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

被引:151
作者
Brossier, Florence [1 ,2 ]
Veziris, Nicolas [1 ,2 ]
Aubry, Alexandra [1 ,2 ]
Jarlier, Vincent [1 ,2 ]
Sougakoff, Wladimir [1 ,2 ,3 ]
机构
[1] Hop La Pitie Salpetriere, Natl Reference Ctr Mycobacteria, AP HP, Paris, France
[2] Univ Paris 06, Fac Med Pitie Salpetriere, Paris, France
[3] INSERM, UMRS 872, Lab Bacteriol Hyg, LRMA, F-75634 Paris 13, France
关键词
FUNCTIONAL-ANALYSIS; CLINICAL SPECIMENS; GYRASE MUTATIONS; MUTANT ENZYMES; EMBB CODON-306; STRAINS; FLUOROQUINOLONE; ASSAY; CAPREOMYCIN; KANAMYCIN;
D O I
10.1128/JCM.01947-09
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The GenoType MTBDRsl 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 MTBDRsl 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 MTBDRsl 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 MTBDRsl test and that one FQ-susceptible strain, identified as resistant by the MTBDRsl 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 MTBDRsl 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 MTBDRsl 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 MTBDRsl test should be confirmed by drug susceptibility testing.
引用
收藏
页码:1683 / 1689
页数:7
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