Quantitative detection of Streptococcus pneumoniae, Haemophilus influenzae, and Moraxella catarrhalis in lower respiratory tract samples by real-time PCR

被引:68
|
作者
Kais, Madeleine
Spindler, Carl
Kalin, Mats
Ortqvist, Ake
Giske, Christian G. [1 ]
机构
[1] Karolinska Inst, Karolinska Univ Hosp Solna, Dept Clin Microbiol, SE-17176 Stockholm, Sweden
[2] Karolinska Inst, Dept Med, Infect Dis Unit, SE-17176 Stockholm, Sweden
[3] Karolinska Inst, Karolinska Hosp Solna, Dept Infect Dis, SE-17176 Stockholm, Sweden
[4] Dept Communicable Dis Control & Prevent, SE-17176 Stockholm, Sweden
[5] Karolinska Inst, Clin Microbiol,Microbiol & Tumor Biol Ctr, Karolinska Univ Hosp Solna, SE-17176 Stockholm, Sweden
关键词
community-acquired pneumonia; etiology; diagnostic methods;
D O I
10.1016/j.diagmicrobio.2006.01.007
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The limitation of polymerase chain reaction (PCR) in diagnosis of lower respiratory tract infections (LRTIs) caused by Streptococcus pneumoniae, Haemophilus infuenzae, and Moraxella catarrhalis has been a distinguishing colonization from infection. We assess here the usefulness of real-time quantitative PCR (RQ-PCR) performed on lower respiratory tract samples to overcome this problem. Consecutive respiratory tract samples from patients with and without signs of infection (n = 203) were subjected to RQ-PCR, targeting the genes pneumolysin (S. pneumoniae), fumarate reductase (H. infuenzae), and outer membrane protein B (M. catarrhalis). DNA from positive controls with predefined colony forming units (CFUs) per milliliter were included to allow estimation of CFU per milliliter for the test samples. In parallel, assessment of quantitative cultures from all samples was performed. In the group of patients with LRTI, significant pathogens (>= 10(5) CFU/mL) were found in 32/135 samples (23.7%) with culture, in 51/135 (37.7%) with RQ-PCR, and in 59/135 (43.7%) when combining the methods. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:169 / 178
页数:10
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