Zhang Shi-Jun, Su Dan, Zhao Shi-Bo, Xing Jia-You, Zeng Lei, Wang Jiang, Ming Sheng-Li, Chu Bei-Bei
College of Veterinary Medicine, Henan Agricultural University, Zhengzhou 450046, China.
Key Laboratory of Animal Biochemistry and Nutrition, Ministry of Agriculture and Rural Affairs, Zhengzhou 450046, China.
Int J Mol Sci. 2025 Mar 13;26(6):2565. doi: 10.3390/ijms26062565.
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 TCID/0.1 mL. Genomic sequencing coupled with phylogenetic reconstruction of the gene revealed a close genetic relation to domestic Chinese strains and international variants, while maintaining distinct evolutionary divergence from other calicivirus genera.
本研究调查了中国河南省郑州市一家兽医机构疑似猫杯状病毒(FCV)爆发的情况。逆转录聚合酶链反应(RT-PCR)分析证实了FCV的存在,随后通过CRFK细胞培养增殖,实现了ZZ202306毒株的分离和鉴定。免疫荧光和蛋白质免疫印迹分析验证了靶向FCV VP1衣壳蛋白的单克隆抗体的特异性。透射电子显微镜显示直径约40 nm的无包膜病毒粒子,呈现典型的杯状病毒结构。病毒复制动力学表明,接种后6至18小时内呈指数增长,达到10 TCID/0.1 mL的峰值滴度。基因组测序结合该基因的系统发育重建显示,其与中国国内毒株和国际变体存在密切的遗传关系,同时与其他杯状病毒属保持明显的进化差异。