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粉防己提取物协同抑制耐氨苄西林和万古霉素的屎肠球菌。

Stephania suberosa Forman extract synergistically inhibits ampicillin- and vancomycin-resistant Enterococcus faecium.

作者信息

Teethaisong Yothin, Chueakwon Piyasiri, Poolpol Kulwara, Ayamuang Intu-Orn, Suknasang Siriporn, Apinundecha Chittadech, Eumkeb Griangsak

机构信息

Department of Medical Sciences, Faculty of Allied Health Sciences, Burapha University, Chon Buri 20131, Thailand.

Research Unit for Sensor Innovation (RUSI), Burapha University, Chon Buri 20131, Thailand.

出版信息

Saudi J Biol Sci. 2023 Feb;30(2):103557. doi: 10.1016/j.sjbs.2023.103557. Epub 2023 Jan 16.

Abstract

Increasing antibiotic resistance in enterococci is among the most serious public health problems worldwide. The new naturally occurring antibacterial agents were explored. This study, therefore, investigated the antibacterial potential of extract (SSE) and its synergism with ampicillin (AMP) or vancomycin (VAN) against AMP- and VAN-resistant . Disc diffusion assay revealed that SSE inhibited DMST 12829, 12852, 12970, and a reference strain of ATCC 29,212 in a dose-dependent manner. The minimum inhibitory concentration (MIC) of SSE against all isolates was 0.5 mg/mL. DMST 12,829 and 12,852 were highly resistant to AMP, as indicated by high MIC values, and DMST 12,829 and 12,970 were resistant to VAN. spp. were killed by SSE at the minimum bactericidal concentrations (MBCs) ranging from 0.5 to 4 mg/mL. Checkerboard determination showed that SSE plus AMP and SSE plus VAN combinations exhibited synergistic interaction against isolates. The killing curve assay of isolates confirmed the antibacterial and synergistic activities of combined agents by dramatically reducing the viable counts compared to a single agent. Scanning electron microscope elucidated the cell damage and abnormal cell division. Enterococcal proteases were also inhibited by SSE. These findings support that SSE could reverse the activity of AMP and VAN. Moreover, it can synergistically inhibit AMP- and VAN-resistant . Our combined agents could be attractive candidates for developing new combinatorial agents to resurrect the efficacy of antibiotics for treating AMP- and VAN-resistant infections.

摘要

肠球菌抗生素耐药性增加是全球最严重的公共卫生问题之一。人们探索了新的天然抗菌剂。因此,本研究调查了提取物(SSE)及其与氨苄西林(AMP)或万古霉素(VAN)联合对耐AMP和耐VAN肠球菌的抗菌潜力。纸片扩散法显示,SSE以剂量依赖方式抑制DMST 12829、12852、12970以及粪肠球菌ATCC 29212参考菌株。SSE对所有分离株的最低抑菌浓度(MIC)为0.5mg/mL。高MIC值表明,DMST 12829和12852对AMP高度耐药,DMST 12829和12970对VAN耐药。肠球菌在最低杀菌浓度(MBC)为0.5至4mg/mL时被SSE杀灭。棋盘法测定表明,SSE加AMP以及SSE加VAN组合对肠球菌分离株表现出协同相互作用。肠球菌分离株的杀菌曲线测定证实了联合用药的抗菌和协同活性,与单一药物相比,活菌数显著减少。扫描电子显微镜阐明了细胞损伤和异常细胞分裂。SSE还抑制了肠球菌蛋白酶。这些发现支持SSE可以逆转AMP和VAN的活性。此外,它可以协同抑制耐AMP和耐VAN的肠球菌。我们的联合用药可能是开发新的组合药物以恢复抗生素治疗耐AMP和耐VAN肠球菌感染疗效的有吸引力的候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/203e/9876979/b0d9f04cf888/gr1.jpg

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