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钠新鱼腥草素与盐酸小檗碱联合对生长和持续耐甲氧西林及万古霉素中介金黄色葡萄球菌的抗菌作用。

The combined antibacterial effects of sodium new houttuyfonate and berberine chloride against growing and persistent methicillin-resistant and vancomycin-intermediate Staphylococcus aureus.

机构信息

Beijing Key Laboratory of Antimicrobial Agents, Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100050, China.

Wuya College of Innovation, Shenyang Pharmaceutical University, Shenyang, 110016, China.

出版信息

BMC Microbiol. 2020 Oct 19;20(1):317. doi: 10.1186/s12866-020-02003-2.

Abstract

BACKGROUND

Infections caused by drug-resistant Staphylococcus aureus, especially vancomycin-intermediate Staphylococcus aureus (VISA), leave clinicians with limited therapeutic options for treatment. Persister cells is a leading cause of recalcitrant infection and antibiotic treatment failure, and there is no drug in clinical use that specifically targets persister cells currently. Here, we report a promising combination therapy of sodium new houttuyfonate (SNH) and berberine chloride (BBR) which is able to eradicate both growing and persistent drug-resistant Staphylococcus aureus.

RESULTS

The susceptibility test showed SNH exhibited anti-MRSA activity with MIC at 64 μg/mL, while BBR showed weak anti-MRSA activity with MIC at 512 μg/mL. MICs of BBR in combination with 1/2 MIC SNH decreased by 4 to 64 folds compared with MICs of BBR alone. The results of time-killing assays revealed that the combined use of sub-MIC SNH and BBR offered an in vitro synergistic action against growing MRSA (including pathogenic MRSA) and VISA strains. More importantly, the combination of SNH and BBR was able to eradicate VISA Mu50 and pathogenic MRSA persister cells. The synergistic effect is likely related to the interruption of the cell membrane caused by SNH, which is confirmed by scanning electron microscope and membrane potential and permeability analysis.

CONCLUSIONS

Our study provide a promising clinical curative strategy for combating drug-resistant S. aureus infections, especially for recalcitrant infections caused by persister cells.

摘要

背景

耐甲氧西林金黄色葡萄球菌(MRSA)引起的感染,尤其是中间耐万古霉素金黄色葡萄球菌(VISA),使得临床医生在治疗方面的选择有限。持留细胞是导致难治性感染和抗生素治疗失败的主要原因,目前临床上没有专门针对持留细胞的药物。在这里,我们报告了一种有前途的钠新虎杖苷(SNH)和盐酸小檗碱(BBR)联合治疗方案,能够根除生长和持续存在的耐药性金黄色葡萄球菌。

结果

药敏试验显示 SNH 对 MRSA 具有抗活性,MIC 为 64μg/ml,而 BBR 对 MRSA 表现出弱抗活性,MIC 为 512μg/ml。与单独使用 BBR 相比,BBR 与 1/2 MIC SNH 联合使用时的 MIC 降低了 4 到 64 倍。时间杀伤试验结果表明,亚 MIC SNH 和 BBR 的联合使用对生长中的 MRSA(包括致病性 MRSA)和 VISA 菌株具有体外协同作用。更重要的是,SNH 和 BBR 的联合使用能够根除 VISA Mu50 和致病性 MRSA 持留细胞。协同作用可能与 SNH 引起的细胞膜中断有关,这一点通过扫描电子显微镜和膜电位及通透性分析得到了证实。

结论

我们的研究为治疗耐甲氧西林金黄色葡萄球菌感染提供了一种有前途的临床治疗策略,特别是对持留细胞引起的难治性感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5096/7574187/ce9a986bfbe0/12866_2020_2003_Fig1_HTML.jpg

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