Unité des Interactions Bactéries-Cellules, Institut Pasteur, U604, Institut National de la Santé et de la Recherche Médicale, Institut National de la Recherche Agronomique, 75015 Paris, France.
Proc Natl Acad Sci U S A. 2011 Mar 1;108(9):3612-7. doi: 10.1073/pnas.1100126108. Epub 2011 Feb 14.
Mitochondria are essential and highly dynamic organelles, constantly undergoing fusion and fission. We analyzed mitochondrial dynamics during infection with the human bacterial pathogen Listeria monocytogenes and show that this infection profoundly alters mitochondrial dynamics by causing transient mitochondrial network fragmentation. Mitochondrial fragmentation is specific to pathogenic Listeria monocytogenes, and it is not observed with the nonpathogenic Listeria innocua species or several other intracellular pathogens. Strikingly, the efficiency of Listeria infection is affected in cells where either mitochondrial fusion or fission has been altered by siRNA treatment, highlighting the relevance of mitochondrial dynamics for Listeria infection. We identified the secreted pore-forming toxin listeriolysin O as the bacterial factor mainly responsible for mitochondrial network disruption and mitochondrial function modulation. Together, our results suggest that the transient shutdown of mitochondrial function and dynamics represents a strategy used by Listeria at the onset of infection to interfere with cellular physiology.
线粒体是至关重要且高度动态的细胞器,不断经历融合和裂变。我们分析了感染人源细菌病原体李斯特菌时的线粒体动力学,结果表明,这种感染通过导致短暂的线粒体网络碎片化,深刻地改变了线粒体动力学。线粒体碎片化是特异性的致病性李斯特菌的现象,在非致病性李斯特菌或几种其他细胞内病原体中观察不到。引人注目的是,在用 siRNA 处理改变线粒体融合或裂变的细胞中,李斯特菌感染的效率受到影响,这突出表明线粒体动力学对李斯特菌感染的重要性。我们确定了分泌的孔形成毒素李斯特菌溶血素 O 是主要负责破坏线粒体网络和调节线粒体功能的细菌因子。总之,我们的结果表明,线粒体功能和动力学的短暂关闭代表了李斯特菌在感染开始时用来干扰细胞生理学的一种策略。