Comparison of the characters of the plaque-purified viruses from foot-and-mouth disease virus O/JPN/2000
At least two biotypes were observed at the 2nd passage stage after the isolation of Foot-and-mouth disease Virus (FMDV) O/JPN/2000 strain. These 2 types of viruses differed from their plaque phenotypes and were distinguishable by using a monoclonal antibody (MAb) 64G8 that was made for the FMDV O/JP...
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Published in | Journal of Veterinary Medical Science Vol. 70; no. 7; pp. 653 - 658 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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Japan
JAPANESE SOCIETY OF VETERINARY SCIENCE
01.07.2008
Japan Science and Technology Agency |
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Abstract | At least two biotypes were observed at the 2nd passage stage after the isolation of Foot-and-mouth disease Virus (FMDV) O/JPN/2000 strain. These 2 types of viruses differed from their plaque phenotypes and were distinguishable by using a monoclonal antibody (MAb) 64G8 that was made for the FMDV O/JPN/2000 strain. One of these 2 biotypes formed small plaque (SP) and with immuno staining showed a positive reaction to MAb 64G8, while the other formed clear large plaque (LP) and did not react with MAb 64G8. The amino acid sequences of the capsid coding region (VP1-VP4) of the SP virus (SPV) and the LP virus (LPV) revealed two substitutions on the 133rd amino acid in VP2, and the 56th amino acid in VP3. These amino acid changes of SPV and LPV are Asn to Asp, Arg to His, respectively. The Arg of the 56th amino acid in VP3 that have been known as critical position of cell culture adapted virus. Only LPV showed high pathogenicity in suckling mice, and its LDsub(50) was calculated to be about 10E2TCIDsub(50)/0.1 ml. These results showed that the SPV that existed at the 2nd passage stage from isolation was a low virulence virus, which may suggest why the pathogenicity of O/JPN/2000 did not show clear symptoms in infected cattle. |
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AbstractList | At least two biotypes were observed at the 2nd passage stage after the isolation of Foot-and-mouth disease Virus (FMDV) O/JPN/2000 strain. These 2 types of viruses differed from their plaque phenotypes and were distinguishable by using a monoclonal antibody (MAb) 64G8 that was made for the FMDV O/JPN/2000 strain. One of these 2 biotypes formed small plaque (SP) and with immuno staining showed a positive reaction to MAb 64G8, while the other formed clear large plaque (LP) and did not react with MAb 64G8. The amino acid sequences of the capsid coding region (VP1-VP4) of the SP virus (SPV) and the LP virus (LPV) revealed two substitutions on the 133rd amino acid in VP2, and the 56th amino acid in VP3. These amino acid changes of SPV and LPV are Asn to Asp, Arg to His, respectively. The Arg of the 56th amino acid in VP3 that have been known as critical position of cell culture adapted virus. Only LPV showed high pathogenicity in suckling mice, and its LD50 was calculated to be about 102 TCID50/0.1 ml. These results showed that the SPV that existed at the 2nd passage stage from isolation was a low virulence virus, which may suggest why the pathogenicity of O/JPN/2000 did not show clear symptoms in infected cattle. At least two biotypes were observed at the 2nd passage stage after the isolation of Foot-and-mouth disease Virus (FMDV) O/JPN/2000 strain. These 2 types of viruses differed from their plaque phenotypes and were distinguishable by using a monoclonal antibody (MAb) 64G8 that was made for the FMDV O/JPN/2000 strain. One of these 2 biotypes formed