Sandhu G S, Kline B C, Espy M J, Stockman L, Smith T F, Limper A H
Department of Biochemistry and Molecular Biology, Mayo Clinic and Foundation, Rochester, MN 55905, USA.
Diagn Microbiol Infect Dis. 1999 Mar;33(3):157-62. doi: 10.1016/s0732-8893(98)00137-0.
PCR with 5S mitochondrial ribosomal RNA (5S) target is a sensitive and specific assay for the detection of Pneumocystis carinii in clinical specimens from the respiratory tract. We developed an oligonucleotide probe directed to a 200 bp amplicon generated by fungal-specific universal primers that anneals with sequences specific for P. carinii in the 28S ribosomal RNA gene (28S). Of 50 archived bronchoalveolar lavage 1(BAL) specimens, 46 of 50 samples (92% agreement) gave the same result (23 positive, 23 negative) by PCR directed to the 5S and 28S assays. Results of calcofluor white staining of BAL smears on slides indicated agreement with the molecular results in 43 of 46 (93.5%) assays. PCR detection of P. carinii by amplification of 28S ribosomal gene target by fungal-specific primers and an organism-specific probe provides an alternate genomic target for the laboratory diagnosis of this organism.
以线粒体核糖体RNA(5S)基因为靶点的聚合酶链反应(PCR)是一种灵敏且特异的检测方法,用于检测呼吸道临床标本中的卡氏肺孢子虫。我们设计了一种寡核苷酸探针,该探针针对真菌特异性通用引物产生的200 bp扩增子,可与28S核糖体RNA基因(28S)中卡氏肺孢子虫的特异性序列退火。在50份存档的支气管肺泡灌洗(BAL)标本中,50份样本中的46份(一致性为92%)通过针对5S和28S检测的PCR得出了相同结果(23份阳性,23份阴性)。玻片上BAL涂片的荧光钙白染色结果表明,46份检测中的43份(93.5%)与分子检测结果一致。通过真菌特异性引物和生物体特异性探针扩增28S核糖体基因靶点来进行卡氏肺孢子虫的PCR检测,为该生物体的实验室诊断提供了另一种基因组靶点。