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青蒿琥酯通过减少α-毒素合成抑制金黄色葡萄球菌生物膜形成。

Artesunate inhibits Staphylococcus aureus biofilm formation by reducing alpha-toxin synthesis.

机构信息

Department of Pharmacy, The Second Affiliated Hospital, Chongqing Medical University, No. 76, Linjiang Road, Yuzhong District, Chongqing, 400010, China.

Department of Liver Disease, Chongqing Traditional Chinese Medicine Hospital, Chongqing, 400021, China.

出版信息

Arch Microbiol. 2021 Mar;203(2):707-717. doi: 10.1007/s00203-020-02077-6. Epub 2020 Oct 10.

Abstract

Staphylococcus aureus is one of the most common pathogens in bacterial biofilm infections. Antibiotic treatment for infection caused by S. aureus biofilms is challenging, and few effective strategies have been developed to combat these infections. The aim of this study was to investigate the effect and possible mechanisms of artesunate on the biofilm formation of S. aureus. Bacterial growth curves were determined by a microtiter plate. Biofilm formation was determined by the crystal violet staining method and confocal laser scanning microscopy. Bacterial adhesion was assayed by the colony-counting method. The expression of virulence and adhesion genes was determined by real-time PCR. The hemolytic activity and expression of ɑ-hemolysin were analyzed using rabbit erythrocytes and Western blotting. The results showed that artesunate could significantly inhibit the biofilm formation of S. aureus in a dose-dependent manner. Artesunate could also inhibit bacterial adhesion and the expression of hla, RNAIII and agrA as well as ɑ-hemolysin production. The effect of artesunate on adhesion genes (clfA, clfB, fnbA, fnbB) had strain specificity, but it did not affect the expression of ica genes. The results indicated that artesunate might inhibit ɑ-hemolysin synthesis by the agr system, which inhibits biofilm formation.

摘要

金黄色葡萄球菌是细菌生物膜感染中最常见的病原体之一。金黄色葡萄球菌生物膜感染的抗生素治疗具有挑战性,目前尚未开发出有效的策略来对抗这些感染。本研究旨在探讨青蒿琥酯对金黄色葡萄球菌生物膜形成的影响及其可能的机制。通过微量板测定细菌生长曲线。结晶紫染色法和共聚焦激光扫描显微镜测定生物膜形成。通过平板计数法测定细菌黏附。实时 PCR 测定毒力和黏附基因的表达。用兔红细胞和 Western blot 分析溶血活性和α-溶血素的表达。结果表明,青蒿琥酯可呈剂量依赖性显著抑制金黄色葡萄球菌生物膜的形成。青蒿琥酯还可抑制细菌黏附和 hla、RNAIII 和 agrA 的表达以及α-溶血素的产生。青蒿琥酯对黏附基因(clfA、clfB、fnbA、fnbB)的作用具有菌株特异性,但不影响 ica 基因的表达。结果表明,青蒿琥酯可能通过 Agr 系统抑制α-溶血素的合成,从而抑制生物膜的形成。

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