Detection by GenoType MTBDR sl Test of Complex Mechanisms of Resistance to Second-Line Drugs and Ethambutol in Multidrug-Resistant Mycobacterium tuberculosis Complex Isolates

Author:

Brossier Florence12,Veziris Nicolas12,Aubry Alexandra12,Jarlier Vincent12,Sougakoff Wladimir123

Affiliation:

1. National Reference Centre for Mycobacteria, Hôpital Pitié-Salpêtrière, AP-HP, Paris, France

2. Université Pierre et Marie Curie (UPMC), Université Paris 06, Faculté de Médecine Pitié-Salpêtrière, Paris, France

3. Institut National de la Santé et de la Recherche Médicale (INSERM), Unité Mixte de Recherche en Santé (UMRS 872, Equipe 12 Pitié-Salpêtrière), Laboratoire de Recherche Moléculaire sur les Antibiotiques (LRMA), Paris, France

Abstract

ABSTRACT The GenoType MTBDR sl test rapidly detects resistance to ethambutol, fluoroquinolones, and second-line aminoglycosides (amikacin and kanamycin) and cyclic peptide (capreomycin) in Mycobacterium tuberculosis . A set of 41 multidrug-resistant (MDR) M. tuberculosis strains, 8 extensively drug-resistant (XDR) M. tuberculosis strains, and 3 non-MDR M. tuberculosis strains were tested by the MTBDR sl test and by DNA sequencing of the resistance-determining regions in gyrA and gyrB (fluoroquinolones [FQ]), rpsL (streptomycin), rrs and tlyA (aminoglycosides and/or cyclic peptide), and embB (ethambutol). The sensitivity and specificity of the MTBDR sl test were as follows: 87% and 96%, respectively, for fluoroquinolones; 100% for both for amikacin; 77% and 100%, respectively, for kanamycin, 80% and 98%, respectively, for capreomycin; and 57% and 92%, respectively, for ethambutol. Analysis of the discrepant results indicated that three FQ-resistant strains (including one XDR strain) with mutations in gyrB were missed by the MTBDR sl test and that one FQ-susceptible strain, identified as resistant by the MTBDR sl test, had a double mutation (T80A-A90G) in GyrA that did not confer resistance to FQ. Five strains (including two XDR strains) without mutations in rrs were monoresistant to aminoglycosides or cyclic peptide and were missed by the MTBDR sl test. Finally, 12/28 ethambutol-resistant strains had no mutation at codon 306 in embB , while 2/24 ethambutol-susceptible strains had such a mutation. In conclusion, the MTBDR sl test efficiently detects the most common mutations involved in resistance to fluoroquinolones, aminoglycosides/cyclic peptide, and ethambutol and accurately assesses susceptibility to amikacin. However, due to mutations not included in the test (particularly in gyrB ) or resistance mechanisms not yet characterized (particularly those related to ethambutol resistance and to monoresistance to aminoglycosides or cyclic peptide), the wild-type results yielded by the MTBDR sl test should be confirmed by drug susceptibility testing.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

Reference34 articles.

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