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      MDR M. tuberculosis outbreak clone in Eswatini missed by Xpert has elevated bedaquiline resistance dated to the pre-treatment era

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          Abstract

          Background

          Multidrug-resistant (MDR) Mycobacterium tuberculosis complex strains not detected by commercial molecular drug susceptibility testing (mDST) assays due to the RpoB I491F resistance mutation are threatening the control of MDR tuberculosis (MDR-TB) in Eswatini.

          Methods

          We investigate the evolution and spread of MDR strains in Eswatini with a focus on bedaquiline (BDQ) and clofazimine (CFZ) resistance using whole-genome sequencing in two collections ((1) national drug resistance survey, 2009–2010; (2) MDR strains from the Nhlangano region, 2014–2017).

          Results

          MDR strains in collection 1 had a high cluster rate (95%, 117/123 MDR strains) with 55% grouped into the two largest clusters (gCL3, n = 28; gCL10, n = 40). All gCL10 isolates, which likely emerged around 1993 (95% highest posterior density 1987–1998), carried the mutation RpoB I491F that is missed by commercial mDST assays. In addition, 21 (53%) gCL10 isolates shared a Rv0678 M146T mutation that correlated with elevated minimum inhibitory concentrations (MICs) to BDQ and CFZ compared to wild type isolates. gCL10 isolates with the Rv0678 M146T mutation were also detected in collection 2.

          Conclusion

          The high clustering rate suggests that transmission has been driving the MDR-TB epidemic in Eswatini for three decades. The presence of MDR strains in Eswatini that are not detected by commercial mDST assays and have elevated MICs to BDQ and CFZ potentially jeopardizes the successful implementation of new MDR-TB treatment guidelines. Measures to limit the spread of these outbreak isolates need to be implemented urgently.

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          Most cited references29

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          The European Nucleotide Archive

          The European Nucleotide Archive (ENA; http://www.ebi.ac.uk/ena) is Europe’s primary nucleotide-sequence repository. The ENA consists of three main databases: the Sequence Read Archive (SRA), the Trace Archive and EMBL-Bank. The objective of ENA is to support and promote the use of nucleotide sequencing as an experimental research platform by providing data submission, archive, search and download services. In this article, we outline these services and describe major changes and improvements introduced during 2010. These include extended EMBL-Bank and SRA-data submission services, extended ENA Browser functionality, support for submitting data to the European Genome-phenome Archive (EGA) through SRA, and the launch of a new sequence similarity search service.
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            Unexpected high prevalence of resistance-associated Rv0678 variants in MDR-TB patients without documented prior use of clofazimine or bedaquiline

            Objectives: Resistance-associated variants (RAVs) in Rv0678, a regulator of the MmpS5-MmpL5 efflux pump, have been shown to lead to increased MICs of bedaquiline (2- to 8- fold) and clofazimine (2- to 4-fold). The prevalence of these Rv0678 RAVs in clinical isolates and their impact on treatment outcomes are important factors to take into account in bedaquiline treatment guidelines. Methods: Baseline isolates from two bedaquiline MDR-TB clinical trials were sequenced for Rv0678 RAVs and corresponding bedaquiline MICs were determined on 7H11 agar. Rv0678 RAVs were also investigated in non-MDR-TB sequences of a population-based cohort. Results: Rv0678 RAVs were identified in 23/347 (6.3%) of MDR-TB baseline isolates. Surprisingly, bedaquiline MICs for these isolates were high (> 0.24 mg/L, n = 8), normal (0.03−0.24 mg/L, n = 11) or low (< 0.03 mg/L, n = 4). A variant at position −11 in the intergenic region mmpS5–Rv0678 was identified in 39 isolates (11.3%) and appeared to increase the susceptibility to bedaquiline. In non-MDR-TB isolates, the frequency of Rv0678 RAVs was lower (6/852 or 0.7%). Competition experiments suggested that rifampicin was not the drug selecting for Rv0678 RAVs. Conclusions: RAVs in Rv0678 occur more frequently in MDR-TB patients than previously anticipated, are not associated with prior use of bedaquiline or clofazimine, and in the majority of cases do not lead to bedaquiline MICs above the provisional breakpoint (0.24 mg/L). Their origin remains unknown. Given the variety of RAVs in Rv0678 and their variable effects on the MIC, only phenotypic drug-susceptibility methods can currently be used to assess bedaquiline susceptibility.
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              Detection of drug-resistant tuberculosis by Xpert MTB/RIF in Swaziland.

