Vancomycin-resistant enterococci exploit antibiotic-induced innate immune deficits

被引:513
作者
Brandl, Katharina [1 ]
Plitas, George [2 ]
Mihu, Coralia N. [1 ]
Ubeda, Carles [1 ]
Jia, Ting [1 ]
Fleisher, Martin [3 ]
Schnabl, Bernd [4 ]
DeMatteo, Ronald P. [2 ]
Pamer, Eric G. [1 ,3 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Infect Dis Serv, Dept Med, Program Immunol,Sloan Kettering Inst, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Hepatobiliary Serv, New York, NY 10021 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Clin Labs, New York, NY 10021 USA
[4] Columbia Univ, Dept Med, New York, NY 10032 USA
关键词
D O I
10.1038/nature07250
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Infection with antibiotic- resistant bacteria, such as vancomycin-resistant Enterococcus ( VRE), is a dangerous and costly complication of broad- spectrum antibiotic therapy(1,2). How antibiotic-mediated elimination of commensal bacteria promotes infection by antibiotic- resistant bacteria is a fertile area for speculation with few defined mechanisms. Here we demonstrate that antibiotic treatment of mice notably downregulates intestinal expression of RegIII gamma ( also known as Reg3g), a secreted C- type lectin that kills Gram- positive bacteria, including VRE. Downregulation of RegIII gamma markedly decreases in vivo killing of VRE in the intestine of antibiotic- treated mice. Stimulation of intestinal Toll- like receptor 4 by oral administration of lipopolysaccharide re-induces RegIII gamma, thereby boosting innate immune resistance of antibiotic-treated mice against VRE. Compromised mucosal innate immune defence, as induced by broad- spectrum antibiotic therapy, can be corrected by selectively stimulating mucosal epithelial Toll- like receptors, providing a potential therapeutic approach to reduce colonization and infection by antibiotic- resistant microbes.
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收藏
页码:804 / U8
页数:5
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