Carl M, Tibbs C W, Dobson M E, Paparello S F, Dasch G A
Naval Medical Research Institute, Naval Medical Command, Bethesda, Maryland 20814-5055.
Ann N Y Acad Sci. 1990;590:439-44. doi: 10.1111/j.1749-6632.1990.tb42252.x.
We used the polymerase chain reaction (PCR) for the diagnosis of an acute rickettsial infection. A primer pair derived from the 17-kDa antigen sequence of Rickettsia rickettsii amplified specifically a 434-bp DNA fragment from the genome of Rocky Mountain spotted fever and endemic and epidemic typhus. The assay was able to detect as few as 30 rickettsiae. Detection of PCR-amplified DNA with a digoxigenin-labeled DNA probe confirmed an acute human infection with Rickettsia prowazekii.
我们使用聚合酶链反应(PCR)来诊断急性立克次体感染。一对源自立氏立克次体17-kDa抗原序列的引物,能从落基山斑疹热、地方性斑疹伤寒和流行性斑疹伤寒的基因组中特异性扩增出一个434-bp的DNA片段。该检测方法能够检测到低至30个立克次体。用地高辛标记的DNA探针检测PCR扩增的DNA,证实了急性人类普氏立克次体感染。