Henry Katherine M, Jiang Ju, Rozmajzl Patrick J, Azad Abdu F, Macaluso Kevin R, Richards Allen L
Rickettsial Diseases Department, Naval Medical Research Center, 503 Robert Grant Avenue, Silver Spring, MD 20910-7500, USA.
Mol Cell Probes. 2007 Feb;21(1):17-23. doi: 10.1016/j.mcp.2006.06.002. Epub 2006 Jul 1.
Rickettsia typhi and Rickettsia felis are the etiologic agents of murine typhus and flea-borne spotted fever, respectively. We have constructed two quantitative real-time polymerase chain reaction (qPCR) assays to detect these pathogenic rickettsiae. The qPCR assays were developed utilizing unique sequences of the R. typhi and R. felis outer membrane protein B genes (ompB) to design the specific primers and molecular beacon probes. The assays were found to be species-specific and did not yield false-positive reactions with nucleic acid from other rickettsiae, orientiae, neorickettsiae or unrelated bacteria. In addition, the assays were sensitive enough to detect three target sequence copies per reaction and were capable of detecting R. typhi and R. felis nucleic acid in the cat flea, Ctenocephalides felis. These results demonstrate that two sensitive and specific qPCR assays have been successfully developed to detect and enumerate R. typhi and R. felis.
斑疹伤寒立克次体和猫立克次体分别是鼠型斑疹伤寒和蚤传斑点热的病原体。我们构建了两种定量实时聚合酶链反应(qPCR)检测方法来检测这些致病性立克次体。利用斑疹伤寒立克次体和猫立克次体的外膜蛋白B基因(ompB)的独特序列设计特异性引物和分子信标探针,从而开发出qPCR检测方法。结果发现这些检测方法具有种属特异性,对来自其他立克次体、东方体、新立克次体或无关细菌的核酸不会产生假阳性反应。此外,这些检测方法灵敏度很高,每个反应能够检测到三个目标序列拷贝,并且能够检测猫栉首蚤体内的斑疹伤寒立克次体和猫立克次体核酸。这些结果表明,已成功开发出两种灵敏且特异的qPCR检测方法,用于检测和计数斑疹伤寒立克次体和猫立克次体。