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Virulence-Suppressing Effects of Linezolid on Methicillin-Resistant Staphylococcus aureus: Possible Contribution to Early Defervescence

机译:利奈唑胺对耐甲氧西林金黄色葡萄球菌的毒力抑制作用:可能对早期退热的贡献。

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摘要

In the present study, immunomodulatory effects of linezolid (LZD) on methicillin-resistance Staphylococcus aureus (MRSA) infections were evaluated. We have retrospectively reviewed treatment effects of LZD on 52 patients with severe MRSA infections. Sixty-four percent of the febrile patients demonstrated significant defervescence within 3 days, despite the presence of positive culture results. We speculated that this finding might be due to early anti-inflammatory effects of LZD, and to investigate this further we initiated in vivo experiments using mice MRSA pneumonia models. Mice were treated with either LZD or vancomycin (VCM) immediately after intranasal administration of MRSA. Bacterial numbers and levels of inflammatory cytokines in the lungs were determined. Although the bacterial burden in the lungs was not apparently different between the two groups, LZD but not VCM treatment significantly reduced induction of inflammatory cytokines in the lungs (P < 0.05). To evaluate whether this anti-inflammatory response was due to suppression of virulence factor expression, filter-sterilized supernatants of MRSA incubated in broth overnight with sub-MICs of LZD were subcutaneously administered to mice. To clarify whether LZD possesses direct host-modulating activity, cytokine responses to the supernatants were examined in mice pretreated with LZD. Interestingly, MRSA solutions prepared in the presence of sub-MICs of LZD revealed significant suppression of interleukin 6 (IL-6) in a dose-dependent manner (P < 0.05), but pretreatment of mice with LZD revealed no changes in cytokines. These findings suggest that sub-MICs of LZD might suppress virulence factors of MRSA, which may be associated with a reduction in endogenous pyrogens. These data may explain at least in part early defervescence observed in LZD-treated individuals.
机译:在本研究中,评估了利奈唑胺(LZD)对耐甲氧西林金黄色葡萄球菌(MRSA)感染的免疫调节作用。我们回顾性地回顾了LZD对52例严重MRSA感染患者的治疗效果。尽管有阳性培养结果,但仍有64%的发热患者在3天内表现出明显的退热。我们推测该发现可能是由于LZD的早期抗炎作用所致,为了进一步研究这一点,我们启动了使用小鼠MRSA肺炎模型的体内实验。鼻内施用MRSA后立即用LZD或万古霉素(VCM)治疗小鼠。确定了肺中细菌的数量和炎性细胞因子的水平。尽管两组之间的肺部细菌负担没有明显差异,但是LZD而非VCM治疗显着降低了肺部炎性细胞因子的诱导(P <0.05)。为了评估这种抗炎反应是否是由于毒力因子表达的抑制而引起的,将与LZD亚型MIC在肉汤中孵育过夜的MRSA滤膜灭菌上清液皮下施用给小鼠。为了阐明LZD是否具有直接的宿主调节活性,在用LZD预处理的小鼠中检查了对上清液的细胞因子反应。有趣的是,在LZD亚型MICs存在下制备的MRSA溶液显示出白介素6(IL-6)的剂量依赖性(P <0.05)显着抑制,但是用LZD预处理的小鼠未发现细胞因子发生变化。这些发现表明,LZD的亚MIC可能会抑制MRSA的毒力因子,这可能与内源性热原减少有关。这些数据可以至少部分解释在LZD治疗的个体中观察到的早期去铁质。

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