Department of Small Animal Clinical SciencesCollege of Veterinary Medicine, Michigan State University Veterinary Teaching Hospital, East Lansing, MI, USA.
J Vet Intern Med. 2011 Mar-Apr;25(2):199-205. doi: 10.1111/j.1939-1676.2011.0685.x. Epub 2011 Feb 11.
The epidemiology of feline calicivirus (FCV) infection in cats with idiopathic cystitis (FIC) has not been investigated by contemporary molecular biologic methods.
To determine the prevalence of and evaluate risk factors for FCV viruria, oral carriage, and virus neutralizing (VN) antibodies in cats with and without FIC.
Cats with nonobstructive FIC (n = 47), obstructive FIC (n = 22), and FCV upper respiratory tract infection (URI; n = 25), and healthy client-owned (n = 18) and colony-housed (n = 24) cats.
Oropharyngeal secretions and urine were evaluated with a FCV p30 gene-based real-time reverse-transcriptase polymerase chain reaction (RT-PCR) assay. Serum VN antibody titers were determined by a modified microtiter assay. Associations of risk factors with log-transformed antibody titers were determined by multivariable generalized linear regression.
FCV viruria was detected in 4 (6%) and 3 (12%) cats with FIC and URI, respectively. In 3 FIC cats, viruria was unassociated with detectable oral virus carriage. Oral FCV carriage was detected in 7 (10%) FIC cats. Median antibody titers were significantly higher in cats with obstructive FIC (1 :256), nonobstructive FIC (1:128), and URI (1:512) compared with healthy client-owned (1:16) and colony-housed (1:4) cats (P < .001). Other than disease, multivariate analysis did not identify any other explanatory variables for increased titers in cats with FIC or URI.
FCV viruria was detected in cats with FIC and URI, however, its etiologic significance is uncertain. Serologic results suggest increased FCV exposure in FIC cats compared with controls. Further investigations are needed to clarify the potential role of FCV in FIC.
采用当代分子生物学方法,尚未研究过特发性膀胱炎(FIC)猫中猫杯状病毒(FCV)感染的流行病学。
确定 FIC 和非 FIC 猫中 FCV 尿病毒血症、口腔携带和病毒中和(VN)抗体的流行率,并评估其相关风险因素。
患有非阻塞性 FIC(n = 47)、阻塞性 FIC(n = 22)和 FCV 上呼吸道感染(URI;n = 25)的猫,以及健康的客户拥有的(n = 18)和群体饲养的(n = 24)猫。
采用基于 FCV p30 基因的实时逆转录聚合酶链反应(RT-PCR)检测口咽分泌物和尿液。通过改良微量滴定法测定血清 VN 抗体滴度。采用多变量广义线性回归确定与抗体滴度相关的风险因素。
分别在 4 只(6%)和 3 只(12%)患有 FIC 和 URI 的猫中检测到 FCV 尿病毒血症。在 3 只 FIC 猫中,尿病毒血症与口腔病毒携带无关。在 7 只 FIC 猫中检测到口腔 FCV 携带。与健康的客户拥有的(1:16)和群体饲养的(1:4)猫相比,患有阻塞性 FIC(1:256)、非阻塞性 FIC(1:128)和 URI(1:512)的猫的抗体滴度中位数明显更高(P <.001)。除疾病外,多变量分析未确定 FIC 或 URI 猫中抗体滴度增加的其他解释变量。
在患有 FIC 和 URI 的猫中检测到 FCV 尿病毒血症,但尚不确定其病因学意义。血清学结果表明,与对照组相比,FIC 猫中 FCV 暴露增加。需要进一步研究以阐明 FCV 在 FIC 中的潜在作用。