Sugita T, Nakajima M, Ikeda R, Niki Y, Matsushima T, Shinoda T
Department of Microbiology, Meiji Pharmaceutical University, Kiyose, Tokyo, Japan.
Microbiol Immunol. 2001;45(2):143-8. doi: 10.1111/j.1348-0421.2001.tb01282.x.
Deep-seated trichosporonosis caused by Trichosporon asahii has a high mortality rate and a very poor prognosis. New species-specific oligonucleotide primers for T. asahii were developed from a sequence analysis of rRNA genes that included the internal transcribed spacer regions. A nested PCR assay with specific primers was used to examine 11 serum samples from 7 patients, who were diagnosed with deep-seated trichosporonosis histologically at autopsy. In addition, Trichosporon cell wall polysaccharide (PS) was detected by a latex agglutination (LA) test. Of 11 samples, seven had a positive LA test, and T. asahii DNA was also detected with the nested PCR assay. Of the four samples in which PS antigen was not detected, the nested PCR of two samples was positive. Our new nested PCR assay may be used as an adjunct to conventional methods for diagnosing T. asahii infection.
由阿萨希毛孢子菌引起的深部毛孢子菌病死亡率高,预后极差。基于对包括内部转录间隔区在内的rRNA基因的序列分析,开发了针对阿萨希毛孢子菌的新的种特异性寡核苷酸引物。使用特异性引物的巢式PCR检测法对7例患者的11份血清样本进行检测,这些患者在尸检时经组织学诊断为深部毛孢子菌病。此外,通过乳胶凝集(LA)试验检测毛孢子菌细胞壁多糖(PS)。11份样本中,7份LA试验呈阳性,巢式PCR检测也检测到阿萨希毛孢子菌DNA。在未检测到PS抗原的4份样本中,2份样本的巢式PCR呈阳性。我们新的巢式PCR检测法可作为诊断阿萨希毛孢子菌感染的传统方法的辅助手段。