Molecular epidemiology of coxsackievirus A6 circulating in Hong Kong reveals common neurological manifestations and emergence of novel recombinant groups

•HFMD was the most common diagnosis among patients with CV-A6 infection.•Neurological manifestations were commonly observed (25%).•CV-A6 circulating in Hong Kong mainly belonged to genotype D5.•Three novel recombinant strains (two novel groups RL and RM) were identified.•3D gene was a common recombi...

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Veröffentlicht in:Journal of clinical virology 2018-11, Vol.108, p.43-49
Hauptverfasser: Lau, Susanna K.P., Zhao, Pyrear S.H., Sridhar, Siddharth, Yip, Cyril C.Y., Aw-Yong, Kam Leng, Chow, Elaine Y.Y., Cheung, Kelvin C.M., Hui, Rex W.H., Leung, Ryan Y.H., Lai, Yuki S.K., Wu, Alan K.L., To, Kelvin K.W., Woo, Patrick C.Y., Yuen, Kwok-Yung
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Sprache:eng
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Zusammenfassung:•HFMD was the most common diagnosis among patients with CV-A6 infection.•Neurological manifestations were commonly observed (25%).•CV-A6 circulating in Hong Kong mainly belonged to genotype D5.•Three novel recombinant strains (two novel groups RL and RM) were identified.•3D gene was a common recombination site in CV-A6. Coxsackievirus A6 (CV-A6) represents the predominant enterovirus serotype in Hong Kong, but its epidemiology in our population was unknown. To examine the clinical and molecular epidemiology of CV-A6 and detect emerging recombinant strains in Hong Kong. Nasopharyngeal aspirates (NPAs) from patients with febrile or respiratory illness were subject to RT-PCR for CV-A6 and sequencing of 5′-NCR and VP1. CV-A6-positive samples were further subject to 2C and 3D gene sequencing. Complete genome sequencing was performed on potential recombinant strains. Thirty-six (0.35%) NPAs were positive for CV-A6 by 5′-NCR RT-PCR and sequencing, 28 of which confirmed by partial VP1 gene sequencing. Among the 28 patients (mainly young children) with CV-A6 infection, hand-foot-and-mouth disease (HFMD) (43%), herpangina (18%) and tonsillitis (11%) were the most common diagnoses. Seven (25%) patients had neurological manifestations, including febrile seizures, encephalitis and meningitis. VP1 gene analysis showed that 24 CV-A6 strains circulating in Hong Kong belonged to genotype D5, while 4 strains belonged to D4. Further 2C and 3D gene analysis revealed eight potential recombinant strains. Genome sequencing of five selected strains confirmed four recombinant strains: HK459455/2013 belonging to recombination group RJ arisen from CV-A6/CV-A4, HK458288/2015 and HK446377/2015 representing novel group RL arisen from CV-A6/CV-A4, and HK462069/2015 representing novel group RM arisen from CV-A6/EV-A71. Recombination breakpoints located at 3D were identified in the latter three recombinant strains, with HK462069/2015 (from a child with encephalitis) having acquired 3D region from EV-A71. We identified novel recombinant CV-A6 strains in Hong Kong, with 3D being a common recombination site.
ISSN:1386-6532
1873-5967
DOI:10.1016/j.jcv.2018.09.002