Persistent bacterial infections, antibiotic tolerance, and the oxidative stress response

被引:256
作者
Grant, Sarah Schmidt [1 ,2 ,3 ]
Hung, Deborah T. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Broad Inst MIT & Harvard, Cambridge, MA USA
[2] Brigham & Womens Hosp, Dept Med, Div Pulm & Crit Care Med, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Microbiol & Immunobiol, Boston, MA USA
[4] Massachusetts Gen Hosp, Dept Mol Biol, Boston, MA 02114 USA
[5] Massachusetts Gen Hosp, Ctr Computat & Integrat Biol, Boston, MA 02114 USA
关键词
persistent bacterial infections; antibiotic tolerance; persisters; oxidative stress; small colony variants; biofilms; SMALL-COLONY VARIANTS; UROPATHOGENIC ESCHERICHIA-COLI; MYCOBACTERIUM-TUBERCULOSIS PERSISTENCE; PNEUMONIAE BIOFILM RESISTANCE; URINARY-TRACT INFECTION; STAPHYLOCOCCUS-AUREUS; CYSTIC-FIBROSIS; PSEUDOMONAS-AERUGINOSA; STATIONARY-PHASE; INTRACELLULAR PERSISTENCE;
D O I
10.4161/viru.23987
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Certain bacterial pathogens are able to evade the host immune system and persist within the human host. The consequences of persistent bacterial infections potentially include increased morbidity and mortality from the infection itself as well as an increased risk of dissemination of disease. Eradication of persistent infections is difficult, often requiring prolonged or repeated courses of antibiotics. During persistent infections, a population or subpopulation of bacteria exists that is refractory to traditional antibiotics, possibly in a non-replicating or metabolically altered state. This review highlights the clinical significance of persistent infections and discusses different in vitro models used to investigate the altered physiology of bacteria during persistent infections. We specifically focus on recent work establishing increased protection against oxidative stress as a key element of the altered physiologic state across different in vitro models and pathogens.
引用
收藏
页码:273 / 283
页数:11
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