Affiliation:
1. Department of Applied Microbiology, Institute of Microbiology, Faculty of Biology, University of Warsaw, Warsaw, Poland
2. Department of Medical Microbiology, Radboud University Medical Center, Nijmegen, The Netherlands
3. Department of Internal Medicine, Pulmonary Diseases and Allergy, Medical University of Warsaw, Warsaw, Poland
Abstract
ABSTRACT
Very few studies have examined drug susceptibility of
Mycobacterium kansasii
, and they involve a limited number of strains. The purpose of this study was to determine drug susceptibility profiles of
M. kansasii
isolates representing a spectrum of species genotypes (subtypes) with two different methodologies, i.e., broth microdilution and Etest assays. To confirm drug resistance, drug target genes were sequenced. A collection of 85
M. kansasii
isolates, including representatives of eight different subtypes (I to VI, I/II, and IIB) from eight countries, was used. Drug susceptibility against 13 and 8 antimycobacterial agents was tested by using broth microdilution and Etest, respectively. For drug-resistant or high-MIC isolates, eight structural genes (
rrl
,
katG
,
inhA
,
embB
,
rrs
,
rpsL
,
gyrA
, and
gyrB
) and one regulatory region (
embCA
) were PCR amplified and sequenced in the search for resistance-associated mutations. All isolates tested were susceptible to rifampin (RIF), amikacin (AMK), co-trimoxazole (SXT), rifabutin (RFB), moxifloxacin (MXF), and linezolid (LZD) according to the microdilution method. Resistance to ethambutol (EMB), ciprofloxacin (CIP), and clarithromycin (CLR) was found in 83 (97.7%), 17 (20%), and 1 (1.2%) isolate, respectively. The calculated concordance between the Etest and dilution method was 22.6% for AMK, 4.8% for streptomycin (STR), 3.2% for CLR, and 1.6% for RIF. For EMB, INH, and SXT, not even a single MIC value determined by one method equaled that by the second method. The only mutations disclosed were A2266C transversion at the
rrl
gene (CLR-resistant strain) and A128G transition at the
rpsL
gene (strain with STR MIC of >64 mg/liter). In conclusion, eight drugs, including RIF, CLR, AMK, SXT, RFB, MXF, LZD, and ethionamide (ETO), showed high
in vitro
activity against
M. kansasii
isolates. Discrepancies of the results between the reference microdilution method and Etest preclude the use of the latter for drug susceptibility determination in
M. kansasii
. Drug resistance in
M. kansasii
may have different genetic determinants than resistance to the same drugs in
M. tuberculosis
.
Funder
MNiSW | Narodowe Centrum Badań i Rozwoju
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology