Department of Microbiology and Immunology, College of Veterinary Medicine, Cornell University, Ithaca, New York, USA.
Department of Population Medicine and Diagnostic Sciences, College of Veterinary Medicine, Cornell University, Ithaca, New York, USA Animal Health Diagnostic Center, College of Veterinary Medicine, Cornell University, Ithaca, New York, USA.
J Clin Microbiol. 2014 Dec;52(12):4230-8. doi: 10.1128/JCM.02158-14. Epub 2014 Sep 24.
Emerging canine coronavirus (CCoV) variants that are associated with systemic infections have been reported in the European Union; however, CCoV-associated disease in the United States is incompletely characterized. The purpose of this study was to correlate the clinicopathological findings and viral antigen distribution with the genotypic characteristics of CCoV in 11 puppies from nine premises in five states that were submitted for diagnostic investigation at Cornell University between 2008 and 2013. CCoV antigen was found in epithelial cells of small intestinal villi in all puppies and the colon in 2 of the 10 puppies where colon specimens were available. No evidence of systemic CCoV infection was found. Comparative sequence analyses of viral RNA extracted from intestinal tissues revealed CCoV-II genotype in 9 out of 11 puppies. Of the nine CCoV-IIs, five were subtyped as group IIa and one as IIb, while three CCoVs could not be subtyped. One of the CCoV-IIa variants was isolated in cell culture. Infection with CCoV alone was found in five puppies, of which two also had small intestinal intussusception. Concurrent infections with either parvovirus (n = 1), attaching-effacing Escherichia coli (n = 4), or protozoan parasites (n = 3) were found in the other six puppies. CCoV is an important differential diagnosis in outbreaks of severe enterocolitis among puppies between 4 days and 21 weeks of age that are housed at high population density. These findings will assist with the rapid laboratory diagnosis of enteritis in puppies and highlight the need for continued surveillance for CCoV variants and intestinal viral diseases of global significance.
在欧盟已报告了与全身性感染相关的新兴犬冠状病毒 (CCoV) 变异株;然而,美国的 CCoV 相关疾病尚未得到充分描述。本研究的目的是将临床病理发现和病毒抗原分布与在 2008 年至 2013 年间在康奈尔大学进行诊断研究的来自五个州的九个场所的 11 只幼犬的 CCoV 基因型特征相关联。在所有幼犬的小肠绒毛上皮细胞和 10 只提供结肠标本的幼犬中的 2 只的结肠中均发现了 CCoV 抗原。未发现全身性 CCoV 感染的证据。从肠道组织中提取的病毒 RNA 的比较序列分析显示,11 只幼犬中有 9 只为 CCoV-II 基因型。在这 9 个 CCoV-II 中,有 5 个为 IIa 亚群,1 个为 IIb,而 3 个 CCoV 无法亚群化。其中一个 CCoV-IIa 变体在细胞培养中被分离出来。在 5 只幼犬中仅发现了 CCoV 感染,其中 2 只还患有小肠套叠。在其他 6 只幼犬中,同时感染细小病毒(n=1)、附着性致病变异型大肠杆菌(n=4)或原生动物寄生虫(n=3)。CCoV 是 4 天至 21 周龄、高密度饲养的幼犬中严重肠炎爆发的重要鉴别诊断。这些发现将有助于快速诊断幼犬肠炎,并强调需要持续监测 CCoV 变异株和具有全球意义的肠道病毒病。