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口蹄疫疫苗及攻击病毒的快速工程制作

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

作者信息

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

机构信息

Animal and Plant Quarantine Agency, Gimcheon City, Gyeongsangbuk-do, Republic of Korea.

College of Veterinary Medicine (BK21 Plus Program), Chungnam National University, Gungdong, Daejon City, Republic of Korea.

出版信息

J Virol. 2017 Jul 27;91(16). doi: 10.1128/JVI.00155-17. Print 2017 Aug 15.

Abstract

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. 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.

摘要

口蹄疫病毒(FMDV)有七种抗原性不同的血清型,每种血清型都有亚型变种。在本研究中,我们开发了有效制备针对七种血清型或亚型的有前景疫苗的方法。疫苗株O1/Manisa/土耳其/69的衣壳编码基因(P1)被来自O、A、亚洲1型、C、南非1型、南非2型和南非3型血清型的扩增或合成基因所取代。成功拯救出了七种血清型的病毒。每种替换了P1的嵌合FMDV都表现出血清型特异性抗原性,并且在猪和小鼠中的致病性有所不同。用基于主要血清型O、A和亚洲1型的灭活重组体的实验性三价疫苗对猪进行接种,有效地保护了它们免受病毒攻击。这项技术可能是一种定制疫苗及攻毒工具的潜在策略,以预防由特定血清型或亚型的FMDV引起的 epizootic 疾病。口蹄疫(FMD)病毒(FMDV)造成重大经济损失。对于疫苗制备而言,高抗原变异性使疫苗株的选择变得复杂。在本研究中,我们提出了一种有效策略,用于快速制备和评估针对流行毒株的大规模定制疫苗。编码著名疫苗病毒结构蛋白的P1基因被七种代表性血清型病毒的合成或扩增基因所取代。这些嵌合病毒通常在细胞培养中易于复制,并且颗粒大小与原始疫苗株相似。它们的抗原性反映了其P1基因所源自的原始血清型的抗原性。动物感染实验表明,重组体在致病性方面存在差异。该策略将是快速生成针对所有血清型的定制FMD疫苗或攻毒病毒的有用工具,特别是对于已禁止进口FMDV的无口蹄疫国家。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6cc5/5533925/eecbf6930f39/zjv9991827930001.jpg

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