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肺炎克雷伯菌裂解噬菌体诱导PAO1生物膜形成。

Klebsiella Lytic Phages Induce PAO1 Biofilm Formation.

作者信息

Guła Grzegorz, Majkowska-Skrobek Grazyna, Misterkiewicz Anna, Salwińska Weronika, Piasecki Tomasz, Drulis-Kawa Zuzanna

机构信息

Department of Pathogen Biology and Immunology, University of Wrocław, S. Przybyszewskiego 63/77, 50-148 Wrocław, Poland.

Department of Nanometrology, Wrocław University of Science and Technology, Z. Janiszewskiego 11/17, 50-372 Wrocław, Poland.

出版信息

Viruses. 2025 Apr 25;17(5):615. doi: 10.3390/v17050615.

Abstract

Bacterial biofilms, characterized by complex structures, molecular communication, adaptability to environmental changes, insensitivity to chemicals, and immune response, pose a big problem both in clinics and in everyday life. The increasing bacterial resistance to antibiotics also led to the exploration of lytic bacteriophages as alternatives. Nevertheless, bacteria have co-evolved with phages, developing effective antiviral strategies, notably modification or masking phage receptors as the first line of defense mechanism. This study investigates viral-host interactions between non-host-specific phages and , assessing whether bacteria can detect phage particles and initiate protective mechanisms. Using real-time biofilm monitoring via impedance and optical density techniques, we monitored the phage effects on biofilm and planktonic populations. Three Klebsiella phages, KP15, KP34, and KP36, were tested against the PAO1 population, as well as Pseudomonas KTN6. The results indicated that Klebsiella phages (non-specific to ), particularly podovirus KP34, accelerated biofilm formation without affecting planktonic cultures. Our hypothesis suggests that bacteria sense phage virions, regardless of specificity, triggering biofilm matrix formation to block potential phage adsorption and infection. Nevertheless, further research is needed to understand the ecological and evolutionary dynamics between phages and bacteria, which is crucial for developing novel antibiofilm therapies.

摘要

细菌生物膜具有结构复杂、分子通讯、适应环境变化、对化学物质不敏感以及免疫反应等特征,在临床和日常生活中都构成了重大问题。细菌对抗生素的耐药性不断增加,也促使人们探索溶菌性噬菌体作为替代方案。然而,细菌与噬菌体共同进化,形成了有效的抗病毒策略,尤其是修饰或掩盖噬菌体受体作为第一道防御机制。本研究调查了非宿主特异性噬菌体与[未提及的细菌名称]之间的病毒-宿主相互作用,评估细菌是否能够检测到噬菌体颗粒并启动保护机制。通过阻抗和光密度技术进行实时生物膜监测,我们监测了噬菌体对生物膜和浮游菌群的影响。使用三种克雷伯氏菌噬菌体KP15、KP34和KP36对PAO1菌群以及铜绿假单胞菌KTN6进行测试。结果表明,克雷伯氏菌噬菌体(对[未提及的细菌名称]非特异性),特别是短尾噬菌体KP34,加速了生物膜的形成,而不影响浮游培养物。我们的假设表明,细菌能够感知噬菌体病毒粒子,无论其特异性如何,都会触发生物膜基质的形成,以阻止潜在的噬菌体吸附和感染。然而,需要进一步研究来了解噬菌体与细菌之间的生态和进化动态,这对于开发新型抗生物膜疗法至关重要。

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