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

J Clin Virol. 2018 Nov:108:43-49. doi: 10.1016/j.jcv.2018.09.002. Epub 2018 Sep 8.

Abstract

Background: Coxsackievirus A6 (CV-A6) represents the predominant enterovirus serotype in Hong Kong, but its epidemiology in our population was unknown.

Objectives: To examine the clinical and molecular epidemiology of CV-A6 and detect emerging recombinant strains in Hong Kong.

Study design: 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.

Results: 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.

Conclusions: We identified novel recombinant CV-A6 strains in Hong Kong, with 3D being a common recombination site.

Keywords: Coxsackievirus A6; Epidemiology; Hand-foot-and-mouth disease; Hong Kong; Novel; Recombination.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antigens, Viral / genetics
  • Capsid Proteins / genetics
  • Carrier Proteins / genetics
  • Child
  • Child, Preschool
  • Enterovirus B, Human / genetics
  • Enterovirus B, Human / isolation & purification*
  • Female
  • Genome, Viral
  • Genotype
  • Hand, Foot and Mouth Disease / complications*
  • Hand, Foot and Mouth Disease / diagnosis
  • Hand, Foot and Mouth Disease / epidemiology*
  • Hong Kong / epidemiology
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Nasopharynx / virology
  • Nervous System Diseases / epidemiology*
  • Nervous System Diseases / virology*
  • Phylogeny
  • RNA, Viral / genetics
  • Reassortant Viruses / genetics
  • Reassortant Viruses / isolation & purification
  • Sequence Analysis, DNA
  • Viral Nonstructural Proteins / genetics

Substances

  • Antigens, Viral
  • Capsid Proteins
  • Carrier Proteins
  • RNA, Viral
  • VP1 protein, enterovirus B
  • Viral Nonstructural Proteins
  • virus-infection-associated antigen, Foot-and-mouth disease virus
  • 2C protein, viral