Decaro Nicola, Pratelli Annamaria, Campolo Marco, Elia Gabriella, Martella Vito, Tempesta Maria, Buonavoglia Canio
Department of Animal Health and Well-being, Faculty of Veterinary Medicine of Bari, S.p. per Casamassima km 3, Valenzano, Bari 70010, Italy.
J Virol Methods. 2004 Aug;119(2):145-50. doi: 10.1016/j.jviromet.2004.03.012.
A TaqMan fluorogenic reverse transcriptase-polymerase chain reaction (RT-PCR) assay was developed for the detection and quantitation of canine coronavirus (CCoV) RNA in the faeces of naturally or experimentally infected dogs. The CCoV fluorogenic RT-PCR assay, which targeted the ORF5 (M gene), was more sensitive than a conventional RT-PCR assay targeting the same gene, showing a detection limit of 10 copies of CCoV standard RNA, and was linear from 10 to 10(8) copies, allowing quantitation of samples with a wide range of CCoV RNA loads. A total of 78 faecal samples of diarrhoeic dogs were tested simultaneously by conventional and fluorogenic RT-PCR: 29 were negative by both techniques, whereas 27 tested positive by conventional RT-PCR and 48 by the established CCoV fluorogenic assay. One sample, which was positive by conventional RT-PCR, gave no signal in the fluorogenic assay. In addition, by the fluorogenic assay CCoV shedding in the faecal samples of an experimentally infected dog was monitored for 28 days. The high sensitivity, simplicity and reproducibility of the CCoV fluorogenic RT-PCR assay, combined with its wide dynamic range and high throughput, make this method especially suitable for efficacy trials on CCoV vaccines.
开发了一种TaqMan荧光逆转录-聚合酶链反应(RT-PCR)检测方法,用于检测和定量自然感染或实验感染犬粪便中的犬冠状病毒(CCoV)RNA。针对开放阅读框5(M基因)的CCoV荧光RT-PCR检测方法比针对同一基因的传统RT-PCR检测方法更灵敏,检测限为10拷贝的CCoV标准RNA,在10至10⁸拷贝范围内呈线性,可对具有广泛CCoV RNA载量的样本进行定量。同时采用传统RT-PCR和荧光RT-PCR对78份腹泻犬粪便样本进行检测:两种技术检测均为阴性的有29份,传统RT-PCR检测呈阳性的有27份,而建立的CCoV荧光检测呈阳性的有48份。一份传统RT-PCR检测呈阳性的样本在荧光检测中未给出信号。此外,通过荧光检测对一只实验感染犬粪便样本中的CCoV排毒情况进行了28天的监测。CCoV荧光RT-PCR检测方法具有高灵敏度、简单性和可重复性,结合其宽动态范围和高通量,使其特别适用于CCoV疫苗的效力试验。