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2014 年至 2016 年间,泰国曼谷地区婴幼儿中诺如病毒基因型的动态变化及新型重组 GII.P12-GII.3 的基因分析。

The dynamics of norovirus genotypes and genetic analysis of a novel recombinant GII.P12-GII.3 among infants and children in Bangkok, Thailand between 2014 and 2016.

机构信息

Thailand-Japan Research Collaboration Center on Emerging and Re-emerging Infections (RCC-ERI), Nonthaburi 11000, Thailand.

National Institute of Health, Department of Medical Sciences, Ministry of Public Health, Nonthaburi 11000, Thailand.

出版信息

Infect Genet Evol. 2018 Jun;60:133-139. doi: 10.1016/j.meegid.2018.02.028. Epub 2018 Feb 20.

Abstract

Norovirus (NoV) is the leading cause of viral acute gastroenteritis among all age groups in the world. We performed a molecular epidemiological study of the NoVs prevalent in Bangkok between November 2014 and July 2016 to investigate the emergence of new NoV variants in Thailand. A total of 332 stool specimens were collected from hospitalized pediatric patients with acute gastroenteritis in Bangkok, Thailand. NoVs were detected by real-time PCR. The genome of the N-terminal/shell domain was amplified, the nucleotide sequence was determined, and phylogenetic analyses were performed. GII NoV was detected in 58 (17.5%) of the 332 specimens. GII.17, a genotype strain prevalent from 2014 to mid-2015, was hardly detected and replaced by the GII.3 genotype strain. Entire genome sequencing followed by phylogenetic analysis of the GII.3 genotype strains indicated that they are new recombinant viruses, because the genome encoding ORF1 is derived from a GII.12 genotype strain, whereas that encoding ORF2-3 is from a GII.3 genotype strain. The putative recombination breakpoints with the highest statistical significance were located around the border of 3D and ORF2. The change in the prevalent strain of NoV seems to be linked to the emergence of new forms of recombinant viruses. These findings suggested that the swapping of the structural and non-structural proteins of NoV is a common mechanism by which new epidemic variants are generated in nature.

摘要

诺如病毒(NoV)是全球所有年龄段人群病毒性急性肠胃炎的主要病因。我们对 2014 年 11 月至 2016 年 7 月期间曼谷流行的 NoV 进行了分子流行病学研究,以调查泰国新 NoV 变异株的出现情况。从泰国曼谷住院的小儿急性肠胃炎患者中采集了 332 份粪便标本。采用实时 PCR 检测 NoV。扩增 N 端/壳区基因组,测定核苷酸序列,并进行系统进化分析。在 332 份标本中检测到 58 份(17.5%)GII NoV。2014 年至 2015 年年中流行的 GII.17 基因型菌株几乎检测不到,取而代之的是 GII.3 基因型菌株。对 GII.3 基因型菌株进行全基因组测序和系统进化分析表明,它们是新的重组病毒,因为编码 ORF1 的基因组来源于 GII.12 基因型菌株,而编码 ORF2-3 的基因组来源于 GII.3 基因型菌株。具有最高统计学意义的假定重组断点位于 3D 和 ORF2 的边界附近。NoV 流行株的变化似乎与新重组病毒形式的出现有关。这些发现表明,NoV 的结构蛋白和非结构蛋白的交换是自然界中产生新流行变异株的常见机制。

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