensitivity was > 1.8 TCID50/ml.
- a full-length infectious clone (IC) of the virulent Brescia isolate (pBIC) (17) was used as a template in which six residues of the WH303 epitope (TAVSPTTLR; SEQ ID NO:1) between residues 829 to 837 of E2 were mutated to reflect those of homologous residues present in the BVDV isolate NADL (TSFNMDTLA; SEQ ID NO:2) (Lin et a/., supra).
- Reverse primers correspond to the complementary sequence.
- RNA products were precipitated with LiCI and transfected into SK6 cells by electroporation at 500 volts, 720 ohms, 100 watts with a BTX 630 electroporator (BTX, San Diego, CA).
- Cells were plated in 12 well plates and 25 cm 2 flasks, and incubated for 4 days at 37EC and 5% CO 2 atmosphere.
- Virus was detected by immunoperoxidase staining using a CSFV E2 specific monoclonal antibody (WH308). Stocks of rescued viruses were stored at -70C. Accuracy of the introduced mutations was verified by sequencing the E2 gene of the mutated viruses.
- T1v-T5v In vitro growth characteristics of T1v-T5v relative to parental pBICv were evaluated in a multistep growth curve (Fig. 2A).
- SK6 cell cultures were infected at a multiplicity of infection (MOI) of 0.01 TCID 50 per cell.
- Virus was adsorbed for 1 h (time zero), and samples were collected at times post infection through 72 h. While mutants TIv T2v. and T3 exhibited growth characteristics practically indistinguishable from pBICv, T4 and T5v exhibited a 10-fold decrease in the final virus yield.
- T4v and T5v also exhibited an 80-90% reduction in plaque size relative to BICv, T1v, T2v, and T3v (Fig. 2B).
- T1v-T5v mutants appeared to have virulence phenotypes that were increasingly attenuated (Table 2, Figure 3).
- T1v and T2v were also highly pathogenic, inducing fever and death in swine in a manner similar to that of BICv (Table 2); however, T2v demonstrated a slight delay in clinical scores relative to BICv (Table 3).
- T3v induced lethal disease but with delayed kinetics relative to BICv, as death occurred 4-8 days later (Table 2).
- T4v and T5v failed to induce lethal disease, with T4v inducing only a mild and transient fever and T5v inducing almost no clinical disease (Table 2, Figure 3).
- BICv, Z Z TD C D C 1v, T2v and T3v infection resulted Q C Q C by 6 DPI in a drastic reduction in white blood cell (WBC) and platelet counts which remained low until death, while T4v and T5v-infected induced a transient and much less dramatic effect (Fig. 4).
- Table 3 Virus titers 1 in clinical samples and tissues following infection with T5v or BICv.
- T1v-T5v Attenuation of T1v-T5v was also reflected in viremia and virus shedding. While T1v and T2v induced viremic titers comparable to those induced by BICv, T3v titers were reduced by 10 1 to 10 2 log-io, and T4v and T5v induced titers 10 3 to 10 5 logi 0 lower than BICv titers at similar times post-infection (Fig. 5A). A similar pattern was observed for virus titers from nasal swabs and tonsil-scrapings (Fig. 5B and C, respectively), with T3v, T4v and T5v titers falling below detectible levels at later DPI.
- T5v and BICv-infected animals were euthanized at 2, 4, 6, 8, and 14 DPI (one animal/time point/group) and virus titers determined for tissue samples of tonsils, submandibular lymph node, spleen, blood and kidney tissue samples and for nasal swab and tonsil scraping samples (Table 3).
- T5v exhibited significantly lower levels of virus replication in tonsils (approximately 10 2 to 10 4 logio) relative to BICv. Similar differences between T5v and BICv were observed in virus titers from the regional draining mandibular lymph node, spleen and kidney between (Table 3).
- Each of the T1v-T5v mutants was initially screened for its virulence phenotype in swine relative to virulent Brescia virus. Swine used in all animal studies here were 10 to 12 week old, forty-pound pigs inoculated intranasally with 10 5 TCID 50 of either mutant or wild-type virus. For screening, 12 pigs were randomly allocated into 6 groups of 2 animals each, and pigs in each group were inoculated with one of the T1v-T5v mutants or pBICv. Clinical signs (anorexia, depression, fever, purple skin discoloration, staggering gait, diarrhea and cough) were observed daily throughout the experiment and scored as previously described with modifications.
