Development of quantitative real-time PCR assays to detect Rickettsia typhi and Rickettsia felis, the causative agents of murine typhus and flea-borne spotted fever

被引:91
作者
Henry, Katherine M.
Jiang, Ju
Rozmajzl, Patrick J.
Azad, Abdu F.
Macaluso, Kevin R.
Richards, Allen L.
机构
[1] USN, Res Ctr, Rickettsial Dis Dept, Silver Spring, MD 20910 USA
[2] Univ Maryland, Sch Med, Baltimore, MD 21201 USA
[3] Louisiana State Univ, Baton Rouge, LA 70803 USA
关键词
Rickettsia typhi; Rickettsia felis; murine typhus; flea-borne spotted fever; quantitative real-time polymerase chain reaction;
D O I
10.1016/j.mcp.2006.06.002
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
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. Published by Elsevier Ltd.
引用
收藏
页码:17 / 23
页数:7
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