抗生素
微生物学
多粘菌素
抗菌剂
达托霉素
细菌细胞结构
多粘菌素B
多重耐药
抗生素耐药性
生物
肽聚糖
磷霉素
细菌
革兰氏阴性菌
致病菌
金黄色葡萄球菌
万古霉素
生物化学
大肠杆菌
基因
遗传学
出处
期刊:Revue Scientifique Et Technique De L Office International Des Epizooties
[O.I.E (World Organisation for Animal Health)]
日期:2012-04-01
卷期号:31 (1): 43-56
被引量:74
标识
DOI:10.20506/rst.31.1.2096
摘要
Antimicrobial agents that target the bacterial cell wall or cell membrane have been used effectively for the past 70 years. Among the agents that inhibit bacterial cell wall synthesis, the beta-lactam antibiotics have emerged into broad-spectrum agents that inhibit most pathogenic bacteria, but are now being threatened by the rapid spread of drug-inactivating beta-lactamases. Glycopeptides still retain high activity against staphylococci, but resistance among the enterococci has become a major problem. Recently, fosfomycin has been used in the treatment of multidrug-resistant Gram-negative bacteria. Daptomycin, which targets both membrane function and peptidoglycan synthesis, is especially effective in treating staphylococcal infections. The polymyxin antibiotics that target cell membranes are being used more frequently to treat multidrug-resistant Gram-negative infections. The ionophore antibiotics, used in veterinary medicine, target membranes in many microbial and animal species. Although increasing resistance is a continuing concern, these classes of bactericidal agents can provide highly effective antibiotics.
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