Dramsi Shaynoor, Cossart Pascale
Unité des Interactions Bactéries Cellules, Institut Pasteur, 75724 Paris Cedex 15, France.
J Cell Biol. 2002 Mar 18;156(6):943-6. doi: 10.1083/jcb.200202121.
Cholesterol-dependent cytolysins (CDCs)* are produced by a large number of pathogenic gram-positive bacteria. A member of this family, listeriolysin O (LLO), is produced by the intracellular pathogen Listeria monocytogenes. A unique feature of LLO is its low optimal pH activity (approximately 6) which permits escape of the bacterium from the phagosome into the host cell cytosol without damaging the plasma membrane of the infected cell. In a recent study (Glomski et al., 2002, this issue), Portnoy's group has addressed the molecular mechanism underlying the pH sensitivity of LLO. Unexpectedly, a single amino acid substitution in LLO L461T results in a molecule more active at neutral pH and promoting premature permeabilization of the infected cells, leading to attenuated virulence. This finding highlights how subtle changes in proteins can be exploited by bacterial pathogens to establish and maintain the integrity of their specific niches.
胆固醇依赖性细胞溶素(CDCs)*由大量致病性革兰氏阳性细菌产生。该家族的一个成员,李斯特菌溶血素O(LLO),由细胞内病原体单核细胞增生李斯特菌产生。LLO的一个独特特征是其最佳pH活性较低(约为6),这使得细菌能够从吞噬体逃逸到宿主细胞胞质溶胶中,而不会损害被感染细胞的质膜。在最近的一项研究(Glomski等人,2002年,本期)中,波特诺伊的研究小组探讨了LLO对pH敏感性的分子机制。出乎意料的是,LLO L461T中的单个氨基酸取代导致一个在中性pH下更具活性的分子,并促进被感染细胞的过早通透化,从而导致毒力减弱。这一发现突出了细菌病原体如何利用蛋白质中的细微变化来建立和维持其特定生态位的完整性。