Bacterial autolysins trim cell surface peptidoglycan to prevent detection by the Drosophila innate immune system

被引:30
作者
Atilano, Magda Luciana [1 ,2 ]
Pereira, Pedro Matos [3 ]
Vaz, Filipa [1 ]
Catalao, Maria Joao [1 ]
Reed, Patricia [3 ]
Grilo, Ines Ramos [4 ]
Sobral, Rita Goncalves [5 ]
Ligoxygakis, Petros [2 ]
Pinho, Mariana Gomes [3 ]
Filipe, Sergio Raposo [1 ]
机构
[1] Univ Nova Lisboa, Inst Tecnol Quim & Biol, Lab Bacterial Cell Surfaces & Pathogenesis, Oeiras, Portugal
[2] Univ Oxford, Dept Biochem, Genes & Dev Lab, Oxford OX1 3QU, England
[3] Univ Nova Lisboa, Inst Tecnol Quim & Biol, Lab Bacterial Cell Biol, Oeiras, Portugal
[4] Univ Nova Lisboa, Inst Tecnol Quim & Biol, Mol Genet Lab, P-2780156 Oeiras, Portugal
[5] Univ Nova Lisboa, Fac Ciencias & Tecnol, Ctr Recursos Microbiol CREM, Dept Ciencias Vida, Caparica, Portugal
基金
欧洲研究理事会; 英国惠康基金;
关键词
D O I
10.7554/eLife.02277
中图分类号
Q [生物科学];
学科分类号
090105 [作物生产系统与生态工程];
摘要
Bacteria have to avoid recognition by the host immune system in order to establish a successful infection. Peptidoglycan, the principal constituent of virtually all bacterial surfaces, is a specific molecular signature recognized by dedicated host receptors, present in animals and plants, which trigger an immune response. Here we report that autolysins from Gram-positive pathogenic bacteria, enzymes capable of hydrolyzing peptidoglycan, have a major role in concealing this inflammatory molecule from Drosophila peptidoglycan recognition proteins (PGRPs). We show that autolysins trim the outermost peptidoglycan fragments and that in their absence bacterial virulence is impaired, as PGRPs can directly recognize leftover peptidoglycan extending beyond the external layers of bacterial proteins and polysaccharides. The activity of autolysins is not restricted to the producer cells but can also alter the surface of neighboring bacteria, facilitating the survival of the entire population in the infected host.
引用
收藏
页数:23
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