Coxsackievirus B: The important agent of hand, foot, and mouth disease

Yuhan Liu1,2, Junwei Chen1,3, Ming Zhang1,2

  • 1Institute of Medical Biology, Chinese Academy of Medical Sciences, Peking Union Medical College, Kunming, People's Republic of China.

Insights

Enteroviruses (EVs) cause hand, foot, and mouth disease (HFMD). This study found enterovirus B (EV-B), particularly coxsackievirus B (CV-B) strains, are significant agents in severe pediatric HFMD cases in China.

Area of Science:

  • Virology
  • Infectious Diseases
  • Pediatrics

Background:

  • Hand, foot, and mouth disease (HFMD) is a common pediatric illness primarily caused by enteroviruses (EVs), with EV-A serotypes frequently implicated.
  • Previous research has focused on EV-A, but the role of other enterovirus types, such as EV-B, in severe HFMD cases requires further investigation.

Purpose of the Study:

  • To retrospectively analyze stool samples from children with severe HFMD in Yunnan, China, to identify and characterize enterovirus infections, with a specific focus on EV-B.
  • To determine the prevalence of different EV serotypes and investigate potential associations between EV-B infections and severe HFMD.

Main Methods:

  • Retrospective analysis of 213 stool samples collected from children diagnosed with severe HFMD in Yunnan, China, during 2013, 2015, and 2016.
  • Enterovirus detection and serotyping using molecular methods.
  • Genotyping of specific coxsackievirus B isolates.

Main Results:

  • Enteroviruses were detected in 70.0% of the samples, with 20 distinct serotypes identified.
  • Enterovirus A (EV-A) and Enterovirus B (EV-B) were prevalent, accounting for 45.1% and 41.3% of infections, respectively.
  • Coxsackievirus B (CV-B) species represented 28.6% of positive specimens, with CV-B4 and CV-B5 being significant, alongside the predominant EV-A71. Co-infections were observed in 19.3% of cases.

Conclusions:

  • Enterovirus B (EV-B), particularly coxsackievirus B (CV-B) strains, may play a more significant role in severe pediatric HFMD than previously recognized.
  • These findings contribute to understanding the complex etiology of HFMD and can inform future prevention and treatment strategies.
  • Further research into EV-B epidemiology and pathogenicity is warranted for comprehensive HFMD control.

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