Detection of Haemophilus influenzae in respiratory secretions from pneumonia patients by quantitative real-time polymerase chain reaction

被引:46
作者
Abdeldaim, Guma M. K. [1 ]
Stralin, Kristoffer [2 ]
Kirsebom, Leif A. [3 ]
Olcen, Per [4 ]
Blomberg, Jonas [1 ]
Hermann, Bjorn [1 ]
机构
[1] Univ Uppsala Hosp, Dept Clin Microbiol, S-75185 Uppsala, Sweden
[2] Orebro Univ Hosp, Dept Infect Dis, S-70185 Orebro, Sweden
[3] Biomed Ctr, Dept Cell & Mol Biol, S-75124 Uppsala, Sweden
[4] Orebro Univ Hosp, Dept Clin Microbiol, S-70185 Orebro, Sweden
关键词
H; influenzae; Pneumonia; Real-time PCR; Outer membrane protein P6; fucK; mpB; RNASE-P RNA; STREPTOCOCCUS-PNEUMONIAE; PHYLOGENETIC-RELATIONSHIPS; PNEUMOCOCCAL PNEUMONIA; BACTERIAL PATHOGENS; ANTIGEN-DETECTION; BLOOD CULTURES; MULTIPLEX PCR; STRAINS; GENE;
D O I
10.1016/j.diagmicrobio.2009.03.030
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
A quantitative real-time polymerase chain reaction (PCR) based on the omp P6 gene was developed to detect Haemophilus influenzae. Its specificity was determined by analysis of 29 strains of 11 different Haemophilus spp. and was compared with PCR assays having other target genes: mpB, 16S rRNA, and bexA. The method was evaluated on nasopharyngeal aspirates from 166 adult patients with community-acquired pneumonia. When 104 DNA copies/mL was used as cutoff limit for the method, P6 PCR had a sensitivity of 97.5% and a specificity of 96.0% compared with the culture. Of 20 culture-negative but P6 PCR-positive cases, 18 were confirmed by, fucK PCR as H. influenzae. Five (5.9%) of 84 nasopharyngeal aspirates from adult controls tested PCR positive. We conclude that the P6 real-time PCR is both sensitive and specific for identification of H. influenzae in respiratory secretions. Quantification facilitates discrimination between disease-causing H. influenzae strains and commensal colonization. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:366 / 373
页数:8
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