- T5v mutations were randomly allocated into 2 groups of 5 animals each and inoculated with T5v or pBICv. One pig per group was sacrificed at 2, 4, 6, 8 and 14 DPI. Blood, nasal swabs and tonsil scraping samples were obtained from pigs at necropsy. Tissue samples (tonsil, mandibular lymph node, spleen and kidney) were snap-frozen in liquid nitrogen for virus titration.
- T5v induced by 3 DPI complete protection against BICv-induced clinical disease. All pigs survived infection and remained clinically normal, with only two animals presenting with a transient fever at 4 DPC (Table 4) and without significant changes in their hematological values (Fig. 6). Similarly, pigs challenged at 21 days post T5v infection remained clinically normal (Table 4).
- Viremia and virus shedding of BICv challenge virus as specifically detected with mAb WH303 was also examined at 4, 6, 8, 14 and 21 DPC (data not shown).
- BICv viremia was observed by 5 DPC, with virus titers remaining high (10 6 TCID 50 /ml by 8 DPC) until death, and BICv was titrated from nasal swabs and tonsil scrapings by 4 DPC, reaching titers of 10 4 -10 5 TCID 50 /ml) by 8 DPC.
- BICv was absent in all clinical samples (blood, nasal swabs, or tonsil scrapings) from T5v-vaccinated swine following challenge.
- T5v is able to rapidly induce complete protection against lethal CSFV challenge, that T5v-immune swine demonstrate no detectible viremia or shedding from challenge virus.
- T5v is able to induce in experimentally vaccinated animals complete protection against both the presence of clinical disease and the replication of the challenge virus when challenged with the virulent parental virus Brescia either at 3 or 28 days after T5 vaccination.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Genetics & Genomics (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Virology (AREA)
- Zoology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Wood Science & Technology (AREA)
- Medicinal Chemistry (AREA)
- Biomedical Technology (AREA)
- Microbiology (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- General Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Immunology (AREA)
- Biophysics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Gastroenterology & Hepatology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Mycology (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Physics & Mathematics (AREA)
- Plant Pathology (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Peptides Or Proteins (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
Abstract
Description
Claims
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
UAA200815018A UA98620C2 (en) | 2006-05-30 | 2007-05-29 | Attenuated classic swine fever virus containing modified glycoprotein e2 |
BRPI0712558-5A BRPI0712558A2 (en) | 2006-05-30 | 2007-05-29 | virulence determinant within classical fever virus structural glycoprotein e2 |
KR1020087031827A KR101432840B1 (en) | 2006-05-30 | 2007-05-29 | Novel virulence determinant within the e2 structural glycoprotein of classical swine fever virus |
CA002656560A CA2656560A1 (en) | 2006-05-30 | 2007-05-29 | A novel virulence determinant within the e2 structural glycoprotein of classical swine fever virus |
EP07797826.0A EP2023953B1 (en) | 2006-05-30 | 2007-05-29 | A novel virulence determinant within the e2 structural glycoprotein of classical swine fever virus |
MX2008015215A MX2008015215A (en) | 2006-05-30 | 2007-05-29 | A novel virulence determinant within the e2 structural glycoprotein of classical swine fever virus. |
JP2009513411A JP5377296B2 (en) | 2006-05-30 | 2007-05-29 | Novel virulence determinants in the E2 structural glycoprotein of swine cholera virus |
CN2007800235147A CN101478985B (en) | 2006-05-30 | 2007-05-29 | Virulence determinant within E2 structural glycoprotein of classical swine fever virus |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/443,132 US8846055B2 (en) | 2006-05-30 | 2006-05-30 | Virulence determinant within the E2 structural glycoprotein of classical swine fever virus |
US11/443,132 | 2006-05-30 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2007143442A2 true WO2007143442A2 (en) | 2007-12-13 |
