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
Reference34 articles.
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