A single upstream mutation of whiB7 underlies amikacin and clarithromycin resistance in Mycobacterium abscessus

被引:0
|
作者
De Boeck, Nathan [1 ,2 ,3 ]
Villellas, Cristina [3 ,4 ]
Crespo-Yuste, Estefania [4 ,5 ]
Gonzalo-Asensio, Jesus [4 ,5 ]
Buckley, Peter T. [3 ]
Thys, Kim [3 ]
Vuong, Cuong [3 ]
Lounis, Nacer [3 ]
Verstraeten, Natalie [1 ,2 ]
Michiels, Jan [1 ,2 ]
机构
[1] VIB KU Leuven, Ctr Microbiol, B-3001 Leuven, Belgium
[2] Katholieke Univ Leuven, Ctr Microbial & Plant Genet, B-3001 Leuven, Belgium
[3] Janssen Pharmaceut NV, Infect Dis Therapeut Area LLC, B-2340 Beerse, Belgium
[4] Univ Zaragoza, IIS Aragon, Fac Med, Grp Genet Micobacterias,Dept Microbiol, Zaragoza 50009, Spain
[5] Inst Salud Carlos III, CIBER Enfermedades Resp, Madrid 28029, Spain
关键词
Mycobacterium abscessus; amikacin; clarithromycin; whiB7; antimicrobial resistance; experimental evolution; 23S RIBOSOMAL-RNA; TUBERCULOSIS; TERMINATION; GENE; 16S;
D O I
10.1093/jambio/lxae286
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aims: We aimed to investigate the molecular mechanisms underlying the survival of Mycobacterium abscessus when faced with antibiotic combination therapy. By conducting evolution experiments and whole-genome sequencing (WGS), we sought to identify genetic variants associated with stress response mechanisms, with a particular focus on drug survival and resistance. Methods and results: We conducted evolution experiments on M. abscessus, exposing the bacteria to a combination therapy of amikacin and rifabutin. Genetic mutations associated with increased antibiotic survival and altered susceptibility were subsequently identified by WGS. We focused on mutations that contribute to stress response mechanisms and tolerance. Of particular interest was a novel frameshift mutation in MAB_3509c, a gene of unknown function within the upstream open reading frame of whiB7. A MAB_3509c knockout mutant was constructed, and expression of downstream drug resistance genes was assessed by RT-qPCR. Mutation of MAB_3509c results in increased RNA levels of whiB7and downstream stress response genes such as eis2, which is responsible for aminoglycoside resistance. Conclusion: Our findings demonstrate the importance of whiB7in the adaptive stress response in M. abscessus. Moreover, our results highlight the complexity of M. abscessus adapting to drug stress and underscore the need for further research. Impact Statement Interventional therapy options for Mycobacterium abscessus infections are severely limited, and antimicrobial resistance further restricts available treatments, leading to prolonged, poorly tolerated regimens with suboptimal outcomes. Here, we investigate a polymorphism in the upstream open reading frame of whiB7, which contributes to increased resistance in M. abscessus. Understanding the mechanisms behind WhiB7 induction offers novel insights into intrinsic resistance and may serve as a valuable tool in drug discovery.
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页数:13
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