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2012/2013年在越南由共同流行毒株产生的重配型DS-1样G1P[4] A组轮状病毒毒株

Reassortant DS-1-like G1P[4] Rotavirus A strains generated from co-circulating strains in Vietnam, 2012/2013.

作者信息

Agbemabiese Chantal Ama, Nakagomi Toyoko, Nguyen Minh Quang, Gauchan Punita, Nakagomi Osamu

机构信息

Leading Program, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan.

Department of Molecular Epidemiology, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan.

出版信息

Microbiol Immunol. 2017 Aug;61(8):328-336. doi: 10.1111/1348-0421.12501.

Abstract

One major mechanism by which Rotavirus A (RVA) evolves is genetic reassortment between strains with different genotype constellations. However, the parental strains of the reassortants generated have seldom been identified. Here, the whole genome of two suspected reassortants, RVA/Human-wt/VNM/SP127/2013/G1P[4] and RVA/Human-wt/VNM/SP193/2013/G1P[4], with short RNA electropherotypes were examined by Illumina MiSeq sequencing and their ancestral phylogenies reconstructed. Their genotype constellation, G1-P[4]-I2-R2-C2-M2-A2-N2-T2-E2-H2, indicated that they were G1 VP7 mono-reassortants possessing DS-1-like genetic backbones. The two strains were ≧99.7% identical across the genome. While their VP7 genes were ≧99.7 identical to that of a Wa-like strain RVA/Human-wt/VNM/SP110/2012/G1P[8] which co-circulated during the 2012/2013 season, 10 genes were ≧99.8% identical to that of the DS-1-like strains RVA/Human-wt/VNM/SP015/2012/G2P[4] (and SP108) that co-circulated during the season. The identities were consistent with the phylogenetic relationships observed between the genes of the reassortants and those of the afore-mentioned strains. Consequently, the G1P[4] strains appear to have been generated by genetic reassortment between SP110-like and SP015-like strains. In conclusion, this study provides robust molecular evidence for the first time that G1P[4] strains detected in Hanoi Vietnam were generated by inter-genogroup reassortment between co-circulating G1P[8] and G2P[4] strains within the same place and season.

摘要

A组轮状病毒(RVA)进化的一个主要机制是具有不同基因型组合的毒株之间发生基因重配。然而,很少能鉴定出重配毒株的亲代毒株。在此,通过Illumina MiSeq测序检测了两个疑似重配毒株RVA/人类-wt/越南/SP127/2013/G1P[4]和RVA/人类-wt/越南/SP193/2013/G1P[4]的全基因组,并重建了它们的祖先系统发育树。它们的基因型组合G1-P[4]-I2-R2-C2-M2-A2-N2-T2-E2-H2表明,它们是具有DS-1样遗传背景的G1 VP7单重配毒株。这两个毒株在全基因组上的相似度≧99.7%。虽然它们的VP7基因与2012/2013季节共同流行的Wa样毒株RVA/人类-wt/越南/SP110/2012/G1P[8]的VP7基因相似度≧99.7%,但有10个基因与该季节共同流行的DS-1样毒株RVA/人类-wt/越南/SP015/2012/G2P[4](和SP108)的基因相似度≧99.8%。这些相似度与在重配毒株基因和上述毒株基因之间观察到的系统发育关系一致。因此,G1P[4]毒株似乎是由SP110样毒株和SP015样毒株之间的基因重配产生的。总之,本研究首次提供了有力的分子证据,表明在越南河内检测到的G1P[4]毒株是由同一地点和季节共同流行的G1P[8]和G2P[4]毒株之间的基因组间重配产生的。

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