广东省18株柯萨奇病毒A6全序列分析

Hanri Zeng, Jing Lu, Huanying Zheng, Xiaoli Chen, Leng Liu, Xue Guo, Changwen Ke, Hui Li
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摘要

本研究对2013年广东省手足口病感染的柯萨奇病毒A6 (coxsackievirus A6, CVA6)全基因组进行检测,探讨CVA6流行株与非流行株的遗传异同。对18株CVA6进行全基因组测序,采用DNASTAR6.0、mega5.2和SimPlot3.5.1软件对序列进行系统发育分析、序列比对分析和基因重组分析。结果显示,18株广东cva6菌株的全基因组长度在7390bp ~ 732bp之间。在编码区未检测到插入或删除。在5'UTR和3'UTR中有一些插入和删除。系统进化分析表明,18个全基因组的核苷酸和氨基酸序列同源性分别为90.5% ~ 99.6%和97.5% ~ 99.9%。2013年分离的菌株可进一步分为III和IV两类,而2011年分离的菌株仅存在于IV类。基因重组分析显示,CVA6广东代表菌株GD870/2013在P2和p3区存在基因重组,而GD839/2013菌株未表现出明显的基因重组。对2013年广东省流行株CVA6的全基因组分析显示,CVA6可能存在III和IV两条传播链。传播链Ⅲ来自P2和p3区基因重组的菌株,与IV链完全不同。CVA6的IV链传播仅在2011年未流行的菌株中观察到。
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[The Complete Sequence Analysis of 18 Strains of Coxsackievirus A6 in Guangdong Province of China].

In this study, we examined the complete genome of coxsackievirus A6 (CVA6) from hand, foot, and mouth disease in Guangdong Province from 2013,and explored the genetic similarities and differences in epidemic and non-epidemic stains of CVA6.Eighteen strains of CVA6 were included in complete genome sequencing, and the sequences were subject to phylogenetic analysis,sequence alignment analysis and genetic recombination analysis using the software DNASTAR6.0,MEGA5.2and SimPlot3.5.1.The results showed that the complete genome of 18 Guangdong CVA6strains ranged from 7390bp to 7392bp.No insertions or deletions were detected in the coding region. There were several insertions and deletions in 5′UTR and 3′UTR.Phylogenetic analysis indicated that the nucleotide and amino acid sequence identity between the 18 complete genomes were 90.5%-99.6% and 97.5%-99.9%,respectively.The strains isolated in2013 could be further divided into two clusters, III and IV, while the strains isolated in 2011 were only present in the IV cluster. Genetic recombination analysis revealed that the Guangdong representative strain of CVA6,GD870/2013,had gene recombination in the P2 and P3regions,while the GD839/2013 strain did not show obvious genetic recombination. Genome-wide analysis of CVA6 revealed that there are two possible transmitted chains, III and IV, in epidemic strains from Guangdong Province in 2013.The transmitted chain Ⅲ originated from the strain with genetic recombination in the P2 and P3regions,whichwas completely different from the chain IV. Transmission of chain IV of CVA6 was only observed in the nonepidemic 2011 strain.

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