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Molecular characterisation of the NSP4 gene of group A human rotavirusG2P4 strains circulating in São Paulo Brazil from 1994 and 2006 to2010

机译:A群人轮状病毒NSP4基因的分子特征从1994年至2006年在巴西圣保罗传播的G2P 4菌株2010年

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摘要

Group A human rotaviruses (HuRVA) are causative agents of acute gastroenteritis. Six viral structural proteins (VPs) and six nonstructural proteins (NSPs) are produced in RV-infected cells. NSP4 is a diarrhoea-inducing viral enterotoxin and NSP4 gene analysis revealed at least 15 (E1-E15) genotypes. This study analysed the NSP4 genetic diversity of HuRVA G2P[4] strains collected in the state of São Paulo (SP) from 1994 and 2006-2010 using reverse transcription-polymerase chain reaction, sequencing and phylogenetic analysis. Forty (97.6%) G2P[4] strains displayed genotype E2; one strain (2.4%) displayed genotype E1. These results are consistent with the proposed linkage between VP4/VP7 (G2P[4]) and the NSP4 (E2) genotype of HuRVA. NSP4 phylogenetic analysis showed distinct clusters, with grouping of most strains by their genotype and collection year, and most strains from SP were clustered together with strains from other Brazilian states. A deduced amino acid sequence alignment for E2 showed many variations in the C-terminal region, including the VP4-binding domain. Considering the ability of NSP4 to generate host immunity, monitoring NSP4 variations, along with those in the VP4 or VP7 protein, is important for evaluating the circulation and pathogenesis of RV. Finally, the presence of one G2P[4]E1 strain reinforces the idea that new genotype combinations emerge through reassortment andindependent segregation.
机译:A组人类轮状病毒(HuRVA)是急性胃肠炎的病原体。在RV感染的细胞中产生了六个病毒结构蛋白(VP)和六个非结构蛋白(NSP)。 NSP4是一种引起腹泻的病毒肠毒素,NSP4基因分析显示至少有15种(E1-E15)基因型。本研究使用逆转录-聚合酶链反应,测序和系统发育分析分析了1994年和2006-2010年在圣保罗州(SP)采集的HuRVA G2P [4]菌株的NSP4遗传多样性。 40株(97.6%)G2P [4]菌株显示出基因型E2。一株(2.4%)显示出基因型E1。这些结果与VP4 / VP7(G2P [4])和HuRVA的NSP4(E2)基因型之间的拟议连锁关系一致。 NSP4的系统发育分析显示出明显的簇,大多数菌株按其基因型和收集年份分组,并且来自SP的大多数菌株与来自其他巴西州的菌株聚在一起。推导的E2氨基酸序列比对显示C端区域有许多变异,包括VP4结合结构域。考虑到NSP4产生宿主免疫的能力,监测NSP4变异以及VP4或VP7蛋白中的变异对于评估RV的循环和发病机理很重要。最后,一种G2P [4] E1菌株的存在强化了这样的观念,即新基因型组合通过重排和独立隔离。

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