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用于设计机制导向性抗生物膜药物的生物学和计算方法概述

An Overview of Biological and Computational Methods for Designing Mechanism-Informed Anti-biofilm Agents.

作者信息

An Andy Y, Choi Ka-Yee Grace, Baghela Arjun S, Hancock Robert E W

机构信息

Centre for Microbial Diseases and Immunity Research, University of British Columbia, Vancouver, BC, Canada.

出版信息

Front Microbiol. 2021 Apr 13;12:640787. doi: 10.3389/fmicb.2021.640787. eCollection 2021.

Abstract

Bacterial biofilms are complex and highly antibiotic-resistant aggregates of microbes that form on surfaces in the environment and body including medical devices. They are key contributors to the growing antibiotic resistance crisis and account for two-thirds of all infections. Thus, there is a critical need to develop anti-biofilm specific therapeutics. Here we discuss mechanisms of biofilm formation, current anti-biofilm agents, and strategies for developing, discovering, and testing new anti-biofilm agents. Biofilm formation involves many factors and is broadly regulated by the stringent response, quorum sensing, and c-di-GMP signaling, processes that have been targeted by anti-biofilm agents. Developing new anti-biofilm agents requires a comprehensive systems-level understanding of these mechanisms, as well as the discovery of new mechanisms. This can be accomplished through omics approaches such as transcriptomics, metabolomics, and proteomics, which can also be integrated to better understand biofilm biology. Guided by mechanistic understanding, techniques such as virtual screening and machine learning can discover small molecules that can inhibit key biofilm regulators. To increase the likelihood that these candidate agents selected from approaches are efficacious in humans, they must be tested in biologically relevant biofilm models. We discuss the benefits and drawbacks of and biofilm models and highlight organoids as a new biofilm model. This review offers a comprehensive guide of current and future biological and computational approaches of anti-biofilm therapeutic discovery for investigators to utilize to combat the antibiotic resistance crisis.

摘要

细菌生物膜是复杂且具有高度抗生素抗性的微生物聚集体,它们在包括医疗设备在内的环境和身体表面形成。它们是日益严重的抗生素耐药性危机的关键因素,占所有感染的三分之二。因此,迫切需要开发针对生物膜的特异性治疗方法。在此,我们讨论生物膜形成的机制、当前的抗生物膜药物以及开发、发现和测试新型抗生物膜药物的策略。生物膜形成涉及许多因素,并受到严谨反应、群体感应和环二鸟苷酸信号传导的广泛调控,这些过程已成为抗生物膜药物的作用靶点。开发新型抗生物膜药物需要对这些机制有全面的系统层面理解,同时还需要发现新的机制。这可以通过转录组学、代谢组学和蛋白质组学等组学方法来实现,这些方法也可以整合起来以更好地理解生物膜生物学。在机制理解的指导下,虚拟筛选和机器学习等技术可以发现能够抑制关键生物膜调节因子的小分子。为了提高从这些方法中选出的候选药物在人体中有效的可能性,必须在生物学相关的生物膜模型中对其进行测试。我们讨论了体外和体内生物膜模型的优缺点,并强调类器官作为一种新型生物膜模型。本综述为当前和未来抗生物膜治疗发现的生物学和计算方法提供了全面指南,供研究人员用于应对抗生素耐药性危机。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9be3/8076610/33670c75bf03/fmicb-12-640787-g001.jpg

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