Department of Microbiology and Excellent Research Laboratory on Natural Products and Natural Product Research Center of Excellence, Faculty of Science, Prince of Songkla University, Songkhla, Thailand.
Departamento de Bioquímica y Biología Molecular, Universidad de Córdoba, Campus de Excelencia Internacional CeiA3, Córdoba, Spain; Department of Engineering of Technological Equipment, National University of Science and Technology "MISiS", Moscow, Russia.
Microb Pathog. 2019 Mar;128:112-118. doi: 10.1016/j.micpath.2018.12.019. Epub 2018 Dec 21.
Sigma factor B (SigB) controls the expression of Staphylococcus aureus genes including virulence factors and plays a role in the bacterial secretion system through membrane vesicle production. Inhibition of SigB could attenuate SigB dependent virulence and secretion system. The objective of this study was to determine the effects of rhodomyrtone on SigB and virulence factors related to SigB. Minimal inhibitory concentration (MIC) and minimal bactericidal concentration (MBC) values of rhodomyrtone against 67 clinical methicillin-resistant S. aureus isolates were 0.25-8 μg/ml, which were similar to those of vancomycin. Using luciferase gene fused to SigB dependent promoters of asp23, five time reduction in SigB activity was observed when the bacteria were treated with rhodomyrtone for 3 h. Rhodomyrtone significantly reduced SigB activity in a concentration dependent manner in exponentially growing cells (P < 0.05). In addition, sigB mutant was more sensitive towards increasing concentrations of rhodomyrtone than the wild type and yabJ-spoVG mutant. Rhodomyrtone at 0.625 μg/ml reduced the growth of sigB mutant by approximately 99%, compared with the yabJ-spoVG mutant and the wild type. Membrane vesicles were significantly reduced in the bacterial cells when treated with 0.5 × MIC rhodomyrtone (P < 0.05). Decreased haemolytic activity was detected within rhodomyrtone-treated membrane vesicles. The results indicated that rhodomyrtone inhibited S. aureus SigB activity during exponentially growing phase and inhibited haemolytic activity within membrane vesicles.
σB 因子(SigB)控制金黄色葡萄球菌基因的表达,包括毒力因子,并通过膜泡产生在细菌分泌系统中发挥作用。SigB 的抑制可减弱 SigB 依赖性毒力和分泌系统。本研究旨在确定罗地莫酮对 SigB 和与 SigB 相关的毒力因子的影响。罗地莫酮对 67 株临床耐甲氧西林金黄色葡萄球菌分离株的最小抑菌浓度(MIC)和最小杀菌浓度(MBC)值为 0.25-8μg/ml,与万古霉素相似。用荧光素酶基因融合到 SigB 依赖性 asp23 启动子,当细菌用罗地莫酮处理 3 小时时,SigB 活性降低了五倍。罗地莫酮在对数生长期细胞中以浓度依赖性方式显著降低 SigB 活性(P<0.05)。此外,与野生型和 yabJ-spoVG 突变体相比,sigB 突变体对罗地莫酮浓度的增加更为敏感。与 yabJ-spoVG 突变体和野生型相比,罗地莫酮在 0.625μg/ml 时可使 sigB 突变体的生长减少约 99%。用 0.5×MIC 罗地莫酮处理细菌细胞时,膜泡明显减少(P<0.05)。在罗地莫酮处理的膜泡中检测到溶血活性降低。结果表明,罗地莫酮在指数生长期抑制金黄色葡萄球菌 SigB 活性,并抑制膜泡内的溶血活性。
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