Department of Sanitary Toxicology and Chemistry, Tianjin Medical University, Tianjin, 300070, China.
Tianjin Key Laboratory of Environment Nutrition and Public Health, Tianjin Medical University, Tianjin, 300070, China.
Mol Biol Rep. 2024 Jun 14;51(1):761. doi: 10.1007/s11033-024-09698-w.
Methicillin-resistant Staphylococcus aureus (MRSA) poses a great health threat to humans. Looking for compounds that could reduce the resistance of S. aureus towards methicillin is an effective way to alleviate the antimicrobial resistance crisis.
Minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC), Time-killing growth curve, staphyloxanthin and penicillin-binding protein 2a (PBP2a) were detected. A quantitative polymerase chain reaction was used to measure the effect of BBH on the gene transcription profiles of MRSA. The MIC of MRSA-ST59-t437 towards oxacillin was 8 µg/ml, and MBC was 128 µg/ml. After adding a sub-inhibitory concentration of BBH, the MIC and MBC of MRSA-ST59-t478 towards oxacillin went down to 0.125 and 32 µg/ml respectively. The amount of PBP2a and staphyloxanthin were reduced after treatment with BBH. Moreover, the transcription levels of sarA, mecA and fni genes were downregulated.
It is for the first time reported that BBH could inhibit staphyloxanthin synthesis by inhibiting fni gene. Moreover, fni might be the target gene of sarA, and there might be another regulatory pathway to inhibit staphyloxanthin biosynthesis. BBH could effectively reduce the methicillin resistance of MRSA-ST59-t437 by downregulating fni, sarA and mecA genes.
耐甲氧西林金黄色葡萄球菌(MRSA)对人类健康构成了巨大威胁。寻找能够降低金黄色葡萄球菌对甲氧西林耐药性的化合物是缓解抗菌药物耐药性危机的有效方法。
检测最低抑菌浓度(MIC)、最低杀菌浓度(MBC)、时程杀菌生长曲线、葡萄球菌黄素和青霉素结合蛋白 2a(PBP2a)。采用定量聚合酶链反应检测 BBH 对 MRSA 基因转录谱的影响。MRSA-ST59-t437 对苯唑西林的 MIC 为 8μg/ml,MBC 为 128μg/ml。加入亚抑菌浓度的 BBH 后,MRSA-ST59-t478 对苯唑西林的 MIC 和 MBC 分别降至 0.125 和 32μg/ml。BBH 处理后 PBP2a 和葡萄球菌黄素的含量减少。此外,sarA、mecA 和 fni 基因的转录水平下调。
首次报道 BBH 可通过抑制 fni 基因抑制葡萄球菌黄素的合成。此外,fni 可能是 sarA 的靶基因,可能存在另一种抑制葡萄球菌黄素生物合成的调控途径。BBH 通过下调 fni、sarA 和 mecA 基因,可有效降低 MRSA-ST59-t437 的甲氧西林耐药性。