Department of Molecular Biology and Biochemistry, Simon Fraser University, Burnaby, BC, Canada.
Department of Molecular Biology and Biochemistry, Simon Fraser University, Burnaby, BC, Canada.
EBioMedicine. 2023 Feb;88:104429. doi: 10.1016/j.ebiom.2022.104429. Epub 2023 Jan 9.
Novel therapeutics to manage bacterial infections are urgently needed as the impact and prevalence of antimicrobial resistance (AMR) grows. Antivirulence therapeutics are an alternative approach to antibiotics that aim to attenuate virulence rather than target bacterial essential functions, while minimizing microbiota perturbation and the risk of AMR development. Beyond known virulence factors, pathogen-associated genes (PAGs; genes found only in pathogens to date) may play an important role in virulence or host association. Many identified PAGs encode uncharacterized hypothetical proteins and represent an untapped wealth of novel drug targets. Here, we review current advances in antivirulence drug research and development, including PAG identification, and provide a comprehensive workflow from the discovery of antivirulence drug targets to drug discovery. We highlight the importance of integrating bioinformatic/genomic-based methods for novel virulence factor discovery, coupled with experimental characterization, into existing drug screening platforms to develop novel and effective antivirulence drugs.
由于抗菌药物耐药性(AMR)的影响和流行程度不断增加,迫切需要新的治疗方法来治疗细菌感染。抗毒力治疗是一种替代抗生素的方法,旨在减弱毒力,而不是针对细菌的必需功能,同时最大限度地减少微生物群的扰动和 AMR 发展的风险。除了已知的毒力因子外,病原体相关基因(PAG;迄今为止仅在病原体中发现的基因)可能在毒力或宿主关联中发挥重要作用。许多已识别的 PAG 编码未表征的假设蛋白,代表着尚未开发的新型药物靶点的巨大财富。在这里,我们综述了抗毒力药物研究和开发的最新进展,包括 PAG 的鉴定,并提供了从抗毒力药物靶点的发现到药物发现的全面工作流程。我们强调了将基于生物信息学/基因组的新毒力因子发现方法与实验特征相结合,纳入现有的药物筛选平台,以开发新型有效的抗毒力药物的重要性。