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开发抗生物膜治疗策略以克服抗菌药物耐药性。

Development of Antibiofilm Therapeutics Strategies to Overcome Antimicrobial Drug Resistance.

作者信息

Nadar Sahaya, Khan Tabassum, Patching Simon G, Omri Abdelwahab

机构信息

Department of Pharmaceutical Chemistry, St. John Institute of Pharmacy and Research, Mumbai 400056, India.

Department of Pharmaceutical Chemistry & Quality Assurance, SVKM's Dr. Bhanuben Nanavati College of Pharmacy, Mumbai 400056, India.

出版信息

Microorganisms. 2022 Jan 27;10(2):303. doi: 10.3390/microorganisms10020303.

Abstract

A biofilm is a community of stable microorganisms encapsulated in an extracellular matrix produced by themselves. Many types of microorganisms that are found on living hosts or in the environment can form biofilms. These include pathogenic bacteria that can serve as a reservoir for persistent infections, and are culpable for leading to a broad spectrum of chronic illnesses and emergence of antibiotic resistance making them difficult to be treated. The absence of biofilm-targeting antibiotics in the drug discovery pipeline indicates an unmet opportunity for designing new biofilm inhibitors as antimicrobial agents using various strategies and targeting distinct stages of biofilm formation. The strategies available to control biofilm formation include targeting the enzymes and proteins specific to the microorganism and those involved in the adhesion pathways leading to formation of resistant biofilms. This review primarily focuses on the recent strategies and advances responsible for identifying a myriad of antibiofilm agents and their mechanism of biofilm inhibition, including extracellular polymeric substance synthesis inhibitors, adhesion inhibitors, quorum sensing inhibitors, efflux pump inhibitors, and cyclic diguanylate inhibitors. Furthermore, we present the structure-activity relationships (SAR) of these agents, including recently discovered biofilm inhibitors, nature-derived bioactive scaffolds, synthetic small molecules, antimicrobial peptides, bioactive compounds isolated from fungi, non-proteinogenic amino acids and antibiotics. We hope to fuel interest and focus research efforts on the development of agents targeting the uniquely complex, physical and chemical heterogeneous biofilms through a multipronged approach and combinatorial therapeutics for a more effective control and management of biofilms across diseases.

摘要

生物膜是由微生物自身产生的胞外基质包裹的稳定微生物群落。在活体宿主或环境中发现的多种微生物都能形成生物膜。这些微生物包括致病性细菌,它们可作为持续性感染的储存库,并导致多种慢性疾病以及抗生素耐药性的出现,致使这些疾病难以治疗。药物研发流程中缺乏针对生物膜的抗生素,这表明存在一个尚未满足的机会,即利用各种策略并针对生物膜形成的不同阶段设计新型生物膜抑制剂作为抗菌剂。可用于控制生物膜形成的策略包括靶向微生物特有的酶和蛋白质以及参与导致耐药生物膜形成的黏附途径的那些酶和蛋白质。本综述主要关注近期用于鉴定众多抗生物膜剂及其生物膜抑制机制的策略和进展,包括胞外聚合物合成抑制剂、黏附抑制剂、群体感应抑制剂、外排泵抑制剂和环二鸟苷酸抑制剂。此外,我们还介绍了这些药剂的构效关系(SAR),包括最近发现的生物膜抑制剂、天然来源的生物活性支架、合成小分子、抗菌肽、从真菌中分离出的生物活性化合物、非蛋白质氨基酸和抗生素。我们希望通过多管齐下的方法和联合疗法激发人们的兴趣,并将研究工作聚焦于开发针对独特复杂、物理和化学性质各异的生物膜的药剂,以便更有效地控制和管理各种疾病中的生物膜。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa51/8879831/ce7571d29a4e/microorganisms-10-00303-g001.jpg

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