Postgenomic strategies in antibacterial drug discovery

被引:60
作者
Broetz-Oesterhelt, Heike [1 ]
Sass, Peter [2 ]
机构
[1] AiCuris, Wuppertal, Germany
[2] Univ Bonn, Pharmaceut Microbiol Sect, Inst Med Microbiol Immunol & Parasitol, D-5300 Bonn, Germany
关键词
antibiotic; development; drug discovery; genomics; natural product; rational design; resistance; screening; structure; target; RESISTANT STAPHYLOCOCCUS-AUREUS; CELL-WALL BIOSYNTHESIS; GRAM-POSITIVE BACTERIA; IN-VITRO ACTIVITY; INFECTIOUS-DISEASES-SOCIETY; PSEUDOMONAS-AERUGINOSA; STREPTOCOCCUS-PNEUMONIAE; DIHYDROFOLATE-REDUCTASE; NATURAL-PRODUCTS; BACILLUS-SUBTILIS;
D O I
10.2217/FMB.10.119
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
During the last decade the field of antibacterial drug discovery has changed in many aspects including bacterial organisms of primary interest, discovery strategies applied and pharmaceutical companies involved. Target-based high-throughput screening had been disappointingly unsuccessful for antibiotic research. Understanding of this lack of success has increased substantially and the lessons learned refer to characteristics of targets, screening libraries and screening strategies. The 'genomics' approach was replaced by a diverse array of discovery strategies, for example, searching for new natural product leads among previously abandoned compounds or new microbial sources, screening for synthetic inhibitors by targeted approaches including structure-based design and analyses of focused libraries and designing resistance-breaking properties into antibiotics of established classes. Furthermore, alternative treatment options are being pursued including anti-virulence strategies and immunotherapeutic approaches. This article summarizes the lessons learned from the genomics era and describes discovery strategies resulting from that knowledge.
引用
收藏
页码:1553 / 1579
页数:27
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