small plaque (SP) and with immuno staining showed a positive reaction to MAb 64G8, while the other formed clear large plaque (LP) and did not react with MAb 64G8. The amino acid sequences of the capsid coding region (VP1-VP4) of the SP virus (SPV) and the LP virus (LPV) revealed two substitutions on the 133rd amino acid in VP2, and the 56th amino acid in VP3. These amino acid changes of SPV and LPV are Asn to Asp, Arg to His, respectively. The Arg of the 56th amino acid in VP3 that have been known as critical position of cell culture adapted virus. Only LPV showed high pathogenicity in suckling mice, and its LD(50) was calculated to be about 10(2) TCID(50)/0.1 ml. These results showed that the SPV that existed at the 2nd passage stage from isolation was a low virulence virus, which may suggest why the pathogenicity of O/JPN/2000 did not show clear symptoms in infected cattle.At least two biotypes were observed at the 2nd passage stage after the isolation of Foot-and-mouth disease Virus (FMDV) O/JPN/2000 strain. These 2 types of viruses differed from their plaque phenotypes and were distinguishable by using a monoclonal antibody (MAb) 64G8 that was made for the FMDV O/JPN/2000 strain. One of these 2 biotypes formed small plaque (SP) and with immuno staining showed a positive reaction to MAb 64G8, while the other formed clear large plaque (LP) and did not react with MAb 64G8. The amino acid sequences of the capsid coding region (VP1-VP4) of the SP virus (SPV) and the LP virus (LPV) revealed two substitutions on the 133rd amino acid in VP2, and the 56th amino acid in VP3. These amino acid changes of SPV and LPV are Asn to Asp, Arg to His, respectively. The Arg of the 56th amino acid in VP3 that have been known as critical position of cell culture adapted virus. Only LPV showed high pathogenicity in suckling mice, and its LD(50) was calculated to be about 10(2) TCID(50)/0.1 ml. These results showed that the SPV that existed at the 2nd passage stage from isolation was a low virulence virus, which may suggest why the pathogenicity of O/JPN/2000 did not show clear symptoms in infected cattle. At least two biotypes were observed at the 2nd passage stage after the isolation of Foot-and-mouth disease Virus (FMDV) O/JPN/2000 strain. These 2 types of viruses differed from their plaque phenotypes and were distinguishable by using a monoclonal antibody (MAb) 64G8 that was made for the FMDV O/JPN/2000 strain. One of these 2 biotypes formed small plaque (SP) and with immuno staining showed a positive reaction to MAb 64G8, while the other formed clear large plaque (LP) and did not react with MAb 64G8. The amino acid sequences of the capsid coding region (VP1-VP4) of the SP virus (SPV) and the LP virus (LPV) revealed two substitutions on the 133rd amino acid in VP2, and the 56th amino acid in VP3. These amino acid changes of SPV and LPV are Asn to Asp, Arg to His, respectively. The Arg of the 56th amino acid in VP3 that have been known as critical position of cell culture adapted virus. Only LPV showed high pathogenicity in suckling mice, and its LD(50) was calculated to be about 10(2) TCID(50)/0.1 ml. These results showed that the SPV that existed at the 2nd passage stage from isolation was a low virulence virus, which may suggest why the pathogenicity of O/JPN/2000 did not show clear symptoms in infected cattle. At least two biotypes were observed at the 2nd passage stage after the isolation of Foot-and-mouth disease Virus (FMDV) O/JPN/2000 strain. These 2 types of viruses differed from their plaque phenotypes and were distinguishable by using a monoclonal antibody (MAb) 64G8 that was made for the FMDV O/JPN/2000 strain. One of these 2 biotypes