畜牧兽医学报 ›› 2024, Vol. 55 ›› Issue (6): 2560-2568.doi: 10.11843/j.issn.0366-6964.2024.06.027

• 预防兽医 • 上一篇    下一篇

猫泛白细胞减少症病毒A91S变异株对猫的致病性及基因组特征研究

周宁(), 汤承, 许佳, 岳华, 陈曦*()   

  1. 西南民族大学畜牧兽医学院, 成都 610041
  • 收稿日期:2023-10-13 出版日期:2024-06-23 发布日期:2024-06-28
  • 通讯作者: 陈曦 E-mail:1443230028@qq.com;cx15591859198@163.com
  • 作者简介:周宁(1999-),男,四川自贡人,硕士生,主要从事小动物疾病研究,E-mail:1443230028@qq.com
  • 基金资助:
    西南民族大学中央高校基本科研业务费专项基金资助(ZYN2023040);人才类(自科)-引进人才科研启动金资助项目(RQD2023035)

Pathogenicity and Genomic Characteristics of Feline Panleukopenia Virus A91S Variant in Cats

Ning ZHOU(), Cheng TANG, Jia XU, Hua YUE, Xi CHEN*()   

  1. College of Animal Husbandry and Veterinary Medicine, Southwest University for Nationalities, Chengdu 610041, China
  • Received:2023-10-13 Online:2024-06-23 Published:2024-06-28
  • Contact: Xi CHEN E-mail:1443230028@qq.com;cx15591859198@163.com

摘要:

猫泛白细胞减少症病毒(feline panleukopenia virus, FPV)是一种对猫危害严重的病原。近年来,一种VP2 91位氨基酸残基由A突变为S的FPV变异株(FPV A91S变异株)已经在国内广泛流行,但目前还未见该变异株对猫致病性的报道,本试验旨在探究FPV A91S变异株对猫的感染特性及其分子特征。利用F81细胞分离FPV A91S变异株,并研究其血凝特性、对猫的致病性及其基因组特征。成功分离到一株FPV A91S变异株,纯化后病毒滴度为104.6 TCID50·mL-1;该毒株能在pH 6.0~6.5、4和37 ℃条件下有效凝集猪红细胞;分离株经口服成功感染幼猫,引起呕吐、腹泻、白细胞急剧降低、眼睑脓性分泌物等症状,并在5 d内导致猫死亡;大体和组织病理变化发现严重的肠道和肺出血。获得该毒株近乎全长的基因组序列,其VP2蛋白的关键位点氨基酸符合典型FPV特征。除了VP2 A91S的突变外,其NS1蛋白也有3个独特的氨基酸突变(D23N、I443V和H596Q),这些特征导致FPV A91S毒株在进化树中单独聚为一支,具有独特的遗传进化趋势。本研究首次探究了FPV A91S变异株的血凝性和对猫的致病性,为进一步了解FPV的生物学特性和遗传变异提供参考。

关键词: 猫泛白细胞减少症病毒, FPV VP2 A91 S变异体, 血凝性, 致病性, 遗传进化

Abstract:

Feline panleukopenia virus (FPV) is a highly pathogenic threat to cats. In recent years, an FPV variant harboring an amino acid mutation at the VP2 91 site (A to S) has emerged prominently in China, however, information regarding on its pathogenicity is lacking. The aim of this study was to investigate the infection and molecular characteristics of the FPV A91S variant. F81 cells were used to isolate the FPV A91S variant, and the hemagglutination properties, pathogenicity and genomic characteristics were determined. An FPV A91S variant was successfully isolated, with a virus titer of 104.6 TCID50·mL-1 after viral purification. This isolate could effectively agglutinate porcine erythrocytes at pH 6.0-6.5 and temperatures of 4 ℃ and 37 ℃. When orally administered to kittens, the isolate caused a spectrum of clinical manifestations including vomiting, diarrhea, severe leukopenia, purulent discharge from the eyes, and cat death within 5 days. Gross and histopathological examinations unveiled severe hemorrhaging in the intestines and lungs. The nearly full genome sequence of this isolate was obtained, and the key amino acid residues were consistent with those of the typical FPV. In addition to the A91S mutation in VP2, three distinctive amino acid mutations (D23N, I443V and H596Q) were observed in the NS1 protein. These amino acid mutations caused the FPV A91S strains to form a discrete branch on all the evolutionary trees. This study, for the first time, investigated the hemagglutination properties and pathogenicity of the FPV A91S variant, which contribute valuable insights into the biological characteristics and genetic variations of FPV.

Key words: feline panleukopenia virus, VP2 A91 S variant, hemagglutination, pathogenicity, genetic evolution

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