WO2007143442A3 WO2007143442A3 (en) | 2008-03-13 |
Family
ID=38790491
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2007/069852 WO2007143442A2 (en) | 2006-05-30 | 2007-05-29 | A novel virulence determinant within the e2 structural glycoprotein of classical swine fever virus |
Country Status (14)
Country | Link |
---|---|
US (1) | US8846055B2 (en) |
EP (1) | EP2023953B1 (en) |
JP (1) | JP5377296B2 (en) |
KR (1) | KR101432840B1 (en) |
CN (1) | CN101478985B (en) |
BR (1) | BRPI0712558A2 (en) |
CA (1) | CA2656560A1 (en) |
CR (1) | CR10508A (en) |
GT (1) | GT200800269A (en) |
MX (1) | MX2008015215A (en) |
RU (1) | RU2451746C2 (en) |
UA (1) | UA98620C2 (en) |
WO (1) | WO2007143442A2 (en) |
ZA (1) | ZA200810285B (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009091720A2 (en) * | 2008-01-15 | 2009-07-23 | The United States Of America, As Represented By The Secretary Of Agriculture | N-linked glycosylation alteration in e1 glycoprotein of classical swine fever virus and novel classical swine fever virus vaccine |
WO2010047955A2 (en) * | 2008-10-24 | 2010-04-29 | The United States Of America, As Represented By The Secretary Of Agriculture | N-linked glycosylation alteration in e0 and e2 glycoprotein of classical swine fever virus and novel classical swine fever virus vaccine |
EP2202298A1 (en) * | 2008-12-23 | 2010-06-30 | Stichting Dienst Landbouwkundig Onderzoek | Recombinant classical swine fever virus (CSFV) comprising a modified E2 protein and methods for generating said recombinant CSFV |
WO2011144360A1 (en) | 2010-05-18 | 2011-11-24 | Riemser Arzneimittelag | Marker vaccine for classical swine fever |
CN104483490A (en) * | 2014-12-09 | 2015-04-01 | 武汉科前生物股份有限公司 | Hog cholera virus inhibition ELISA antibody detection kit and application thereof |
WO2015177369A1 (en) * | 2014-05-23 | 2015-11-26 | Boehringer Ingelheim Vetmedica Gmbh | Recombinant classical swine fever virus (csfv) comprising substitution in the tav epitope of the e2 protein |
CN109324193A (en) * | 2018-12-07 | 2019-02-12 | 中国农业科学院兰州兽医研究所 | A kind of the visualization quick detection kit and its application of antibody against swine fever virus |
EP4105225A1 (en) * | 2021-06-18 | 2022-12-21 | Institut de Recerca i Tecnologia Agroalimentàries | Peptide-based assay to differentiate animals infected with csfv from vaccinated animals |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102175849B (en) * | 2010-12-22 | 2013-07-03 | 江苏出入境检验检疫局动植物与食品检测中心 | Kit for quickly detecting swine fever antibody and preparation method thereof |
CN102268079B (en) * | 2011-05-03 | 2013-04-03 | 新乡学院 | (Classical swine fever virus) CSFV E2 protein ligand epitope peptide and application thereof |
CN103499693A (en) * | 2013-10-11 | 2014-01-08 | 重庆出入境检验检疫局检验检疫技术中心 | Competitive Alpha LISA (linked immuno sorbent assay) detection kit for classical swine fever virus (CSFV) antibody and detection method thereof |
CN105829892B (en) | 2013-12-19 | 2018-06-12 | 英特维特国际股份有限公司 | The improved diagnostic test of CSFV antibody |
US9814771B2 (en) * | 2015-09-11 | 2017-11-14 | The United States Of America, As Represented By The Secretary Of Agriculture | Live attenuated classical swine fever vaccine based in genetic manipulation of a putative fusion peptide area in the virus structural glycoprotein E2 |
RU2727847C2 (en) * | 2016-05-12 | 2020-07-24 | Биоэппликейшнз Инк. | Herbal composition for swine fever vaccination and a method for preparation thereof |
US9808520B1 (en) * | 2016-07-01 | 2017-11-07 | The United States Of America As Represented By The Secretary Of Agriculture | Rationally developed african swine fever attenuated virus strain protects against challenge with parental virus georgia 2007 isolate |
CN106749519B (en) * | 2016-11-15 | 2020-04-07 | 河南省农业科学院 | Peptide ligand sequence design and application based on computer simulation and used for CSFV E2 protein targeted combination |
CN112961224B (en) * | 2021-03-26 | 2022-09-27 | 中国农业大学 | Preparation and application of bovine viral diarrhea virus type 1 virus-like particles |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0982402A1 (en) * | 1998-08-14 | 2000-03-01 | Stichting Instituut voor Dierhouderij en Diergezondheid (ID-DLO) | Pestivirus vaccination |
