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Genomic and molecular characterization of a cyprinid herpesvirus 2 YC-01 strain isolated from gibel carp. | LitMetric

Genomic and molecular characterization of a cyprinid herpesvirus 2 YC-01 strain isolated from gibel carp.

Heliyon

National Pathogen Collection Center for Aquatic Animals, Shanghai Ocean University, Shanghai, 201306, China.

Published: July 2024

Cyprinid herpesvirus 2 (CyHV-2) is the pathogen of herpesviral hematopoietic necrosis (HVHN), causing the severe economic losses in farmed gibel carp (). Further exploration of the genome structure and potential molecular pathogenesis of CyHV-2 through complete genome sequencing, comparative genomics, and molecular characterization is required. Herein, the genome of a CyHV-2 YC-01 strain isolated from diseased gibel carp collected in Yancheng, Jiangsu Province, China was sequenced, then we analyzed the genomic structure, genetic properties, and molecular characterization. First, the complete YC-01 genome comprises 275,367 bp without terminal repeat (TR) regions, with 151 potential open reading frames (ORFs). Second, compared with other representative published strains of the genus , several evident variations are found in YC-01, particularly the orientation and position of and . and are considered as potential molecular genetic markers for YC-01. (encoding thymidine kinase) might be used to distinguish YC-01 and ST-J1 from other CyHV-2 isolates. Third, phylogenetically, YC-01 clusters with the members of the genus (together with the other six CyHV-2 isolates). Fourth, 43 putative proteins are predicted to be functional and are mainly divided into five categories. Several conserved motifs are found in nucleotide, amino acid, and promoter sequences including -acting elements identification of YC-01. Finally, the potential virulence factors and linear B cell epitopes of CyHV-2 are predicted to supply possibilities for designing novel vaccines rationally. Our results provide insights for further understanding genomic structure, genetic evolution, and potential molecular mechanisms of CyHV-2.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11259805PMC
http://dx.doi.org/10.1016/j.heliyon.2024.e32811DOI Listing

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