Rapid Membrane Disruption by a Perforin-Like Protein Facilitates Parasite Exit from Host Cells

被引:216
|
作者
Kafsack, Bjorn F. C. [1 ,2 ]
Pena, Janethe D. O. [3 ]
Coppens, Isabelle [2 ]
Ravindran, Sandeep [4 ]
Boothroyd, John C. [4 ]
Carruthers, Vern B. [1 ]
机构
[1] Univ Michigan, Sch Med, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USA
[2] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Mol Microbiol & Immunol, Baltimore, MD 21205 USA
[3] Univ Fed Uberlandia, Dept Immunol, BR-38400 Uberlandia, MG, Brazil
[4] Stanford Univ, Sch Med, Dept Microbiol & Immunol, Stanford, CA 94305 USA
关键词
PORE-FORMING TOXINS; TOXOPLASMA-GONDII; ATTACK; MECHANISM; DOMAIN; FAMILY; SPOROZOITES; INFECTION; DEFENSE; DEATH;
D O I
10.1126/science.1165740
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Perforin-like proteins are expressed by many bacterial and protozoan pathogens, yet little is known about their function or mode of action. Here, we describe Toxoplasma perforin- like protein 1 ( TgPLP1), a secreted perforin- like protein of the intracellular protozoan pathogen Toxoplasma gondii that displays structural features necessary for pore formation. After intracellular growth, TgPLP1- deficient parasites failed to exit normally, resulting in entrapment within host cells. We show that this defect is due to an inability to rapidly permeabilize the parasitophorous vacuole membrane and host plasma membrane during exit. TgPLP1 ablation had little effect on growth in culture but resulted in a reduction greater than five orders of magnitude of acute virulence in mice. Perforin- like proteins from other intracellular pathogens may play a similar role in microbial egress and virulence.
引用
收藏
页码:530 / 533
页数:4
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