-
2006
- 2006-05-30 US US11/443,132 patent/US8846055B2/en active Active
-
2007
- 2007-05-29 MX MX2008015215A patent/MX2008015215A/en active IP Right Grant
- 2007-05-29 EP EP07797826.0A patent/EP2023953B1/en not_active Not-in-force
- 2007-05-29 RU RU2008150400/10A patent/RU2451746C2/en not_active IP Right Cessation
- 2007-05-29 CA CA002656560A patent/CA2656560A1/en not_active Abandoned
- 2007-05-29 ZA ZA200810285A patent/ZA200810285B/en unknown
- 2007-05-29 JP JP2009513411A patent/JP5377296B2/en not_active Expired - Fee Related
- 2007-05-29 CN CN2007800235147A patent/CN101478985B/en not_active Expired - Fee Related
- 2007-05-29 KR KR1020087031827A patent/KR101432840B1/en not_active IP Right Cessation
- 2007-05-29 BR BRPI0712558-5A patent/BRPI0712558A2/en not_active Application Discontinuation
- 2007-05-29 WO PCT/US2007/069852 patent/WO2007143442A2/en active Application Filing
- 2007-05-29 UA UAA200815018A patent/UA98620C2/en unknown
-
2008
- 2008-12-01 GT GT200800269A patent/GT200800269A/en unknown
- 2008-12-15 CR CR10508A patent/CR10508A/en unknown
Non-Patent Citations (3)
Title |
---|
KONIG, J. VIRAL., vol. 69, 1995, pages 6479 - 6486 |
LIN, J. VIRAL., vol. 74, 2000, pages 11619 - 11625 |
See also references of EP2023953A4 |
Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009091720A3 (en) * | 2008-01-15 | 2009-10-08 | The United States Of America, As Represented By The Secretary Of Agriculture | N-linked glycosylation alteration in e1 glycoprotein of classical swine fever virus and novel classical swine fever virus vaccine |
WO2009091720A2 (en) * | 2008-01-15 | 2009-07-23 | The United States Of America, As Represented By The Secretary Of Agriculture | N-linked glycosylation alteration in e1 glycoprotein of classical swine fever virus and novel classical swine fever virus vaccine |
WO2010047955A3 (en) * | 2008-10-24 | 2010-07-08 | The United States Of America, As Represented By The Secretary Of Agriculture | N-linked glycosylation alteration in e0 and e2 glycoprotein of classical swine fever virus and novel classical swine fever virus vaccine |
WO2010047955A2 (en) * | 2008-10-24 | 2010-04-29 | The United States Of America, As Represented By The Secretary Of Agriculture | N-linked glycosylation alteration in e0 and e2 glycoprotein of classical swine fever virus and novel classical swine fever virus vaccine |
JP2012513212A (en) * | 2008-12-23 | 2012-06-14 | インターベツト・インターナシヨナル・ベー・ベー | Recombinant swine fever virus (CSFV) comprising a modified E2 protein and methods for forming said recombinant CSFV |
WO2010074575A3 (en) * | 2008-12-23 | 2010-08-26 | Stichting Dienst Landbouwkundig Onderzoek | Recombinant classical swine fever virus (csfv) comprising a modified e2 protein and methods for generating said recombinant csfv. |
US20110287044A1 (en) * | 2008-12-23 | 2011-11-24 | Jeroen Alexander Kortekaas | Recombinant classical swine fever virus (csfv) comprising a modified e2 protein and methods for generating said recombinant csfv |
EP2202298A1 (en) * | 2008-12-23 | 2010-06-30 | Stichting Dienst Landbouwkundig Onderzoek | Recombinant classical swine fever virus (CSFV) comprising a modified E2 protein and methods for generating said recombinant CSFV |
US8911744B2 (en) | 2008-12-23 | 2014-12-16 | Intervet International B.V. | Recombinant classical swine fever virus (CSFV) comprising a modified E2 protein and methods for generating said recombinant CSFV |
WO2011144360A1 (en) | 2010-05-18 | 2011-11-24 | Riemser Arzneimittelag | Marker vaccine for classical swine fever |
WO2015177369A1 (en) * | 2014-05-23 | 2015-11-26 | Boehringer Ingelheim Vetmedica Gmbh | Recombinant classical swine fever virus (csfv) comprising substitution in the tav epitope of the e2 protein |
US9993544B2 (en) | 2014-05-23 | 2018-06-12 | Boehringer Ingelheim Vetmedica Gmbh | Recombinant classical swine fever virus (CSFV) comprising substitution in the TAV epitope of the E2 protein |
