The role of uropathogenic Escherichia coli biofilms in antibiotic-resistant urinary tract infections: Nanoparticle-based, phage therapy, and quorum-sensing inhibitor approaches.

IF 1.3 4区 医学 Q4 UROLOGY & NEPHROLOGY
Current Urology Pub Date : 2026-03-01 Epub Date: 2025-10-02 DOI:10.1097/CU9.0000000000000308
Kirolos Eskandar
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引用次数: 0

Abstract

Background: Urinary tract infections (UTIs) caused by uropathogenic E. coli (UPEC) pose a global health challenge, largely due to UPEC biofilms that drive persistent infections and antibiotic resistance.

Materials and methods: To explore the role of UPEC biofilms in antibiotic-resistant UTIs and summarize emerging therapeutic strategies, this study conducted a systematic review adhering to PRISMA guidelines and registered in PROSPERO (CRD420251040212). A structured search of PubMed, Google Scholar, Scopus, and Web of Science identified English-language studies published up to 2024, with 57 eligible studies selected after three-stage screening and analyzed via thematic synthesis.

Results: This study explored UPEC biofilms enhance resistance through extracellular matrix barriers, persister cell formation, efflux pump upregulation, and horizontal gene transfer; emerging therapies including bacteriophage therapy, quorum-sensing inhibitors, and nanoparticle-based drug delivery effectively target biofilms by penetration, signaling disruption, and improved drug efficacy. Additional approaches such as antibiofilm peptides, probiotics, and immunotherapy also demonstrate potential.

Conclusions: The UPEC biofilms are key to chronic UTIs, and novel targeted therapies offer promising solutions, but clinical validation, regulatory hurdles, and combination therapy optimization are critical for translation to clinical practice.

尿路致病性大肠杆菌生物膜在耐药尿路感染中的作用:纳米颗粒、噬菌体治疗和群体感应抑制剂方法。
背景:尿路致病性大肠杆菌(UPEC)引起的尿路感染(uti)是一个全球性的健康挑战,主要是由于UPEC生物膜驱动持续感染和抗生素耐药性。材料和方法:为了探索UPEC生物膜在抗生素耐药UTIs中的作用,总结新兴的治疗策略,本研究遵循PRISMA指南进行了系统综述,并在PROSPERO注册(CRD420251040212)。对PubMed、b谷歌Scholar、Scopus和Web of Science进行结构化搜索,确定了截至2024年发表的英语研究,经过三个阶段的筛选,选择了57项符合条件的研究,并通过主题综合进行分析。结果:UPEC生物膜通过细胞外基质屏障、持久性细胞形成、外排泵上调和水平基因转移增强耐药性;新兴疗法包括噬菌体疗法、群体感应抑制剂和基于纳米颗粒的药物递送,通过渗透、信号中断和改善药物疗效有效地靶向生物膜。其他方法,如抗生素膜肽、益生菌和免疫疗法也显示出潜力。结论:UPEC生物膜是慢性uti的关键,新的靶向治疗提供了有希望的解决方案,但临床验证、监管障碍和联合治疗优化对于转化为临床实践至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Current Urology
Current Urology Medicine-Urology
CiteScore
2.30
自引率
0.00%
发文量
96
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