Classification of genotypes based on the VP1 gene of feline calicivirus and study of cross-protection between different genotypes

文献类型： 外文期刊

第一作者： Yang, Yupeng

作者： Yang, Yupeng;Liu, Zhe;Feng, Kexin;Qi, Ruibin;Zheng, Yating;Kang, Hongtao;Jiang, Qian;Yang, Mingfa;Qu, Liandong;Liu, Jiasen;Chen, Mengru;Wang, Ying

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关键词： FCV; VP1; cross-neutralization assay; genotype; challenge tests; broad-spectrum neutralization

期刊名称：FRONTIERS IN MICROBIOLOGY （ 影响因子：5.2； 五年影响因子：6.2 ）

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年卷期： 2023 年 14 卷

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收录情况： SCI

摘要： Feline calicivirus (FCV) causes upper respiratory tract diseases and even death in cats, thereby acting as a great threat to feline animals. Currently, FCV prevention is mainly achieved through vaccination, but the effectiveness of vaccination is limited. In this study, 105 FCV strain VP1 sequences with clear backgrounds were downloaded from the NCBI and subjected to a maximum likelihood method for systematic evolutionary analysis. Based on the genetic analysis results, FCV-positive sera were prepared using SPF mice and Chinese field cats as target animals, followed by a cross-neutralization assay conducted on the different genotype strains and in vivo challenge tests were carried out to further verify with the strain with best cross-protection effect. The results revealed that FCV was mainly divided into two genotypes: GI and GII. The GI genotype strains are prevalent worldwide, but all GII genotype strains were isolated from Asia, indicating a clear geographical feature. This may form resistance to FCV prevention in Asia. The in vitro neutralization assay conducted using murine serum demonstrated that the cross-protection effect varied among strains. A strain with broad-spectrum neutralization properties, DL39, was screened. This strain could produce neutralizing titers (10 x 2(3.08)-10 x 2(0.25)) against all strains used in this study. The antibody titers against the GI strains were 10 x 2(3.08)-10 x 2(0.5) and those against the GII strains were 10 x 2(0.75)-10 x 2(0.25). Preliminary evidence suggested that the antibody titer of the DL39 strain against GI was higher than that against GII. Subsequent cross-neutralization assays with cat serum prepared with the DL39 strain and each strain simultaneously yielded results similar to those described above. In vivo challenge tests revealed that the DL39 strain-immunized cats outperformed the positive controls in all measures. The results of several trials demonstrated that strain DL39 can potentially be used as a vaccine strain. The study attempted to combine the genetic diversity and phylogenetic analysis of FCV with the discovery of potential vaccines, which is crucial for developing highly effective FCV vaccines.

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