CN104483490A (en) * | 2014-12-09 | 2015-04-01 | 武汉科前生物股份有限公司 | Hog cholera virus inhibition ELISA antibody detection kit and application thereof |
CN104483490B (en) * | 2014-12-09 | 2016-06-08 | 武汉科前生物股份有限公司 | A kind of Pestivirus suis stop band restrain antibody assay kit and application |
CN109324193A (en) * | 2018-12-07 | 2019-02-12 | 中国农业科学院兰州兽医研究所 | A kind of the visualization quick detection kit and its application of antibody against swine fever virus |
EP4105225A1 (en) * | 2021-06-18 | 2022-12-21 | Institut de Recerca i Tecnologia Agroalimentàries | Peptide-based assay to differentiate animals infected with csfv from vaccinated animals |
WO2022263647A1 (en) * | 2021-06-18 | 2022-12-22 | Institut de Recerca i Tecnologia Agroalimentàries (IRTA) | Peptide-based assay to differentiate animals infected with csfv from vaccinated animals |
Also Published As
Publication number | Publication date |
---|---|
US20070280955A1 (en) | 2007-12-06 |
RU2451746C2 (en) | 2012-05-27 |
RU2008150400A (en) | 2010-07-10 |
KR20090025291A (en) | 2009-03-10 |
CN101478985A (en) | 2009-07-08 |
GT200800269A (en) | 2009-05-04 |
EP2023953A4 (en) | 2010-01-20 |
CN101478985B (en) | 2013-10-30 |
CR10508A (en) | 2009-02-23 |
BRPI0712558A2 (en) | 2012-11-20 |
EP2023953A2 (en) | 2009-02-18 |
JP2009538628A (en) | 2009-11-12 |
JP5377296B2 (en) | 2013-12-25 |
MX2008015215A (en) | 2009-02-06 |
US8846055B2 (en) | 2014-09-30 |
EP2023953B1 (en) | 2014-11-19 |
ZA200810285B (en) | 2010-07-28 |
WO2007143442A3 (en) | 2008-03-13 |
KR101432840B1 (en) | 2014-09-22 |
UA98620C2 (en) | 2012-06-11 |
CA2656560A1 (en) | 2007-12-13 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US8846055B2 (en) | Virulence determinant within the E2 structural glycoprotein of classical swine fever virus | |
Risatti et al. | Identification of a novel virulence determinant within the E2 structural glycoprotein of classical swine fever virus | |
JP5868182B2 (en) | Recombinant swine fever virus (CSFV) comprising a modified E2 protein and methods for forming said recombinant CSFV | |
Van Gennip et al. | Determinants of virulence of classical swine fever virus strain Brescia | |
US20150290314A1 (en) | Marker vaccine | |
Holinka et al. | Development of a live attenuated antigenic marker classical swine fever vaccine | |
Wehrle et al. | Chimeric pestiviruses: candidates for live-attenuated classical swine fever marker vaccines | |
US8133495B2 (en) | Live attenuated antigenically marked classical swine fever virus | |
SK18232000A3 (en) | Attenuated pestiviruses | |
Kortekaas et al. | Rational design of a classical swine fever C-strain vaccine virus that enables the differentiation between infected and vaccinated animals | |
US7332170B1 (en) | Classical swine fever virus virulence determinant and a novel classical swine fever vaccine | |
US7244434B2 (en) | Replicons of pestviruses that do not express C and or E1 protein and infectious viral particles containing same, that can be used in vaccines | |
US9352032B2 (en) | Live attenuated antigenically marked classical swine fever vaccine |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 200780023514.7 Country of ref document: CN |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 07797826 Country of ref document: EP Kind code of ref document: A2 |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2009513411 Country of ref document: JP Ref document number: 12008502636 Country of ref document: PH Ref document number: MX/A/2008/015215 Country of ref document: MX |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: CR2008-010508 Country of ref document: CR |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2007797826 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 1020087031827 Country of ref document: KR |
|
ENP | Entry into the national phase |
Ref document number: 2656560 Country of ref document: CA |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2008150400 Country of ref document: RU Ref document number: A200815018 Country of ref document: UA |
|
ENP | Entry into the national phase |
Ref document number: PI0712558 Country of ref document: BR Kind code of ref document: A2 Effective date: 20081201 |