Use of different PCR-based techniques integrated into a non-tuberculous identification algorithm

被引:6
作者
Esparcia, Oscar [1 ,2 ]
Espanol, Montserrat [1 ]
Garrigo, Montserrat [1 ,2 ]
Moreno, Carmen [1 ]
Montemayor, Michel [1 ]
Navarro, Ferran [1 ,2 ]
Coll, Pere [1 ,2 ]
机构
[1] Hosp Santa Creu & Sant Pau, Microbiol Serv, Barcelona, Spain
[2] Univ Autonoma Barcelona, Dept Genet & Microbiol, E-08193 Barcelona, Spain
来源
ENFERMEDADES INFECCIOSAS Y MICROBIOLOGIA CLINICA | 2012年 / 30卷 / 01期
关键词
16S rRNA gene; AccuProbe; Mycobacterium avium complex; hsp6S; LENGTH POLYMORPHISM ANALYSIS; 16S RIBOSOMAL-RNA; MYCOBACTERIUM-AVIUM COMPLEX; SP-NOV; RAPID IDENTIFICATION; SEQUENCE-ANALYSIS; HSP65; GENE; RESTRICTION; LEVEL;
D O I
10.1016/j.eimc.2011.06.014
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Introduction: The aim of the present work was to demonstrate the utility of a non-tuberculous mycobacteria (NTM) identification algorithm, which integrates different PCR-based techniques and basic phenotypic features. Moreover, the algorithm for pattern restriction analysis of hsp65 (hsp65 PRA) interpretation has been updated. Methods: The workflow chosen consisted of the identification by a DNA hybridization probe method, followed by PCR-restriction enzyme analysis of hsp65 (hsp65 PRA) in those isolates that cannot be identified by hybridization probes. If necessary, 16S rRNA gene and hsp65 gene sequencing were used for speciation. Results: A total of 236 NTM were collected, in which 102 (43.2%) isolates were identified by DNA specific probes and 76 (32.2%) isolates were identified with hsp65 PRA. Partial sequencing of the 165 rRNA gene was used for species identification of the remaining 58 (24.5%) isolates. Fifty-three (22.4%) were identified using this method. Five isolates (2.1%) were submitted for partial sequencing of hsp65 gene and one isolate was identified with this method. Four strains (1.7%) could not be identified at species level. Three new PRA patterns were found. Seven isolates tested positive with the AccuProbe Mycobacterium avium complex identification test but did not test positive with the M. avium or Mycobacterium intracellulare specific probes. Five and two of these isolates were identified as M. intracellulare and Mycobacterium colombiense, respectively. Conclusion: This approach allowed us to identify almost all NTM isolates found in this study, including some recently described species. (C) 2011 Elsevier Espana, S.L. All rights reserved.
引用
收藏
页码:3 / 10
页数:8
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