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多微生物生物膜:跨界相互作用、耐药性及治疗策略

Polymicrobial Biofilms: Interkingdom Interactions, Resistance and Therapeutic Strategies.

作者信息

Nithyanand Paramasivam, Boya Bharath Reddy, Lee Jin-Hyung, Lee Jintae

机构信息

School of Chemical Engineering, Yeungnam University, Gyeongsan, Republic of Korea.

出版信息

Microb Biotechnol. 2025 Aug;18(8):e70218. doi: 10.1111/1751-7915.70218.

DOI:10.1111/1751-7915.70218
PMID:40847578
Abstract

Polymicrobial biofilms are a conglomeration of diverse microbial consortia encased in a self-produced exopolysaccharide layer that forms on any biotic or abiotic surface. They are more resilient and persistent due to their enhanced drug resistance compared to monospecies biofilms, making it more difficult to eliminate using standard antimicrobial therapies. The present review discusses various inter- and intra-kingdom interactions taking place in polymicrobial biofilms and accounts for the various underlying drug resistance mechanisms in this complex and heterogeneous niche. In addition, this review provides insights into developing new diagnostic approaches by exploiting metabolites and byproducts produced by drug-resistant pathogens and other microorganisms in polymicrobial biofilms. As drug resistance is an ever-evolving mechanism in polymicrobial biofilms, synergistic combinations of natural products and antibiotics alone are not a panacea for eradicating these drug-resistant polymicrobial biofilms. Therefore, this review summarises both chemical and physical measures undertaken to combat these drug-resistant biofilms and stresses the need to employ 'omics' approaches, gene editing technologies and the integration of artificial intelligence/machine learning tools as future perspectives to eradicate these complex biofilms.

摘要

多微生物生物膜是多种微生物群落的聚集体,包裹在自生的胞外多糖层中,形成于任何生物或非生物表面。与单一物种生物膜相比,它们具有更强的耐药性,因此更具弹性和持久性,使得使用标准抗菌疗法更难消除。本综述讨论了多微生物生物膜中发生的各种界间和界内相互作用,并阐述了这个复杂且异质生态位中各种潜在的耐药机制。此外,本综述还介绍了通过利用多微生物生物膜中耐药病原体和其他微生物产生的代谢物和副产物来开发新诊断方法的见解。由于耐药性是多微生物生物膜中不断演变的机制,仅靠天然产物和抗生素的协同组合并非根除这些耐药多微生物生物膜的万灵药。因此,本综述总结了对抗这些耐药生物膜所采取的化学和物理措施,并强调需要采用“组学”方法、基因编辑技术以及整合人工智能/机器学习工具,作为根除这些复杂生物膜的未来方向。

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本文引用的文献

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Current Applications and the Future of Phage Therapy for Periprosthetic Joint Infections.噬菌体疗法在人工关节感染中的当前应用及未来发展
Antibiotics (Basel). 2025 Jun 6;14(6):581. doi: 10.3390/antibiotics14060581.
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Multifunctional Nanocarriers in Bacteriophage Delivery: A Paradigm Shift in Treating Multidrug-Resistant Infections.噬菌体递送中的多功能纳米载体:治疗多重耐药感染的范式转变
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Bacteriophage-antibiotic synergy enhances therapeutic efficacy against multidrug-resistant Klebsiella pneumoniae infections.
噬菌体-抗生素协同作用增强了对多重耐药肺炎克雷伯菌感染的治疗效果。
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Long-Read Sequencing for the Rapid Response to Infectious Diseases Outbreaks.用于传染病爆发快速响应的长读长测序
Curr Clin Microbiol Rep. 2025;12(1):10. doi: 10.1007/s40588-025-00247-y. Epub 2025 May 15.
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Flavonoids as Promising Natural Compounds for Combating Bacterial Infections.黄酮类化合物作为对抗细菌感染的有前景的天然化合物。
Int J Mol Sci. 2025 Mar 10;26(6):2455. doi: 10.3390/ijms26062455.
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Pilocarpine inhibits biofilm maturation by altering lipid, sphingolipid, and protein content.毛果芸香碱通过改变脂质、鞘脂和蛋白质含量来抑制生物膜成熟。
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Microb Pathog. 2025 Jun;203:107481. doi: 10.1016/j.micpath.2025.107481. Epub 2025 Mar 13.
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Integrated Co-extraction Protocol for Transcriptomic and H NMR Metabolomic Analysis of Multi-species Biofilms.用于多物种生物膜转录组学和核磁共振代谢组学分析的综合共提取方案
Bio Protoc. 2025 Mar 5;15(5):e5237. doi: 10.21769/BioProtoc.5237.
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Antimicrobial peptide biological activity, delivery systems and clinical translation status and challenges.抗菌肽的生物活性、递送系统以及临床转化现状与挑战。
J Transl Med. 2025 Mar 7;23(1):292. doi: 10.1186/s12967-025-06321-9.
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Advancing Nanotechnology: Targeting Biofilm-Forming Bacteria with Antimicrobial Peptides.推进纳米技术:用抗菌肽靶向生物膜形成细菌。
BME Front. 2025 Mar 4;6:0104. doi: 10.34133/bmef.0104. eCollection 2025.