Jaglan Anu Bala, Verma Ravikant, Vashisth Medhavi, Virmani Nitin, Bera B C, Vaid R K, Anand Taruna
ICAR - National Research Centre on Equines, Hisar, Haryana, 125 001, India; Department of Zoology and Aquaculture, Chaudhary Charan Singh Haryana Agricultural University, Hisar, Haryana, 125 004, India.
Department of Zoology and Aquaculture, Chaudhary Charan Singh Haryana Agricultural University, Hisar, Haryana, 125 004, India.
Microb Pathog. 2025 Sep;206:107761. doi: 10.1016/j.micpath.2025.107761. Epub 2025 Jun 2.
In recent years, Escherichia coli is frequently associated with food borne infections causing colibacillosis in both food animals and humans. Therefore, to secure a safe and healthy foods, there is a need of an alternative strategy. Bacteriophages due to their ability serve as a promising strategy for combating drug-resistant bacteria. In this study, a lytic Escherichia phage phiEco273 was isolated from a pond water sample targeting multidrug-resistant strain of E. coli. Escherichia phage phiEco273 showed lytic activity against 13/50 tested strains of E. coli of animal origin. Escherichia phage phiEco273 exhibit activity in acidic environment (pH3) and elevated temperature (70 °C). Escherichia phage phiEco273 is classified as the member of class Caudoviricetes based on their Electron micrograph and genome analysis. The Genome of Escherichia phage phiEco273 is 44.7 kb in size with 54.4 % GC content. Genome analysis predicted 59 open reading frames (ORFs), which were subsequently assigned to four functional categories based on their annotations: nucleotide regulation, structural, proteins involved in lysis mechanisms, and hypothetical proteins. Escherichia phage phiEco273 also eradicated the biofilm developed by the VTCCBAA252 bacterium on glass surface. Despite the narrow host range of Escherichia phage phiEco273, it could serve as a good candidate for targeting biofilm forming multidrug resistant bacteria. Also, the presence of a unique tail fiber domain containing protein distinct it from other known Dhillinovirus. However, further investigations required to clearly find out how the presence of CD35 affect the host range and infectivity of bacteriophage phiEco273, which might be helpful in enhancing the therapeutic potential of phiEco273.
近年来,大肠杆菌经常与食源性感染相关,在食用动物和人类中均会引发大肠杆菌病。因此,为确保食品安全与健康,需要一种替代策略。噬菌体因其自身能力,有望成为对抗耐药菌的策略。在本研究中,从一份池塘水样中分离出一种裂解性大肠杆菌噬菌体phiEco273,其靶向多重耐药的大肠杆菌菌株。大肠杆菌噬菌体phiEco273对50株受试动物源大肠杆菌菌株中的13株显示出裂解活性。大肠杆菌噬菌体phiEco273在酸性环境(pH3)和高温(70°C)下均表现出活性。基于电子显微镜和基因组分析,大肠杆菌噬菌体phiEco273被归类为有尾噬菌体目成员。大肠杆菌噬菌体phiEco273的基因组大小为44.7kb,GC含量为54.4%。基因组分析预测有59个开放阅读框(ORF),随后根据注释将其分为四个功能类别:核苷酸调控、结构、参与裂解机制的蛋白质以及假设蛋白。大肠杆菌噬菌体phiEco273还能清除VTCCBAA252细菌在玻璃表面形成的生物膜。尽管大肠杆菌噬菌体phiEco273的宿主范围较窄,但它可作为靶向形成生物膜的多重耐药菌的良好候选者。此外,其存在一个独特的含尾丝结构域蛋白,使其有别于其他已知的迪林诺病毒。然而,需要进一步研究以明确CD35的存在如何影响噬菌体phiEco273的宿主范围和感染性,这可能有助于提高phiEco273的治疗潜力。