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活的结核分枝杆菌导致吞噬溶酶体生物发生受阻的机制。

Mechanism of phagolysosome biogenesis block by viable Mycobacterium tuberculosis.

作者信息

Vergne Isabelle, Chua Jennifer, Lee Hwang-Ho, Lucas Megan, Belisle John, Deretic Vojo

机构信息

Department of Molecular Genetics and Microbiology , University of New Mexico School of Medicine, Albuquerque, NM 87131, USA.

出版信息

Proc Natl Acad Sci U S A. 2005 Mar 15;102(11):4033-8. doi: 10.1073/pnas.0409716102. Epub 2005 Mar 7.

Abstract

Live Mycobacterium tuberculosis persists in macrophage phagosomes by interfering with phagolysosome biogenesis. Here, using four-dimensional microscopy and in vitro assays, we report the principal difference between phagosomes containing live and dead mycobacteria. Phosphatidylinositol 3-phosphate (PI3P), a membrane trafficking regulatory lipid essential for phagosomal acquisition of lysosomal constituents, is retained on phagosomes harboring dead mycobacteria but is continuously eliminated from phagosomes with live bacilli. We show that the exclusion of PI3P from live mycobacterial phagosomes can be only transiently reversed by Ca2+ fluxes, and that live M. tuberculosis secretes a lipid phosphatase, SapM, that hydrolyzes PI3P, inhibits phagosome-late endosome fusion in vitro, and contributes to inhibition of phagosomal maturation.

摘要

活的结核分枝杆菌通过干扰吞噬溶酶体的生物发生而持续存在于巨噬细胞吞噬体中。在此,我们利用四维显微镜和体外试验,报告了含有活的和死的分枝杆菌的吞噬体之间的主要差异。磷脂酰肌醇3-磷酸(PI3P)是一种对吞噬体获取溶酶体成分至关重要的膜运输调节脂质,它保留在含有死分枝杆菌的吞噬体上,但会从含有活杆菌的吞噬体中持续消除。我们表明,Ca2+通量只能短暂逆转活分枝杆菌吞噬体中PI3P的排除,并且活的结核分枝杆菌分泌一种脂质磷酸酶SapM,它能水解PI3P,在体外抑制吞噬体-晚期内体融合,并有助于抑制吞噬体成熟。

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