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Rapid Engineering of Foot-and-Mouth Disease Vaccine and Challenge Viruses

There are seven antigenically distinct serotypes of foot-and-mouth disease virus (FMDV), each of which has intratypic variants. In the present study, we have developed methods to efficiently generate promising vaccines against seven serotypes or subtypes. The capsid-encoding gene (P1) of the vaccine...

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Autores principales: Lee, Seo-Yong, Lee, Yeo-Joo, Kim, Rae-Hyung, Park, Jeong-Nam, Park, Min-Eun, Ko, Mi-Kyeong, Choi, Joo-Hyung, Chu, Jia-Qi, Lee, Kwang-Nyeong, Kim, Su-Mi, Tark, Dongseob, Lee, Hyang-Sim, Ko, Young-Joon, Seo, Min-Goo, Park, Jung-Won, Kim, Byounghan, Lee, Myoung-Heon, Lee, Jong-Soo, Park, Jong-Hyeon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5533925/
https://www.ncbi.nlm.nih.gov/pubmed/28566375
http://dx.doi.org/10.1128/JVI.00155-17
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author Lee, Seo-Yong
Lee, Yeo-Joo
Kim, Rae-Hyung
Park, Jeong-Nam
Park, Min-Eun
Ko, Mi-Kyeong
Choi, Joo-Hyung
Chu, Jia-Qi
Lee, Kwang-Nyeong
Kim, Su-Mi
Tark, Dongseob
Lee, Hyang-Sim
Ko, Young-Joon
Seo, Min-Goo
Park, Jung-Won
Kim, Byounghan
Lee, Myoung-Heon
Lee, Jong-Soo
Park, Jong-Hyeon
author_facet Lee, Seo-Yong
Lee, Yeo-Joo
Kim, Rae-Hyung
Park, Jeong-Nam
Park, Min-Eun
Ko, Mi-Kyeong
Choi, Joo-Hyung
Chu, Jia-Qi
Lee, Kwang-Nyeong
Kim, Su-Mi
Tark, Dongseob
Lee, Hyang-Sim
Ko, Young-Joon
Seo, Min-Goo
Park, Jung-Won
Kim, Byounghan
Lee, Myoung-Heon
Lee, Jong-Soo
Park, Jong-Hyeon
author_sort Lee, Seo-Yong
collection PubMed
description There are seven antigenically distinct serotypes of foot-and-mouth disease virus (FMDV), each of which has intratypic variants. In the present study, we have developed methods to efficiently generate promising vaccines against seven serotypes or subtypes. The capsid-encoding gene (P1) of the vaccine strain O1/Manisa/Turkey/69 was replaced with the amplified or synthetic genes from the O, A, Asia1, C, SAT1, SAT2, and SAT3 serotypes. Viruses of the seven serotype were rescued successfully. Each chimeric FMDV with a replacement of P1 showed serotype-specific antigenicity and varied in terms of pathogenesis in pigs and mice. Vaccination of pigs with an experimental trivalent vaccine containing the inactivated recombinants based on the main serotypes O, A, and Asia1 effectively protected them from virus challenge. This technology could be a potential strategy for a customized vaccine with challenge tools to protect against epizootic disease caused by specific serotypes or subtypes of FMDV. IMPORTANCE Foot-and-mouth disease (FMD) virus (FMDV) causes significant economic losses. For vaccine preparation, the selection of vaccine strains was complicated by high antigenic variation. In the present study, we suggested an effective strategy to rapidly prepare and evaluate mass-produced customized vaccines against epidemic strains. The P1 gene encoding the structural proteins of the well-known vaccine virus was replaced by the synthetic or amplified genes of viruses of seven representative serotypes. These chimeric viruses generally replicated readily in cell culture and had a particle size similar to that of the original vaccine strain. Their antigenicity mirrored that of the original serotype from which their P1 gene was derived. Animal infection experiments revealed that the recombinants varied in terms of pathogenicity. This strategy will be a useful tool for rapidly generating customized FMD vaccines or challenge viruses for all serotypes, especially for FMD-free countries, which have prohibited the import of FMDVs.
