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首页> 外文期刊>Infection, Genetics and Evolution: Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases >Human G9P[8] rotavirus strains circulating in Cameroon, 1999-2000: Genetic relationships with other G9 strains and detection of a new G9 subtype
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Human G9P[8] rotavirus strains circulating in Cameroon, 1999-2000: Genetic relationships with other G9 strains and detection of a new G9 subtype

机译:1999-2000年在喀麦隆流通的人G9P [8]轮状病毒株:与其他G9株的遗传关系和新G9亚型的检测

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摘要

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
机译:A组轮状病毒(RV-A)是全世界儿童病毒性肠胃炎的主要原因,基因型G9P [8]是人类检测到的五种最常见的基因型之一。为了深入了解在喀麦隆流通的G9P [8]菌株的遗传变异程度,在1999-2000年轮状病毒季节期间在喀麦隆的两个不同地理区域(西南和西部地区)收集了粪便样本。通过RT-PCR,鉴定了15个G9P [8]菌株(15/89 = 16.8%),其菌株的基因组构型随后通过全部或部分基因测序确定。总的来说,所有喀麦隆G9菌株都聚集成当前VP7基因的全球传播子系,它们之间显示86.6-100%的核苷酸同一性,与全球G9菌株显示81.2-99.5%的核苷酸同一性。喀麦隆所有菌株的全基因组分类为G9-P [8] -I1-R1-C1-M1-A1-N1-T1-E1-H1,但对每个基因的系统发育分析表明,该菌株分布在4个或更多不同的地方血统。一个不常见的菌株RVA / Human-wt / CMR / 6788/1999 / G9P [8],与其他喀麦隆G9P [8]菌株具有相同的基因组构象,它含有一个新的G9亚型,其显着不同(18.8%核苷酸和19%氨基酸距离)。核苷酸和氨基酸比对表明,该基因的3'端与其他G9 VP7基因高度不同,表明它是通过大量积累的点突变而产生的。这项研究的结果表明,1999-2000年间喀麦隆传播了多种G9菌株

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