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猪流行性腹泻病毒刺突基因的突变与体外生长适应性及体内毒力减弱相关。

Mutations in the spike gene of porcine epidemic diarrhea virus associated with growth adaptation in vitro and attenuation of virulence in vivo.

作者信息

Sato Tetsuo, Takeyama Natsumi, Katsumata Atsushi, Tuchiya Kotaro, Kodama Toshiaki, Kusanagi Ko-ichi

机构信息

Nippon Institute for Biological Science, 9-2221-1 Shin-machi, Ome, Tokyo, 198-0024, Japan.

出版信息

Virus Genes. 2011 Aug;43(1):72-8. doi: 10.1007/s11262-011-0617-5. Epub 2011 May 11.

Abstract

Previously, we have reported that a serial passage of 83P-5 strain of porcine epidemic diarrhea virus (PEDV) in Vero cells resulted in a growth adaptation of the virus in cultured cells at the 22nd passage. In this study, we further maintained the 83P-5 in Vero cells up to the 100th passage and analyzed changes in the spike (S), membrane (M), and nucleocapsid (N) gene sequences and pathogenicity of the virus at the 34th, 61st, and 100th passage levels. Sequence analyses revealed a strong selection for the S gene of 83P-5 in Vero cells, and virtually all mutations occurring at the 34th and 61st passages had been carried over to the 100th-passaged virus. In contrast, the viral M and N genes showed a strong conservation during the serial passage. Pigs experimentally infected with the 34th- or 61st-passaged virus, but not the 100th-passaged virus, exhibited diarrhea, indicating an attenuation of the 83P-5 at the 100th passage. Interestingly, S protein of the attenuated 100th-passaged 83P-5 showed a remarkable sequence similarity to that of previously reported DR-13 strain of attenuated PEDV that also had been established by serial passage in Vero cells. Further studies will be required to define whether the mutations in the S gene of 83P-5 that had been selected and accumulated during the serial passages are indeed the causalities of the growth adaptation in vitro and the attenuation of virulence in vivo.

摘要

此前,我们曾报道,猪流行性腹泻病毒(PEDV)83P - 5毒株在Vero细胞中连续传代,在第22代时病毒在培养细胞中出现生长适应性。在本研究中,我们将83P - 5在Vero细胞中进一步传代至第100代,并分析了第34代、第61代和第100代时病毒的刺突(S)、膜(M)和核衣壳(N)基因序列变化以及病毒致病性。序列分析显示,Vero细胞对83P - 5的S基因有强烈选择作用,第34代和第61代出现的几乎所有突变都传递到了第100代病毒中。相比之下,病毒的M和N基因在连续传代过程中表现出高度保守性。用第34代或第61代传代病毒而非第100代传代病毒实验感染猪,猪出现腹泻,表明83P - 5在第100代时毒力减弱。有趣的是,第100代减毒的83P - 5的S蛋白与先前报道的同样通过在Vero细胞中连续传代建立的减毒PEDV DR - 13毒株的S蛋白具有显著的序列相似性。需要进一步研究来确定83P - 5在连续传代过程中选择和积累的S基因中的突变是否确实是其体外生长适应性和体内毒力减弱的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03f8/7088782/27fecadb47f8/11262_2011_617_Fig1_HTML.jpg

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