Suppr超能文献

I3-Ag85对结核菌酸二霉菌酸酯合成的影响。

I3-Ag85 effect on phthiodiolone dimycocerosate synthesis.

作者信息

Rens Céline, Laval Françoise, Wattiez Ruddy, Lefèvre Philippe, Dufrasne François, Daffé Mamadou, Fontaine Véronique

机构信息

Université Libre de Bruxelles (ULB), Unit of Pharmaceutical Microbiology and Hygiene, CP205/2, Boulevard du Triomphe, 1050 Brussels, Belgium.

Institute of Pharmacology and Structural Biology, University of Toulouse, CNRS, University Paul Sabatier (UMR 5089), Department of "Tuberculosis and Infection Biology", 205 route de Narbonne, BP64182, 31077 Toulouse cedex 04, France.

出版信息

Tuberculosis (Edinb). 2018 Jan;108:93-95. doi: 10.1016/j.tube.2017.10.007. Epub 2017 Oct 24.

Abstract

The multiplicity of drug resistant Mycobacterium tuberculosis (Mtb) strains is a growing health issue. New therapies are needed, acting on new targets. The I3-Ag85 was already reported to reduce the amount of trehalose dimycolate lipid of the mycobacterial cell wall. This inhibitor of Ag85C increased the mycobacterial wall permeability. We previously showed that M. tuberculosis strains, even multi-drug resistant and extensively-drug resistant strains, can be susceptible to vancomycin when concomitantly treated with a drug altering the cell envelope integrity. We investigated the effect of the I3-Ag85 on vancomycin susceptibility of M. tuberculosis. Although no synergy was observed, a new target of this drug was discovered: the production of phthiodiolone dimycocerosate (PDIM B).

摘要

耐药结核分枝杆菌(Mtb)菌株的多样性是一个日益严重的健康问题。需要作用于新靶点的新疗法。I3-Ag85已被报道可减少分枝杆菌细胞壁中海藻糖二霉菌酸脂的含量。这种Ag85C抑制剂增加了分枝杆菌细胞壁的通透性。我们之前表明,结核分枝杆菌菌株,即使是耐多药和广泛耐药菌株,在与改变细胞壁完整性的药物联合治疗时,也可能对万古霉素敏感。我们研究了I3-Ag85对结核分枝杆菌万古霉素敏感性的影响。虽然未观察到协同作用,但发现了这种药物的一个新靶点:邻苯二酚二霉菌酸酯(PDIM B)的产生。

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