Synergistic effects of quorum-sensing molecules and antimicrobials against Candida albicans and Pseudomonas aeruginosa biofilms: in vitro and in vivo studies.

IF 3.9 2区 医学 Q1 INFECTIOUS DISEASES
Mayram Hacioglu, Fatima Nur Yilmaz, Hande Ipek Yetke, Ebru Haciosmanoglu-Aldogan
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引用次数: 0

Abstract

Background: Candida albicans can form polymicrobial biofilms with other microorganisms, such as Pseudomonas aeruginosa, at infection sites.

Objectives: As biofilms are highly resistant to antibiotics there is a need for new antibiofilm agents that have unique targets and modes of action.

Methods: In this study the antibiofilm effects of two quorum-sensing molecules (QSMs), farnesol and tyrosol, were investigated alone and in combination with antibiotics (aztreonam, colistin, tobramycin) and antifungals (fluconazole, amphotericin B, caspofungin), against single- and dual-species biofilms of C. albicans and P. aeruginosa in in vitro and in vivo systems.

Results: It was observed that QSMs alone, especially farnesol, showed at least a 1-log reduction against preformed single- and dual-species biofilms of C. albicans and P. aeruginosa. Combination of QSMs with colistin or fluconazole was found to be effective against both single- and dual-species biofilms in vitro. Increased survival was observed in C. elegans when treated with colistin or fluconazole in combination with QSMs, compared with no treatment. Additionally, the QSMs and colistin and farnesol combinations effectively inhibited biofilm formation by C. albicans and P. aeruginosa on bronchial epithelial cells, and reduced IL-1β expression in lung bronchial epithelial cells.

Conclusions: There is a need for effective treatments for bacterial-fungal biofilm infections and, to our knowledge, there have been no studies of QSMs and antimicrobial combinations against dual-species biofilms involving C. albicans and P. aeruginosa. Hence these findings will make a significant contribution to the literature.

法定人数感应分子和抗菌剂对白色念珠菌和铜绿假单胞菌生物膜的协同作用:体外和体内研究。
背景:白色念珠菌可在感染部位与铜绿假单胞菌等其他微生物形成多微生物生物膜:由于生物膜对抗生素具有高度耐药性,因此需要具有独特靶点和作用模式的新型抗生物膜药物:方法:本研究在体外和体内系统中研究了两种法定量感应分子(QSMs)--法呢醇和酪醇--单独或与抗生素(阿曲南、可乐定、妥布霉素)和抗真菌药(氟康唑、两性霉素B、卡泊芬净)联用对白僵菌和铜绿假单胞菌单种和双种生物膜的抗生物膜作用:结果:观察发现,单独使用 QSMs,尤其是法尼醇,对预先形成的白僵菌和铜绿假单胞菌单种和双种生物膜的抑制作用至少降低 1 个菌落。在体外将 QSMs 与可乐定或氟康唑结合使用,对单种和双种生物膜均有效。与不使用 QSMs 的情况相比,在使用可乐定或氟康唑与 QSMs 联合治疗时,可乐菌的存活率有所提高。此外,QSMs 和可乐定与法尼醇的组合能有效抑制支气管上皮细胞上白僵菌和铜绿假单胞菌生物膜的形成,并减少肺支气管上皮细胞中 IL-1β 的表达:据我们所知,目前还没有针对涉及白僵菌和铜绿假单胞菌的双种生物膜的 QSMs 和抗菌药组合研究。因此,这些研究结果将为相关文献做出重大贡献。
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来源期刊
CiteScore
9.20
自引率
5.80%
发文量
423
审稿时长
2-4 weeks
期刊介绍: The Journal publishes articles that further knowledge and advance the science and application of antimicrobial chemotherapy with antibiotics and antifungal, antiviral and antiprotozoal agents. The Journal publishes primarily in human medicine, and articles in veterinary medicine likely to have an impact on global health.
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