Abstract

Abstract

Background: Identification of the Mycobacterium tuberculosis complex organisms to the species level is important for diagnostic, therapeutic and epidemiologic perspectives. Indeed, isolates are routinely identified as belonging to the M. tuberculosis complex without further discrimination in agreement with the high genomic similarity of the M. tuberculosis complex members and the resulting complex available identification tools.

Findings: We herein develop a pyrosequencing assay analyzing polymorphisms within glpK , pykA and gyrB genes to identify members of the M. tuberculosis complex at the species level. The assay was evaluated with 22 M. tuberculosis , 21 M. bovis , 3 M. caprae , 3 M. microti , 2 M. bovis BCG, 2 M. pinnipedii , 1 M. canettii and 1 M. africanum type I isolates. The resulted pyrograms were consistent with conventional DNA sequencing data and successfully identified all isolates. Additionally, 127 clinical M. tuberculosis complex isolates were analyzed and were unambiguously identified as M. tuberculosis .

Conclusion: We proposed a pyrosequencing-based scheme for the rapid identification of M. tuberculosis complex isolates at the species level. The assay is robust, specific, rapid and can be easily introduced in the routine activity.

Details

Title
Pyrosequencing assay for rapid identification of Mycobacterium tuberculosis complex species
Author
Kahla, Imen Ben; Henry, Mireille; Boukadida, Jalel; Drancourt, Michel
Pages
423
Publication year
2011
Publication date
2011
Publisher
BioMed Central
e-ISSN
17560500
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
904003394
Copyright
© 2011 Drancourt et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.