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Mechanisms of Antibiotic Tolerance in Mycobacterium avium Complex: Lessons From Related Mycobacteria
- Source :
- Frontiers in Microbiology, Vol 11 (2020)
- Publication Year :
- 2020
- Publisher :
- Frontiers Media SA, 2020.
-
Abstract
- Mycobacterium avium complex (MAC) species are the most commonly isolated nontuberculous mycobacteria to cause pulmonary infections worldwide. The lengthy and complicated therapy required to cure lung disease due to MAC is at least in part due to the phenomenon of antibiotic tolerance. In this review, we will define antibiotic tolerance and contrast it with persistence and antibiotic resistance. We will discuss physiologically relevant stress conditions that induce altered metabolism and antibiotic tolerance in mycobacteria. Next, we will review general molecular mechanisms underlying bacterial antibiotic tolerance, particularly those described for MAC and related mycobacteria, including Mycobacterium tuberculosis, with a focus on genes containing significant sequence homology in MAC. An improved understanding of antibiotic tolerance mechanisms can lay the foundation for novel approaches to target antibiotic-tolerant mycobacteria, with the goal of shortening the duration of curative treatment and improving survival in patients with MAC.
- Subjects :
- Microbiology (medical)
Tuberculosis
Multidrug tolerance
antibiotic tolerance
lcsh:QR1-502
macrophage
Microbiology
lcsh:Microbiology
Mycobacterium tuberculosis
models
03 medical and health sciences
Antibiotic resistance
medicine
Mycobacterium avium complex
030304 developmental biology
0303 health sciences
biology
030306 microbiology
business.industry
persistence
biology.organism_classification
medicine.disease
tuberculosis
Lung disease
Nontuberculous mycobacteria
Stress conditions
business
Mycobacterium avium
Subjects
Details
- ISSN :
- 1664302X
- Volume :
- 11
- Database :
- OpenAIRE
- Journal :
- Frontiers in Microbiology
- Accession number :
- edsair.doi.dedup.....7081aa0e405765fa42a5813e7d5287de
- Full Text :
- https://doi.org/10.3389/fmicb.2020.573983