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首页> 外文期刊>Journal of Clinical Microbiology >Analysis of the Serotype and Genotype Correlation of VP1 and the 5′ Noncoding Region in an Epidemiological Survey of the Human Enterovirus B Species
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Analysis of the Serotype and Genotype Correlation of VP1 and the 5′ Noncoding Region in an Epidemiological Survey of the Human Enterovirus B Species

机译:人类肠道病毒B流行病学调查中VP1和5'非编码区的血清型和基因型相关性分析。

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The sequence identity of the enterovirus VP1 gene has been shown to correlate with the serotype concept. Enterovirus molecular typing methods are therefore often based on sequencing of the VP1 genomic region and monophyletic clustering of VP1 sequences of a homologous serotype. For epidemiological surveillance, 342 enterovirus samples obtained from patients with aseptic meningitis in Belgium from 1999 to 2002 were first diagnosed as being enterovirus positive by amplification of the 5′ noncoding region (5′NCR) by reverse transcription (RT)-PCR. Subsequently, samples were molecularly typed by RT-nested PCR amplification and sequencing of a portion of the VP1 gene. Phylogenetic analyses were performed to investigate enteroviral evolution and to examine the serotype and genotype correlation of the two genomic regions. Our typing results demonstrated echovirus 30, echovirus 13, echovirus 18, and echovirus 6 to be the most predominant types. Echoviruses 13 and 18 were considered to be emerging human serotypes since 2000 and 2001, respectively, as they had been rarely reported before. Several serotypes existed as multiple genotypes (subtypes) from 1999 to 2002, but genomic differences mainly resided at synonymous sites; these results strongly suggest that the subtypes exhibit similar antigenic properties. Phylogenetic analyses confirmed that VP1 is an adequate region for molecular typing. Serotype-specific clusters are not observed commonly in phylogenetic trees based on the 5′NCR, and the phylogenetic signal in the 5′NCR was found to be particularly low. However, some substructure in the 5′NCR tree made a tentative prediction of the enterovirus type possible and was therefore helpful in PCR strategies for VP1 (e.g., primer choice), provided some background knowledge on the local spectrum of enteroviruses already exists.
机译:肠病毒VP1基因的序列同一性已显示与血清型概念相关。因此,肠道病毒分子分型方法通常基于VP1基因组区域的测序和同源血清型VP1序列的单系聚类。为了进行流行病学监测,首先通过逆转录(RT)-PCR扩增5'非编码区(5'NCR),从1999年至2002年从比利时的无菌性脑膜炎患者中获得了342份肠道病毒样本,被诊断为肠道病毒阳性。随后,通过RT巢式PCR扩增和部分VP1基因的测序对样品进行分子分型。进行了系统发育分析,以调查肠病毒的进化,并检查两个基因组区域的血清型和基因型相关性。我们的打字结果表明,echovirus 30,echovirus 13,echovirus 18和echovirus 6是最主要的类型。自2000年和2001年以来,回声病毒13和18分别被认为是新兴的人类血清型,因为以前很少报道。从1999年到2002年,有几种血清型作为多种基因型(亚型)存在,但基因组差异主要存在于同义位点。这些结果强烈表明亚型表现出相似的抗原特性。系统发育分析证实,VP1是分子分型的适当区域。在基于5'NCR的系统发育树中通常没有观察到血清型特异性簇,并且发现5'NCR中的系统发育信号特别低。但是,5'NCR树中的某些子结构使得可能初步预测肠病毒类型,因此,如果已经存在关于肠病毒局部光谱的一些背景知识,则有助于VP1的PCR策略(例如引物选择)。

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