Isolation, Identification, and Genetic Evolution Analysis of VP1 Gene of Feline Calicivirus Strain ZZ202306

This study investigated a suspected Feline calicivirus (FCV) outbreak at a veterinary facility in Zhengzhou, Henan Province, China. RT-PCR analysis confirmed the FCV presence, with subsequent CRFK cell culture propagation leading to the isolation and characterization of strain ZZ202306. Immunofluorescence and Western blot analyses validated the specificity of monoclonal antibodies targeting the FCV VP1 capsid protein. Transmission electron microscopy revealed non-enveloped virions of ~40 nm in diameter, exhibiting typical caliciviral architecture. Viral replication kinetics demonstrated exponential growth between 6 and 18 h post-inoculation, reaching a peak titer of 10<sup>7.96</sup> TCID<sub>50</sub>/0.1 mL. Genomic sequencing coupled with phylogenetic reconstruction of the <i>VP1</i> gene revealed a close genetic relation to domestic Chinese strains and international variants, while maintaining distinct evolutionary divergence from other calicivirus genera.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2025-03-13
DOI
https://doi.org/10.3390/ijms26062565
Citations
1
Primary Topic
Viral gastroenteritis research and epidemiology
Type
article
Field-Weighted Citation Impact
1.40

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article

Isolation, Identification, and Genetic Evolution Analysis of VP1 Gene of Feline Calicivirus Strain ZZ202306

Shibo Zhao, Dan Su, Shijun Zhang, Jie Xing et al.
1 citations
International Journal of Molecular Sciences
Viral gastroenteritis research and epidemiology
1.40
article

Isolation, Identification, and Genetic Evolution Analysis of VP1 Gene of Feline Calicivirus Strain ZZ202306

Shibo Zhao, Dan Su, Shijun Zhang, Jie Xing, Sheng‐Li Ming, Bei‐Bei Chu, Jiang Wang, Lei Zeng
article en
1 citations

Abstract

This study investigated a suspected Feline calicivirus (FCV) outbreak at a veterinary facility in Zhengzhou, Henan Province, China. RT-PCR analysis confirmed the FCV presence, with subsequent CRFK cell culture propagation leading to the isolation and characterization of strain ZZ202306. Immunofluorescence and Western blot analyses validated the specificity of monoclonal antibodies targeting the FCV VP1 capsid protein. Transmission electron microscopy revealed non-enveloped virions of ~40 nm in diameter, exhibiting typical caliciviral architecture. Viral replication kinetics demonstrated exponential growth between 6 and 18 h post-inoculation, reaching a peak titer of 10<sup>7.96</sup> TCID<sub>50</sub>/0.1 mL. Genomic sequencing coupled with phylogenetic reconstruction of the <i>VP1</i> gene revealed a close genetic relation to domestic Chinese strains and international variants, while maintaining distinct evolutionary divergence from other calicivirus genera.

International Journal of Molecular SciencesVol. 26(6)
Ministry of Agriculture and Rural Affairs (CN), Henan Agricultural University (CN)
Henan Provincial Science and Technology Research Project
Openalex Percentile: Top 23%
Viral gastroenteritis research and epidemiology
1.40
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Isolation, Identification, and Genetic Evolution Analysis of VP1 Gene of Feline Calicivirus Strain ZZ202306 — Shibo Zhao, Dan Su, et al. · International Journal of Molecular Sciences (2025) | TGRS Research Map | TGRS