formed small plaque (SP) and with immuno staining showed a positive reaction to MAb 64G8, while the other formed clear large plaque (LP) and did not react with MAb 64G8. The amino acid sequences of the capsid coding region (VP1-VP4) of the SP virus (SPV) and the LP virus (LPV) revealed two substitutions on the 133rd amino acid in VP2, and the 56th amino acid in VP3. These amino acid changes of SPV and LPV are Asn to Asp, Arg to His, respectively. The Arg of the 56th amino acid in VP3 that have been known as critical position of cell culture adapted virus. Only LPV showed high pathogenicity in suckling mice, and its LD sub(50) was calculated to be about 10 super(2) TCID sub(50)/0.1 ml. These results showed that the SPV that existed at the 2nd passage stage from isolation was a low virulence virus, which may suggest why the pathogenicity of O/JPN/2000 did not show clear symptoms in infected cattle. At least two biotypes were observed at the 2nd passage stage after the isolation of Foot-and-mouth disease Virus (FMDV) O/JPN/2000 strain. These 2 types of viruses differed from their plaque phenotypes and were distinguishable by using a monoclonal antibody (MAb) 64G8 that was made for the FMDV O/JPN/2000 strain. One of these 2 biotypes formed small plaque (SP) and with immuno staining showed a positive reaction to MAb 64G8, while the other formed clear large plaque (LP) and did not react with MAb 64G8. The amino acid sequences of the capsid coding region (VP1-VP4) of the SP virus (SPV) and the LP virus (LPV) revealed two substitutions on the 133rd amino acid in VP2, and the 56th amino acid in VP3. These amino acid changes of SPV and LPV are Asn to Asp, Arg to His, respectively. The Arg of the 56th amino acid in VP3 that have been known as critical position of cell culture adapted virus. Only LPV showed high pathogenicity in suckling mice, and its LDsub(50) was calculated to be about 10E2TCIDsub(50)/0.1 ml. These results showed that the SPV that existed at the 2nd passage stage from isolation was a low virulence virus, which may suggest why the pathogenicity of O/JPN/2000 did not show clear symptoms in infected cattle. |
Author | Morioka, K.(National Inst. of Animal Health, Kodaira, Tokyo (Japan)) Tsuda, T Yoshida, K Fukai, K Sakamoto, K Ohashi, S |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/18685235$$D View this record in MEDLINE/PubMed |
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Efficient infection of cells in culture by type O foot-and-mouth disease virus requires binding to cell surface heparan sulfate. J. Virol. 70: 5282-5287. 13. Marquardt, O., Adam, K.H. and Staub, O.C. 1991. Detection and localization of single-base sequence difference in foot-and-mouth disease virus genomes by the RNase mismatch cleavage method. J. Virol. Methods 33: 267-282. 20. Samuel, A.R. and Knowles, N.J. 2001. Foot-and-mouth disease virus: cause of the recent crisis for the UK livestock industry. TRENDS Genetics 17: 421-424. 7. Jackson T., King, A.M., Stuart, D.I. and Fry, E. 2003. Structure and receptor binding. Virus Research 91: 33-46. 19. Sakamoto, K., Kanno, T., Yamakawa, M. and Yoshida, K. 2002. Isolation of foot-and-mouth disease virus from Japanese black cattle in Miyazaki prefecture, Japan, 2000. J. Vet. Med. Sci. 64: 91-94. 18. Sakamoto, K., Yamakawa, M., Kanno, T. and Yoshida, K. 2001. 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Kitson, J.D.A., Mccahon, D. and Belsham, G.J. 1990. Sequence analysis of resistant mutant of type O foot and mouth disease virus: evidence for the involvement of the three surface exposed proteins in four antigenic sites. Virology 179: 26-34. 21. Shin, J.H., Sohn, H.J., Choi, K.S., Kwon, B.J., Ko, Y.J., An, D.J., Cha, S.H., Park, J.H., Jeong, W.S., Park, J.Y., Choi, C.U., Kweon, C.H., Song, J.Y., Kim, J.Y., An, S.H., Kim, S.J. and Joo, Y.S. 2003. Molecular epidemiological investigation of foot-and-mouth disease virus in Korea in 2000. J. Vet. Med. Sci. 65: 9-16. 11 22 12 JACKSON T (5) 2000; 81 13 14 15 16 18 19 (1) 1998; 72 2 3 6 7 8 9 (4) 1996; 70 (17) 1997; 71 20 10 21 |
