Endopeptidase-Mediated Beta Lactam Tolerance

被引:43
作者
Doerr, Tobias [1 ,2 ,3 ]
Davis, Brigid M. [1 ,2 ,3 ]
Waldor, Matthew K. [1 ,2 ,3 ]
机构
[1] Brigham & Womens Hosp, Div Infect Dis, Boston, MA 02115 USA
[2] Howard Hughes Med Inst, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Microbiol & Immunobiol, Boston, MA USA
关键词
BACTERIAL-CELL-WALL; D-AMINO ACIDS; ESCHERICHIA-COLI; PSEUDOMONAS-AERUGINOSA; PERSISTER CELLS; VIBRIO-CHOLERAE; PEPTIDOGLYCAN; SEPARATION; MUREIN; ANTIBIOTICS;
D O I
10.1371/journal.ppat.1004850
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In many bacteria, inhibition of cell wall synthesis leads to cell death and lysis. The pathways and enzymes that mediate cell lysis after exposure to cell wall-acting antibiotics (e.g. beta lactams) are incompletely understood, but the activities of enzymes that degrade the cell wall ('autolysins') are thought to be critical. Here, we report that Vibrio cholerae, the cholera pathogen, is tolerant to antibiotics targeting cell wall synthesis. In response to a wide variety of cell wall-acting antibiotics, this pathogen loses its rod shape, indicative of cell wall degradation, and becomes spherical. Genetic analyses revealed that paradoxically, V. cholerae survival via sphere formation required the activity of D,D endopeptidases, enzymes that cleave the cell wall. Other autolysins proved dispensable for this process. Our findings suggest the enzymes that mediate cell wall degradation are critical for determining bacterial cell fate - sphere formation vs. lysis - after treatment with antibiotics that target cell wall synthesis.
引用
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页数:16
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