噬菌体鸡尾酒、环丙沙星和卡泊芬金序贯给药对金黄色葡萄球菌和白色念珠菌双种生物膜的影响。

IF 2.6 4区 医学 Q3 IMMUNOLOGY
Marta Gliźniewicz, Barbara Dołęgowska, Adrian Augustyniak, Rafał Rakoczy, Tomasz Kędzierski, Ewa Mijowska, Bartłomiej Grygorcewicz
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引用次数: 0

摘要

多微生物生物膜,包括跨界生物膜,是后抗生素时代的另一个威胁。因此,许多替代方案正在研究中,包括噬菌体-抗生素协同作用(PAS),由于药物和噬菌体的作用机制不同,它可能更有效。在这项研究中,我们评估了噬菌体混合物、环丙沙星和卡泊芬金不同的给药顺序对体外(浮游培养和生物膜)根除金黄色葡萄球菌和白色念珠菌的影响。在液体培养中,噬菌体→卡泊真菌素→环丙沙星处理完全根除这两种微生物。在生物膜中,最有效的方案是同时应用所有三种药物或噬菌体+环丙沙星再加卡泊芬金。因此,药物和噬菌体的给药顺序是实现有效治疗和揭示最协同的组合的关键因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of sequential administration of phage cocktail, ciprofloxacin, and caspofungin on Staphylococcus aureus and Candida albicans dual-species biofilms.

Polymicrobial biofilms, including inter-kingdom ones, represent another threat in the post-antibiotic era. Therefore, many alternative solutions are being investigated, including phage-antibiotic synergy (PAS), which may be more effective due to the differing mechanisms of action of drugs and phages. In this study, we evaluated how different sequences of administering a bacteriophage cocktail, ciprofloxacin, and caspofungin affect the eradication of S. aureus and C. albicans in vitro (planktonic culture and in biofilms). In liquid culture, the phage → caspofungin → ciprofloxacin treatment completely eradicated both organisms. In biofilms, the most effective regimens were either the simultaneous application of all three agents or phages + ciprofloxacin followed by caspofungin. Therefore, the sequence of administration of drugs and phages is a key factor in achieving effective therapy and revealing the most synergistic combinations.

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来源期刊
Microbes and Infection
Microbes and Infection 医学-病毒学
CiteScore
12.60
自引率
1.70%
发文量
90
审稿时长
40 days
期刊介绍: Microbes and Infection publishes 10 peer-reviewed issues per year in all fields of infection and immunity, covering the different levels of host-microbe interactions, and in particular: the molecular biology and cell biology of the crosstalk between hosts (human and model organisms) and microbes (viruses, bacteria, parasites and fungi), including molecular virulence and evasion mechanisms. the immune response to infection, including pathogenesis and host susceptibility. emerging human infectious diseases. systems immunology. molecular epidemiology/genetics of host pathogen interactions. microbiota and host "interactions". vaccine development, including novel strategies and adjuvants. Clinical studies, accounts of clinical trials and biomarker studies in infectious diseases are within the scope of the journal. Microbes and Infection publishes articles on human pathogens or pathogens of model systems. However, articles on other microbes can be published if they contribute to our understanding of basic mechanisms of host-pathogen interactions. Purely descriptive and preliminary studies are discouraged.
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