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一种抗火鸡关节炎呼肠孤病毒的重组皮钦德病毒载体疫苗的研制及其在接种动物中的免疫反应特性分析

Development of a Recombinant Pichinde Virus-Vectored Vaccine against Turkey Arthritis Reovirus and Its Immunological Response Characterization in Vaccinated Animals.

作者信息

Kumar Pawan, Sharafeldin Tamer A, Kumar Rahul, Huang Qinfeng, Liang Yuying, Goyal Sagar M, Porter Robert E, Ly Hinh, Mor Sunil K

机构信息

Department of Veterinary Population Medicine, College of Veterinary Medicine, University of Minnesota, Saint Paul, MN 55108, USA.

Department of Animal Biotechnology, College of Veterinary Sciences, Lala Lajpat Rai University of Veterinary & Animal Sciences, Hisar, Haryana 125001, India.

出版信息

Pathogens. 2021 Feb 13;10(2):197. doi: 10.3390/pathogens10020197.

Abstract

Vaccination may be an effective way to reduce turkey arthritis reovirus (TARV)-induced lameness in turkey flocks. However, there are currently no commercial vaccines available against TARV infection. Here, we describe the use of reverse genetics technology to generate a recombinant Pichinde virus (PICV) that expresses the Sigma C and/or Sigma B proteins of TARV as antigens. Nine recombinant PICV-based TARV vaccines were developed carrying the wild-type S1 (Sigma C) and/or S3 (Sigma B) genes from three different TARV strains. In addition, three recombinant PICV-based TARV vaccines were produced carrying codon-optimized S1 and/or S3 genes of a TARV strain. The S1 and S3 genes and antigens were found to be expressed in virus-infected cells via reverse transcriptase polymerase chain reaction (RT-PCR) and the direct fluorescent antibody (DFA) technique, respectively. Turkey poults inoculated with the recombinant PICV-based TARV vaccine expressing the bivalent TARV S1 and S3 antigens developed high anti-TARV antibody titers, indicating the immunogenicity (and safety) of this vaccine. Future in vivo challenge studies using a turkey reovirus infection model will determine the optimum dose and protective efficacy of this recombinant virus-vectored candidate vaccine.

摘要

接种疫苗可能是减少火鸡群中火鸡关节炎呼肠孤病毒(TARV)引起的跛行的有效方法。然而,目前尚无针对TARV感染的商业疫苗。在此,我们描述了利用反向遗传学技术生成一种重组皮钦德病毒(PICV),该病毒表达TARV的西格玛C和/或西格玛B蛋白作为抗原。基于重组PICV的9种TARV疫苗被开发出来,它们携带来自三种不同TARV毒株的野生型S(西格玛C)和/或S(西格玛B)基因。此外,还生产了三种基于重组PICV的TARV疫苗,它们携带一种TARV毒株的密码子优化的S和/或S基因。通过逆转录聚合酶链反应(RT-PCR)和直接荧光抗体(DFA)技术分别发现,S和S基因及抗原在病毒感染细胞中表达。接种表达二价TARV S和S抗原的基于重组PICV的TARV疫苗的小火鸡产生了高抗TARV抗体滴度,表明该疫苗具有免疫原性(和安全性)。未来使用火鸡呼肠孤病毒感染模型进行的体内攻毒研究将确定这种重组病毒载体候选疫苗的最佳剂量和保护效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acc0/7918942/4ca012893925/pathogens-10-00197-g001.jpg

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