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通过连续细胞传代衰减和鉴定猪肠道α冠状病毒 GDS04 株。

Attenuation and characterization of porcine enteric alphacoronavirus strain GDS04 via serial cell passage.

机构信息

State Key Laboratory of Biocontrol, School of Life Science, Sun Yat-sen University, Guangzhou, 510006, China.

College of Animal Science and Veterinary Medicine, Henan Agricultural University, Zhengzhou, 450046, China.

出版信息

Vet Microbiol. 2019 Dec;239:108489. doi: 10.1016/j.vetmic.2019.108489. Epub 2019 Nov 4.

Abstract

Porcine enteric alphacoronavirus (PEAV) is a newly identified swine enteropathogenic coronavirus that causes watery diarrhea in newborn piglets. In this study, an original, highly virulent PEAV strain GDS04 was serially passaged in Vero cells. The virus titers and sizes of syncytia increased gradually with the cell passages. Newborn piglets were orally inoculated with PEAV P15, P67 and P100. Compared with P15 and P67, P100 resulted in only mild clinical signs and intestinal lesions in piglets. The virus shedding in feces and viral antigens in intestinal tract were markedly reduced in P100-inoculated piglets. Importantly, all P100-inoculated newborn piglets survived, indicating that P100 was an attenuated variant. Sequence analysis revealed that the virulent strain GDS04 had four, one, six and eleven amino acid differences in membrane, nucleocapsid, spike and ORF1ab proteins, respectively, from P100. Furthermore, more differences in the predicted three-dimensional structure of S protein between GDS04 and P100 were observed, indicating that these differences might be associated with the pathogenicity of PEAV. Collectively, our research successfully prepared a PEAV attenuated variant which might serve as a live attenuated vaccine candidate against PEAV infection.

摘要

猪肠道冠状病毒(PEAV)是一种新鉴定的猪肠道致病性冠状病毒,可引起新生仔猪水样腹泻。在本研究中,我们将原始的、高毒力的 PEAV 株 GDS04 在 Vero 细胞中连续传代。随着细胞传代,病毒滴度和合胞体大小逐渐增加。新生仔猪经口接种 PEAV P15、P67 和 P100。与 P15 和 P67 相比,P100 仅导致仔猪出现轻微的临床症状和肠道病变。P100 感染仔猪的粪便病毒脱落和肠道病毒抗原明显减少。重要的是,所有 P100 感染的新生仔猪均存活,表明 P100 是一种减毒变体。序列分析显示,毒力株 GDS04 在膜蛋白、核衣壳蛋白、刺突蛋白和 ORF1ab 蛋白上分别有四个、一个、六个和十一个氨基酸差异,而 P100 则没有。此外,还观察到 GDS04 和 P100 之间 S 蛋白的预测三维结构存在更多差异,表明这些差异可能与 PEAV 的致病性有关。总之,我们的研究成功制备了一种 PEAV 减毒变体,可能可作为针对 PEAV 感染的活减毒疫苗候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9459/7117411/871e97837230/gr1_lrg.jpg

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