Molecular identification and analysis of human enteroviruses isolated from healthy children in Shenzhen, China from 2010 to 2011

PLoS One. 2013 Jun 6;8(6):e64889. doi: 10.1371/journal.pone.0064889. Print 2013.

Abstract

Objective: To determine the prevalence and distribution of human enteroviruses (HEVs) among healthy children in Shenzhen, China.

Method: Clinical specimens were obtained from 320 healthy children under 5 years old in Shenzhen, China from 2010 to 2011. The specimens were evaluated using real-time PCR and cell cultures. The positive specimens were further tested using reverse transcription-seminested PCR (RT-snPCR). Molecular typing and phylogenetic analysis were based on the sequence determined.

Results: Among the 320 samples, 34 were tested positive for HEVs (10.6%) and 22 different serotypes were identified using RT-snPCR. PV1 and PV2 were also detected. The predominant serotype observed was EV71 (17.6%), followed by CV-B4 (14.7%). HEV-B was detected most frequently, with an overall prevalence of 47.1%. HEV-A and HEV-C were found in 32.3% and 20.6% of the samples, respectively. No HEV-D was identified. Molecular phylogeny indicated that all EV71 strains were of C4 genotype.

Conclusion: Although a variety of HEVs was detected in healthy children, HEV-B was relatively more prevalent than other HEV species. Considering HEV-A is more prevalent than HEV-B among patients with hand-foot-mouth disease, additional long-term surveillance of HEV is warranted in both asymptomatic and symptomatic populations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Asymptomatic Diseases
  • Child, Preschool
  • China / epidemiology
  • Enterovirus A, Human / genetics*
  • Enterovirus A, Human / isolation & purification
  • Enterovirus B, Human / genetics*
  • Enterovirus B, Human / isolation & purification
  • Enterovirus C, Human / genetics*
  • Enterovirus C, Human / isolation & purification
  • Enterovirus Infections / diagnosis
  • Enterovirus Infections / epidemiology
  • Enterovirus Infections / virology*
  • Female
  • Humans
  • Male
  • RNA, Viral / genetics*
  • RNA, Viral / isolation & purification

Substances

  • RNA, Viral

Grants and funding

This study was financed by the Key Projects in the National Science and Technology Pillar Program in the Eleventh Five-year Plan Period. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.