Bacterial Persister Cell Formation and Dormancy

被引:468
作者
Wood, Thomas K. [1 ,2 ]
Knabel, Stephen J. [3 ]
Kwan, Brian W. [1 ]
机构
[1] Penn State Univ, Dept Chem Engn, University Pk, PA 16802 USA
[2] Penn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USA
[3] Penn State Univ, Dept Food Sci, University Pk, PA 16802 USA
关键词
ESCHERICHIA-COLI BIOFILMS; GENERAL STRESS-RESPONSE; TOXIN-ANTITOXIN SYSTEMS; PSEUDOMONAS-AERUGINOSA; MULTIDRUG TOLERANCE; ANTIMICROBIAL PEPTIDES; ANTIBIOTIC TOLERANCE; RNA-POLYMERASE; MESSENGER-RNA; MECHANISMS;
D O I
10.1128/AEM.02636-13
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
Bacterial cells may escape the effects of antibiotics without undergoing genetic change; these cells are known as persisters. Unlike resistant cells that grow in the presence of antibiotics, persister cells do not grow in the presence of antibiotics. These persister cells are a small fraction of exponentially growing cells (due to carryover from the inoculum) but become a significant fraction in the stationary phase and in biofilms (up to 1%). Critically, persister cells may be a major cause of chronic infections. The mechanism of persister cell formation is not well understood, and even the metabolic state of these cells is debated. Here, we review studies relevant to the formation of persister cells and their metabolic state and conclude that the best model for persister cells is still dormancy, with the latest mechanistic studies shedding light on how cells reach this dormant state.
引用
收藏
页码:7116 / 7121
页数:6
相关论文
共 61 条
  • [1] An Escherichia coli chromosomal ''addiction module'' regulated by 3',5'-bispyrophosphate: A model for programmed bacterial cell death
    Aizenman, E
    EngelbergKulka, H
    Glaser, G
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (12) : 6059 - 6063
  • [2] Metabolite-enabled eradication of bacterial persisters by aminoglycosides
    Allison, Kyle R.
    Brynildsen, Mark P.
    Collins, James J.
    [J]. NATURE, 2011, 473 (7346) : 216 - +
  • [3] Metabolic Control of Persister Formation in Escherichia coli
    Amato, Stephanie M.
    Orman, Mehmet A.
    Brynildsen, Mark P.
    [J]. MOLECULAR CELL, 2013, 50 (04) : 475 - 487
  • [4] Escherichia coli MazF Leads to the Simultaneous Selective Synthesis of Both "Death Proteins'' and "Survival Proteins''
    Amitai, Shahar
    Kolodkin-Gal, Ilana
    Hananya-Meltabashi, Mirit
    Sacher, Ayelet
    Engelberg-Kulka, Hanna
    [J]. PLOS GENETICS, 2009, 5 (03):
  • [5] Bacterial persistence as a phenotypic switch
    Balaban, NQ
    Merrin, J
    Chait, R
    Kowalik, L
    Leibler, S
    [J]. SCIENCE, 2004, 305 (5690) : 1622 - 1625
  • [6] The bacterial signal indole increases epithelial-cell tight-junction resistance and attenuates indicators of inflammation
    Bansal, Tarun
    Alaniz, Robert C.
    Wood, Thomas K.
    Jayaraman, Arul
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (01) : 228 - 233
  • [7] Autoinducer 2 controls biofilm formation in Escherichia coli through a novel motility quorum-sensing regulator (MqsR, B3022)
    Barrios, AFG
    Zuo, RJ
    Hashimoto, Y
    Yang, L
    Bentley, WE
    Wood, TK
    [J]. JOURNAL OF BACTERIOLOGY, 2006, 188 (01) : 305 - 316
  • [8] Bigger JW, 1944, LANCET, V2, P497
  • [9] Three Dimensional Structure of the MqsR: MqsA Complex: A Novel TA Pair Comprised of a Toxin Homologous to RelE and an Antitoxin with Unique Properties
    Brown, Breann L.
    Grigoriu, Simina
    Kim, Younghoon
    Arruda, Jennifer M.
    Davenport, Andrew
    Wood, Thomas K.
    Peti, Wolfgang
    Page, Rebecca
    [J]. PLOS PATHOGENS, 2009, 5 (12):
  • [10] INFLUENCE OF GROWTH-RATE ON SUSCEPTIBILITY TO ANTIMICROBIAL AGENTS - MODIFICATION OF THE CELL-ENVELOPE AND BATCH AND CONTINUOUS CULTURE STUDIES
    BROWN, MRW
    COLLIER, PJ
    GILBERT, P
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1990, 34 (09) : 1623 - 1628