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

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          Abstract

          Background

          Resistance 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.

          Methods

          Sputum samples obtained from DTT-TB cases from health facilities across Ghana were processed for rapid diagnosis and detection of drug resistance using the Genotype MTBDR plus and Genotype MTBDR sl. v2 from Hain Life science.

          Results

          A 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 (ANY r); 16.8% (50/298) were isoniazid-mono-resistant (INH r), 16.8% (50/298) were rifampicin-mono-resistant (RIF r), and 25.2% (75/298) were MDR. 24 (13.7%) of the ANY r were additionally resistant to at least one second line drug: 7.4% (2 RIF r, 1 INH r, and 10 MDR samples) resistant to only FQs and 2.3% (2 RIF r, 1 INH r, and 1 MDR samples) resistant to AMG drugs kanamycin (KAN), amikacin (AMK), capreomycin (CAP), and viomycin (VIO). Additionally, there were 4.0% (5 RIF r and 2 MDR samples) resistant to both FQs and AMGs. 81 (65.6%) out of 125 INH-resistant samples including INH r 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.

          Conclusion

          The 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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          Most cited references28

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          COVID-19 as the Leading Cause of Death in the United States

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            Global Tuberculosis Report 2020.

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              Fluoroquinolone resistance in Mycobacterium tuberculosis and mutations in gyrA and gyrB.

              This study evaluated cross-resistance of Mycobacterium tuberculosis strains to ofloxacin, moxifloxacin, and gatifloxacin and investigated the presence of mutations in gyrA and gyrB. Fluoroquinolone susceptibilities were determined for 41 M. tuberculosis strains by the proportion method on 7H11, and MICs were determined by the resazurin microtiter assay. Forty strains shared the same resistance results for the three fluoroquinolones. However, one strain, with an Asn-533 --> Thr mutation in gyrB, was susceptible to ofloxacin but resistant to moxifloxacin and gatifloxacin.
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                Author and article information

                Contributors
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                12 January 2023
                2022
                : 13
                : 1069292
                Affiliations
                [1] 1Noguchi Memorial Institute for Medical Research, College of Health Sciences, University of Ghana , Accra, Ghana
                [2] 2Institute for Environment and Sanitation Studies, College of Basic and Applied Sciences, University of Ghana , Accra, Ghana
                [3] 3Eastern Regional Hospital , Koforidua, Ghana
                [4] 4Chest Department, 37 Military Hospital , Accra, Ghana
                [5] 5National Tuberculosis Control Program, Ghana Health Service , Accra, Ghana
                [6] 6Medical Parasitology and Infection Biology, Swiss Tropical and Public Health Institute, University of Basel , Basel, Switzerland
                Author notes

                Edited by: Maria Rosalia Pasca, University of Pavia, Italy

                Reviewed by: Okon Okwong Kenneth, Federal Medical Centre Makurdi, Nigeria; Uma Devi Ranganathan, National Institute of Research in Tuberculosis (ICMR), India

                *Correspondence: Isaac Darko Otchere, iotchere@ 123456noguchi.ug.edu.gh

                This article was submitted to Antimicrobials, Resistance and Chemotherapy, a section of the journal Frontiers in Microbiology

                Article
                10.3389/fmicb.2022.1069292
                9878308
                36713197
                54d5cb13-14a7-44f8-97c3-e0026834a408
                Copyright © 2023 Otchere, Morgan, Asare, Osei-Wusu, Aboagye, Yirenkyi, Musah, Danso, Tetteh-Ocloo, Afum, Asante-Poku, Laryea, Poku, Bonsu, Gagneux and Yeboah-Manu.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 13 October 2022
                : 28 December 2022
                Page count
                Figures: 2, Tables: 5, Equations: 0, References: 31, Pages: 9, Words: 5149
                Funding
                This study was funded by the Swiss-African Research Cooperation (SARECO) grant SA_IO110 to IO and the WANETAM-2 funded by EDCTP.
                Categories
                Microbiology
                Original Research

                Microbiology & Virology
                pre-xdr-tb,drug resistance,ghana,monitoring,tuberculosis,screening,treatment
                Microbiology & Virology
                pre-xdr-tb, drug resistance, ghana, monitoring, tuberculosis, screening, treatment

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