Herrewegh A A, Mähler M, Hedrich H J, Haagmans B L, Egberink H F, Horzinek M C, Rottier P J, de Groot R J
Department of Infectious Diseases and Immunology, Faculty of Veterinary Medicine, Utrecht University, The Netherlands.
Virology. 1997 Aug 4;234(2):349-63. doi: 10.1006/viro.1997.8663.
Feline coronavirus (FCoV) persistence and evolution were studied in a closed cat-breeding facility with an endemic serotype I FCoV infection. Viral RNA was detected by reverse transcriptase polymerase chain reaction (RT-PCR) in the feces and/or plasma of 36 of 42 cats (86%) tested. Of 5 cats, identified as FCoV shedders during the initial survey, 4 had detectable viral RNA in the feces when tested 111 days later. To determine whether this was due to continuous reinfection or to viral persistence, 2 cats were placed in strict isolation and virus shedding in the feces was monitored every 2-4 days. In 1 of the cats, virus shedding continued for up to 7 months. The other animal was sacrificed after 124 days of continuous virus shedding in order to identify the sites of viral replication. Viral mRNA was detected only in the ileum, colon, and rectum. Also in these tissues, FCoV-infected cells were identified by immunohistochemistry. These findings provide the first formal evidence that FCoV causes chronic enteric infections. To assess FCoV heterogeneity in the breeding facility and to study viral evolution during chronic infection, FCoV quasispecies sampled from individual cats were characterized by RT-PCR amplification of selected regions of the viral genome followed by sequence analysis. Phylogenetic comparison of nucleotides 7-146 of ORF7b to corresponding sequences obtained for independent European and American isolates indicated that the viruses in the breeding facility form a clade and are likely to have originated from a single founder infection. Comparative consensus sequence analysis of the more variable region formed by residues 79-478 of the S gene revealed that each cat harbored a distinct FCoV quasispecies. Moreover, FCoV appeared to be subject to immune selection during chronic infection. The combined data support a model in which the endemic infection is maintained by chronically infected carriers. Virtually every cat born to the breeding facility becomes infected, indicating that FCoV is spread very efficiently. FCoV-infected cats, however, appear to resist superinfection by closely related FCoVs.
在一个存在地方性I型猫冠状病毒(FCoV)感染的封闭猫繁育设施中,对FCoV的持续性和进化进行了研究。通过逆转录聚合酶链反应(RT-PCR)在42只接受检测的猫中的36只(86%)的粪便和/或血浆中检测到了病毒RNA。在初始调查中被确定为FCoV排泄者的5只猫中,4只在111天后接受检测时,粪便中可检测到病毒RNA。为了确定这是由于持续再感染还是病毒持续性所致,将2只猫严格隔离,并每2 - 4天监测一次粪便中的病毒排泄情况。在其中1只猫中,病毒排泄持续了长达7个月。另一只动物在持续病毒排泄124天后被处死,以确定病毒复制的部位。仅在回肠、结肠和直肠中检测到病毒mRNA。同样在这些组织中,通过免疫组织化学鉴定出了FCoV感染的细胞。这些发现提供了首个正式证据,证明FCoV可引起慢性肠道感染。为了评估繁育设施中FCoV的异质性,并研究慢性感染期间的病毒进化,从个体猫中采集的FCoV准种通过对病毒基因组选定区域进行RT-PCR扩增,随后进行序列分析来进行表征。对开放阅读框7b(ORF7b)的核苷酸7 - 146与独立的欧洲和美国分离株的相应序列进行系统发育比较表明,繁育设施中的病毒形成一个进化枝,并且很可能源自单一的初始感染。对由刺突蛋白(S基因)的79 - 478位残基形成的更多可变区域进行比较共有序列分析显示,每只猫都携带独特的FCoV准种。此外,FCoV在慢性感染期间似乎受到免疫选择。综合数据支持一种模型,即地方性感染由慢性感染携带者维持。繁育设施中出生的几乎每只猫都会被感染,这表明FCoV传播非常高效。然而,FCoV感染的猫似乎能抵抗密切相关FCoV的重复感染。