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近期肠道病毒30型谱系的出现以一系列基因重组事件为特征。

Emergence of recent echovirus 30 lineages is marked by serial genetic recombination events.

作者信息

Mirand Audrey, Henquell Cécile, Archimbaud Christine, Peigue-Lafeuille Hélène, Bailly Jean-Luc

机构信息

CHU Clermont-Ferrand, Laboratoire de Virologie, Centre de Biologie, F-63003 Clermont-Ferrand, France.

Université d'Auvergne, Laboratoire de Virologie-EA3843, UFR Médecine, 28 place Henri-Dunant, F-63001 Clermont-Ferrand, France.

出版信息

J Gen Virol. 2007 Jan;88(Pt 1):166-176. doi: 10.1099/vir.0.82146-0.

Abstract

In an earlier report, different variants of echovirus 30 (E-30), an enterovirus serotype, were identified during two outbreaks in 1997 and 2000. Here, the diversity of E-30 was investigated over a longer period (1991-2005) and the variations in four genomic segments were determined in 52 isolates involved in meningitis cases, to characterize the evolutionary processes underlying the emergence of lineages. Phylogenetic analysis of the VP1 sequences showed that five phylogenetic variants succeeded one another. When a partial 3CD segment was examined, the five variants split further into 10 lineages. Phylogenetic groupings observed with both the VP1 and 3CD sequences were clearly related to the calendar time of virus isolation. The rapid turnover of lineages during the study period was not associated with variations in amino acid residues in either the VP1 or the 3CD sequences, indicating major evolutionary contraints in E-30. The variation patterns were examined further along a subgenomic segment of 4878 nt in 13 virus isolates, representative of the 10 lineages. Breakpoints detected in the similarity profiles were investigated by bootscanning and maximum-likelihood phylogenetic analysis of virus genes. Evidence of several past recombination events was observed in the middle of the genome and predicted recombination crossover sites were mapped with precision. The contribution of recombination to the evolution of E-30 is substantial. It is associated tightly with the emergence of new genetic lineages and certain recombinants have undergone epidemic spread.

摘要

在一份早期报告中,肠道病毒血清型埃可病毒30(E-30)的不同变体在1997年和2000年的两次疫情爆发期间被鉴定出来。在此,对E-30的多样性进行了更长时间(1991 - 2005年)的研究,并确定了52株涉及脑膜炎病例的分离株中四个基因组片段的变异情况,以表征谱系出现背后的进化过程。VP1序列的系统发育分析表明,五个系统发育变体相继出现。当检查部分3CD片段时,这五个变体进一步分为10个谱系。用VP1和3CD序列观察到的系统发育分组与病毒分离的日历时间明显相关。研究期间谱系的快速更替与VP1或3CD序列中氨基酸残基的变异无关,这表明E-30存在主要的进化限制。沿着13株病毒分离株(代表10个谱系)中4878 nt的亚基因组片段进一步检查变异模式。通过对病毒基因进行自展扫描和最大似然系统发育分析,研究了相似性图谱中检测到的断点。在基因组中部观察到了几次过去重组事件的证据,并精确绘制了预测的重组交叉位点。重组对E-30进化的贡献很大。它与新遗传谱系的出现紧密相关,并且某些重组体已经经历了流行传播。

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