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Published on: September 13, 2024
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.
Abstract:
Human parechovirus (HPeV), which is a member of the Picornavirus group of viruses, is a pathogen that is reported to be associated with manifestations that include respiratory tract involvement, gastroenteritis, sepsis-like symptom, and central nervous system complication. Until now, nineteen genotypes have been identified. The lack of proofreading property of viral RNA-dependent RNA polymerase (RdRp) together with recombination among the intra- and inter-genotypes of the virus results in high diversity. However, data specific to the molecular evolutionary perspective of the complete genome of HPeV remains limited. This study aimed to analyze the phylogenetic, molecular evolution, and recombination characteristics of the complete genome of HPeV strains isolated in Thailand during 2009-2012. Fifty-eight samples that were previously confirmed to be HPeV positive and then evaluated for genotyping were subjected to complete genome amplification to generate ten overlapping PCR fragments using a set of in-house designed primers. The same position of the viral genome was read in triplicate using direct Sanger sequencing. All samples were classified into the same previously defined genotypes in both whole-genome and VP1 phylogenic tree. However, sample B1091/HPeV14/2011 exhibited discordant grouping between whole-genome and VP1 on the phylogenetic tree. Bootscan analysis revealed that B1091/HPeV14/2011 inherited from two genotypic viruses, including VP1 from HPeV14, and the rest of the genome from HPeV1B. The results of this study provide important insights into the molecular evolution of and recombination in the viral genome of HPeV that will improve and accelerate our ability to develop treatment and prophylactic strategies in the future.
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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