De Vos D, Lim A, Pirnay J P, Struelens M, Vandenvelde C, Duinslaeger L, Vanderkelen A, Cornelis P
Flanders Interuniversity Institute for Biotechnology, Vrije Universiteit Brussel, Sint-Genesius-Rode, Belgium.
J Clin Microbiol. 1997 Jun;35(6):1295-9. doi: 10.1128/jcm.35.6.1295-1299.1997.
A multiplex PCR test based on the simultaneous amplification of two lipoprotein genes, oprI and oprL, was designed and evaluated for its ability to directly detect fluorescent pseudomonads (amplification of oprI open reading frame, 249 bp) and Pseudomonas aeruginosa (amplification of oprL open reading frame, 504 bp) in clinical material. A collection of reference strains including 20 different species of fluorescent pseudomonads was tested. Positive PCR results for both genes were observed only for P. aeruginosa isolates (n = 150), including strains of clinical and environmental origin, while only one gene, oprI, was amplified from the other fluorescent pseudomonads. All other bacteria tested (n = 15) were negative by the amplification test. The lower detection level for P. aeruginosa was estimated to be 10(2) cells/ml. Preliminary evaluation on testing skin biopsy specimens from patients with burns (n = 14) and sputum samples from cystic fibrosis patients (n = 49) and other patients (n = 19) showed 100% sensitivity and 74% specificity in comparison with culture. This multiplex PCR assay appears promising for the rapid and sensitive detection of P. aeruginosa in clinical specimens. Further evaluation of its specificity in longitudinal clinical studies is warranted.
设计了一种基于同时扩增两个脂蛋白基因oprI和oprL的多重PCR检测方法,并评估了其直接检测临床材料中荧光假单胞菌(oprI开放阅读框扩增,249 bp)和铜绿假单胞菌(oprL开放阅读框扩增,504 bp)的能力。对包括20种不同荧光假单胞菌的参考菌株进行了检测。仅在铜绿假单胞菌分离株(n = 150)中观察到两个基因的PCR阳性结果,包括临床来源和环境来源的菌株,而从其他荧光假单胞菌中仅扩增出一个基因oprI。所有其他检测的细菌(n = 15)通过扩增试验均为阴性。铜绿假单胞菌的最低检测水平估计为10(2) 个细胞/ml。对烧伤患者(n = 14)的皮肤活检标本、囊性纤维化患者(n = 49)和其他患者(n = 19)的痰液样本进行检测的初步评估显示,与培养相比,其灵敏度为100%,特异性为74%。这种多重PCR检测方法在临床标本中快速、灵敏地检测铜绿假单胞菌方面似乎很有前景。有必要在纵向临床研究中进一步评估其特异性。