Suppr超能文献

VFDB 2025:一个用于探索抗毒力化合物的综合资源库。

VFDB 2025: an integrated resource for exploring anti-virulence compounds.

作者信息

Zhou Siyu, Liu Bo, Zheng Dandan, Chen Lihong, Yang Jian

机构信息

NHC Key Laboratory of Systems Biology of Pathogens, National Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, P.R. China.

出版信息

Nucleic Acids Res. 2025 Jan 6;53(D1):D871-D877. doi: 10.1093/nar/gkae968.

Abstract

With the escalating crisis of bacterial multidrug resistance, anti-virulence therapeutic strategies have emerged as a highly promising alternative to conventional antibiotic treatments. Anti-virulence compounds are specifically designed to target virulence factors (VFs), disarming pathogens without affecting bacterial growth and thus reduce the selective pressure for resistance development. However, due to the complexity of bacterial pathogenesis, no anti-virulence small molecules have been approved for clinical use thus far, despite the documentation of hundreds of potential candidates. To provide valuable reference resources for drug design, repurposing, and target selection, the virulence factor database (VFDB, http://www.mgc.ac.cn/VFs/) has systematically collected public data on anti-virulence compounds through extensive literature mining, and further integrated this information with its existing knowledge of bacterial VFs. To date, the VFDB has curated a comprehensive dataset of 902 anti-virulence compounds across 17 superclasses reported by 262 studies worldwide. By cross-linking the current knowledge of bacterial VFs with information on relevant compounds (e.g. classification, chemical structure, molecular targets and mechanisms of action), the VFDB aims to bridge the gap between chemists and microbiologists, providing crucial insights for the development of innovative and effective antibacterial therapies to combat bacterial infections and address antibiotic resistance.

摘要

随着细菌多重耐药危机的不断升级,抗毒力治疗策略已成为传统抗生素治疗极具前景的替代方案。抗毒力化合物专门设计用于靶向毒力因子(VF),在不影响细菌生长的情况下使病原体失活,从而降低耐药性发展的选择压力。然而,由于细菌致病机制的复杂性,尽管有数百种潜在候选药物的记录,但迄今为止尚无抗毒力小分子被批准用于临床。为了为药物设计、重新利用和靶点选择提供有价值的参考资源,毒力因子数据库(VFDB,http://www.mgc.ac.cn/VFs/)通过广泛的文献挖掘系统地收集了抗毒力化合物的公开数据,并将这些信息与现有的细菌毒力因子知识进一步整合。迄今为止,VFDB已整理了一个综合数据集,包含全球262项研究报告的17个超类中的902种抗毒力化合物。通过将当前细菌毒力因子知识与相关化合物信息(如分类、化学结构、分子靶点和作用机制)进行交叉关联,VFDB旨在弥合化学家和微生物学家之间的差距,为开发创新有效的抗菌疗法以对抗细菌感染和解决抗生素耐药性问题提供关键见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b1/11701737/3237e17db91e/gkae968figgra1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验