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抗大肠杆菌ATCC 25922噬菌体的分离鉴定及其生物膜抑制研究。

Isolation and identification of bacteriophage against Escherichia coli ATCC 25922 and their biofilm Inhibition studies.

作者信息

Sivakumar Lakshminarayanan, John Durai Kumar Jeya Vignesh, Madhavan Subadarshini, Mina Parvesh K U, Arunagiri Santhosh Kumar, Rajadesingu Suriyaprakash, Sugumar Shobana, Jayaraman Narenkumar, Leela Kagithakara Vajravelu, Karthik A, Malik Tabarak, Punniyakotti Parthipan

机构信息

Department of Biotechnology, Faculty of Science and Humanities, SRM Institute of Science and Technology, Kattankulathur, Chengalpattu, 603203, Tamil Nadu, India.

Centre for Research in Environment, Sustainability Advocacy and Climate CHange (REACH), Directorate of Research, SRM Institute of Science and Technology, Kattankulathur, Chengalpattu, 603203, Tamil Nadu, India.

出版信息

Sci Rep. 2025 Jul 24;15(1):26964. doi: 10.1038/s41598-025-12366-z.

Abstract

Bacterial biofilm development plays a crucial role in causing serious health concerns in the medical sector. The adhesion of germs on living and non-living surfaces can lead to damage as well as diseases in humans, and other animals. To address this problem, researchers focus exclusively on bacteriophage therapy. In the present study, lytic phage with 10 PFU/mL was isolated from hospital sewage samples by targeting Escherichia coli (ATCC 25922). The morphological study of the isolated phage was examined under high-resolution transmission electron microscopy (HR-TEM) by using 2% of uranyl acetate as a negative staining, which revealed that the isolated phage belonged to the Myoviridae family. Bacterial turbidity assay showed reduced optical density (OD) in 0.01 multiplicity of infection (MOI) and no growth in 0.1 and 1.0 MOI phage concentration which was compared with control (without phage-treated E. coli cells). The phage-host interaction was investigated using an HR-TEM after treating the phage for 30 min, which showed the lytic cycle of the phage. Further, the E. coli biofilm was assessed using a microplate reader after 24 and 48 h on 96 titer plates with crystal violet staining to confirm the inhibition efficiency of phage-treated biofilm quantitatively (83%). Then the compound and fluorescence microscopy were used for qualitative measurement of inhibition activity. Further, the biofilm formation of E. coli on a coverslip surface was analysed using scanning electron microscopy, comparing samples treated with 0.1 MOI of phage to untreated controls. About 10% of countable cells only present over the phage-treated surface (90% of biofilm inhibition). The outcome of this study revealed that phage treatment effectively suppressed the E. coli biofilm development, and it can be used as a sustainable and eco-friendly approach for the control of biofilm formation on surfaces specifically in hospital environments.

摘要

细菌生物膜的形成在医疗领域引发严重健康问题方面起着关键作用。细菌在生物和非生物表面的粘附会对人类及其他动物造成损害并引发疾病。为解决这一问题,研究人员专门聚焦于噬菌体疗法。在本研究中,通过靶向大肠杆菌(ATCC 25922)从医院污水样本中分离出了浓度为10 PFU/mL的裂解性噬菌体。使用2%的醋酸铀作为负染剂,在高分辨率透射电子显微镜(HR-TEM)下对分离出的噬菌体进行形态学研究,结果表明该分离出的噬菌体属于肌尾噬菌体科。细菌浊度测定显示,在感染复数(MOI)为0.01时光密度(OD)降低,在MOI为0.1和1.0的噬菌体浓度下无生长,这与对照(未用噬菌体处理的大肠杆菌细胞)相比。在处理噬菌体30分钟后,使用HR-TEM研究噬菌体与宿主的相互作用,结果显示了噬菌体的裂解周期。此外,在96孔滴定板上培养24小时和48小时后用结晶紫染色,使用酶标仪评估大肠杆菌生物膜,以定量确认噬菌体处理生物膜的抑制效率(83%)。然后使用化合物和荧光显微镜对抑制活性进行定性测量。此外,使用扫描电子显微镜分析大肠杆菌在盖玻片表面的生物膜形成情况,将用0.1 MOI噬菌体处理的样品与未处理的对照进行比较。在经噬菌体处理的表面上仅存在约10%的可计数细胞(生物膜抑制率为90%)。本研究结果表明,噬菌体处理可有效抑制大肠杆菌生物膜的形成,并且它可以作为一种可持续且环保的方法,用于控制特别是医院环境中表面生物膜的形成。

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