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Selection and evolutionary analysis in the nonstructural protein NSP2 of rotavirus A

机译:轮状病毒A非结构蛋白NSP2的选择与进化分析

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摘要

Rotavirus A is the leading cause of acute gastroenteritis in infants and young children worldwide. The nonstructural protein 2 (NSP2) plays essential roles in the replication cycle of rotavirus and may play a role in protective immunity against rotavirus disease. Using a Bayesian approach, we measured the mutation rate of genotype N1 NSP2 gene sequences. The N1 genotype is the main NSP2 genotype associated with rotavirus strains causing severe disease, and was found to have a high mutation rate (8.7 × 10?4 substitutions/site/year) in comparison to the rotavirus VP4 gene and rates of mutation in other RNA viruses. NSP2 has traditionally been considered as a conserved rotavirus protein and selection analysis indicated that the NSP2 protein was under strong negative selection, suggesting that most nucleotide substitutions were synonymous. This conservation is likely a result of functional constraints of NSP2 in the rotavirus replication cycle. Four sites of positive selection were identified; two of these (positions 249 and 255) were located in a previously characterised antibody binding epitope. The remaining sites were not located in known functional regions, and the reason for variation at these sites remains to be elucidated.
机译:轮状病毒A是全世界婴幼儿急性胃肠炎的主要原因。非结构蛋白2(NSP2)在轮状病毒的复制周期中起重要作用,并可能在针对轮状病毒疾病的保护性免疫中发挥作用。使用贝叶斯方法,我们测量了基因型N1 NSP2基因序列的突变率。 N1基因型是与轮状病毒株引起严重疾病的主要NSP2基因型,与轮状病毒VP4基因和其他突变率相比,具有较高的突变率(8.7×10?4替换/位点/年)。 RNA病毒。 NSP2传统上一直被视为保守的轮状病毒蛋白,选择分析表明NSP2蛋白处于强阴性选择下,这表明大多数核苷酸取代是同义的。这种保护可能是轮状病毒复制周期中NSP2功能受限的结果。确定了四个阳性选择位点;其中两个(位置249和255)位于先前表征的抗体结合表位中。其余位点不在已知的功能区中,这些位点变异的原因还有待阐明。

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