Genetic Variation of Multiple Serotypes of Enteroviruses Associated with Hand, Foot and Mouth Disease in Southern China

被引:13
作者
Zhou, Yonghong [1 ]
Le Van Tan [2 ]
Luo, Kaiwei [3 ]
Liao, Qiaohong [1 ,4 ]
Wang, Lili [1 ]
Qiu, Qi [1 ]
Zou, Gang [5 ]
Liu, Ping [6 ]
Nguyen To Anh [2 ]
Nguyen Thi Thu Hong [2 ]
He, Min [6 ]
Wei, Xiaoman [7 ]
Yu, Shuanbao [4 ]
Lam, Tommy Tsan-Yuk [8 ,9 ]
Cui, Jie [10 ]
van Doorn, H. Rogier [2 ,11 ]
Yu, Hongjie [1 ]
机构
[1] Fudan Univ, Sch Publ Hlth, Key Lab Publ Hlth Safety, Minist Educ, Shanghai 200032, Peoples R China
[2] Univ Oxford, Clin Res Unit, Ho Chi Minh City 700000, Vietnam
[3] Hunan Prov Ctr Dis Control & Prevent, Changsha 410005, Peoples R China
[4] Chinese Ctr Dis Control & Prevent, Div Infect Dis, Key Lab Surveillance & Early Warning Infect Dis, Beijing 102206, Peoples R China
[5] Chinese Acad Sci, Inst Pasteur Shanghai, Shanghai 200032, Peoples R China
[6] Anhua Cty Ctr Dis Control & Prevent, Anhua 413000, Peoples R China
[7] Chinese Acad Sci, Ctr Emerging Infect Dis, Wuhan Inst Virol, CAS Key Lab Special Pathogens & Biosafety, Wuhan 430071, Peoples R China
[8] Univ Hong Kong, Ctr Influenza Res, Sch Publ Hlth, Hong Kong 999077, Peoples R China
[9] Univ Hong Kong, Sch Publ Hlth, State Key Lab Emerging Infect Dis, Hong Kong 999077, Peoples R China
[10] Chinese Acad Sci, Inst Pasteur Shanghai, CAS Key Lab Mol Virol & Immunol, Shanghai 200032, Peoples R China
[11] Univ Oxford, Ctr Trop Med, Nuffield Dept Med, Oxford OX3 7DQ, England
基金
中国国家自然科学基金;
关键词
Enteroviruses (EVs); Hand; foot and mouth disease (HFMD); Enterovirus A71 (EV-A71); Coxsackievirus A16 (CVA16); Coxsackievirus A6 (CVA6); COXSACKIEVIRUS A16; FREQUENT RECOMBINATION; EMERGENCE; STRAINS; VP1; A6; EVOLUTION; EPIDEMIC; PROTEIN; HFMD;
D O I
10.1007/s12250-020-00266-7
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Enteroviruses (EVs) species A are a major public health issue in the Asia-Pacific region and cause frequent epidemics of hand, foot and mouth disease (HFMD) in China. Mild infections are common in children; however, HFMD can also cause severe illness that affects the central nervous system. To molecularly characterize EVs, a prospective HFMD virological surveillance program was performed in China between 2013 and 2016. Throat swabs, rectal swabs and stool samples were collected from suspected HFMD patients at participating hospitals. EVs were detected using generic real-time and nested reverse transcription-polymerase chain reactions (RT-PCRs). Then, the complete VP1 regions of enterovirus A71 (EV-A71), coxsackievirus A16 (CVA16) and CVA6 were sequenced to analyze amino acid changes and construct a viral molecular phylogeny. Of the 2836 enrolled HFMD patients, 2,517 (89%) were EV positive. The most frequently detected EVs were CVA16 (32.5%, 819), CVA6 (31.2%, 785), and EV-A71 (20.4%, 514). The subgenogroups CVA16_B1b, CVA6_D3a and EV-A71_C4a were predominant in China and recombination was not observed in the VP1 region. Sequence analysis revealed amino acid variations at the 30, 29 and 44 positions in the VP1 region of EV-A71, CVA16 and CVA6 (compared to the respective prototype strains BrCr, G10 and Gdula), respectively. Furthermore, in 21 of 24 (87.5%) identified EV-A71 samples, a known amino acid substitution (D31N) that may enhance neurovirulence was detected. Our study provides insights about the genetic characteristics of common HFMD-associated EVs. However, the emergence and virulence of the described mutations require further investigation.
引用
收藏
页码:61 / 74
页数:14
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