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Subinhibitory Concentrations of Linezolid Reduce Staphylococcus aureus Virulence Factor Expression

机译:亚抑制浓度的利奈唑胺降低金黄色葡萄球菌毒力因子表达

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摘要

The influence of the antibiotic linezolid on the secretion of exotoxins by Staphylococcus aureus was analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis combined with matrix-assisted laser desorption ionization-time of flight mass spectrometry and Western blot analysis. S. aureus suspensions were treated with grading subinhibitory concentrations of linezolid (12.5, 25, 50, and 90% of MIC) at different stages of bacterial growth (i.e., an optical density at 540 nm [OD540] of 0.05 or 0.8). When added to S. aureus cultures at an OD540 of 0.05, linezolid reduced in a dose-dependent manner the secretion of specific virulence factors, including staphylococcal enterotoxin A (SEA) and SEB, bifunctional autolysin, autolysin, protein A, and alpha- and beta-hemolysins. In contrast, other presumably nontoxic exoproteins remained unchanged or even accumulated in supernatants in the presence of linezolid at a 90% MIC. Similarily, when added at OD540 of 0.8, that is, after quorum sensing, linezolid reduced the release of virulence factors, whereas the relative abundance of nontoxic exoproteins such as triacylglycerol lipase, glycerol ester hydrolase, DnaK, or translation elongation factor EF-Tu was found to be increased. Consistently, linezolid reduced in a dose-dependent manner the tumor necrosis factor-inducing activity secreted by S. aureus into the culture supernatants. The results of our study suggest that the expression of virulence factors in S. aureus is especially sensitive to the inhibition of protein synthesis by linezolid, which should be an advantage in the treatment of infections with toxin-producing S. aureus.
机译:通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳结合基质辅助激光解吸电离-飞行时间质谱和Western印迹分析来分析抗生素利奈唑胺对金黄色葡萄球菌分泌外毒素的影响。在细菌生长的不同阶段(即540 nm [OD540]的光密度为0.05或0.8),用亚抑制浓度的利奈唑胺(MIC的12.5%,25%,50%和90%)处理金黄色葡萄球菌悬浮液。当以540的OD540加入金黄色葡萄球菌培养物中时,利奈唑胺以剂量依赖性方式减少特定毒力因子的分泌,包括葡萄球菌肠毒素A(SEA)和SEB,双功能自溶素,自溶素,蛋白A和α-和β-溶血素。相反,在存在利奈唑胺的情况下,在90%MIC下,其他可能无毒的外蛋白保持不变,甚至在上清液中积累。类似地,当以OD540的0.8加入时,即在群体感应后,利奈唑胺减少了毒力因子的释放,而无毒外泌蛋白(如三酰甘油脂肪酶,甘油酯水解酶,DnaK或翻译延伸因子EF-Tu)的相对丰度却很高。发现增加。一致地,利奈唑胺以剂量依赖性方式降低由金黄色葡萄球菌分泌到培养上清液中的肿瘤坏死因子诱导活性。我们的研究结果表明,金黄色葡萄球菌中毒力因子的表达对利奈唑胺抑制蛋白质合成特别敏感,这在治疗产生毒素的金黄色葡萄球菌感染中应该是一个优势。

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