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Mechanisms of antimicrobial resistance in Serratia marcescens

机译:粘质沙雷氏菌的抗药性机制

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Serratia marcescens, one of the Enterobacteriaceae, was considered originally to be non-pathogenic. But in recent decades, nosocomial infections caused by this organism are often hard to treat because of both the intrinsic resistance of this species and its abilities to acquire further resistance to multiple groups of antimicrobial agents, including?β-lactams, aminoglycosides and fluoroquinolones.?S. marcescens?have their own ways to become resistant in common with other Enterobacteriaceae: production of?β-lactamasesincluding extended-spectrum β-lactamases, AmpC-type cephalosporinase and carbapenemases; diminished outer membrane permeability;?modification of the target site-PBPs; overexpression of active efflux systems; synthesis of aminoglycoside-modifying enzymes; and structural alterations of?the GyrA protein. This review will show a brief history, the virulence factors and the known resistance mechanisms to the most frequently administrated?antimicrobial agents:?β-lactams, aminoglycosides and fluoroquinolones in?S. marcescens.
机译:粘质沙雷氏菌是肠杆菌科之一,最初被认为是非致病性的。但是在最近几十年中,由于该生物的内在抗性及其对包括β-内酰胺类,氨基糖苷类和氟喹诺酮类在内的多种抗菌剂的进一步抗性的能力,常常难以治疗由该生物体引起的医院感染。 S.粘菌具有与其他肠杆菌科一样的抗药性:产生β-内酰胺酶,包括广谱β-内酰胺酶,AmpC型头孢菌素酶和碳青霉烯酶;外膜通透性降低;靶位点-PBP的修饰;主动外排系统的过表达;氨基糖苷修饰酶的合成;和GyrA蛋白的结构改变。这篇综述将简要介绍病史,毒力因子和已知的对最常用的抗菌剂:β-内酰胺,氨基糖苷类和氟喹诺酮类药物的耐药机制。 marcescens。

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