Illuminating the landscape of host-pathogen interactions with the bacterium Listeria monocytogenes, Proc. Natl. Acad. Sci, 2011. ,
DOI : 10.1016/j.smim.2010.02.002
Conjugated action of two species-specific invasion proteins for fetoplacental listeriosis, Nature, vol.37, issue.7216, pp.1114-1118, 2008. ,
DOI : 10.1038/nature07303
Entry of Listeria monocytogenes in mammalian epithelial cells: an updated view, Cold Spring Harb, Perspect. Med, vol.2, 2012. ,
Actin-based motility of intracellular pathogens, Current Opinion in Microbiology, vol.8, issue.1, pp.35-45, 2005. ,
DOI : 10.1016/j.mib.2004.12.013
across the intestinal barrier upon specific targeting of goblet cell accessible E-cadherin, The Journal of Experimental Medicine, vol.276, issue.11, pp.2263-2277, 2011. ,
DOI : 10.1016/S0092-8674(00)00071-4
Listeriolysin O allows Listeria monocytogenes replication in macrophage vacuoles, Nature, vol.99, issue.7176, pp.350-354, 2008. ,
DOI : 10.4161/auto.4450
Surface proteins and the pathogenic potential of Listeria monocytogenes, Trends in Microbiology, vol.10, issue.5, pp.238-245, 2002. ,
DOI : 10.1016/S0966-842X(02)02342-9
E-Cadherin Is the Receptor for Internalin, a Surface Protein Required for Entry of L. monocytogenes into Epithelial Cells, Cell, vol.84, issue.6, pp.923-932, 1996. ,
DOI : 10.1016/S0092-8674(00)81070-3
A Transgenic Model for Listeriosis: Role of Internalin in Crossing the Intestinal Barrier, Science, vol.292, issue.5522, pp.1722-1725, 2001. ,
DOI : 10.1126/science.1059852
Targeting and crossing of the human maternofetal barrier by Listeria monocytogenes: Role of internalin interaction with trophoblast E-cadherin, Proceedings of the National Academy of Sciences, vol.285, issue.1, pp.6152-6157, 2004. ,
DOI : 10.1007/s004410050625
InlB-Dependent Internalization of Listeria Is Mediated by the Met Receptor Tyrosine Kinase, Cell, vol.103, issue.3, pp.501-510, 2000. ,
DOI : 10.1016/S0092-8674(00)00141-0
into host cells, The Journal of Cell Biology, vol.327, issue.5, pp.743-753, 2004. ,
DOI : 10.1126/science.1068539
Clathrin phosphorylation is required for actin recruitment at sites of bacterial adhesion and internalization, The Journal of Cell Biology, vol.195, issue.3, pp.525-536, 2011. ,
DOI : 10.1091/mbc.E04-09-0774
Endocytosis of Viruses and Bacteria, Cold Spring Harb, Perspect. Biol, vol.6, issue.8, p.25085912, 2014. ,
Clathrin-mediated endocytosis: What works for small, also works for big, BioEssays, vol.418, issue.Pt 12, pp.496-504, 2010. ,
DOI : 10.1002/bies.200900172
Membrane Trafficking and Lifestyle: The Exception or the Rule?, Annual Review of Cell and Developmental Biology, vol.25, issue.1, pp.649-670, 2009. ,
DOI : 10.1146/annurev.cellbio.042308.113331
A Common Clathrin-Mediated Machinery Co-ordinates Cell-Cell Adhesion and Bacterial Internalization, Traffic, vol.4, issue.12, pp.1653-1666, 2012. ,
DOI : 10.1091/mbc.4.6.647
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3760411
PI3-kinase activation is critical for host barrier permissiveness to Listeria monocytogenes, The Journal of Cell Biology, vol.208, issue.3, pp.165-183, 2015. ,
DOI : 10.1084/jem.20141406
URL : https://hal.archives-ouvertes.fr/pasteur-01128770
Protein InlB Is an Agonist of Mammalian Phosphoinositide 3-Kinase, Journal of Biological Chemistry, vol.10, issue.24, pp.17025-17032, 1999. ,
DOI : 10.1126/science.274.5295.2115
The carboxyl-terminal SH3 domain of the mammalian adaptor CrkII promotes internalization of Listeria monocytogenes through activation of host phosphoinositide 3-kinase, Cellular Microbiology, vol.15, issue.10, pp.2497-2516, 2007. ,
DOI : 10.1038/sj.onc.1204173
Listeria hijacks the clathrin-dependent endocytic machinery to invade mammalian cells, Nature Cell Biology, vol.16, issue.9, pp.894-900, 2005. ,
