{"title":"生物黄酮黄芩素通过抑制金黄色葡萄球菌的外排泵调节四环素耐药性","authors":"Soumitra Moulick, Dijendra Nath Roy","doi":"10.1089/mdr.2024.0099","DOIUrl":null,"url":null,"abstract":"<p><p>The rise in antibiotic resistance among bacterial pathogens, particularly <i>Staphylococcus aureus</i>, has become a critical global health issue, necessitating the search for novel antimicrobial agents. <i>S. aureus</i> uses various mechanisms to resist antibiotics, including the activation of efflux pumps, biofilm formation, and enzymatic modification of drugs. This study explores the potential of baicalein, a bioflavonoid from <i>Scutellaria baicalensis</i>, in modulating tetracycline resistance in <i>S. aureus</i> by inhibiting efflux pumps. The synergistic action of baicalein and tetracycline was evaluated through various assays. The minimum inhibitory concentration (MIC) of baicalein and tetracycline against <i>S. aureus</i> was 256 and 1.0 μg/mL, respectively. Baicalein at 64 μg/mL reduced the MIC of tetracycline by eightfold, indicating a synergistic effect (fractional inhibitory concentration index: 0.375). Time-kill kinetics demonstrated a 1.0 log CFU/mL reduction in bacterial count after 24 hours with the combination treatment. The ethidium bromide accumulation assay showed that baicalein mediated significant inhibition of efflux pumps, with a dose-dependent increase in fluorescence. In addition, baicalein inhibited DNA synthesis by 73% alone and 92% in combination with tetracycline. It also markedly reduced biofilm formation and the invasiveness of <i>S. aureus</i> into HeLa cells by 52% at 64 μg/mL. These findings suggest that baicalein enhances tetracycline efficacy and could be a promising adjunct therapy to combat multidrug-resistant <i>S. aureus</i> infections.</p>","PeriodicalId":18701,"journal":{"name":"Microbial drug resistance","volume":" ","pages":"363-371"},"PeriodicalIF":2.3000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Bioflavonoid Baicalein Modulates Tetracycline Resistance by Inhibiting Efflux Pump in <i>Staphylococcus aureus</i>.\",\"authors\":\"Soumitra Moulick, Dijendra Nath Roy\",\"doi\":\"10.1089/mdr.2024.0099\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The rise in antibiotic resistance among bacterial pathogens, particularly <i>Staphylococcus aureus</i>, has become a critical global health issue, necessitating the search for novel antimicrobial agents. <i>S. aureus</i> uses various mechanisms to resist antibiotics, including the activation of efflux pumps, biofilm formation, and enzymatic modification of drugs. This study explores the potential of baicalein, a bioflavonoid from <i>Scutellaria baicalensis</i>, in modulating tetracycline resistance in <i>S. aureus</i> by inhibiting efflux pumps. The synergistic action of baicalein and tetracycline was evaluated through various assays. The minimum inhibitory concentration (MIC) of baicalein and tetracycline against <i>S. aureus</i> was 256 and 1.0 μg/mL, respectively. Baicalein at 64 μg/mL reduced the MIC of tetracycline by eightfold, indicating a synergistic effect (fractional inhibitory concentration index: 0.375). Time-kill kinetics demonstrated a 1.0 log CFU/mL reduction in bacterial count after 24 hours with the combination treatment. The ethidium bromide accumulation assay showed that baicalein mediated significant inhibition of efflux pumps, with a dose-dependent increase in fluorescence. In addition, baicalein inhibited DNA synthesis by 73% alone and 92% in combination with tetracycline. It also markedly reduced biofilm formation and the invasiveness of <i>S. aureus</i> into HeLa cells by 52% at 64 μg/mL. These findings suggest that baicalein enhances tetracycline efficacy and could be a promising adjunct therapy to combat multidrug-resistant <i>S. aureus</i> infections.