Emerging enterococcus pore-forming toxins with MHC/HLA-I as receptors

被引:37
|
作者
Xiong, Xiaozhe [1 ,2 ]
Tian, Songhai [1 ,2 ]
Yang, Pan [2 ]
Lebreton, Francois [2 ,3 ,4 ,5 ]
Bao, Huan [6 ]
Sheng, Kuanwei [7 ]
Yin, Linxiang [1 ,2 ]
Chen, Pengsheng [1 ,2 ]
Zhang, Jie [1 ]
Qi, Wanshu [8 ,9 ]
Ruan, Jianbin [10 ,11 ,14 ]
Wu, Hao [10 ,11 ,12 ,13 ]
Chen, Hong [12 ,13 ]
Breault, David T. [8 ,9 ,15 ]
Wu, Hao [10 ,11 ,12 ,13 ]
Earl, Ashlee M. [4 ]
Gilmore, Michael S. [2 ,3 ,4 ]
Abraham, Jonathan [2 ,4 ,16 ]
Dong, Min [1 ,2 ]
机构
[1] Harvard Med Sch, Boston Childrens Hosp, Dept Urol, Dept Surg, Boston, MA 02115 USA
[2] Harvard Med Sch, Dept Microbiol, Boston, MA 02115 USA
[3] Harvard Med Sch, Massachusetts Eye & Ear Infirm, Dept Ophthalmol, Boston, MA 02114 USA
[4] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
[5] Walter Reed Army Inst Res, Multidrug Resistant Organism Repository & Surveil, Silver Spring, MD 20910 USA
[6] Scripps Res Inst, Dept Mol Med, Jupiter, FL 33458 USA
[7] Harvard Univ, Wyss Inst Biol Inspired Engn, Boston, MA 02115 USA
[8] Boston Childrens Hosp, Div Endocrinol, Boston, MA 02115 USA
[9] Harvard Med Sch, Dept Pediat, Boston, MA 02115 USA
[10] Boston Childrens Hosp, Program Cellular & Mol Med, Boston, MA 02115 USA
[11] Harvard Med Sch, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[12] Boston Childrens Hosp, Dept Surg, Vasc Biol Program, Boston, MA 02115 USA
[13] Harvard Med Sch, Boston, MA 02115 USA
[14] Univ Connecticut, Hlth Sch Med, Dept Immunol, Farmington, CT 06030 USA
[15] Harvard Stem Cell Inst, Cambridge, MA 02138 USA
[16] Brigham & Womens Hosp, Dept Med, Div Infect Dis, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
MHC CLASS-I; CRYSTAL-STRUCTURE; ALPHA-HEMOLYSIN; REVEALS; INTERFERON; MOLECULE; ANTIGEN; PREDICTION; COMPONENT; MECHANISM;
D O I
10.1016/j.cell.2022.02.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Enterococci are a part of human microbiota and a leading cause of multidrug resistant infections. Here, we identify a family of Enterococcus pore-forming toxins (Epxs) in E. faecalis, E. faecium, and E. hirae strains isolated across the globe. Structural studies reveal that Epxs form a branch of 0-barrel pore-forming toxins with a 0-barrel protrusion (designated the top domain) sitting atop the cap domain. Through a genome-wide CRISPR-Cas9 screen, we identify human leukocyte antigen class I (HLA-I) complex as a receptor for two members (Epx2 and Epx3), which preferentially recognize human HLA-I and homologous MHC-I of equine, bovine, and porcine, but not murine, origin. Interferon exposure, which stimulates MHC-I expression, sensitizes human cells and intestinal organoids to Epx2 and Epx3 toxicity. Co-culture with Epx2-harboring E. faecium damages human peripheral blood mononuclear cells and intestinal organoids, and this toxicity is neutralized by an Epx2 antibody, demonstrating the toxin-mediated virulence of Epx-carrying Enterococcus.
引用
收藏
页码:1157 / +
页数:38
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