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Duck hepatitis a virus: Full-length genome-based phylogenetic and phylogeographic view during 1986-2020.
Yang, Caiting; Shah, Pir Tariq; Bahoussi, Amina Nawal; Wu, Changxin; Wang, Li; Xing, Li.
Afiliación
  • Yang C; Institutes of Biomedical Sciences, Shanxi University, 92 Wucheng Road, Taiyuan, Shanxi 030006, China.
  • Shah PT; Institutes of Biomedical Sciences, Shanxi University, 92 Wucheng Road, Taiyuan, Shanxi 030006, China.
  • Bahoussi AN; Institute of Environmental Science, Shanxi University, 63 Nanzhonghuan East Street, Taiyuan 030031, China.
  • Wu C; Institutes of Biomedical Sciences, Shanxi University, 92 Wucheng Road, Taiyuan, Shanxi 030006, China.
  • Wang L; Institute of Environmental Science, Shanxi University, 63 Nanzhonghuan East Street, Taiyuan 030031, China.
  • Xing L; Institutes of Biomedical Sciences, Shanxi University, 92 Wucheng Road, Taiyuan, Shanxi 030006, China; Shanxi Provincial Key Laboratory for Prevention and Treatment of Major Infectious Diseases, 92 Wucheng Road, Taiyuan 030006, China; The Key Laboratory of Chemical Biology and Molecular Engineering o
Virus Res ; 336: 199216, 2023 Oct 15.
Article en En | MEDLINE | ID: mdl-37657508
ABSTRACT
Duck hepatitis A virus (DHAV) is one of key pathogens for duck viral hepatitis, especially in Asian duck industry. Currently, two main genotypes (DHAV-1 and -3) exist. To explore insightfully the evolutionary character, we assessed the available 141 full-length genome sequences of DHAV isolated in 1986-2020 globally and divided DHAV-1 and DHAV-3 into further seven (DHAV-1 a-g) and five (DHAV-3 a-e) sub-clades, respectively. Phylogenetic and phylogeographic network analyses indicated great genetic diversity of DHAV identified in China, where the DHAV-1 cluster and DHAV-3 cluster were linked by virus strain HDHV1-BJ (GenBank ID FJ157172.1) and Du_CH_LSD_090612 (GenBank ID JF828995.1) via a long mutational branch and intermediate strains. Several strains previously identified as DHAV-1 according to the partial gene sequences were actually clustered within DHAV-3 in full-length genome-based analysis. Furthermore, we identified 32 recombination events across virus genome with the recombination hotspot at the 5' end and upstream of the capsid coding region. The highest variability of DHAV polyprotein was shown at the upstream region of the N terminus P-loop region, e.g., amino acids 672-716, followed by the aa 334-359 in the Capsid encoding region. The results presented here provides a robust insight into the genetic exchange patterns of DHAV genomes during the past decades, which may be used to map the evolutionary history and facilitate preventive measures of DHAVs.
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Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Virus Res Asunto de la revista: VIROLOGIA Año: 2023 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Virus Res Asunto de la revista: VIROLOGIA Año: 2023 Tipo del documento: Article País de afiliación: China