Fish Eric J, Diniz Pedro Paulo Vp, Juan Yen-Chen, Bossong Frank, Collisson Ellen W, Drechsler Yvonne, Kaltenboeck Bernhard
1 College of Veterinary Medicine, Western University of Health Sciences, Pomona, CA, USA.
2 Department of Pathobiology, College of Veterinary Medicine, Auburn University, Auburn, AL, USA.
J Feline Med Surg. 2018 Apr;20(4):295-301. doi: 10.1177/1098612X17705227. Epub 2017 Apr 20.
Objectives The objectives of this study were to determine the prevalence of feline coronavirus (FCoV) viremia, and its replication in peripheral blood using quantitative RT-PCR (qRT-PCR) methodology in a population of 205 healthy shelter cats in Southern California, as well as to assess any possible connection to longitudinal development of feline infectious peritonitis (FIP). Methods The study was performed on buffy-coat samples from EDTA-anticoagulated whole blood samples of 205 healthy shelter cats. From 50 of these cats, fecal samples were also examined. FCoV genomic and subgenomic RNA in the buffy coats was amplified by a total FCoV RNA qRT-PCR. Evidence for FCoV replication in peripheral blood and feces was obtained by M gene mRNA qRT-PCR. Results Nine of 205 cats (4.4%) were viremic by the total FCoV RNA qRT-PCR, and one of these cats had evidence of peripheral FCoV blood replication by an FCoV mRNA qRT-PCR. The single cat with peripheral blood replication had a unique partial M gene sequence distinct from positive controls and previously published FCoV sequences. Neither seven of the nine viremic cats with follow-up nor the single cat with replicating FCoV with positive qRT-PCR results developed signs compatible with FIP within 6 months of sample collection. Conclusions and relevance FCoV viremia and peripheral blood replication in healthy shelter cats have a low prevalence and do not correlate with later development of FIP in this study population, but larger case-control studies evaluating the prognostic accuracy of the qRT-PCR assays are needed.
目的 本研究的目的是使用定量逆转录聚合酶链反应(qRT-PCR)方法,确定南加州205只健康收容所猫群体中猫冠状病毒(FCoV)病毒血症的患病率及其在外周血中的复制情况,并评估其与猫传染性腹膜炎(FIP)纵向发展的任何可能联系。方法 本研究对205只健康收容所猫的乙二胺四乙酸(EDTA)抗凝全血样本的血沉棕黄层样本进行检测。其中50只猫还进行了粪便样本检测。通过总FCoV RNA qRT-PCR扩增血沉棕黄层中的FCoV基因组和亚基因组RNA。通过M基因mRNA qRT-PCR获得FCoV在外周血和粪便中复制的证据。结果 通过总FCoV RNA qRT-PCR检测,205只猫中有9只(4.4%)存在病毒血症,其中1只猫通过FCoV mRNA qRT-PCR有外周FCoV血液复制的证据。外周血复制的这只猫具有独特的部分M基因序列,与阳性对照和先前发表的FCoV序列不同。9只病毒血症猫中有7只进行了随访,在样本采集后6个月内,无论是这7只猫还是qRT-PCR结果为阳性的有FCoV复制的那只猫,均未出现与FIP相符的症状。结论及相关性 在本研究群体中,健康收容所猫的FCoV病毒血症和外周血复制患病率较低,且与FIP的后期发展无关,但需要开展更大规模的病例对照研究来评估qRT-PCR检测的预后准确性。