Abstract

BackgroundHuman enterovirus 71 (EV-71) is a common causative agent of hand, foot and mouth disease (HFMD). In recent years, the virus has caused several outbreaks with high numbers of deaths and severe neurological complications. Several new EV-71 subgenotypes were identified from these outbreaks. The mechanisms that contributed to the emergence of these subgenotypes are unknown.ResultsSix EV-71 isolates from an outbreak in Malaysia, in 1997, were sequenced completely. These isolates were identified as EV-71 subgenotypes, B3, B4 and C2. A phylogenetic tree that correlated well with the present enterovirus classification scheme was established using these full genome sequences and all other available full genome sequences of EV-71 and human enterovirus A (HEV-A). Using the 5' UTR, P2 and P3 genomic regions, however, isolates of EV-71 subgenotypes B3 and C4 segregated away from other EV-71 subgenotypes into a cluster together with coxsackievirus A16 (CV-A16/G10) and EV-71 subgenotype C2 clustered with CV-A8. Results from the similarity plot analyses supported the clustering of these isolates with other HEV-A. In contrast, at the same genomic regions, a CV-A16 isolate, Tainan5079, clustered with EV-71. This suggests that amongst EV-71 and CV-A16, only the structural genes were conserved. The 3' end of the virus genome varied and consisted of sequences highly similar to various HEV-A viruses. Numerous recombination crossover breakpoints were identified within the non-structural genes of some of these newer EV-71 subgenotypes.ConclusionPhylogenetic evidence obtained from analyses of the full genome sequence supports the possible occurrence of inter-typic recombination involving EV-71 and various HEV-A, including CV-A16, the most common causal agent of HFMD. It is suggested that these recombination events played important roles in the emergence of the various EV-71 subgenotypes.

Highlights

  • Human enterovirus 71 (EV-71) is a common causative agent of hand, foot and mouth disease (HFMD)

  • Phylogenetic relationships between EV-71 and other HEVA viruses The complete genome sequences of all the EV-71 isolates were aligned with other available human enterovirus A (HEV-A) complete genome sequences obtained from the Genbank

  • An unrooted phylogenetic tree constructed using the whole genome sequences of all EV-71 and HEV-A viruses had all the EV71 isolates subdivided into three genotypes, A, B (B2, B3 and B4) and C (C2 and C4)

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Summary

Introduction

Human enterovirus 71 (EV-71) is a common causative agent of hand, foot and mouth disease (HFMD). CV-A2, CV-A6, CV-A8 and CV-A10 are known to cause herpangina [2]; CV-A2, CV-A4, CV-A7 and CV-A10 cause aseptic meningitis [2] and CV-A5, CVA10, CV-A16 and EV-71 usually cause hand, foot and mouth disease (HFMD) [2] Amongst these HEV-A (page number not for citation purposes). The C2 isolates were identified as the main causal agent of the HFMD-associated severe and fatal infections during the 1998 Taiwan outbreak [6,10]. These isolates caused severe infections in the Perth 1999 outbreak [7,9] but no report of serious infection or death attributed to these isolates was recorded from the Malaysia 1997 outbreak [8,12]. The potential mechanisms that could play important role in the emergence of the different EV-71 subgenotypes are phylogenetically investigated

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