小调控rna作为病原菌抗生素耐药性的关键调节剂。

IF 3.3 4区 生物学 Q2 MICROBIOLOGY
Journal of Microbiology Pub Date : 2025-04-01 Epub Date: 2025-04-02 DOI:10.71150/jm.2501027
Yubin Yang, Hana Hyeon, Minju Joo, Kangseok Lee, Eunkyoung Shin
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引用次数: 0

摘要

不断升级的抗生素耐药性危机对全球公共卫生构成重大挑战,威胁到当前治疗方法的效力,并推动耐多药病原体的出现。在与细菌抗生素耐药性相关的各种因素中,小调控rna (sRNAs)已成为关键的转录后调控因子,通过多种机制协调细菌对抗生素压力的适应。本文综述了目前关于rna介导机制的知识,重点是药物摄取、药物外排系统、脂多糖、细胞壁修饰、生物膜形成和突变。转录组学和功能分析的最新进展揭示了新的srna及其调控网络,扩大了我们对耐药机制的理解。这些发现突出了靶向srna介导途径作为对抗抗生素耐药性的创新治疗策略的潜力,并为管理挑战性细菌感染提供了有希望的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Small regulatory RNAs as key modulators of antibiotic resistance in pathogenic bacteria.

The escalating antibiotic resistance crisis poses a significant challenge to global public health, threatening the efficacy of current treatments and driving the emergence of multidrug-resistant pathogens. Among the various factors associated with bacterial antibiotic resistance, small regulatory RNAs (sRNAs) have emerged as pivotal post-transcriptional regulators which orchestrate bacterial adaptation to antibiotic pressure via diverse mechanisms. This review consolidates the current knowledge on sRNA-mediated mechanisms, focusing on drug uptake, drug efflux systems, lipopolysaccharides, cell wall modification, biofilm formation, and mutagenesis. Recent advances in transcriptomics and functional analyses have revealed novel sRNAs and their regulatory networks, expanding our understanding of resistance mechanisms. These findings highlight the potential of targeting sRNA-mediated pathways as an innovative therapeutic strategy to combat antibiotic resistance, and offer promising avenues for managing challenging bacterial infections.

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来源期刊
Journal of Microbiology
Journal of Microbiology 生物-微生物学
CiteScore
5.70
自引率
3.30%
发文量
0
审稿时长
3 months
期刊介绍: Publishes papers that deal with research on microorganisms, including archaea, bacteria, yeasts, fungi, microalgae, protozoa, and simple eukaryotic microorganisms. Topics considered for publication include Microbial Systematics, Evolutionary Microbiology, Microbial Ecology, Environmental Microbiology, Microbial Genetics, Genomics, Molecular Biology, Microbial Physiology, Biochemistry, Microbial Pathogenesis, Host-Microbe Interaction, Systems Microbiology, Synthetic Microbiology, Bioinformatics and Virology. Manuscripts dealing with simple identification of microorganism(s), cloning of a known gene and its expression in a microbial host, and clinical statistics will not be considered for publication by JM.
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