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      Rifabutin Is Active against Mycobacterium abscessus Complex

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          ABSTRACT

          Lung infections caused by Mycobacterium abscessus are emerging as a global threat to individuals with cystic fibrosis and to other patient groups. Recent evidence for human-to-human transmission worsens the situation. M. abscessus is an intrinsically multidrug-resistant pathogen showing resistance to even standard antituberculosis drugs, such as rifampin. Here, our objective was to identify existing drugs that may be employed for the treatment of M. abscessus lung disease. A collection of more than 2,700 approved drugs was screened at a single-point concentration against an M. abscessus clinical isolate. Hits were confirmed with fresh solids in dose-response experiments. For the most attractive hit, growth inhibition and bactericidal activities against reference strains of the three M. abscessus subspecies and a collection of clinical isolates were determined. Surprisingly, the rifampin derivative rifabutin had MICs of 3 ± 2 μM (3 μg/ml) against the screening strain, the reference strains M. abscessus subsp. abscessus ATCC 19977, M. abscessus subsp. bolletii CCUG 50184-T, and M. abscessus subsp. massiliense CCUG 48898-T, as well as against a collection of clinical isolates. Furthermore, rifabutin was active against clarithromycin-resistant strains. In conclusion, rifabutin, in contrast to rifampin, is active against the Mycobacterium abscessus complex bacteria in vitro and may be considered for treatment of M. abscessus lung disease.

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          A novel gene, erm(41), confers inducible macrolide resistance to clinical isolates of Mycobacterium abscessus but is absent from Mycobacterium chelonae.

          Mycobacterium abscessus infections tend to respond poorly to macrolide-based chemotherapy, even though the organisms appear to be susceptible to clarithromycin. Circumstantial evidence suggested that at least some M. abscessus isolates might be inducibly resistant to macrolides. Thus, the purpose of this study was to investigate the macrolide phenotype of M. abscessus clinical isolates. Inducible resistance to clarithromycin (MIC > 32 microg/ml) was found for 7 of 10 clinical isolates of M. abscessus previously considered susceptible; the remaining 3 isolates were deemed to be susceptible (MIC
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            Mycobacterium abscessus Complex Infections in Humans

            New treatments, rapid and inexpensive identification methods, and measures to contain nosocomial transmission and outbreaks are urgently needed.
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              Antimicrobial susceptibility testing, drug resistance mechanisms, and therapy of infections with nontuberculous mycobacteria.

              Within the past 10 years, treatment and diagnostic guidelines for nontuberculous mycobacteria have been recommended by the American Thoracic Society (ATS) and the Infectious Diseases Society of America (IDSA). Moreover, the Clinical and Laboratory Standards Institute (CLSI) has published and recently (in 2011) updated recommendations including suggested antimicrobial and susceptibility breakpoints. The CLSI has also recommended the broth microdilution method as the gold standard for laboratories performing antimicrobial susceptibility testing of nontuberculous mycobacteria. This article reviews the laboratory, diagnostic, and treatment guidelines together with established and probable drug resistance mechanisms of the nontuberculous mycobacteria.
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                Author and article information

                Journal
                Antimicrob Agents Chemother
                Antimicrob. Agents Chemother
                aac
                aac
                AAC
                Antimicrobial Agents and Chemotherapy
                American Society for Microbiology (1752 N St., N.W., Washington, DC )
                0066-4804
                1098-6596
                10 April 2017
                24 May 2017
                June 2017
                24 May 2017
                : 61
                : 6
                : e00155-17
                Affiliations
                [a ]Department of Microbiology and Immunology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore
                [b ]Department of Laboratory Medicine, National University Hospital, Singapore
                [c ]Public Health Research Institute, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, New Jersey, USA
                Author notes
                Address correspondence to Thomas Dick, td367@ 123456njms.rutgers.edu .

                Citation Aziz DB, Low JL, Wu M-L, Gengenbacher M, Teo JWP, Dartois V, Dick T. 2017. Rifabutin is active against Mycobacterium abscessus complex. Antimicrob Agents Chemother 61:e00155-17. https://doi.org/10.1128/AAC.00155-17.

                Author information
                http://orcid.org/0000-0002-9321-3341
                http://orcid.org/0000-0002-9604-9452
                Article
                00155-17
                10.1128/AAC.00155-17
                5444174
                28396540
                e1691b41-9263-457f-98de-fe34c13df7d8
                Copyright © 2017 Aziz et al.

                This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.

                History
                : 24 January 2017
                : 19 March 2017
                : 31 March 2017
                Page count
                Figures: 2, Tables: 4, Equations: 0, References: 64, Pages: 10, Words: 7080
                Funding
                Funded by: MOH | National Medical Research Council (NMRC) https://doi.org/10.13039/501100001349
                Award ID: NMRC/TCR/011-NUHS/2014
                Award Recipient : Thomas Dick
                Categories
                Susceptibility
                Custom metadata
                June 2017

                Infectious disease & Microbiology
                mycobacterium abscessus,ntm,rifabutin,repurposing
                Infectious disease & Microbiology
                mycobacterium abscessus, ntm, rifabutin, repurposing

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