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双子阳离子两亲分子控制细菌性阴道病病原体的生物膜形成。

Gemini Cationic Amphiphiles Control Biofilm Formation by Bacterial Vaginosis Pathogens.

机构信息

Department of Biochemistry and Microbiology, Rutgers State University, New Brunswick, New Jersey, USA.

Department of Biology and Biotechnology, College of Science, Diyala University, Baqubah, Iraq.

出版信息

Antimicrob Agents Chemother. 2017 Nov 22;61(12). doi: 10.1128/AAC.00650-17. Print 2017 Dec.

Abstract

Antibiotic resistance and recurrence of bacterial vaginosis (BV), a polymicrobial infection, justify the need for novel antimicrobials to counteract microbial resistance to conventional antibiotics. Previously, two series of cationic amphiphiles (CAms) which self-assemble into supramolecular nanostructures with membrane-lytic properties were designed with hydrophilic head groups and nonpolar domains. The combination of CAms and commonly prescribed antibiotics is suggested as a promising strategy for targeting microorganisms that are resistant to conventional antibiotics. Activities of the CAms against ATCC 14018, a representative BV pathogen, ranged from 1.1 to 24.4 μM. Interestingly, the tested healthy species, especially ATCC 39268, were significantly more tolerant of CAms than the selected pathogens. In addition, CAms prevented biofilm formation at concentrations which did not influence the normal growth ability of ATCC 14018. Furthermore, the biofilm minimum bactericidal concentration (MBC-Bs) of CAms against ATCC 14018 ranged from 58.8 to 425.6 μM, while much higher concentrations (≥850 μM) were required to produce ≥3-log reductions in the number of biofilm-associated lactobacilli. The conventional antibiotic metronidazole synergized strongly with all tested CAms against planktonic cells and biofilms of ATCC 14018. The synergism between CAms and the tested conventional antibiotic may be considered a new, effective, and beneficial method of controlling biofilm-associated bacterial vaginosis.

摘要

抗生素耐药性和细菌性阴道病(BV)的复发是一种多微生物感染,这证明需要新型抗菌药物来对抗对抗生素的微生物耐药性。此前,设计了两类阳离子两亲物(CAms),它们具有亲水头基和非极性结构域,可自组装成具有膜裂解特性的超分子纳米结构。CAms 与常用的抗生素联合使用被认为是一种很有前途的策略,可以靶向对抗生素耐药的微生物。CAms 对代表 BV 病原体的 ATCC 14018 的活性范围为 1.1-24.4μM。有趣的是,与选定的病原体相比,测试的健康种属,特别是 ATCC 39268,对 CAms 的耐受性明显更高。此外,CAms 可以防止生物膜形成,而不会影响 ATCC 14018 的正常生长能力。此外,CAms 对 ATCC 14018 的生物膜最低杀菌浓度(MBC-Bs)范围为 58.8-425.6μM,而要使生物膜相关乳酸杆菌减少≥3 对数级,则需要更高的浓度(≥850μM)。传统抗生素甲硝唑与所有测试的 CAms 对 ATCC 14018 的浮游细胞和生物膜均表现出强烈的协同作用。CAms 与测试的常规抗生素之间的协同作用可能被认为是控制与生物膜相关的细菌性阴道病的一种新的、有效和有益的方法。

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