A chimeric Mla-Pqi lipid transport system is required for Brucella abortus survival in macrophages.

IF 8.3 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
EMBO Journal Pub Date : 2025-09-01 Epub Date: 2025-08-13 DOI:10.1038/s44318-025-00511-3
Adélie Lannoy, Alexi Ronneau, Miguel Fernández-García, Marc Dieu, Patricia Renard, Antonia García Fernández, Raquel Condez-Alvarez, Xavier De Bolle
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引用次数: 0

Abstract

The cell envelope of gram-negative bacteria is composed of an inner and an outer membrane. In Escherichia coli, several pathways mediate phospholipid transport between the two membranes, including the Mla (i.e., maintenance of lipid asymmetry) and Pqi (i.e., paraquat inducible) systems. Here, we identify and characterise in the intracellular pathogen Brucella abortus a complex named Mpc, which exhibits homology to both Mla and Pqi components. Mpc is required for bacterial growth under envelope stress conditions, and for survival within macrophages during the early stages of infection. Analyses of protein-protein interactions and structural predictions suggest that the Mpc complex bridges the two membranes of the bacterial cell envelope. Absence of this system results in altered lipid composition of the outer membrane vesicles, indicating that Mpc plays a role in lipid transport between the membranes. Our sequence comparisons reveal that Mpc is conserved across numerous species of Hyphomicrobiales. The discovery of this novel lipid-trafficking system expands our understanding of the diversity and evolution of lipid-transport mechanisms in diderm bacteria.

嵌合Mla-Pqi脂质转运系统是流产布鲁氏菌在巨噬细胞中存活所必需的。
革兰氏阴性菌的细胞膜由内膜和外膜组成。在大肠杆菌中,有几种途径介导两种膜之间的磷脂转运,包括Mla(即维持脂质不对称)和Pqi(即百草草诱导)系统。在这里,我们在胞内病原体布鲁氏菌中鉴定和表征了一个名为Mpc的复合物,它与Mla和Pqi成分具有同源性。Mpc是细菌在包膜应激条件下生长所必需的,也是感染早期巨噬细胞存活所必需的。蛋白质-蛋白质相互作用的分析和结构预测表明,Mpc复合物连接了细菌细胞包膜的两层膜。该系统的缺失导致外膜囊泡的脂质组成改变,表明Mpc在膜间的脂质运输中起作用。我们的序列比较显示Mpc在许多菌丝微生物种中是保守的。这种新的脂质运输系统的发现扩大了我们对脂质运输机制的多样性和进化的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
EMBO Journal
EMBO Journal 生物-生化与分子生物学
CiteScore
18.90
自引率
0.90%
发文量
246
审稿时长
1.5 months
期刊介绍: The EMBO Journal has stood as EMBO's flagship publication since its inception in 1982. Renowned for its international reputation in quality and originality, the journal spans all facets of molecular biology. It serves as a platform for papers elucidating original research of broad general interest in molecular and cell biology, with a distinct focus on molecular mechanisms and physiological relevance. With a commitment to promoting articles reporting novel findings of broad biological significance, The EMBO Journal stands as a key contributor to advancing the field of molecular biology.
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