Learning from bacterial competition in the host to develop antimicrobials

被引:93
作者
Raffatellu, Manuela [1 ,2 ,3 ,4 ]
机构
[1] Univ Calif Irvine, Dept Microbiol & Mol Genet, Irvine, CA 92717 USA
[2] Univ Calif San Diego, Dept Pediat, Div Host Microbe Syst & Therapeut, La Jolla, CA 92093 USA
[3] Chiba Univ Univ Calif San Diego Ctr Mucosal Immun, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Ctr Microbiome Innovat, La Jolla, CA 92093 USA
关键词
CARBAPENEM-RESISTANT ENTEROBACTERIACEAE; PSEUDOMONAS-AERUGINOSA; GUT MICROBIOTA; STAPHYLOCOCCUS-AUREUS; ESCHERICHIA-COLI; COLONIZATION RESISTANCE; ANTIBACTERIAL ACTIVITY; CLOSTRIDIUM-DIFFICILE; SIDEROPHORE CEPHALOSPORIN; INTESTINAL COLONIZATION;
D O I
10.1038/s41591-018-0145-0
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
In recent years, the alarming increase of antibiotic resistance, compounded by the simultaneous decrease in development of new antibiotics, has created serious concerns for public health. Moreover, current antibiotics also target the beneficial commensal microbes (microbiota) that inhabit our body, sometimes with significant health consequences. The answer to the antibiotic crisis thus involves broad, creative efforts to develop new treatments for infectious agents. Here I discuss what can be learned from investigating microbial competition in vivo and how this knowledge can be utilized to devise new narrow-spectrum therapeutics that target bacterial pathogens while minimizing deleterious effects to the microbiota.
引用
收藏
页码:1097 / 1103
页数:7
相关论文
共 110 条
[1]   Clostridium difficile colitis: pathogenesis and host defence [J].
Abt, Michael C. ;
McKenney, Peter T. ;
Pamer, Eric G. .
NATURE REVIEWS MICROBIOLOGY, 2016, 14 (10) :609-620
[2]  
Alteri CJ, 2016, VIRULENCE MECH BACTE, V4, P337
[3]   The antibiotic alarm [J].
不详 .
NATURE, 2013, 495 (7440) :141-141
[4]  
[Anonymous], 2001, Expert Consultation on Energy in Human Nutrition. Interim Report
[5]  
[Anonymous], 2017, WHO | Global priority list of antibiotic-resistant bacteria to guide research, discovery, and development of new antibiotics
[6]   Contact-dependent inhibition of growth in Escherichia coli [J].
Aoki, SK ;
Pamma, R ;
Hernday, AD ;
Bickham, JE ;
Braaten, BA ;
Low, DA .
SCIENCE, 2005, 309 (5738) :1245-1248
[7]   A widespread family of polymorphic contact-dependent toxin delivery systems in bacteria [J].
Aoki, Stephanie K. ;
Diner, Elie J. ;
de Roodenbeke, Claire t'Kint ;
Burgess, Brandt R. ;
Poole, Stephen J. ;
Braaten, Bruce A. ;
Jones, Allison M. ;
Webb, Julia S. ;
Hayes, Christopher S. ;
Cotter, Peggy A. ;
Low, David A. .
NATURE, 2010, 468 (7322) :439-442
[8]   NEW FAMILY OF LOW-MOLECULAR WEIGHT ANTIBIOTICS FROM ENTEROBACTERIA [J].
ASENSIO, C ;
PEREZDIAZ, JC ;
MARTINEZ, MC ;
BAQUERO, F .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1976, 69 (01) :7-14
[9]  
BAQUERO F, 1984, FEMS MICROBIOL LETT, V23, P117
[10]   The Cytokine IL-22 Promotes Pathogen Colonization by Suppressing Related Commensal Bacteria [J].
Behnsen, Judith ;
Jellbauer, Stefan ;
Wong, Christina P. ;
Edwards, Robert A. ;
George, Michael D. ;
Ouyang, Wenjun ;
Raffatellu, Manuela .
IMMUNITY, 2014, 40 (02) :262-273