姜法春, 赵超, 董鸿铭, 贾静, 王霞, 王衍海, 高晨, 韩俊. 2019年冬季青岛市手足口病患者感染柯萨奇病毒A组16型基因特征分析[J]. 疾病监测, 2022, 37(6): 755-759. DOI: 10.3784/jbjc.202111100577
引用本文: 姜法春, 赵超, 董鸿铭, 贾静, 王霞, 王衍海, 高晨, 韩俊. 2019年冬季青岛市手足口病患者感染柯萨奇病毒A组16型基因特征分析[J]. 疾病监测, 2022, 37(6): 755-759. DOI: 10.3784/jbjc.202111100577
Jiang Fachun, Zhao Chao, Dong Hongming, Jia Jing, Wang Xia, Wang Yanhai, Gao Chen, Han Jun. Genetic characteristics of Coxsackievirus A16 isolated from hand foot and mouth disease cases in Qingdao in winter of 2019[J]. Disease Surveillance, 2022, 37(6): 755-759. DOI: 10.3784/jbjc.202111100577
Citation: Jiang Fachun, Zhao Chao, Dong Hongming, Jia Jing, Wang Xia, Wang Yanhai, Gao Chen, Han Jun. Genetic characteristics of Coxsackievirus A16 isolated from hand foot and mouth disease cases in Qingdao in winter of 2019[J]. Disease Surveillance, 2022, 37(6): 755-759. DOI: 10.3784/jbjc.202111100577

2019年冬季青岛市手足口病患者感染柯萨奇病毒A组16型基因特征分析

Genetic characteristics of Coxsackievirus A16 isolated from hand foot and mouth disease cases in Qingdao in winter of 2019

  • 摘要:
      目的  调查2019年冬季青岛市妇幼医院和中心医院手足口病(HFMD)住院患儿病原感染情况,分析柯萨奇病毒A组16型(Cox A16)基因进化特征。
      方法  收集2019年冬季青岛地区HFMD住院患儿104份咽拭子,采用实时荧光定量PCR进行肠道病毒核酸检测。 使用肠道病毒通用分型引物扩增阳性样本,扩增序列测序后进行Blast比对。 设计Cox A16 VP1全长引物,通过半巢式PCR扩增测序,使用DNAStar进行核苷酸和氨基酸的基因分析,使用MEGA软件构建进化树。
      结果   HFMD住院患儿的咽拭子样本肠道病毒总体阳性率为57.7%(60/104)。 其中Cox A16阳性率为30.8%(32/104),Cox A6阳性率为26.9%(28/104)。 对32份Cox A16阳性的样本进行VP1区全长扩增、测序并进行比对和同源性分析,其核苷酸同源性为87.0%~100%,氨基酸同源性为98.3%~100%。 系统进化分析表明,32株Cox A16中有17株为Cox A16 B1a基因型,另外15株为Cox A16 B1b基因型。
      结论  引起2019年冬季青岛地区住院HFMD的病原体之一是Cox A16,且同时流行Cox A16的B1a和B1b型。

     

    Abstract:
      Objective  To investigate the etiological and genetic characteristics of hand foot and mouth disease (HFMD) cases in Women and Children Hospital and Central Hospital of Qingdao in the winter of 2019, and analyze the genetic evolution of coxsackievirus A16 (Cox A16).
      Methods  After the collection of 104 throat swabs from hospitalized children with HFMD in Qingdao in the winter of 2019, enterovirus nucleic acid test was conducted by real-time fluorescent quantitative PCR (RT-qPCR), the positive samples were amplified with general typing primers of entrovirus. Blast alignment was conducted after sequence amplification. The full-length of Cox A16 VP1 gene was amplified by using semi-nested PCR with designed Cox A16 VP1 full length primers, and genetic analysis of nucleotides and amino acids was conducted by using DNAstar, and a phylogenetic tree was constructed by using MEGA software with reference sequences.
      Results  In the 104 throat swabs from the hospitalized children with HFMD, 60 were positive for enterovirus, and the overall positive rate was 57.7%. The positive rate of Cox A16 was 30.8% (32/104), and the positive rate of Coxsackievirus A6 (Cox A6) was 26.9% (28/104). After Cox A16 VP1 of 32 positive samples were amplified and sequenced, it was found that the nucleotide homology was 87.0%–100%, and the amino acid homology was 98.3%–100%. Phylogenetic analysis showed that 17 of the 32 Cox A16 strains belonged to Cox A16 B1a genotype, and the other 15 strains belonged to Cox A16 B1b genotype.
      Conclusion  The pathogens that caused HFMD hospitalizations in Qingdao in the winter of 2019 included Cox A16, and Cox A16 types B1a and B1b spread at the same time.

     

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