An emerging and expanding clade accounts for the persistent outbreak of Coxsackievirus A6-associated hand, foot, and mouth disease in China since 2013

被引:18
作者
He, Shuizhen [1 ]
Chen, Mengyuan [2 ,3 ,4 ]
Wu, Wenhui [2 ,3 ,4 ]
Yan, Qiang [3 ]
Zhuo, Zhihao [2 ,3 ]
Su, Xiaosong [2 ,3 ,4 ]
Zhang, Shiyin [2 ,3 ,4 ]
Ge, Shengxiang [2 ,3 ,4 ]
Xia, Ningshao [2 ,3 ,4 ]
机构
[1] Xiamen Ctr Dis Control & Prevent, Shengguang Rd, Xiamen, Peoples R China
[2] Xiamen Univ, State Key Lab Mol Vaccinol & Mol Diagnost, Xiangan Campus,South Xiangan Rd, Xiamen, Peoples R China
[3] Xiamen Univ, Natl Inst Diagnost & Vaccine Dev Infect Dis, Xiangan Campus,South Xiangan Rd, Xiamen, Peoples R China
[4] Xiamen Univ, Sch Publ Hlth, Xiangan Campus,South Xiangan Rd, Xiamen, Peoples R China
关键词
Hand; foot; and mouth disease (HFMD); Human enteroviruses (human EVs); Coxsackievirus A6 (CV-A6); Epidemic; Evolution analysis; ENTEROVIRUS; 71; A6; EPIDEMIOLOGY; VP1; VIRULENCE; ETIOLOGY;
D O I
10.1016/j.virol.2018.03.012
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Enterovirus (EV)-A71 and Coxsackievirus (CV)-A16 have historically been the major pathogens of hand, foot, and mouth disease (HMFD) in China; however, CV-A6, which had previously received little attention, became the predominant pathogen in 2013, and has remained one of the common pathogens since then. In this work, we conducted a molecular epidemiology study of CV-A6-associated HFMD in Xiamen from 2009 to 2015. The data showed CV-A6 pandemics had a certain periodicity rather than occurring randomly. Evolution analysis based on near-complete VP1 nucleotide sequences showed subgenotype D5 lineage 4 strains account for the persistent outbreak of CV-A6-associated HFMD in China since 2013. Alignment analysis revealed eight candidate amino acid substitutions in VP1, which may provide useful information for the research of CV-A6 virulence enhancement. This study contributed to elucidating the circulation patterns and genetic characteristics of CV-A6 in China; however, further surveillance and intervention in CV-A6 epidemics is recommended.
引用
收藏
页码:328 / 334
页数:7
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