DOI : 10.1046/j.1365-2958.1997.4621825.x
Invasive and Adherent Bacterial Pathogens Co-Opt Host Clathrin for Infection, Cell Host & Microbe, vol.2, issue.5, pp.340-351, 2007. ,
DOI : 10.1016/j.chom.2007.10.001
URL : http://doi.org/10.1016/j.chom.2007.10.001
A Role for Phosphoinositide 3-Kinase in Bacterial Invasion, Science, vol.274, issue.5288, pp.780-782, 1996. ,
DOI : 10.1126/science.274.5288.780
A FRET analysis to unravel the role of cholesterol in Rac1 and PI 3-kinase activation in the InlB/Met signalling pathway, Cellular Microbiology, vol.11, issue.3, pp.790-803, 2007. ,
DOI : 10.1126/science.1068539
WASP-related proteins, Abi1 and Ena/VASP are required for Listeria invasion induced by the Met receptor, Journal of Cell Science, vol.118, issue.7, pp.1537-1547, 2005. ,
DOI : 10.1242/jcs.02285
-induced phagocytosis, The Journal of Cell Biology, vol.151, issue.1, pp.101-112, 2001. ,
DOI : 10.1083/jcb.151.5.1119
URL : https://hal.archives-ouvertes.fr/hal-00898551
The Human Arp2/3 Complex Is Composed of Evolutionarily Conserved Subunits and Is Localized to Cellular Regions of Dynamic Actin Filament Assembly, The Journal of Cell Biology, vol.101, issue.2, pp.375-384, 1997. ,
DOI : 10.1038/378578a0
Genome-wide siRNA screen identifies complementary signaling pathways involved in Listeria infection and reveals different actin nucleation mechanisms during Listeria cell invasion and actin comet tail formation, pp.598-613, 2015. ,
Septins: the fourth component of the cytoskeleton, Nature Reviews Molecular Cell Biology, vol.22, pp.183-194, 2012. ,
DOI : 10.1016/j.cub.2011.11.034
A Role for Septins in the Interaction between the Listeria monocytogenes Invasion Protein InlB and the Met Receptor, Biophysical Journal, vol.100, issue.8, pp.1949-1959, 2011. ,
DOI : 10.1016/j.bpj.2011.02.040
Distinct protein patterns associated with Listeria monocytogenes InlA- or InlB-phagosomes, Cellular Microbiology, vol.59, issue.2, pp.101-115, 2002. ,
DOI : 10.1038/35052055
Septin 11 restricts InlB-mediated invasion by Listeria, J. Biol. Chem, vol.284, pp.11613-11621, 2009. ,
Septins Regulate Bacterial Entry into Host Cells, PLoS ONE, vol.15, issue.1, 2009. ,
DOI : 10.1371/journal.pone.0004196.s003
URL : http://doi.org/10.1371/journal.pone.0004196
Type II phosphatidylinositol 4-kinases promote Listeria monocytogenes entry into target cells, Cellular Microbiology, vol.31, issue.10, pp.2381-2390, 2007. ,
DOI : 10.1074/jbc.M206860200
Phosphoinositides and host???pathogen interactions, Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids, vol.1851, issue.6, 2014. ,
DOI : 10.1016/j.bbalip.2014.09.011
Simultaneous analysis of large-scale RNAi screens for pathogen entry, BMC Genom, vol.15, issue.1162, 2014. ,
Tetraspanin CD81 Is Required for Listeria monocytogenes Invasion, Infection and Immunity, vol.78, issue.1, pp.204-20900661, 2010. ,
DOI : 10.1128/IAI.00661-09
URL : http://iai.asm.org/content/78/1/204.full.pdf
Hepatocyte CD81 is required for Plasmodium falciparum and Plasmodium yoelii sporozoite infectivity, Nature Medicine, vol.6, issue.1, pp.93-96, 2003. ,
DOI : 10.1016/0309-1651(82)90187-4
Initiation of Hepatitis C Virus Infection Is Dependent on Cholesterol and Cooperativity between CD81 and Scavenger Receptor B Type I, Journal of Virology, vol.81, issue.1, pp.374-38301134, 2006. ,
DOI : 10.1128/JVI.01134-06
Infection through Rac-Dependent Inhibition of Proinflammatory Mediator Release and Activation of Cytotoxic T Cells, The Journal of Immunology, vol.194, issue.12, pp.6090-6101, 2015. ,
DOI : 10.4049/jimmunol.1402957
Infection, Journal of Biological Chemistry, vol.41, issue.16, pp.13128-13136, 2012. ,
DOI : 10.1038/emboj.2011.60
GILT is a critical host factor for Listeria monocytogenes infection, Nature, vol.8, issue.7217, pp.1244-1247, 2008. ,
DOI : 10.1093/infdis/142.4.594
