The type VI secretion system deploys antifungal effectors against microbial competitors

被引:164
作者
Trunk, Katharina [1 ]
Peltier, Julien [2 ,3 ]
Liu, Yi-Chia [1 ]
Dill, Brian D. [2 ]
Walker, Louise [4 ]
Gow, Neil A. R. [4 ]
Stark, Michael J. R. [5 ]
Quinn, Janet [3 ]
Strahl, Henrik [6 ]
Trost, Matthias [2 ,3 ]
Coulthurst, Sarah J. [1 ]
机构
[1] Univ Dundee, Sch Life Sci, Div Mol Microbiol, Dundee, Scotland
[2] Univ Dundee, Sch Life Sci, MRC Prot Phosphorylat & Ubiquitylat Unit, Dundee, Scotland
[3] Newcastle Univ, Inst Cell & Mol Biosci, Newcastle Upon Tyne, Tyne & Wear, England
[4] Univ Aberdeen, Aberdeen Fungal Grp, Inst Med Sci, MRC Ctr Med Mycol, Aberdeen, Scotland
[5] Univ Dundee, Ctr Gene Regulat & Express, Sch Life Sci, Dundee, Scotland
[6] Newcastle Univ, Ctr Bacterial Cell Biol, Newcastle Upon Tyne, Tyne & Wear, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
SACCHAROMYCES-CEREVISIAE; CANDIDA-ALBICANS; AMINO-ACID; TRANSCRIPTIONAL RESPONSE; VIRULENCE FACTORS; YEAST; PERMEASE; GENE; PATHOGEN; PROTEIN;
D O I
10.1038/s41564-018-0191-x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Interactions between bacterial and fungal cells shape many polymicrobial communities. Bacteria elaborate diverse strategies to interact and compete with other organisms, including the deployment of protein secretion systems. The type VI secretion system (T6SS) delivers toxic effector proteins into host eukaryotic cells and competitor bacterial cells, but, surprisingly, T6SS-delivered effectors targeting fungal cells have not been reported. Here we show that the 'antibacterial' T6SS of Serratia marcescens can act against fungal cells, including pathogenic Candida species, and identify the previously undescribed effector proteins responsible. These antifungal effectors, Tfel and Tfe2, have distinct impacts on the target cell, but both can ultimately cause fungal cell death. 'In competition' proteomics analysis revealed that T6SS-mediated delivery of Tfe2 disrupts nutrient uptake and amino acid metabolism in fungal cells, and leads to the induction of autophagy. Intoxication by Tfel, in contrast, causes a loss of plasma membrane potential. Our findings extend the repertoire of the T6SS and suggest that antifungal T6SSs represent widespread and important determinants of the outcome of bacterial-fungal interactions.
引用
收藏
页码:920 / 931
页数:12
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