Tuanthap Supansa, Chiteafea Natdaroon, Rattanasrisomporn Jatuporn, Choowongkomon Kiattawee
Department of Biochemistry, Faculty of Science, Kasetsart University, Bangkok, 10900, Thailand.
Department of Companion Animal Clinical Sciences, Faculty of Veterinary Medicine, Kasetsart University, Bangkok, 10900, Thailand.
Arch Virol. 2021 Oct;166(10):2779-2787. doi: 10.1007/s00705-021-05188-7. Epub 2021 Aug 7.
Feline infectious peritonitis (FIP) is a lethal infectious disease of domestic cats caused by feline coronavirus (FCoV) infection. Feline infectious peritonitis virus (FIPV) is a mutant type of FCoV that is characterized by causing fibrinous serositis with effusions in the pleural and abdominal cavities (wet form) and/or granulomatous-necrotizing inflammatory lesions in several organs (dry form). There have been numerous studies on FIP worldwide, whereas information about this disease in Thailand is still limited. Most studies involving molecular surveillance and evaluation of FCoV field strains have examined the genetic diversity of the spike and accessory ORF3c coding regions. Of these, the S gene is more divergent and is responsible for the two FCoV serotypes, while ORF3c harbors mutations that result either in early termination or destruction of the protein. In this study, we investigated the genetic diversity and genetic relationships among the current Thai and global FCoV strains in the accessory and nucleocapsid genes using a virus-specific PCR method. Comparative sequence analysis suggested that the Thai FCoV isolates were most closely related to strains reported in the Netherlands, the USA, and China. In the ORF3ab sequences, some Thai strains were more than 99% identical to the DF-2 prototype strain. Truncation of the 3a gene product was found in Thai FCoV strains of group 2. Amino acid deletions were observed in the N, ORF3c, and ORF7b proteins of Thai FCoV sequences. The accessory gene sequence divergence may be responsible for driving the periodic emergence and continued persistence of FCoVs in Thai domestic cat populations. Our findings provide updated information about the molecular characteristics of the accessory and nucleocapsid genes of FCoV strains in circulation that were not previously documented in this country.
猫传染性腹膜炎(FIP)是由猫冠状病毒(FCoV)感染引起的家猫致死性传染病。猫传染性腹膜炎病毒(FIPV)是FCoV的一种突变型,其特征是引起胸膜和腹腔纤维素性浆膜炎并伴有积液(湿性形式)和/或多个器官的肉芽肿性坏死性炎症病变(干性形式)。全球对FIP已有大量研究,但泰国关于这种疾病的信息仍然有限。大多数涉及FCoV野外毒株分子监测和评估的研究都检测了刺突蛋白和辅助开放阅读框3c(ORF3c)编码区的遗传多样性。其中,S基因差异更大,决定了两种FCoV血清型,而ORF3c存在导致蛋白质提前终止或破坏的突变。在本研究中,我们使用病毒特异性PCR方法研究了泰国和全球当前FCoV毒株在辅助基因和核衣壳基因中的遗传多样性及遗传关系。比较序列分析表明,泰国FCoV分离株与荷兰、美国和中国报道的毒株关系最为密切。在ORF3ab序列中,一些泰国毒株与DF-2原型毒株的同一性超过99%。在第2组泰国FCoV毒株中发现了3a基因产物的截短。在泰国FCoV序列的N、ORF3c和ORF7b蛋白中观察到氨基酸缺失。辅助基因序列差异可能是FCoV在泰国家猫群体中周期性出现并持续存在的原因。我们的研究结果提供了关于该国此前未记录的流行FCoV毒株辅助基因和核衣壳基因分子特征的最新信息。