Park Hyo-Soon, Lee Jung-Hee, Jeong Eun-Ju, Kim Jung-Eun, Hong Sung-Jin, Park Tae-Kyu, Kim Tae-Yung, Jang Won-Jong, Park Kyung-Hee, Kim Bum-Joon, Kook Yoon-Hoh, Lee Seung-Hyun
Department of Microbiology, Konkuk University, Chungju, Chungchongbuk-Do, Korea.
Microbiol Immunol. 2005;49(6):545-9. doi: 10.1111/j.1348-0421.2005.tb03760.x.
In this study, two new duplex PCR methods based on the groEL gene were developed and investigated for the diagnosis of rickettsiae. The first duplex PCR assay amplified the 229-bp and the 366-bp DNAs of 6 strains including typhus group (TG) and spotted fever group (SFG) rickettsiae, and 5 scrub typhus group (STG) rickettsiae, respectively. The second duplex PCR assay amplified the 397-bp and the 213-bp DNAs of 6 Rickettsia strains and 5 STG strains. These duplex PCR methods could simultaneously perform the rapid identification of rickettsiae and the differential diagnosis of STG and other group rickettsiae in a single reaction.
在本研究中,开发并研究了两种基于groEL基因的新型双重PCR方法用于立克次体的诊断。第一种双重PCR检测法分别扩增了包括斑疹伤寒群(TG)和斑点热群(SFG)立克次体的6个菌株以及5个恙虫病群(STG)立克次体的229bp和366bp的DNA。第二种双重PCR检测法扩增了6个立克次体菌株和5个STG菌株的397bp和213bp的DNA。这些双重PCR方法能够在单一反应中同时对立克次体进行快速鉴定以及对STG和其他群立克次体进行鉴别诊断。