Yoshida Y, Furuya Y, Katayama T, Kaiho I, Yamamoto S
Kanagawa Prefectural Public Health Laboratory.
Kansenshogaku Zasshi. 1994 May;68(5):601-6. doi: 10.11150/kansenshogakuzasshi1970.68.601.
Polymerase chain reaction (PCR) with nested primer pairs was used to diagnose Tsutsugamushi disease and identify the Rickettsia tsutsugamushi serotype. The primer pairs used for PCR were designed on the basis of the nucleotide sequence of the gene that encodes the 56-kDa antigen. Five serovariants, the Gilliam, Karp, Kato, Kawasaki, and Kuroki strains of Rickettsia tsutsugamushi were detected and identified by nested PCR. The serotypes of patients registered during 1990 to 1992 in Kanagawa Prefecture were identified by nested PCR. Sixty percentage of patients showed Kawasaki types, 20% Karp types, and 20% Kuroki types. This result suggested that the recent Tsutsugamushi disease were mostly caused by Kawasaki types in Kanagawa Prefecture.
采用巢式引物对的聚合酶链反应(PCR)来诊断恙虫病并鉴定恙虫病东方体血清型。用于PCR的引物对是根据编码56 kDa抗原的基因的核苷酸序列设计的。通过巢式PCR检测并鉴定了恙虫病东方体的5个血清变种,即Gilliam、Karp、Kato、Kawasaki和Kuroki株。通过巢式PCR鉴定了1990年至1992年在神奈川县登记的患者的血清型。60%的患者为Kawasaki型,20%为Karp型,20%为Kuroki型。这一结果表明,神奈川县近期的恙虫病大多由Kawasaki型引起。