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了解噬菌体受体结合蛋白与宿主表面受体的相互作用:噬菌体介导检测和消除铜绿假单胞菌的关键。

Understanding phage Receptor-binding protein interaction with host surface receptor: the key for phage-Mediated detection and elimination of Pseudomonas aeruginosa.

作者信息

Peng Shihui, Liu Ying, Liu Huiqing, Chen Lili, Niu Xiangheng, Liang Hao, Higgins Paul G, Bai Qinqin

机构信息

Department of Public Health Laboratory Sciences, School of Public Health, Hengyang Medical School, University of South China, Hengyang, Hunan, China.

Institute for Medical Microbiology, Immunology and Hygiene, Faculty of Medicine, University Hospital Cologne, University of Cologne, Cologne, Germany.

出版信息

Eur J Clin Microbiol Infect Dis. 2025 Sep 18. doi: 10.1007/s10096-025-05262-x.

Abstract

Pseudomonas aeruginosa poses a significant clinical challenge due to its intrinsic and acquired antimicrobial resistance and robust biofilm formation, which complicates treatment. Bacteriophages (phages), viruses targeting bacteria, are emerging as a promising alternative or adjunct to combat multidrug-resistant P. aeruginosa infections. This review systematically examines the taxonomic diversity of phages infecting P. aeruginosa, with emphasis on those that remain unclassified at the family taxonomic level, such as Pbunavirus and Pakpunavirus. It comprehensively synthesizes current knowledge on phage receptor-binding proteins (RBPs) - the molecular determinants of host specificity - and their corresponding receptors on the P. aeruginosa surface, such as lipopolysaccharide (LPS), pili, flagella, outer membrane proteins, and alginate. Critically, the review underscores the urgent need to decipher the precise molecular mechanisms governing RBP-receptor interactions. A deeper understanding of these specific recognition events is paramount. This knowledge is essential not only for rationally optimizing phage therapy efficacy, including through engineered phages or RBP-based antimicrobials, but also for developing highly sensitive and specific phage-derived diagnostic tools, utilizing whole phages or purified RBPs as recognition elements for rapid P. aeruginosa detection.

摘要

铜绿假单胞菌因其内在的和获得性的抗菌耐药性以及强大的生物膜形成能力而带来重大临床挑战,这使得治疗变得复杂。噬菌体,即靶向细菌的病毒,正成为对抗多重耐药铜绿假单胞菌感染的一种有前景的替代或辅助手段。本综述系统地研究了感染铜绿假单胞菌的噬菌体的分类多样性,重点关注那些在科分类水平上仍未分类的噬菌体,如Pbunavirus和Pakpunavirus。它全面综合了关于噬菌体受体结合蛋白(RBPs)——宿主特异性的分子决定因素——及其在铜绿假单胞菌表面相应受体的现有知识,如脂多糖(LPS)、菌毛、鞭毛、外膜蛋白和藻酸盐。至关重要的是,该综述强调迫切需要破译控制RBP - 受体相互作用的精确分子机制。深入了解这些特异性识别事件至关重要。这些知识不仅对于合理优化噬菌体治疗效果(包括通过工程噬菌体或基于RBP的抗菌剂)至关重要,而且对于开发高度敏感和特异的噬菌体衍生诊断工具也至关重要,利用完整噬菌体或纯化的RBPs作为识别元件来快速检测铜绿假单胞菌。

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