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从筛选到靶点:抗毒力化合物开发的见解与方法

From screen to target: insights and approaches for the development of anti-virulence compounds.

作者信息

Beckham Katherine S H, Roe Andrew J

机构信息

Glasgow Biomedical Research Centre, Institute of Infection, Immunity and Inflammation, College of Medical, Veterinary and Life Sciences, University of Glasgow Glasgow, UK.

出版信息

Front Cell Infect Microbiol. 2014 Sep 30;4:139. doi: 10.3389/fcimb.2014.00139. eCollection 2014.

Abstract

A detailed understanding of host-pathogen interactions provides exciting opportunities to interfere with the infection process. Anti-virulence compounds aim to modulate or pacify pathogenesis by reducing expression of critical virulence determinants. In particular, prevention of attachment by inhibiting adhesion mechanisms has been the subject of intense research. Whilst it has proven relatively straightforward to develop robust screens for potential anti-virulence compounds, understanding their precise mode of action has proven much more challenging. In this review we illustrate this challenge from our own experiences working with the salicylidene acylhydrazide group of compounds. We aim to provide a useful perspective to guide researchers interested in this field and to avoid some of the obvious pitfalls.

摘要

对宿主-病原体相互作用的深入理解为干扰感染过程提供了令人兴奋的机会。抗毒力化合物旨在通过降低关键毒力决定因素的表达来调节或缓和发病机制。特别是,通过抑制黏附机制来防止病原体附着一直是深入研究的主题。虽然已证明开发针对潜在抗毒力化合物的强大筛选方法相对简单,但了解它们的确切作用方式却被证明更具挑战性。在本综述中,我们根据自己研究水杨醛酰肼类化合物的经验来说明这一挑战。我们旨在提供一个有用的视角,以指导该领域的研究人员,并避免一些明显的陷阱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d73f/4179734/6bd812f1f1e4/fcimb-04-00139-g0001.jpg

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