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1999-2000 年喀麦隆流行的人 G9P[8] 轮状病毒株:与其他 G9 株的遗传关系及新 G9 亚型的检测。

Human G9P[8] rotavirus strains circulating in Cameroon, 1999-2000: Genetic relationships with other G9 strains and detection of a new G9 subtype.

机构信息

Gastroenteritis and Respiratory Viruses Laboratory Branch, Centers for Disease Control and Prevention, Atlanta, USA.

出版信息

Infect Genet Evol. 2013 Aug;18:315-24. doi: 10.1016/j.meegid.2013.06.005. Epub 2013 Jun 14.

Abstract

Group A rotaviruses (RV-A) are the leading cause of viral gastroenteritis in children worldwide and genotype G9P[8] is one of the five most common genotypes detected in humans. In order to gain insight into the degree of genetic variability of G9P[8] strains circulating in Cameroon, stool samples were collected during the 1999-2000 rotavirus season in two different geographic regions in Cameroon (Southwest and Western Regions). By RT-PCR, 15 G9P[8] strains (15/89=16.8%) were identified whose genomic configurations was subsequently determined by complete or partial gene sequencing. In general, all Cameroonian G9 strains clustered into current globally-spread sublineages of the VP7 gene and displayed 86.6-100% nucleotide identity amongst themselves and 81.2-99.5% nucleotide identity with global G9 strains. The full genome classification of all Cameroonian strains was G9-P[8]-I1-R1-C1-M1-A1-N1-T1-E1-H1 but phylogenetic analysis of each gene revealed that the strains were spread across 4 or more distinct lineages. An unusual strain, RVA/Human-wt/CMR/6788/1999/G9P[8], which shared the genomic constellation of other Cameroonian G9P[8] strains, contained a novel G9 subtype which diverged significantly (18.8% nucleotide and 19% amino acid distance) from previously described G9 strains. Nucleotide and amino acid alignments revealed that the 3' end of this gene is highly divergent from other G9 VP7 genes suggesting that it arose through extensive accumulation of point mutations. The results of this study demonstrate that diverse G9 strains circulated in Cameroon during 1999-2000.

摘要

A 组轮状病毒(RV-A)是全世界导致儿童病毒性肠胃炎的主要病原体,基因型 G9P[8]是人类中检测到的五种最常见基因型之一。为了深入了解喀麦隆流行的 G9P[8]毒株的遗传变异程度,在喀麦隆两个不同地理区域(西南区和西区)于 1999-2000 年轮状病毒流行季节采集了粪便样本。通过 RT-PCR,鉴定出 15 株 G9P[8](15/89=16.8%),随后通过完整或部分基因测序确定了其基因组结构。一般来说,所有喀麦隆 G9 株都聚类到当前全球流行的 VP7 基因亚谱系中,彼此之间的核苷酸同一性为 86.6-100%,与全球 G9 株的核苷酸同一性为 81.2-99.5%。所有喀麦隆株的全基因组分类均为 G9-P[8]-I1-R1-C1-M1-A1-N1-T1-E1-H1,但各基因的系统进化分析显示,这些毒株分布在 4 个或更多不同的谱系中。一株罕见的毒株,RVA/Human-wt/CMR/6788/1999/G9P[8],与其他喀麦隆 G9P[8]株具有相同的基因组结构,包含一个新型的 G9 亚型,与之前描述的 G9 株明显分化(核苷酸差异 18.8%,氨基酸差异 19%)。核苷酸和氨基酸比对显示,该基因的 3'末端与其他 G9 VP7 基因高度分化,表明它是通过大量点突变积累而产生的。本研究结果表明,1999-2000 年喀麦隆流行多种 G9 株。

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