首页> 美国卫生研究院文献>Antimicrobial Agents and Chemotherapy >Old Drugs To Treat Resistant Bugs: Methicillin-Resistant Staphylococcus aureus Isolates with mecC Are Susceptible to a Combination of Penicillin and Clavulanic Acid
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Old Drugs To Treat Resistant Bugs: Methicillin-Resistant Staphylococcus aureus Isolates with mecC Are Susceptible to a Combination of Penicillin and Clavulanic Acid

机译:用于治疗抗药性细菌的旧药:耐甲氧西林金黄色葡萄球菌与mecC的分离株易受青霉素和克拉维酸的联合使用

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摘要

β-Lactam resistance in methicillin-resistant Staphylococcus aureus (MRSA) is mediated by the expression of an alternative penicillin-binding protein 2a (PBP2a) (encoded by mecA) with a low affinity for β-lactam antibiotics. Recently, a novel variant of mecA, known as mecC, was identified in MRSA isolates from both humans and animals. In this study, we demonstrate that mecC-encoded PBP2c does not mediate resistance to penicillin. Rather, broad-spectrum β-lactam resistance in MRSA strains carrying mecC (mecC-MRSA strains) is mediated by a combination of both PBP2c and the distinct β-lactamase encoded by the blaZ gene of strain LGA251 (blaZLGA251), which is part of mecC-encoding staphylococcal cassette chromosome mec (SCCmec) type XI. We further demonstrate that mecC-MRSA strains are susceptible to the combination of penicillin and the β-lactam inhibitor clavulanic acid in vitro and that the same combination is effective in vivo for the treatment of experimental mecC-MRSA infection in wax moth larvae. Thus, we demonstrate how the distinct biological differences between mecA- and mecC-encoded PBP2a and PBP2c have the potential to be exploited as a novel approach for the treatment of mecC-MRSA infections.
机译:耐甲氧西林金黄色葡萄球菌(MRSA)中的β-内酰胺耐药性是由对青霉素结合蛋白2a(PBP2a)(由mecA编码)的表达介导的,该蛋白对β-内酰胺抗生素的亲和力低。最近,在来自人类和动物的MRSA分离物中鉴定出一种称为mecC的新型mecA变体。在这项研究中,我们证明mecC编码的PBP2c不会介导对青霉素的抗性。相反,携带mecC的MRSA菌株(mecC-MRSA菌株)的广谱β-内酰胺抗性是由PBP2c和LGA251菌株blaZ基因(blaZLGA251)编码的独特β-内酰胺酶的组合介导的mecC编码葡萄球菌盒式染色体mec(SCCmec)XI型。我们进一步证明了mecC-MRSA菌株在体外对青霉素和β-内酰胺抑制剂克拉维酸的组合敏感,并且该组合在体内对蜡蛾幼虫的实验性mecC-MRSA感染的治疗有效。因此,我们证明了 mecA -和 mecC 编码的PBP2a和PBP2c之间的独特生物学差异如何有可能被开发为治疗的新方法mecC -MRSA感染。

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