Thiel Volker, Thiel Heinz-Jürgen, Tekes Gergely
a Institute of Virology; Justus-Liebig-University Giessen ; Giessen , Germany.
Bioengineered. 2014;5(6):396-400. doi: 10.4161/bioe.32133. Epub 2014 Oct 30.
Feline infectious peritonitis (FIP) is caused by feline coronaviruses (FCoVs) and represents one of the most important lethal infectious diseases of cats. To date, there is no efficacious prevention and treatment, and our limited knowledge on FIP pathogenesis is mainly based on analysis of experiments with field isolates. In a recent study, we reported a promising approach to study FIP pathogenesis using reverse genetics. We generated a set of recombinant FCoVs and investigated their pathogenicity in vivo. The set included the type I FCoV strain Black, a type I FCoV strain Black with restored accessory gene 7b, two chimeric type I/type II FCoVs and the highly pathogenic type II FCoV strain 79-1146. All recombinant FCoVs and the reference strain isolates were found to establish productive infections in cats. While none of the type I FCoVs and chimeric FCoVs induced FIP, the recombinant type II FCoV strain 79-1146 was as pathogenic as the parental isolate. Interestingly, an intact ORF 3c was confirmed to be restored in all viruses (re)isolated from FIP-diseased animals.
猫传染性腹膜炎(FIP)由猫冠状病毒(FCoV)引起,是猫最重要的致死性传染病之一。迄今为止,尚无有效的预防和治疗方法,而我们对FIP发病机制的了解有限,主要基于对野外分离株的实验分析。在最近的一项研究中,我们报道了一种利用反向遗传学研究FIP发病机制的有前景的方法。我们构建了一组重组FCoV,并在体内研究了它们的致病性。该组包括I型FCoV毒株Black、恢复了辅助基因7b的I型FCoV毒株Black、两种I型/II型嵌合FCoV以及高致病性II型FCoV毒株79-1146。所有重组FCoV和参考毒株分离株均能在猫体内建立有效的感染。虽然I型FCoV和嵌合FCoV均未诱导FIP,但重组II型FCoV毒株79-1146与亲本分离株一样具有致病性。有趣的是,在从患有FIP的动物中(重新)分离出的所有病毒中,均证实完整的开放阅读框3c得以恢复。