Environmental, mechanistic and evolutionary landscape of antibiotic persistence

被引:24
作者
Bollen, Celien [1 ,2 ]
Louwagie, Elen [1 ,2 ]
Verstraeten, Natalie [1 ,2 ]
Michiels, Jan [1 ,2 ]
Ruelens, Philip [1 ,2 ,3 ]
机构
[1] Katholieke Univ Leuven, Ctr Microbial & Plant Genet, Leuven, Belgium
[2] Ctr Microbiol VIB, Leuven, Belgium
[3] Katholieke Univ Leuven, Lab Socioecol & Social Evolut, Leuven, Belgium
关键词
antibiotic persistence; evolution; persistent infections; persister recovery; tolerance; ESCHERICHIA-COLI; PSEUDOMONAS-AERUGINOSA; MYCOBACTERIUM-TUBERCULOSIS; DRUG TOLERANCE; STAPHYLOCOCCUS-AUREUS; PHENOTYPIC HETEROGENEITY; BACTERIAL PERSISTENCE; CONTROLLED EXPRESSION; GENE-EXPRESSION; DNA GYRASE;
D O I
10.15252/embr.202357309
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recalcitrant infections pose a serious challenge by prolonging antibiotic therapies and contributing to the spread of antibiotic resistance, thereby threatening the successful treatment of bacterial infections. One potential contributing factor in persistent infections is antibiotic persistence, which involves the survival of transiently tolerant subpopulations of bacteria. This review summarizes the current understanding of antibiotic persistence, including its clinical significance and the environmental and evolutionary factors at play. Additionally, we discuss the emerging concept of persister regrowth and potential strategies to combat persister cells. Recent advances highlight the multifaceted nature of persistence, which is controlled by deterministic and stochastic elements and shaped by genetic and environmental factors. To translate in vitro findings to in vivo settings, it is crucial to include the heterogeneity and complexity of bacterial populations in natural environments. As researchers continue to gain a more holistic understanding of this phenomenon and develop effective treatments for persistent bacterial infections, the study of antibiotic persistence is likely to become increasingly complex.
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页数:16
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共 220 条
[1]   A functional perspective on phenotypic heterogeneity in microorganisms [J].
Ackermann, Martin .
NATURE REVIEWS MICROBIOLOGY, 2015, 13 (08) :497-508
[2]   Drug Tolerance in Replicating Mycobacteria Mediated by a Macrophage-Induced Efflux Mechanism [J].
Adams, Kristin N. ;
Takaki, Kevin ;
Connolly, Lynn E. ;
Wiedenhoft, Heather ;
Winglee, Kathryn ;
Humbert, Olivier ;
Edelstein, Paul H. ;
Cosma, Christine L. ;
Ramakrishnan, Lalita .
CELL, 2011, 145 (01) :39-53
[3]   Stationary phase persister formation in Escherichia coli can be suppressed by piperacillin and PBP3 inhibition [J].
Aedo, Sandra J. ;
Orman, Mehmet A. ;
Brynildsen, Mark P. .
BMC MICROBIOLOGY, 2019, 19 (1)
[4]   RecA Inhibitors Potentiate Antibiotic Activity and Block Evolution of Antibiotic Resistance [J].
Alam, Md Kausar ;
Alhhazmi, Areej ;
DeCoteau, John F. ;
Luo, Yu ;
Geyer, C. Ronald .
CELL CHEMICAL BIOLOGY, 2016, 23 (03) :381-391
[5]   In-depth Profiling of MvfR-Regulated Small Molecules in Pseudomonas aeruginosa after Quorum Sensing Inhibitor Treatment [J].
Allegretta, Giuseppe ;
Maurer, Christine K. ;
Eberhard, Jens ;
Maura, Damien ;
Hartmann, Rolf W. ;
Rahme, Laurence ;
Empting, Martin .
FRONTIERS IN MICROBIOLOGY, 2017, 8
[6]   Metabolite-enabled eradication of bacterial persisters by aminoglycosides [J].
Allison, Kyle R. ;
Brynildsen, Mark P. ;
Collins, James J. .
NATURE, 2011, 473 (7346) :216-+
[7]   Persister Heterogeneity Arising from a Single Metabolic Stress [J].
Amato, Stephanie M. ;
Brynildsen, Mark P. .
CURRENT BIOLOGY, 2015, 25 (16) :2090-2098
[8]   Metabolic Control of Persister Formation in Escherichia coli [J].
Amato, Stephanie M. ;
Orman, Mehmet A. ;
Brynildsen, Mark P. .
MOLECULAR CELL, 2013, 50 (04) :475-487
[9]   Host subversion by formation of intracellular bacterial communities in the urinary tract [J].
Anderson, GG ;
Martin, SM ;
Hultgren, SJ .
MICROBES AND INFECTION, 2004, 6 (12) :1094-1101
[10]   Microbial cell individuality and the underlying sources of heterogeneity [J].
Avery, Simon V. .
NATURE REVIEWS MICROBIOLOGY, 2006, 4 (08) :577-587