依拉环素耐药机制的研究进展

Research progresson the mechanism of resistance to eravacycline

  • 摘要: 近年来泛耐药和全耐药临床分离株呈逐年递增的趋势,作为治疗多药耐药菌感染最后的选择之一的半合成四环素类药物替加环素的耐药性也随之出现,外排泵表达上调及质粒介导传播耐药基因等机制已被报道。依拉环素是一种人工合成构建四环结构的新型四环素类药物,可避免很多革兰阴性菌中经典四环素耐药基因的影响,并且具有较好的对病原体的体外抑制活性,但一些临床分离株对依拉环素的耐药性仍然是存在的。因此对依拉环素耐药性的发生发展机制进行全面的阐述是非常有必要的,以便在现有研究基础上对其做进一步的探究,帮助临床加强对依拉环素耐药的监测和防控以防止其耐药性的传播,并探索出对依拉环素耐药菌株感染更具针对性的治疗措施。

     

    Abstract: OBJECTIVE In recent years, extensively drug-resistant and pandrug-resistant strains isolated in the clinic have been increasing year by year. As one of the last choices for the treatment of multidrug-resistant bacterial infections, the drug resistance of the strains to tigecycline,which belongs to semi-synthetic tetracycline drug has also appeared. The mechanisms of up-regulation of efflux pumps and plasmid-mediated transmission of drug resistance genes have been reported. Eravacycline is a new type of tetracycline drug containing a tetracyclic structure which is artificially synthesized. It can avoid the influence of classical drug resistance genes to tetracycline in many gram-negative bacteria, and has good inhibitory activity against pathogens in vitro. However, some strains are still drug-resistant to eravacycline. Therefore, it is very necessary to comprehensively elaborate the occurrence mechanism of the drug resistance to eravacycline for the further study. Clinical monitoring should be strengthened to control the spread of drug-resistant strains to eravacycline, and more targeted treatment of the infection should be administered.

     

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