Quantitation of Pseudomonas aeruginosa in wound biopsy samples:: from bacterial culture to rapid 'real-time' polymerase chain reaction

被引:40
作者
Pirnay, JP
De Vos, D
Duinslaeger, L
Reper, P
Vandenvelde, C
Cornelis, P
Vanderkelen, A
机构
[1] Queen Astrid Mil Hosp, Burn Wound Ctr, B-1120 Neder Over Heembeek, Belgium
[2] Flanders Interuniv, Inst Biotechnol, Sint Genesius Rode, Belgium
[3] Innogenetics, Neder Over Heembeek, Belgium
来源
CRITICAL CARE | 2000年 / 4卷 / 04期
关键词
burn wound; polymerase chain reaction; Pseudomonas aeruginosa; quantitation; sepsis;
D O I
10.1186/cc702
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
We developed a real-time detection (RTD) polymerase chain reaction (PCR) with rapid thermal cycling to detect and quantify Pseudomonas aeruginosa in wound biopsy samples. This method produced a linear quantitative detection range of 7 logs, with a lower detection limit of 10(3) colony-forming units (CFU)/g tissue or a few copies per reaction. The time from sample collection to result was less than 1 h. RTD-PCR has potential for rapid quantitative detection of pathogens in critical care patients, enabling early and individualized treatment.
引用
收藏
页码:255 / 261
页数:7
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