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皮钦德沙粒病毒强毒株和无毒株的基因组比较

Genome comparison of virulent and avirulent strains of the Pichinde arenavirus.

作者信息

Lan Shuiyun, McLay Lisa, Aronson Judy, Ly Hinh, Liang Yuying

机构信息

Department of Pathology and Laboratory Medicine, Emory University School of Medicine, 615 Michael Street, 105P Whitehead Bldg., Atlanta, GA 30322, USA.

出版信息

Arch Virol. 2008;153(7):1241-50. doi: 10.1007/s00705-008-0101-2. Epub 2008 May 28.

Abstract

A virulent (P18) strain of the Pichinde arenavirus produces a disease in guinea pigs that somewhat mimics human Lassa fever, whereas an avirulent (P2) strain of this virus is attenuated in infected animals. It has been speculated that the composition of viral genomes may confer the degree of virulence in an infected host; the complete sequence of the viral genomes, however, is not known. Here, we provide for the first time genomic sequences of the S and L segments for both the P2 and P18 strains. Sequence comparisons identify three mutations in the GP1 subunit of the viral glycoprotein, one in the nucleoprotein NP, and five in the viral RNA polymerase L protein. These mutations, alone or in combination, may contribute to the acquired virulence of Pichinde virus infection in animals. The three amino acid changes in the variable region of the GP1 glycoprotein subunit may affect viral entry by altering its receptor-binding activity. While NP has previously been shown to modulate host immune responses to viral infection, we found that the R374 K change in this protein does not affect the NP function of suppressing interferon-beta expression. Four out of the five amino acid changes in the L protein occur in a small region of the protein that may contribute to viral virulence by enhancing its function in viral genomic RNA synthesis.

摘要

皮钦德沙粒病毒的一种强毒株(P18)在豚鼠中引发的疾病在一定程度上类似于人类拉沙热,而该病毒的一种无毒株(P2)在受感染动物中则表现为减毒。据推测,病毒基因组的组成可能决定了其在受感染宿主中的毒力程度;然而,病毒基因组的完整序列尚不清楚。在此,我们首次提供了P2和P18毒株的S和L片段的基因组序列。序列比较确定了病毒糖蛋白GP1亚基中的三个突变、核蛋白NP中的一个突变以及病毒RNA聚合酶L蛋白中的五个突变。这些突变单独或共同作用,可能导致皮钦德病毒感染动物后获得毒力。GP1糖蛋白亚基可变区的三个氨基酸变化可能通过改变其受体结合活性来影响病毒进入。虽然此前已表明NP可调节宿主对病毒感染的免疫反应,但我们发现该蛋白中的R374K变化并不影响其抑制干扰素-β表达的NP功能。L蛋白中的五个氨基酸变化中有四个发生在该蛋白的一个小区域,这可能通过增强其在病毒基因组RNA合成中的功能而导致病毒毒力增强。

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