Thinking Outside the Bug: Molecular Targets and Strategies to Overcome Antibiotic Resistance

被引:65
作者
Monserrat-Martinez, Ana [1 ,2 ]
Gambin, Yann [1 ,2 ]
Sierecki, Emma [1 ,2 ]
机构
[1] European Mol Biol Lab Australia EMBL Australia No, Sydney, NSW 2031, Australia
[2] Univ New South Wales, Sch Med Sci, Sydney, NSW 2031, Australia
基金
澳大利亚研究理事会; 英国医学研究理事会;
关键词
antibiotic resistance; host-pathogen interactions; bacterial effectors; protein-protein interactions; antimicrobial peptides and proteins; ANTIMICROBIAL PEPTIDE LL-37; QUORUM-SENSING SIGNAL; HOST-PATHOGEN INTERACTIONS; RECEPTOR-HISTIDINE KINASE; CELL-DEATH; STAPHYLOCOCCUS-AUREUS; COMBINATORIAL CHEMISTRY; SHIGELLA-FLEXNERI; DNA GYRASE; YERSINIA-PSEUDOTUBERCULOSIS;
D O I
10.3390/ijms20061255
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
Since their discovery in the early 20th century, antibiotics have been used as the primary weapon against bacterial infections. Due to their prophylactic effect, they are also used as part of the cocktail of drugs given to treat complex diseases such as cancer or during surgery, in order to prevent infection. This has resulted in a decrease of mortality from infectious diseases and an increase in life expectancy in the last 100 years. However, as a consequence of administering antibiotics broadly to the population and sometimes misusing them, antibiotic-resistant bacteria have appeared. The emergence of resistant strains is a global health threat to humanity. Highly-resistant bacteria like Staphylococcus aureus (methicillin-resistant) or Enterococcus faecium (vancomycin-resistant) have led to complications in intensive care units, increasing medical costs and putting patient lives at risk. The appearance of these resistant strains together with the difficulty in finding new antimicrobials has alarmed the scientific community. Most of the strategies currently employed to develop new antibiotics point towards novel approaches for drug design based on prodrugs or rational design of new molecules. However, targeting crucial bacterial processes by these means will keep creating evolutionary pressure towards drug resistance. In this review, we discuss antibiotic resistance and new options for antibiotic discovery, focusing in particular on new alternatives aiming to disarm the bacteria or empower the host to avoid disease onset.
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页数:23
相关论文
共 186 条
[1]   Mechanisms of cell death induced by the neutrophil antimicrobial peptides α-defensins and LL-37 [J].
Aarbiou, J ;
Tjabringa, GS ;
Verhoosel, RM ;
Ninaber, DK ;
White, SR ;
Peltenburg, LTC ;
Rabe, KF ;
Hiemstra, PS .
INFLAMMATION RESEARCH, 2006, 55 (03) :119-127
[2]   Integrating research and development: the emergence of retional drug design in the pharmaceutical industry [J].
Adam, Matthias .
STUDIES IN HISTORY AND PHILOSOPHY OF SCIENCE PART C-STUDIES IN HISTORY AND PHILOSOPHY OF BIOLOGICAL AND BIOMEDIAL SCIENCES, 2005, 36 (03) :513-537
[3]   ISOLATION OF 3 ANTIBACTERIAL PEPTIDES FROM PIG INTESTINE - GASTRIC-INHIBITORY POLYPEPTIDE(7-42), DIAZEPAM-BINDING INHIBITOR(32-86) AND A NOVEL FACTOR, PEPTIDE-3910 [J].
AGERBERTH, B ;
BOMAN, A ;
ANDERSSON, M ;
JORNVALL, H ;
MUTT, V ;
BOMAN, HG .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1993, 216 (02) :623-629
[4]   YopH of Yersinia pseudotuberculosis interrupts early phosphotyrosine signalling associated with phagocytosis [J].
Andersson, K ;
Carballeira, N ;
Magnusson, KE ;
Persson, C ;
Stendahl, O ;
WolfWatz, H ;
Fallman, M .
MOLECULAR MICROBIOLOGY, 1996, 20 (05) :1057-1069
[5]  
[Anonymous], M100S22 CLSI
[6]  
[Anonymous], P NATL ACAD SCI US
[7]  
[Anonymous], UN AMP SOD SULB SOD
[8]  
[Anonymous], EMACHMP3016072011
[9]  
[Anonymous], 2016, MODERN IND MICROBIOL
[10]  
[Anonymous], 1996, MED MICROBIOLOGY