References_xml | – reference: 13. Marquardt, O., Adam, K.H. and Staub, O.C. 1991. Detection and localization of single-base sequence difference in foot-and-mouth disease virus genomes by the RNase mismatch cleavage method. J. Virol. Methods 33: 267-282. – reference: 22. Sur, J.H., Shin, J.H., Loubroth, J., Yeh, M., Ku, B.K., Choi, K.S., Kwon, B.J., Sohn, H.J., Ko, Y.J., Choi, C.U., Kweon, C.H., Kim, J.Y., An, S.H., Kim, K.S., Moon,O.K., Kim, J.H., Choi, S.H., Lee, H.G., Hwang, E.K., Kim, S.B., Kang, S.S. and Kim, O.K. 2000. In vivo characterization and transmission of Korean foot and mouth disease virus (FMDV). Kor. J. Vet. Res. 40: 719-727. – reference: 7. Jackson T., King, A.M., Stuart, D.I. and Fry, E. 2003. Structure and receptor binding. Virus Research 91: 33-46. – reference: 9. Kitson, J.D.A., Mccahon, D. and Belsham, G.J. 1990. Sequence analysis of resistant mutant of type O foot and mouth disease virus: evidence for the involvement of the three surface exposed proteins in four antigenic sites. Virology 179: 26-34. – reference: 1. Baranowski, E., Sevilla, N., Verdaguer, N., Ruiz-Jarabo, C.M., Beck, E. and Domingo, E. 1998. Multiple virulence determinants of foot-and-mouth disease virus in cell culture. J. Virol. 72: 6362-6372. – reference: 16. Reed, L.J. and Muench, H. 1938. A simple method of estimating fifty per cent endpoints. Am. J. Hyg. 27: 493. – reference: 3. Huang, C.C., Lin, Y.L., Huang, T.S., Tu, W.J., Lee, S.H., Jong, M.H. and Lin, S.Y. 2001. Molecular characterization of foot-and-mouth disease virus isolated from ruminants in Taiwan in 1999-2000. Vet. Microbiol. 81: 193-205. – reference: 2. Dawe, P.S. and King, A. M. Q. 1983. Point mutations in polypeptide VP1 of foot - and-mouth disease virus affect mouse virulence and BHK21 cell pathogenicity. Arch. Virol. 76: 117-126. – reference: 6. 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Snippet | At least two biotypes were observed at the 2nd passage stage after the isolation of Foot-and-mouth disease Virus (FMDV) O/JPN/2000 strain. These 2 types of... |
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SubjectTerms | Amino Acid Sequence Animals Animals, Suckling Antibodies, Monoclonal - chemistry Antibodies, Monoclonal - immunology ANTICORPS MONOCLONAL ANTICUERPOS MONOCLONALES APHTHOVIRUS BETAIL BIOLOGICAL DIFFERENCES Capsid Proteins - genetics Cattle Cattle Diseases - virology DIFERENCIAS BIOLOGICAS DIFFERENCE BIOLOGIQUE Disease Outbreaks - veterinary FIEBRE AFTOSA FIEVRE APHTEUSE FMDV FOOT AND MOUTH DISEASE Foot-and-Mouth Disease - virology Foot-and-mouth disease virus Foot-and-Mouth Disease Virus - genetics Foot-and-Mouth Disease Virus - pathogenicity Foot-and-Mouth Disease Virus - physiology GANADO Immunoenzyme Techniques - veterinary LIVESTOCK Mice Mice, Inbred BALB C MONOCLONAL ANTIBODIES monoclonal antibody Neutralization Tests - veterinary O/JPN/2000 PATHOGENICITY PATOGENICIDAD plaque POUVOIR PATHOGENE Reverse Transcriptase Polymerase Chain Reaction - veterinary RNA, Viral - chemistry RNA, Viral - genetics Sequence Analysis, DNA Virulence - genetics VIRUS FIEBRE AFTOSA VIRUS FIEVRE APHTEUSE |
Title | Comparison of the characters of the plaque-purified viruses from foot-and-mouth disease virus O/JPN/2000 |
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