Phylogenetic molecular evolution and recombination analysis of complete genome of human parechovirus in Thailand

Thaweesak Chieochansin1,2, Jiratchaya Puenpa3, Yong Poovorawan3

  • 1Siriraj Center of Research Excellence for Cancer Immunotherapy, Research Department, Faculty of Medicine Siriraj Hospital, Mahidol University, 2 Prannok Road, Wanglang, Bangkok Noi, Bangkok, 11170, Thailand. thaweesak.chi@mahidol.ac.th.

Scientific Reports
|April 22, 2021
PubMed

Insights

Human parechovirus (HPeV) shows high genetic diversity due to recombination. This study analyzed HPeV complete genomes from Thailand, revealing a novel recombinant strain, B1091/HPeV14/2011, with implications for future treatments.

Area of Science:

  • Virology
  • Molecular Evolution
  • Genomics

Background:

  • Human parechovirus (HPeV) is a picornavirus causing diverse symptoms, including respiratory, gastrointestinal, and neurological complications.
  • High genetic diversity in HPeV is attributed to its RNA-dependent RNA polymerase (RdRp) lacking proofreading and frequent recombination.
  • Limited data exists on the molecular evolutionary aspects of the complete HPeV genome.

Purpose of the Study:

  • To investigate the phylogenetic, molecular evolution, and recombination patterns of the complete HPeV genome.
  • To analyze HPeV strains isolated in Thailand between 2009 and 2012.
  • To understand the evolutionary dynamics driving HPeV diversity.

Main Methods:

  • Complete genome amplification of 58 HPeV-positive samples using in-house designed primers.
  • Generation of ten overlapping PCR fragments for comprehensive genomic analysis.
  • Direct Sanger sequencing and phylogenetic analysis (whole-genome and VP1), alongside Bootscan analysis for recombination detection.

Main Results:

  • Phylogenetic analysis of complete genomes and VP1 regions generally aligned, confirming established genotypes.
  • A specific strain, B1091/HPeV14/2011, showed discordant phylogenetic placement between whole-genome and VP1 analyses.
  • Bootscan analysis identified B1091/HPeV14/2011 as a recombinant virus, with VP1 from HPeV14 and the remaining genome from HPeV1B.

Conclusions:

  • The study provides crucial insights into the molecular evolution and recombination of HPeV genomes.
  • Identification of a novel recombinant strain highlights the ongoing evolution of HPeV.
  • Findings can accelerate the development of targeted treatment and prophylactic strategies against HPeV infections.

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