TY - JOUR
T1 - Bacterial membrane vesicles deliver peptidoglycan to NOD1 in epithelial cells
AU - Liaskos, Maria
AU - Turnbull, Lynne
AU - Carneiro, Leticia
AU - Firth, Stephen Daryl
AU - Coleman, Harold Arthur
AU - Parkington, Helena Cecilia
AU - Le Bourhis, Lionel
AU - Karrar, Abdul
AU - Viala, Jerome
AU - Mak, Johnson
AU - Hutton, Melanie Lisa
AU - Davies, John Keith
AU - Crack, Peter J
AU - Hertzog, Paul John
AU - Philpott, Dana
AU - Girardin, Stephen E
AU - Whitchurch, Cynthia Beth
AU - Ferrero, Richard Louis
PY - 2010
Y1 - 2010
N2 - Summary Gram negative bacterial peptidoglycan is specifically recognized by the host intracellular sensor NOD1, resulting in the generation of innate immune responses. Although epithelial cells are normally refractory to external stimulation with peptidoglycan, these cells have been shown to respond in a NOD1 dependent manner to Gram negative pathogens that can either invade or secrete factors into host cells. In the present work, we report that Gram negative bacteria can deliver peptidoglycan to cytosolic NOD1 in host cells via a novel mechanism involving outer membrane vesicles (OMVs). We purified OMVs from the Gram negative mucosal pathogens: Helicobacter pylori, Pseudomonasaeruginosa and Neisseria gonorrhoea and demonstrated that these peptidoglycan containing OMVs upregulated NF-kappaB and NOD1 dependent responses in vitro. These OMVs entered epithelial cells through lipid rafts thereby inducing NOD1 dependent responses in vitro. Moreover, OMVs delivered intragastrically to mice induced innate and adaptive immune responses via a NOD1 dependent but TLR independent mechanism. Collectively, our findings identify OMVs as a generalized mechanism whereby Gram-negative bacteria deliver peptidoglycan to cytosolic NOD1. We propose that OMVs released by bacteria in vivo may promote inflammation and pathology in infected hosts.
AB - Summary Gram negative bacterial peptidoglycan is specifically recognized by the host intracellular sensor NOD1, resulting in the generation of innate immune responses. Although epithelial cells are normally refractory to external stimulation with peptidoglycan, these cells have been shown to respond in a NOD1 dependent manner to Gram negative pathogens that can either invade or secrete factors into host cells. In the present work, we report that Gram negative bacteria can deliver peptidoglycan to cytosolic NOD1 in host cells via a novel mechanism involving outer membrane vesicles (OMVs). We purified OMVs from the Gram negative mucosal pathogens: Helicobacter pylori, Pseudomonasaeruginosa and Neisseria gonorrhoea and demonstrated that these peptidoglycan containing OMVs upregulated NF-kappaB and NOD1 dependent responses in vitro. These OMVs entered epithelial cells through lipid rafts thereby inducing NOD1 dependent responses in vitro. Moreover, OMVs delivered intragastrically to mice induced innate and adaptive immune responses via a NOD1 dependent but TLR independent mechanism. Collectively, our findings identify OMVs as a generalized mechanism whereby Gram-negative bacteria deliver peptidoglycan to cytosolic NOD1. We propose that OMVs released by bacteria in vivo may promote inflammation and pathology in infected hosts.
UR - http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=19888989
U2 - 10.1111/j.1462-5822.2009.01404.x
DO - 10.1111/j.1462-5822.2009.01404.x
M3 - Article
SN - 1462-5814
VL - 12
SP - 372
EP - 385
JO - Cellular Microbiology
JF - Cellular Microbiology
ER -