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Journal of Clinical Microbiology, February 2008, p. 689-699, Vol. 46, No. 2
0095-1137/08/$08.00+0     doi:10.1128/JCM.01821-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Development of Multiplex Assay for Rapid Characterization of Mycobacterium tuberculosis{triangledown}

I. L. Bergval,1* R. N. C. P. Vijzelaar,2 E. R. Dalla Costa,3 A. R. J. Schuitema,1 L. Oskam,1 A. L. Kritski,3 P. R. Klatser,1 and R. M. Anthony1

KIT Biomedical Research, Royal Tropical Institute,1 MRC-Holland, Amsterdam, The Netherlands,2 Tuberculosis Research Unit, Internal Medicine Department, Medical School of Federal University of Rio de Janeiro, Rio de Janeiro, Brazil3

Received 13 September 2007/ Returned for modification 28 October 2007/ Accepted 30 November 2007

We have developed a multiplex assay, based on multiplex ligation-dependent probe amplification (MLPA), that allows simultaneous detection of multiple drug resistance mutations and genotype-specific mutations at any location in the Mycobacterium tuberculosis genome. The assay was validated on a reference panel of well-characterized strains, and the results show that M. tuberculosis can be accurately characterized by our assay. Eighteen discriminatory markers identifying drug resistance (rpoB, katG, inhA, embB), members of the M. tuberculosis complex (16S rRNA, IS6110, TbD1), the principal genotypic group (katG, gyrA), and Haarlem and Beijing strains (ogt, mutT2, mutT4) were targeted. A sequence specificity of 100% was reached for 16 of the 18 selected genetic targets. In addition, a panel of 47 clinical M. tuberculosis isolates was tested by MLPA in order to determine the correlation between phenotypic drug resistance and MLPA and between spoligotyping and MLPA. Again, all mutations present in these isolates that were targeted by the 16 functional probes were identified. Resistance-associated mutations were detected by MLPA in 71% of the identified rifampin-resistant strains and in 80% of the phenotypically isoniazid-resistant strains. Furthermore, there was a perfect correlation between MLPA results and spoligotypes. When MLPA is used on confirmed M. tuberculosis clinical specimens, it can be a useful and informative instrument to aid in the detection of drug resistance, especially in laboratories where drug susceptibility testing is not common practice and where the rates of multidrug-resistant and extensively drug resistant tuberculosis are high. The flexibility and specificity of MLPA, along with the ability to simultaneously genotype and detect drug resistance mutations, make MLPA a promising tool for pathogen characterization.

* Corresponding author. Mailing address: KIT Biomedical Research, Royal Tropical Institute, Meibergdreef 39, 1105 AZ Amsterdam, The Netherlands. Phone: 31 (0) 20 5665448. Fax: 31 (0) 20 6971841. E-mail: i.bergval{at}kit.nl

{triangledown} Published ahead of print on 12 December 2007.

Journal of Clinical Microbiology, February 2008, p. 689-699, Vol. 46, No. 2
0095-1137/08/$08.00+0     doi:10.1128/JCM.01821-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.



This article has been cited by other articles:

  • Bergval, I. L., Schuitema, A. R. J., Klatser, P. R., Anthony, R. M. (2009). Resistant mutants of Mycobacterium tuberculosis selected in vitro do not reflect the in vivo mechanism of isoniazid resistance. J Antimicrob Chemother 64: 515-523 [Abstract] [Full Text]  


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