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                Author and article information

                Contributors
                sniemann@fz-borstel.de
                Journal
                Genome Med
                Genome Med
                Genome Medicine
                BioMed Central (London )
                1756-994X
                25 November 2020
                25 November 2020
                2020
                : 12
                : 104
                Affiliations
                [1 ]GRID grid.418187.3, ISNI 0000 0004 0493 9170, Molecular and Experimental Mycobacteriology, , Research Center Borstel, ; Parkallee 1, 23845 Borstel, Germany
                [2 ]GRID grid.452463.2, German Center for Infection Research (DZIF), ; Partner Site Hamburg-Lübeck-Borstel-Riems, Borstel, Germany
                [3 ]GRID grid.452373.4, ISNI 0000 0004 0643 8660, Epicentre, ; Paris, France
                [4 ]GRID grid.5335.0, ISNI 0000000121885934, Department of Genetics, , University of Cambridge, ; Cambridge, UK
                [5 ]Centre for Tuberculosis, National TB Reference Laboratory, WHO TB Supranational Laboratory Network, National Institute for Communicable Diseases/National Health Laboratory Services, Johannesburg, South Africa
                [6 ]GRID grid.49697.35, ISNI 0000 0001 2107 2298, Department of Medical Microbiology, , University of Pretoria, ; Pretoria, South Africa
                [7 ]GRID grid.11951.3d, ISNI 0000 0004 1937 1135, Department of Internal Medicine, , University of Witwatersrand, ; Johannesburg, South Africa
                [8 ]GRID grid.11956.3a, ISNI 0000 0001 2214 904X, DST/NRF Centre of Excellence for Biomedical Tuberculosis Research, Faculty of Medicine and Health Sciences, , Stellenbosch University, ; Cape Town, South Africa
                [9 ]GRID grid.11956.3a, ISNI 0000 0001 2214 904X, South African Medical Research Council Centre for Tuberculosis Research, Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, , Stellenbosch University, ; Cape Town, South Africa
                [10 ]SYNLAB Gauting, Gauting, Germany, IML red GmbH, Institute of Microbiology and Laboratory Medicine, WHO Supranational Reference Laboratory of TB, Gauting, Germany
                [11 ]GRID grid.463475.7, National Tuberculosis Reference Laboratory (NTRL), Ministry of Health, ; Mbabane, Swaziland
                [12 ]GRID grid.11505.30, ISNI 0000 0001 2153 5088, Mycobacteriology Unit, Department of Biomedical Sciences, , Institute of Tropical Medicine, ; Antwerp, Belgium
                [13 ]Médecins Sans Frontières (MSF) - Eswatini, Mbabane, Eswatini
                [14 ]GRID grid.418187.3, ISNI 0000 0004 0493 9170, National and WHO Supranational Reference Center for Mycobacteria, , Research Center Borstel, ; Borstel, Germany
                [15 ]GRID grid.8991.9, ISNI 0000 0004 0425 469X, London School of Hygiene and Tropical Medicine, ; London, United Kingdom of Great Britain and Northern Ireland UK
                [16 ]GRID grid.13648.38, ISNI 0000 0001 2180 3484, Eppendorf, Institute of Medical Microbiology, Virology and Hygiene, , University Medical Center Hamburg, ; Hamburg, Germany
                [17 ]GRID grid.121334.6, ISNI 0000 0001 2097 0141, IRD UMI233/ INSERM U1175/Université de Montpellier, ; Montpellier, France
                [18 ]GRID grid.10598.35, ISNI 0000 0001 1014 6159, Biochemistry & Microbiology, School of Medicine, , University of Namibia, ; Windhoek, Namibia
                Author information
                http://orcid.org/0000-0002-6604-0684
                Article
                793
                10.1186/s13073-020-00793-8
                7687760
                33239092
                7dda57ed-790d-47ca-8091-435bb635021b
                © The Author(s) 2020

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 18 May 2020
                : 27 October 2020
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100000780, European Commission;
                Award ID: FP7-223681
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100001659, Deutsche Forschungsgemeinschaft;
                Award ID: EXC 2167
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100001664, Leibniz-Gemeinschaft;
                Award ID: EvoLung
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100002347, Bundesministerium für Bildung und Forschung;
                Award ID: DZIF
                Award Recipient :
                Categories
                Research
                Custom metadata
                © The Author(s) 2020

                Molecular medicine
                tuberculosis,multidrug resistance,resistance evolution,mdr outbreak strains,diagnostice escape,treatment escape,treatment failure

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