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低剂量β-内酰胺类抗生素诱导耐甲氧西林金黄色葡萄球菌生物膜的形成:特异性、普遍性和剂量反应效应。

Induction of MRSA Biofilm by Low-Dose β-Lactam Antibiotics: Specificity, Prevalence and Dose-Response Effects.

机构信息

Department of Biology, American University, Washington DC, USA.

Division of Infectious Diseases, Department of Medicine, The George Washington University, Washington DC, USA.

出版信息

Dose Response. 2013 Jul 25;12(1):152-61. doi: 10.2203/dose-response.13-021.Kaplan. eCollection 2014 Jan.

Abstract

Methicillin-resistant Staphylococcus aureus (MRSA) is a leading cause of hospital- and community-associated infections. The formation of adherent clusters of cells known as biofilms is an important virulence factor in MRSA pathogenesis. Previous studies showed that subminimal inhibitory (sub-MIC) concentrations of methicillin induce biofilm formation in the community-associated MRSA strain LAC. In this study we measured the ability sub-MIC concentrations of eight other β-lactam antibiotics and six non-β-lactam antibiotics to induce LAC biofilm. All eight β-lactam antibiotics, but none of the non-β-lactam antibiotics, induced LAC biofilm. The dose-response effects of the eight β-lactam antibiotics on LAC biofilm varied from biphasic and bimodal to near-linear. We also found that sub-MIC methicillin induced biofilm in 33 out of 39 additional MRSA clinical isolates, which also exhibited biphasic, bimodal and linear dose-response curves. The amount of biofilm formation induced by sub-MIC methicillin was inversely proportional to the susceptibility of each strain to methicillin. Our results demonstrate that induction of biofilm by sub-MIC antibiotics is a common phenotype among MRSA clinical strains and is specific for β-lactam antibiotics. These findings may have relevance to the use of β-lactam antibiotics in clinical and agricultural settings.

摘要

耐甲氧西林金黄色葡萄球菌(MRSA)是医院和社区相关感染的主要原因。形成被称为生物膜的附着细胞簇是 MRSA 发病机制中的一个重要毒力因素。以前的研究表明,低于最低抑菌浓度(sub-MIC)的甲氧西林浓度会诱导社区相关 MRSA 菌株 LAC 形成生物膜。在这项研究中,我们测量了八种其他β-内酰胺抗生素和六种非β-内酰胺抗生素在 sub-MIC 浓度下诱导 LAC 生物膜的能力。所有八种β-内酰胺抗生素,但没有一种非β-内酰胺抗生素,都能诱导 LAC 生物膜形成。八种β-内酰胺抗生素对 LAC 生物膜的剂量反应效应从双相和双峰到近线性不等。我们还发现,sub-MIC 甲氧西林诱导了 39 个额外的 MRSA 临床分离株中的 33 个形成生物膜,这些分离株也表现出双相、双峰和线性剂量反应曲线。sub-MIC 甲氧西林诱导形成的生物膜量与每种菌株对甲氧西林的敏感性成反比。我们的结果表明,sub-MIC 抗生素诱导生物膜是 MRSA 临床菌株的常见表型,并且特异性针对β-内酰胺抗生素。这些发现可能与β-内酰胺抗生素在临床和农业环境中的应用有关。

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