Induction of cell death after localization to the host cell mitochondria by the Mycobacterium tuberculosis PE_PGRS33 protein

被引:66
作者
Cadieux, Nathalie [1 ,2 ]
Parra, Marcela [2 ]
Cohen, Hannah [2 ]
Maric, Dragan [3 ]
Morris, Sheldon L. [2 ]
Brennan, Michael J. [1 ,2 ]
机构
[1] AERAS Global TB Vaccine Fdn, Rockville, MD USA
[2] US FDA, Ctr Biol Evaluat & Res, Bethesda, MD USA
[3] Natl Inst Neurol Disorders & Stroke, NIH, Flow Cytometry Core Facil, Bethesda, MD USA
来源
MICROBIOLOGY-SGM | 2011年 / 157卷
关键词
PE-PGRS PROTEINS; VII SECRETION; EXPRESSION; APOPTOSIS; NECROSIS; MACROPHAGES; VIRULENCE; SYSTEM; POLYMORPHISM; INFECTION;
D O I
10.1099/mic.0.041996-0
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学];
摘要
PE_PGRS33 is the most studied member of the unique PE family of mycobacterial proteins. These proteins are composed of a PE domain (Pro-Glu motif), a linker region and a PGRS domain (polymorphic GC-rich-repetitive sequence). Previous studies have shown that PE_PGRS33 is surface-exposed, constitutively expressed during growth and infection, involved in creating antigenic diversity, and able to induce death in transfected or infected eukaryotic cells. In this study, we showed that PE_PGRS33 co-localizes to the mitochondria of transfected cells, a phenomenon dependent on the linker region and the PGRS domain, but not the PE domain. Using different genetic fusions and chimeras, we also demonstrated a direct correlation between localization to the host mitochondria and the induction of cell death. Finally, although all constructs localizing to the mitochondria did induce apoptosis, only the wild-type PE_PGRS33 with its own PE domain also induced primary necrosis, indicating a potentially important role for the PE domain. Considering the importance of primary necrosis in Mycobacterium tuberculosis dissemination during natural infection, the PE_PGRS33 protein may play a crucial role in the pathogenesis of tuberculosis.
引用
收藏
页码:793 / 804
页数:12
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