Affiliation:
1. National Reference Center for Mycobacteria, Department of Bacteriology-Hygiene, Faculté de Médecine Pierre & Marie Curie (Paris VI) site Pitié-Salpêtrière, Paris, France
Abstract
ABSTRACT
We assessed the performance of the Genotype MTBDR line probe assay that offers the simultaneous identification of
Mycobacterium tuberculosis
and its resistance to rifampin (RIF) and isoniazid (INH) by detecting the most commonly found mutations in the
rpoB
and
katG
genes. One hundred thirteen
M. tuberculosis
isolates were tested. The nucleotide sequences of the
katG
and
inhA
genes and the
mabA
-
inhA
promoter region were also determined. The MTBDR assay detected 100% and 67% (
n
= 64) of the strains resistant to RIF and INH, respectively. Among the latter, 62 strains carried a Ser315Thr mutation in
katG
, 59 of them displaying a high level of resistance to INH. Two strains with a low level of INH resistance had a Ser315Asn mutation. No mutation was found by the MTBDR assay for 31 INH-resistant strains (33%), of which 24 showed a low level of resistance. By DNA sequencing, we found among them various mutations in the KatG protein for 7 strains, a C→T mutation in position −15 of the
mabA
-
inhA
promoter in 17 strains, and a Ser94Ala mutation in InhA for 7 strains. In conclusion, the MTBDR assay, which fits easily in the workflow of a routine laboratory, enabled the detection of 100% of the RIF-resistant strains and 89% of the INH-resistant strains with a high level of resistance but only 17% of the strains characterized by a low level of INH resistance, indicating that the test can be used as a rapid method to detect in the same experiment the rifampin-resistant and the high-level isoniazid-resistant strains of
M. tuberculosis.
Publisher
American Society for Microbiology
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