Analysis of drug resistance among difficult-to-treat tuberculosis patients in Ghana identifies several pre-XDR TB cases

0301 basic medicine Genotype Epidemiology FOS: Basic medicine FOS: Health sciences Ghana Microbiology Gene Global Challenge of Antibiotic Resistance in Bacteria 03 medical and health sciences Kanamycin Antibiotics Biochemistry, Genetics and Molecular Biology Health Sciences Isoniazid Pathology Genetics Tuberculosis Capreomycin Extensively drug-resistant tuberculosis Ethionamide pre-XDR-TB Amikacin Internal medicine Biology Management and Epidemiology of Pneumonia Rifampicin Pharmacology drug resistance screening Sputum Life Sciences Mycobacterium tuberculosis QR1-502 3. Good health monitoring Infectious Diseases tuberculosis Drug resistance FOS: Biological sciences Medicine Molecular Medicine Antimicrobial Resistance Drug Ethambutol
DOI: 10.3389/fmicb.2022.1069292 Publication Date: 2023-01-12T06:21:05Z
ABSTRACT
BackgroundResistance to tuberculosis (TB) drugs has become a major threat to global control efforts. Early case detection and drug susceptibility profiling of the infecting bacteria are essential for appropriate case management. The objective of this study was to determine the drug susceptibility profiles of difficult-to-treat (DTT) TB patients in Ghana.MethodsSputum samples obtained from DTT-TB cases from health facilities across Ghana were processed for rapid diagnosis and detection of drug resistance using the Genotype MTBDRplus and Genotype MTBDRsl.v2 from Hain Life science.ResultsA total of 298 (90%) out of 331 sputum samples processed gave interpretable bands out of which 175 (58.7%) were resistant to at least one drug (ANYr); 16.8% (50/298) were isoniazid-mono-resistant (INHr), 16.8% (50/298) were rifampicin-mono-resistant (RIFr), and 25.2% (75/298) were MDR. 24 (13.7%) of the ANYr were additionally resistant to at least one second line drug: 7.4% (2 RIFr, 1 INHr, and 10 MDR samples) resistant to only FQs and 2.3% (2 RIFr, 1 INHr, and 1 MDR samples) resistant to AMG drugs kanamycin (KAN), amikacin (AMK), capreomycin (CAP), and viomycin (VIO). Additionally, there were 4.0% (5 RIFr and 2 MDR samples) resistant to both FQs and AMGs. 81 (65.6%) out of 125 INH-resistant samples including INHr and MDR had katG-mutations (MT) whereas 15 (12%) had inhApro-MT. The remaining 28 (22.4%) had both katG and inhA MT. All the 19 FQ-resistant samples were gyrA mutants whereas the 10 AMGs were rrs (3), eis (3) as well as rrs, and eis co-mutants (4). Except for the seven pre-XDR samples, no sample had eis MT.ConclusionThe detection of several pre-XDR TB cases in Ghana calls for intensified drug resistance surveillance and monitoring of TB patients to, respectively, ensure early diagnosis and treatment compliance.
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