Use of 16S rRNA gene sequencing for identification of "Pseudomonas-like" isolates from sputum of patients with cystic fibrosis

被引:18
作者
Moissenet, D
Bingen, E
Arlet, G
Vu-Thien, H
机构
[1] Hop Enfants Armand Trousseau, Bacteriol Lab, AP HP, F-75571 Paris, France
[2] Hop Tenon, Bacteriol Lab, AP HP, Paris, France
来源
PATHOLOGIE BIOLOGIE | 2005年 / 53卷 / 8-9期
关键词
cystic fibrosis; rARN 16S gene; sequencing;
D O I
10.1016/j.patbio.2005.06.004
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Since nonfermenting, Gram negative bacilli recovered from patients with cystic fibrosis could be misidentified with phenotypic procedures, we used partial 16S ribosomal RNA gene (16S gene) sequencing to identify these "Pseudomonas-like" isolates. 473 isolates were recovered from 66 patients in 2003. Sequencing was used to identify 29 (from 24 patients) of the 473 isolates, showing unclear results with routine tests. PCR with specific primers was carried out to amplify a 995 bp fragment, which was then sequenced. The sequences were analyzed with GenBank database for species assignment. Phenotypic and genotypic results were concordant for 20/29 isolates (10 Pseudomonas aeruginosa, 5 Burkholderia cepacia, 3 Stenotrophomonas maltophilia, 2 Achromobacter xylosoxidans). However, 3 of the 5 B. cepacia isolates were then identified as Burkholderia multivorans with a PCR-RFLP procedure. Phenotypic misidentification was observed for 9/29 isolates: 4 A. xylosoxidans, 1 P aeruginosa, 1 Bordetella petrii, 1 Bordetella bronchiseptica, 1 Ralstonia respiraculi and 1 Ralstonia mannitolilytica. Partial 16S gene sequencing improved the identification of "Pseudomonas-like" isolates from cystic fibrosis patients, but the accuracy to distinguish between genomovars of the B. cepacia complex was inadequate. (c) 2005 Elsevier SAS. Tous droits reserves.
引用
收藏
页码:500 / 502
页数:3
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