Sugita Y, Matsuzaki T, Nakajima H, Nakajima H
Department of Dermatology, Yokohama City University, School of Medicine.
Nihon Hifuka Gakkai Zasshi. 1991 Jun;101(7):743-6.
A polymerase chain reaction (PCR) using specific oligonucleotide primers and Taq polymerase was developed for the detection of Rickettsia tsutsugamushi, the causative agent of tsutsugamushi disease. Oligonucleotide primers were synthesized on the basis of DNA sequences encoding 58 kD antigen of R. tsutsugamushi. Specific DNA amplification of 358 bp and 109 bp DNA fragments were demonstrated using patient's blood. This PCR method would enable to make a rapid and sensitive diagnosis of tsutsugamushi disease.
为检测恙虫病的病原体恙虫病东方体,开发了一种使用特异性寡核苷酸引物和Taq聚合酶的聚合酶链反应(PCR)。基于编码恙虫病东方体58 kD抗原的DNA序列合成寡核苷酸引物。使用患者血液证实了358 bp和109 bp DNA片段的特异性DNA扩增。这种PCR方法将能够对恙虫病进行快速、灵敏的诊断。