塔克曼
实时聚合酶链反应
逆转录聚合酶链式反应
分子生物学
生物
聚合酶链反应
逆转录酶
核酸
病毒学
基因
信使核糖核酸
遗传学
作者
Xiangdong Zhu,Yufei Wang,Jianfei Chen,Shouxin Zhang,Hongyan Shi,Da Shi,Jing Gao,Li Feng
标识
DOI:10.1016/j.jviromet.2016.01.016
摘要
Porcine kobuvirus (PKV) is a newly emerging virus that has been detected in diarrheic pigs. Presently, reverse transcription-polymerase chain reaction (RT-PCR) and RT-loop-mediated amplification are the only methods that can be used to detect PKV. To develop a TaqMan real-time RT-PCR for the rapid detection and quantitation of PKV nucleic acid in fecal samples, a pair of primers and a probe were designed to amplify the conserved 3D region of the PKV genome. After optimization, the TaqMan real-time RT-PCR was highly specific and ∼1000 times more sensitive than conventional RT-PCR, and the detection limit was as low as 30 DNA copies. Among the 148 intestinal samples from piglets with diarrhea, 136 and 118 were positive based on the TaqMan and conventional RT-PCR methods, respectively, indicating that the TaqMan RT-PCR was more sensitive than conventional RT-PCR, and the total concordance of the two methods was approximately 87.84%. Thus, the TaqMan real-time RT-PCR should be a useful tool for the early detection and quantitation of PKV.
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