</p>\",\"PeriodicalId\":18701,\"journal\":{\"name\":\"Microbial drug resistance\",\"volume\":\" \",\"pages\":\"363-371\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2024-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Microbial drug resistance\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1089/mdr.2024.0099\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/8/12 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"INFECTIOUS DISEASES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbial drug resistance","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1089/mdr.2024.0099","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/8/12 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0
摘要
细菌病原体(尤其是金黄色葡萄球菌)的抗生素耐药性上升已成为一个严重的全球健康问题,因此有必要寻找新型抗菌剂。金黄色葡萄球菌利用各种机制来抵抗抗生素,包括激活外排泵、形成生物膜和对药物进行酶修饰。本研究探讨了黄芩中的生物黄酮类化合物黄芩素通过抑制外排泵调节金黄色葡萄球菌对四环素耐药性的潜力。黄芩苷和四环素的协同作用通过各种试验进行了评估。黄芩苷和四环素对金黄色葡萄球菌的最小抑菌浓度(MIC)分别为 256 和 1.0 μg/mL。黄芩素的浓度为 64 μg/mL 时,四环素的 MIC 降低了 8 倍,显示出协同效应(分数抑制浓度指数:0.375)。时间杀灭动力学显示,联合处理 24 小时后,细菌数量减少了 1.0 log CFU/mL。溴化乙锭蓄积试验表明,黄芩苷能显著抑制外排泵,荧光的增加与剂量有关。此外,黄芩素对 DNA 合成的单独抑制率为 73%,与四环素联合抑制率为 92%。当黄芩苷的剂量为 64 μg/mL 时,它还能显著减少金黄色葡萄球菌生物膜的形成,并使其对 HeLa 细胞的侵袭性降低 52%。这些研究结果表明,黄芩苷能增强四环素的疗效,可以作为一种很有前景的辅助疗法来对付耐多药金黄色葡萄球菌感染。
Bioflavonoid Baicalein Modulates Tetracycline Resistance by Inhibiting Efflux Pump in Staphylococcus aureus.
The rise in antibiotic resistance among bacterial pathogens, particularly Staphylococcus aureus, has become a critical global health issue, necessitating the search for novel antimicrobial agents. S. aureus uses various mechanisms to resist antibiotics, including the activation of efflux pumps, biofilm formation, and enzymatic modification of drugs. This study explores the potential of baicalein, a bioflavonoid from Scutellaria baicalensis, in modulating tetracycline resistance in S. aureus by inhibiting efflux pumps. The synergistic action of baicalein and tetracycline was evaluated through various assays. The minimum inhibitory concentration (MIC) of baicalein and tetracycline against S. aureus was 256 and 1.0 μg/mL, respectively. Baicalein at 64 μg/mL reduced the MIC of tetracycline by eightfold, indicating a synergistic effect (fractional inhibitory concentration index: 0.375). Time-kill kinetics demonstrated a 1.0 log CFU/mL reduction in bacterial count after 24 hours with the combination treatment. The ethidium bromide accumulation assay showed that baicalein mediated significant inhibition of efflux pumps, with a dose-dependent increase in fluorescence. In addition, baicalein inhibited DNA synthesis by 73% alone and 92% in combination with tetracycline. It also markedly reduced biofilm formation and the invasiveness of S. aureus into HeLa cells by 52% at 64 μg/mL. These findings suggest that baicalein enhances tetracycline efficacy and could be a promising adjunct therapy to combat multidrug-resistant S. aureus infections.
期刊介绍:
Microbial Drug Resistance (MDR) is an international, peer-reviewed journal that covers the global spread and threat of multi-drug resistant clones of major pathogens that are widely documented in hospitals and the scientific community. The Journal addresses the serious challenges of trying to decipher the molecular mechanisms of drug resistance. MDR provides a multidisciplinary forum for peer-reviewed original publications as well as topical reviews and special reports.
MDR coverage includes:
Molecular biology of resistance mechanisms
Virulence genes and disease
Molecular epidemiology
Drug design
Infection control.