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 inJournal of Veterinary Medical Science Vol. 70; no. 7; pp. 653 - 658
Main Authors Morioka, K.(National Inst. of Animal Health, Kodaira, Tokyo (Japan)), Fukai, K, Ohashi, S, Sakamoto, K, Tsuda, T, Yoshida, K
Format Journal Article
LanguageEnglish
Published 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.
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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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.
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– reference: 5. Jackson, T., Blakemore, W., Newman, J., Knowles, N.J., Mould, A.P., Humphries, M.J. and King, A.M.Q. 2000a. Foot-and-mouth disease virus is a ligand for the high-affinity binding conformation of integrin a5b1: influence of the leucine residue within the RGDL motif on selectivity of integrin binding. J. Gen. Virol. 81: 1383-1391.
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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
URI https://www.jstage.jst.go.jp/article/jvms/70/7/70_7_653/_article/-char/en
https://www.ncbi.nlm.nih.gov/pubmed/18685235
https://www.proquest.com/docview/1468713012
https://www.proquest.com/docview/19683614
https://www.proquest.com/docview/69399539
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