Variability of <i>Mycobacterium avium</i> Complex Isolates Drug Susceptibility Testing by Broth Microdilution

Non-tuberculous mycobacteria are widely distributed in environments and are capable of infecting humans, particularly those with a compromised immune system. The most prevalent species that cause nontuberculous mycobacterial lung diseases are slow-growing bacteria from the <i>Mycobacterium avi...

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Main Author: Danila Zimenkov (Author)
Format: Book
Published: MDPI AG, 2022-12-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Danila Zimenkov  |e author 
245 0 0 |a Variability of <i>Mycobacterium avium</i> Complex Isolates Drug Susceptibility Testing by Broth Microdilution 
260 |b MDPI AG,   |c 2022-12-01T00:00:00Z. 
500 |a 10.3390/antibiotics11121756 
500 |a 2079-6382 
520 |a Non-tuberculous mycobacteria are widely distributed in environments and are capable of infecting humans, particularly those with a compromised immune system. The most prevalent species that cause nontuberculous mycobacterial lung diseases are slow-growing bacteria from the <i>Mycobacterium avium</i> complex (MAC), mainly <i>M. avium</i> or <i>M. intracellulare</i>. The key treatment of MAC infections includes macrolides, ethambutol, and rifampicin; however, the therapy outcomes are unsatisfactory. Phenotypic drug susceptibility testing is a conditional recommendation prior to treatment, and critical concentrations for clarithromycin, amikacin, moxifloxacin, and linezolid have been established. In this review, data from studies on the determination of MIC of clinical isolates using the broth microdilution method were summarized. A significant variation in the MIC distributions from different studies was found. The main reasons could impact the findings: insufficient reproducibility of the phenotypic testing and variation in species lineages identified in different laboratories, which could have various intrinsic susceptibility to drugs. For most of the drugs analyzed, the MICs are too high, which could undermine the treatment efficiency. Further improvement of treatment outcomes demands the validation of microbiological resistance criteria together with the identification of molecular mechanisms of resistance. 
546 |a EN 
690 |a nontuberculous mycobacteria 
690 |a avium 
690 |a intracellular 
690 |a MAC complex 
690 |a resistance 
690 |a MIC 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Antibiotics, Vol 11, Iss 12, p 1756 (2022) 
787 0 |n https://www.mdpi.com/2079-6382/11/12/1756 
787 0 |n https://doaj.org/toc/2079-6382 
856 4 1 |u https://doaj.org/article/c578e5ca2a5845f7a9652e9d006b6fd9  |z Connect to this object online.