Evaluation of the efficacy of real-time polymerase chain reaction for the routine early detection of Pseudomonas aeruginosa in cystic fibrosis sputum and throat swab specimens

被引:11
|
作者
Logan, Catriona [1 ]
Habington, Adele [1 ]
Lennon, Grainne [1 ,2 ]
Cronin, Frank [1 ]
O'Sullivan, Niamh [1 ,3 ]
机构
[1] Our Ladys Childrens Hosp, Dept Microbiol, Dublin 12, Ireland
[2] Our Ladys Childrens Hosp, Childrens Res Ctr, Dublin 12, Ireland
[3] Coombe Women & Infants Univ Hosp, Dept Pathol, Dublin 8, Ireland
关键词
Pseudomonas aeruginosa; real-time PCR; cystic fibrosis; SUBTRACTIVE HYBRIDIZATION; PULMONARY-FUNCTION; CHRONIC INFECTION; STRAIN; PCR; COLONIZATION; EPIDEMIC; CHILDREN; SPREAD; ASSAY;
D O I
10.1016/j.diagmicrobio.2010.07.012
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
A longitudinal study of 2099 sputa and throat swabs received from 183 pediatric cystic fibrosis patients over a 29-month period was used to evaluate the efficacy of real-time polymerase chain reaction (PCR) for the early detection of Pseudomonas aeruginosa as compared to microbiologic culture Real-time PCR resulted in an increased number of specimens identified as P aerugmosa positive The sensitivity of culture was 82% (373/453) and of PCR was 93% (420/453) when considering both positive culture and PCR results as true positives Of the 80 specimens identified as PCR positive/culture negative for P aerugmosa, the subsequent patient sample in 32 5% (26/80) of specimens concerned was identified as P aerugmosa culture positive, suggesting that PCR has the potential to detect P aeruginosa earlier than the microbiologic culture Real-time PCR analysis found no evidence of the Liverpool and Manchester epidemic P aerugmosa strains in the cohort examined The findings of this study highlight the importance of specimen collection protocols to ensure that adequate samples are received at the laboratory for testing, thereby minimizing the potential for reporting of false-negative P aerugmosa culture results (C) 2010 Elsevier Inc All rights reserved
引用
收藏
页码:358 / 365
页数:8
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