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2018年至2022年中国中东部地区猫细小病毒的分子特征及遗传多样性

Molecular characterization and genetic diversity of parvoviruses prevalent in cats in Central and Eastern China from 2018 to 2022.

作者信息

Pan Shunshun, Jiao Ruiqi, Xu Xin, Ji Jun, Guo Ge, Yao Lunguang, Kan Yunchao, Xie Qingmei, Bi Yingzuo

机构信息

Henan Provincial Engineering and Technology Center of Animal Disease Diagnosis and Integrated Control, Henan Key Laboratory of Insect Biology in Funiu Mountain, Nanyang Normal University, Nanyang, China.

Guangdong Provincial Laboratory of Lingnan Modern Agricultural Science and Technology, College of Animal Science and Veterinary Medicine, South China Agricultural University, Guangzhou, China.

出版信息

Front Vet Sci. 2023 Jul 31;10:1218810. doi: 10.3389/fvets.2023.1218810. eCollection 2023.

Abstract

Cats are a potential source of genetic diversity for parvoviruses. Herein, 134 samples were collected from cats with clinical gastroenteritis and analyzed for the presence of viral DNA via polymerase chain reaction, which revealed 48 positive samples. Identity analysis of VP2 nucleotide sequences indicated that these 48 strains, belonging to feline panleukopenia virus (FPV) and canine parvovirus type-2 (CPV-2; including new CPV-2a and CPV-2c genotypes), shared 94.59-99.94% nucleotide identity with the reference strains. The FPV strain F8 (isolated from Vietnam) appeared to be a recombinant of strains HB2003 and JS1901, whereas the Chinese CPV-2b strain BM-(11) isolated in 2011 was believed to be a recombinant of strains AH2008 and JS1901. In phylogenetic tree analysis based on VP2 nucleotide sequences, all obtained FPV strains and most reference FPV strains were clustered together, except strain BJ-22, which originated from monkeys. Further, two new CPV-2a strains (AH2005 and AH2008) were close to the newly reported Chinese CPV-2a strains but were distant from the other CPV-2a strains, namely CPV-339 (from the United States) and K022 (from South Korea). Additionally, the FPV and CPV-2 strains had high mutation rates in the antigenic regions of the VP2 protein. According to model prediction of the CPV-VP2 protein, these mutations may cause changes in the tertiary structure of VP2. The findings of this study can be used to improve the pre-evaluation of vaccination efficacy against diseases caused by FPV and CPV-2 in domestic cats and understand their genotypic transmission and mutation trends.

摘要

猫是细小病毒遗传多样性的一个潜在来源。在此,从患有临床肠胃炎的猫身上收集了134份样本,并通过聚合酶链反应分析病毒DNA的存在情况,结果显示有48份阳性样本。VP2核苷酸序列的同一性分析表明,这48个毒株属于猫泛白细胞减少症病毒(FPV)和犬细小病毒2型(CPV-2;包括新的CPV-2a和CPV-2c基因型),与参考毒株的核苷酸同一性为94.59%-99.94%。FPV毒株F8(从越南分离)似乎是HB2003和JS1901毒株的重组体,而2011年分离的中国CPV-2b毒株BM-(11)被认为是AH2008和JS1901毒株的重组体。在基于VP2核苷酸序列的系统发育树分析中,所有获得的FPV毒株和大多数参考FPV毒株聚集在一起,但来自猴子的BJ-22毒株除外。此外,两个新的CPV-2a毒株(AH2005和AH2008)与新报道的中国CPV-2a毒株接近,但与其他CPV-2a毒株,即来自美国的CPV-339和来自韩国的K022距离较远。此外,FPV和CPV-2毒株在VP2蛋白的抗原区域具有较高的突变率。根据CPV-VP2蛋白的模型预测,这些突变可能导致VP2三级结构的变化。本研究结果可用于改进对家猫中由FPV和CPV-2引起的疾病的疫苗接种效果的预评估,并了解它们的基因型传播和突变趋势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/168b/10434225/3a3d613deff2/fvets-10-1218810-g001.jpg

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