Molecular epidemiology of enteroviruses associated with severe hand, foot and mouth disease in Shenzhen, China, 2014-2018

被引:32
作者
Chen, Long [1 ,2 ]
Xu, Shao-Jian [3 ]
Yao, Xiang-Jie [1 ,2 ]
Yang, Hong [1 ,2 ]
Zhang, Hai-Long [1 ,2 ]
Meng, Jun [1 ,2 ]
Zeng, Han-Ri [4 ]
Huang, Xu-He [4 ]
Zhang, Ren-Li [1 ,2 ]
He, Ya-Qing [1 ,2 ]
机构
[1] Shenzhen Ctr Dis Control & Prevent, Inst Pathogen Biol, Major Infect Dis Control Key Lab, Shenzhen 518055, Peoples R China
[2] Shenzhen Ctr Dis Control & Prevent, Inst Pathogen Biol, Shenzhen Publ Serv Platform Pathogen Microorganis, Shenzhen 518055, Peoples R China
[3] Longhua Dist Ctr Dis Control & Prevent, Dist Key Lab Infect Dis Prevent & Control, Shenzhen 518109, Peoples R China
[4] Guangdong Prov Ctr Dis Control & Prevent, Guangdong Prov Inst Publ Hlth, Guangzhou 511430, Peoples R China
基金
中国国家自然科学基金;
关键词
71; INFECTION; DIVERSITY; SEQUENCES; REVEALS;
D O I
10.1007/s00705-020-04734-z
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In this study, we investigated the epidemiology and molecular characteristics of enteroviruses associated with severe hand, foot and mouth disease (HFMD) in Shenzhen, China, during 2014-2018. A total of 137 fecal specimens from patients with severe HFMD were collected. Enterovirus (EV) types were determined using real-time reverse transcription polymerase chain reaction (RT-PCR), RT nested PCR, and sequencing. Sequences were analyzed using bioinformatics programs. Of 137 specimens tested, 97 (70.8%), 12 (8.8%), and 10 (7.3%) were positive for EV-A71, coxsackievirus A6 (CVA6), and CVA16, respectively. Other pathogens detected included CVA2 (2.9%, 4/137), CVA10 (2.9%, 4/137), CVA5 (0.7%, 1/137), echovirus 6 (E6) (0.7%, 1/137) and E18 (0.7%, 1/137). The most frequent complication in patients with proven EV infections was myoclonic jerk, followed by aseptic encephalitis, tachypnea, and vomiting. The frequencies of vomiting and abnormal eye movements were higher in EV-A71-infected patients than that in CVA6-infected or CVA16-infected patients. Molecular phylogeny based on the complete VP1 gene revealed no association between the subgenotype of the virus and disease severity. Nevertheless, 12 significant mutations that were likely to be associated with virulence or the clinical phenotype were observed in the 5'UTR, 2A(pro), 2C, 3A, 3D(pol)and 3'UTR of CVA6. Eight significant mutations were observed in the 5'UTR, 2B, 3A, 3D(pol)and 3'UTR of CVA16, and 10 significant mutations were observed in the 5'UTR, VP1, 3A and 3C(pro)of CVA10. In conclusion, EV-A71 is still the main pathogen causing severe HFMD, although other EV types can also cause severe complications. Potential virulence or phenotype-associated sites were identified in the genomes of CVA6, CVA16, and CVA10.
引用
收藏
页码:2213 / 2227
页数:15
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