On the in vivo significance of bacterial resistance to antimicrobial peptides

被引:51
作者
Bauer, Margaret E. [1 ]
Shafer, William M. [2 ,3 ]
机构
[1] Indiana Univ Sch Med, Dept Microbiol & Immunol, Indianapolis, IN 46254 USA
[2] Vet Affairs Med Ctr, Labs Bacterial Pathogenesis, Decatur, GA 30033 USA
[3] Emory Univ, Sch Med, Dept Microbiol & Immunol, Atlanta, GA 30322 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2015年 / 1848卷 / 11期
关键词
Antimicrobial peptides; Cell envelope modifications; In vivo models; Pathogenesis; Resistance mechanisms; Transporters; NONTYPABLE HAEMOPHILUS-INFLUENZAE; ENTERICA SEROVAR TYPHIMURIUM; COMMON PATHOGENIC BACTERIA; ALANYL-LIPOTEICHOIC ACID; NEISSERIA-GONORRHOEAE; STAPHYLOCOCCUS-AUREUS; CONFERS RESISTANCE; YERSINIA-PESTIS; SAP TRANSPORTER; PHOSPHOETHANOLAMINE MODIFICATION;
D O I
10.1016/j.bbamem.2015.02.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Antimicrobial peptides (AMPs) are at the front-line of host defense during infection and play critical roles both in reducing the microbial load early during infection and in linking innate to adaptive immunity. However, successful pathogens have developed mechanisms to resist AMPs. Although considerable progress has been made in elucidating AMP-resistance mechanisms of pathogenic bacteria in vitro, less is known regarding the in vivo significance of such resistance. Nevertheless, progress has been made in this area, largely by using murine models and, in two instances, human models of infection. Herein, we review progress on the use of in vivo infection models in AMP research and discuss the AMP resistance mechanisms that have been established by in vivo studies to contribute to microbial infection. We posit that in vivo infection models are essential tools for investigators to understand the significance to pathogenesis of genetic changes that impact levels of bacterial susceptibility to AMPs. This article is part of a Special Issue entitled: Bacterial Resistance to Antimicrobial Peptides. Published by Elsevier B.V.
引用
收藏
页码:3101 / 3111
页数:11
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