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spelling pubmed-55339252017-08-08 Rapid Engineering of Foot-and-Mouth Disease Vaccine and Challenge Viruses Lee, Seo-Yong Lee, Yeo-Joo Kim, Rae-Hyung Park, Jeong-Nam Park, Min-Eun Ko, Mi-Kyeong Choi, Joo-Hyung Chu, Jia-Qi Lee, Kwang-Nyeong Kim, Su-Mi Tark, Dongseob Lee, Hyang-Sim Ko, Young-Joon Seo, Min-Goo Park, Jung-Won Kim, Byounghan Lee, Myoung-Heon Lee, Jong-Soo Park, Jong-Hyeon J Virol Vaccines and Antiviral Agents There are seven antigenically distinct serotypes of foot-and-mouth disease virus (FMDV), each of which has intratypic variants. In the present study, we have developed methods to efficiently generate promising vaccines against seven serotypes or subtypes. The capsid-encoding gene (P1) of the vaccine strain O1/Manisa/Turkey/69 was replaced with the amplified or synthetic genes from the O, A, Asia1, C, SAT1, SAT2, and SAT3 serotypes. Viruses of the seven serotype were rescued successfully. Each chimeric FMDV with a replacement of P1 showed serotype-specific antigenicity and varied in terms of pathogenesis in pigs and mice. Vaccination of pigs with an experimental trivalent vaccine containing the inactivated recombinants based on the main serotypes O, A, and Asia1 effectively protected them from virus challenge. This technology could be a potential strategy for a customized vaccine with challenge tools to protect against epizootic disease caused by specific serotypes or subtypes of FMDV. IMPORTANCE Foot-and-mouth disease (FMD) virus (FMDV) causes significant economic losses. For vaccine preparation, the selection of vaccine strains was complicated by high antigenic variation. In the present study, we suggested an effective strategy to rapidly prepare and evaluate mass-produced customized vaccines against epidemic strains. The P1 gene encoding the structural proteins of the well-known vaccine virus was replaced by the synthetic or amplified genes of viruses of seven representative serotypes. These chimeric viruses generally replicated readily in cell culture and had a particle size similar to that of the original vaccine strain. Their antigenicity mirrored that of the original serotype from which their P1 gene was derived. Animal infection experiments revealed that the recombinants varied in terms of pathogenicity. This strategy will be a useful tool for rapidly generating customized FMD vaccines or challenge viruses for all serotypes, especially for FMD-free countries, which have prohibited the import of FMDVs. American Society for Microbiology 2017-07-27 /pmc/articles/PMC5533925/ /pubmed/28566375 http://dx.doi.org/10.1128/JVI.00155-17 Text en Copyright © 2017 Lee et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Vaccines and Antiviral Agents
Lee, Seo-Yong
Lee, Yeo-Joo
Kim, Rae-Hyung
Park, Jeong-Nam
Park, Min-Eun
Ko, Mi-Kyeong
Choi, Joo-Hyung
Chu, Jia-Qi
Lee, Kwang-Nyeong
Kim, Su-Mi
Tark, Dongseob
Lee, Hyang-Sim
Ko, Young-Joon
Seo, Min-Goo
Park, Jung-Won
Kim, Byounghan
Lee, Myoung-Heon
Lee, Jong-Soo
Park, Jong-Hyeon
Rapid Engineering of Foot-and-Mouth Disease Vaccine and Challenge Viruses
title Rapid Engineering of Foot-and-Mouth Disease Vaccine and Challenge Viruses
title_full Rapid Engineering of Foot-and-Mouth Disease Vaccine and Challenge Viruses
title_fullStr Rapid Engineering of Foot-and-Mouth Disease Vaccine and Challenge Viruses
title_full_unstemmed Rapid Engineering of Foot-and-Mouth Disease Vaccine and Challenge Viruses
title_short Rapid Engineering of Foot-and-Mouth Disease Vaccine and Challenge Viruses
title_sort rapid engineering of foot-and-mouth disease vaccine and challenge viruses
topic Vaccines and Antiviral Agents
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5533925/
https://www.ncbi.nlm.nih.gov/pubmed/28566375
http://dx.doi.org/10.1128/JVI.00155-17
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