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评估新型 C 型口蹄疫灭活疫苗在牛和猪中的效果。

Evaluation of novel inactivated vaccine for type C foot-and-mouth disease in cattle and pigs.

机构信息

Center for Foot-and-Mouth Disease Vaccine Research, Animal and Plant Quarantine Agency, 177 Hyeoksin 8-ro, Gimcheon, Gyeongsangbuk-do, Republic of Korea.

Center for Foot-and-Mouth Disease Vaccine Research, Animal and Plant Quarantine Agency, 177 Hyeoksin 8-ro, Gimcheon, Gyeongsangbuk-do, Republic of Korea.

出版信息

Vet Microbiol. 2019 Jul;234:44-50. doi: 10.1016/j.vetmic.2019.05.016. Epub 2019 May 23.

Abstract

Foot-and-mouth disease virus (FMDV) is the cause of an economically devastating disease in major cloven-hoofed livestock. Although type C foot-and-mouth disease (FMD) has not occurred anywhere worldwide since 2004, the antigen bank should be preserved in preparation for an unexpected outbreak. We therefore conducted experiments to develop inactivated vaccines that are safer and exhibit improved characteristics over existing vaccines. Our previous study showed that the replacement of the capsid-encoding gene (P1) from the vaccine strain O1 Manisa could be rescued successfully from the vaccine strains. In addition, novel point mutation in the 3C region in the virus genome, for induction of properties with low pathogenesis to create a safe vaccine, and 3BB replacement, for differential diagnosis with the wild type virus, were performed. The modified FMD vaccine strain, C3 Resende-R, was shown to provide lower pathogenesis in young mice than the wild-type virus. To identify the immune responses after vaccination with 146S antigen (15 μg/mL/dose), we conducted a virus neutralization test using serum from pigs and cattle vaccinated with the inactivated vaccine. The neutralizing titers in the cattle were higher than those in the pigs and maintained mean antibody titers of around 1:100 until the end of the experiment. The vaccine showed protection capability of 16 PD against C3 Resende virus in the pigs. The replacement of the structural protein-coding gene for the new FMDV was a useful tool in the development of an effective vaccine candidate strain. This inactivated vaccine will be used for the establishment of a safe vaccine strain for the antigen bank.

摘要

口蹄疫病毒(FMDV)是导致主要偶蹄类牲畜经济上毁灭性疾病的原因。尽管自 2004 年以来,全球范围内没有发生 C 型口蹄疫(FMD),但仍应保存抗原库,为意外爆发做好准备。因此,我们进行了实验,以开发更安全、具有现有疫苗改进特性的灭活疫苗。我们之前的研究表明,可从疫苗株成功拯救出替换疫苗株 O1 Manisa 衣壳编码基因(P1)的嵌合病毒。此外,在病毒基因组的 3C 区进行了新的点突变,以诱导低致病性特性,从而产生安全疫苗,并用 3BB 替换,以与野生型病毒进行鉴别诊断。结果表明,改良的 FMD 疫苗株 C3 Resende-R 在幼鼠中的致病性低于野生型病毒。为了鉴定用 146S 抗原(15μg/mL/剂量)接种后的免疫反应,我们用接种了灭活疫苗的猪和牛的血清进行了病毒中和试验。牛的中和滴度高于猪,且在试验结束前平均抗体滴度保持在 1:100 左右。该疫苗对猪的 C3 Resende 病毒具有 16 PD 的保护能力。新 FMDV 结构蛋白编码基因的替换是开发有效疫苗候选株的有用工具。这种灭活疫苗将用于建立抗原库的安全疫苗株。

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