Chopra Ian
Antimicrobial Research Centre and Division of Microbiology, School of Biochemistry and Molecular Biology, University of Leeds, UK.
Drug Resist Updat. 2002 Jul-Aug;5(3-4):119-25. doi: 10.1016/s1368-7646(02)00051-1.
The tetracyclines, discovered in the 1940s, are a well-established class of antibiotics that still have a role in treating microbial infections in man. However, the widespread emergence of bacterial resistance due to efflux and ribosomal protection mechanisms has severely limited their effectiveness. A new generation of tetracyclines, the glycylcyclines, has been developed to overcome resistance to earlier tetracyclines. One of the new glycylcyclines, 9-t-butylglyclamido-minocycline (GAR-936, tigecycline) is currently undergoing clinical trials. This review considers the current status of glycylcyclines and the possibility that resistance to these agents might arise in the future. Other approaches are also being taken to address the emergence of resistance to tetracyclines. Recently, a number of tetracycline efflux pump inhibitors have been discovered that might be used in combination with earlier tetracyclines to restore their activity against resistant organisms. However, the development of tetracycline efflux pump inhibitors is complicated by the occurrence of several efflux pump sub-families and by the presence of both efflux and ribosomal protection mechanisms in the same organism, especially in naturally occurring, Gram-positive clinical isolates.
四环素于20世纪40年代被发现,是一类成熟的抗生素,在治疗人类微生物感染方面仍发挥着作用。然而,由于外排和核糖体保护机制导致的细菌耐药性广泛出现,严重限制了它们的有效性。为克服对早期四环素的耐药性,已研发出新一代四环素——甘氨酰环素。新型甘氨酰环素之一,9-叔丁基甘氨酰胺米诺环素(GAR-936,替加环素)目前正在进行临床试验。本文综述了甘氨酰环素的现状以及未来可能出现对这些药物耐药的可能性。还采取了其他方法来应对四环素耐药性的出现。最近,已发现多种四环素外排泵抑制剂,它们可能与早期四环素联合使用,以恢复其对耐药菌的活性。然而,四环素外排泵抑制剂的研发因存在多个外排泵亚家族以及同一生物体中同时存在外排和核糖体保护机制(尤其是在天然存在的革兰氏阳性临床分离株中)而变得复杂。