Utilize este identificador para referenciar este registo: http://hdl.handle.net/10362/36409
Título: Bacterial autolysins trim cell surface peptidoglycan to prevent detection by the drosophila innate immune system
Autor: Atilano, Magda Luciana
Pereira, Pedro Matos
Vaz, Filipa
Catalão, Maria João
Reed, Patricia
Grilo, Maria Inês Ramos
Almeida, Rita Gonçalves Sobral de
Ligoxygakis, Petros
Pinho, Mariana Gomes
Filipe, Sérgio Joaquim Raposo
Palavras-chave: Animals
Drosophila
Gram-Positive Bacteria
Hydrolysis
Immunity, Innate
N-Acetylmuramoyl-L-alanine Amidase
Peptidoglycan
Virulence
Biochemistry, Genetics and Molecular Biology(all)
Immunology and Microbiology(all)
Medicine(all)
Neuroscience(all)
Data: 1-Abr-2014
Citação: Atilano, M. L., Pereira, P. M., Vaz, F., Catalão, M. J., Reed, P., Grilo, M. I. R., Almeida, R. G. S. D., Ligoxygakis, P., Pinho, M. G., & Filipe, S. J. R. (2014). Bacterial autolysins trim cell surface peptidoglycan to prevent detection by the drosophila innate immune system. eLife, 2014(3), Article e02277. https://doi.org/10.7554/eLife.02277
Resumo: 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.
Descrição: Fundacao para a Ciencia e Tecnologia PTDC/SAU-IMU/111806/2009 Sergio Raposo Filipe Wellcome Trust WT087680 Petros Ligoxygakis European Research Council ERC-2012-StG-310987 Mariana Gomes Pinho Fundacao para a Ciencia e Tecnologia PTDC/BIA-MIC/111817/2009 Sergio Raposo Filipe Fundacao para a Ciencia e Tecnologia PTDC/BIA-BCM/099152/2008 Mariana Gomes Pinho Fundacao para a Ciencia e Tecnologia PTDC/BIA-MIC/101375/2008 Rita Goncalves Sobral Fundacao para a Ciencia e Tecnologia PEst-OE/EQB/LA0004/2011 Mariana Gomes Pinho, Sergio Raposo Filipe Fundacao para a Ciencia e Tecnologia Fellowship SFRH/BD/28440/2006 Magda Luciana Atilano Fundacao para a Ciencia e Tecnologia Fellowship SFRH/BD/41119/2007 Pedro Matos Pereira Fundacao para a Ciencia e Tecnologia Fellowship SFRH/BD/78748/2011 Filipa Vaz Fundacao para a Ciencia e Tecnologia Fellowship SFRH/BD/77758/2011 Maria Joao Catalao Fundacao para a Ciencia e Tecnologia Fellowship SFRH/BD/23812/2005 Patricia Reed Fundacao para a Ciencia e Tecnologia Fellowship SFRH/BD/70162/2010 Ines Ramos Grilo The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
Peer review: yes
URI: http://www.scopus.com/inward/record.url?scp=84898467936&partnerID=8YFLogxK
DOI: https://doi.org/10.7554/eLife.02277
Aparece nas colecções:FCT: DCV - Artigos em revista internacional com arbitragem científica

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