4.5 Article

Genetic characterization of atypical porcine pestivirus from neonatal piglets with congenital tremor in Hubei province, China

期刊

VIROLOGY JOURNAL
卷 19, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12985-022-01780-8

关键词

Atypical porcine pestivirus; APPV; Congenital tremor; Piglets; Hubei; Phylogenetic analysis

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资金

  1. National Program on Key Research Project of China [2021YFD1801300, 2018YFD0500801]
  2. Fundamental Research Funds for the Central Universities [2662016PY003]

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This study determined the genetic characteristics of APPV in Hubei province, China. The results showed that APPV mainly caused histological lesions in the central nervous system and immune tissues of CT-affected piglets. Furthermore, phylogenetic analysis revealed the close relationship between the CH-HB2020 and CH-HB2021 strains and APPV_CH-GX2016. These findings enhance our understanding of APPV pathogenesis and provide potential molecular evidence for its prevalence and transmission.
Background Atypical porcine pestivirus (APPV) is a single-stranded RNA virus with high genetic variation that causes congenital tremor (CT) in newborn piglets, belonging to the genus Pestivirus of the family Flaviviridae. Increasing cases of APPV infection in China in the past few years would pose severe challenges to the development of pig production. In view of the high genetic variability of APPV, the genetic characteristics of APPV in Hubei province was determined. Methods 52 tissue samples from 8 CT-affected newborn piglets were collected at two different periods in the same pig farm in Hubei province. Viral nucleic acid was extracted to detect pathogens that can cause CT in piglets or other common clinical pathogens by RT-PCR. Haematoxylin and eosin (HE) staining, immunohistochemical (IHC) analysis, and qRT-PCR were performed to observe histopathological changes and histological distribution, and detect the viral load of APPV in CT-affected piglets. The full-length genome of APPV was obtained and sequence analysis was conducted to determine the phylogenetic relationship. Results Histopathological observation and histological distribution analysis showed that the histological lesions and distribution of APPV were mainly in central nervous system (CNS) tissues and immune tissues. Viral load analysis revealed that the viral copy number was higher in the cerebellum, submaxillary lymph nodes, tonsil, and serum than in other tissues. Phylogenetic analysis showed that CH-HB2020 and CH-HB2021 belonged to Clade I.3, and is most closely related to APPV_CH-GX2016. Sequence alignment based on APPV encoding sequences (CDS) showed that the nucleotide identities of CH-HB2020 or CH-HB2021 with Clade I, Clade II, and Clade III strains were 83.5-98.6%, 83.1-83.5%, and 81.1-81.4%, respectively, while the amino acid identities were 91.9-99.2%, 91.2-95.3%, and 90.77-91.4%, respectively. No recombination event was observed in CH-HB2020 or CH-HB2021 strains. Conclusions These findings enhance our understanding of the pathogenesis of APPV and may provide potential molecular evidence for its prevalence and transmission.

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