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2775488
pH-dependent perforation of macrophage phagosomes by listeriolysin O from Listeria monocytogenes, J. Exp. Med, pp.186-1159, 1997. ,
Cytolysin-dependent delay of vacuole maturation in macrophages infected with Listeria monocytogenes, Cellular Microbiology, vol.257, issue.1, 2006. ,
DOI : 10.1021/cr010142r
Membrane perforations inhibit lysosome fusion by altering pH and calcium in Listeria monocytogenes vacuoles, Cellular Microbiology, vol.366, issue.5, pp.781-792, 2006. ,
DOI : 10.1083/jcb.130.4.821
The two distinct phospholipases C of Listeria monocytogenes have overlapping roles in escape from a vacuole and cell-to-cell spread, Infect. Immun, pp.63-4231, 1995. ,
Listeriolysin O-Mediated Calcium Influx Potentiates Entry of Listeria monocytogenes into the Human Hep-2 Epithelial Cell Line, Infection and Immunity, vol.71, issue.6, pp.71-3614, 2003. ,
DOI : 10.1128/IAI.71.6.3614-3618.2003
The Pore-Forming Toxin Listeriolysin O Mediates a Novel Entry Pathway of L. monocytogenes into Human Hepatocytes, PLoS Pathogens, vol.13, issue.11, 2011. ,
DOI : 10.1371/journal.ppat.1002356.s017
Imaging Host Cell-Leishmania Interaction Dynamics Implicates Parasite Motility, Lysosome Recruitment, and Host Cell Wounding in the Infection Process, Cell Host & Microbe, vol.9, issue.4, pp.319-330, 2011. ,
DOI : 10.1016/j.chom.2011.03.011
URL : https://hal.archives-ouvertes.fr/pasteur-01433561
subverts the sphingomyelinase-mediated plasma membrane repair pathway for cell invasion, The Journal of Experimental Medicine, vol.112, issue.5, pp.909-921, 2011. ,
DOI : 10.1083/jcb.140.1.39
URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3092353/pdf
Listeria monocytogenes impairs SUMOylation for efficient infection, Nature, vol.22, issue.7292, pp.1192-1195, 2010. ,
DOI : 10.1038/nature08963
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3627292
Histone modifications induced by a family of bacterial toxins, Proceedings of the National Academy of Sciences, vol.282, issue.20, pp.13467-13472, 2007. ,
DOI : 10.1074/jbc.M610926200
Listeria monocytogenes transiently alters mitochondrial dynamics during infection, Proc. Natl. Acad. Sci, pp.3612-3617, 2011. ,
DOI : 10.1016/j.febslet.2006.03.057
URL : http://www.pnas.org/content/108/9/3612.full.pdf
L. monocytogenes-induced actin assembly requires the actA gene product, a surface protein, Cell, vol.68, issue.3, pp.521-531, 1992. ,
DOI : 10.1016/0092-8674(92)90188-I
Interaction of Human Arp2/3 Complex and the Listeria monocytogenes ActA Protein in Actin Filament Nucleation, Science, vol.281, issue.5373, pp.105-108, 1998. ,
DOI : 10.1126/science.281.5373.105
Listeria Protein ActA Mimics WASP Family Proteins:?? It Activates Filament Barbed End Branching by Arp2/3 Complex, Biochemistry, vol.40, issue.38, pp.11390-11404, 2001. ,
DOI : 10.1021/bi010486b
Isoform diversity in the Arp2/3 complex determines actin filament dynamics, Nature Cell Biology, vol.55, issue.1, pp.76-86, 2015. ,
DOI : 10.1016/j.jsb.2005.06.002
URL : https://hal.archives-ouvertes.fr/hal-01461985
The actin propulsive machinery: The proteome of Listeria monocytogenes tails, Biochemical and Biophysical Research Communications, vol.375, issue.2, pp.194-199, 2008. ,
DOI : 10.1016/j.bbrc.2008.07.152
Cytoplasmic bacteria can be targets for autophagy, Cellular Microbiology, vol.38, issue.7, pp.455-468, 2003. ,
DOI : 10.1177/38.4.2319125
Evades Killing by Autophagy During Colonization of Host Cells, Listeria monocytogenes evades killing by autophagy during colonization of host cells, pp.442-451, 2007. ,
DOI : 10.4161/auto.4450
Listeria monocytogenes ActA-mediated escape from autophagic recognition, Nature Cell Biology, vol.113, issue.10, pp.1233-1240, 2009. ,
DOI : 10.1038/ni.1634
Intracellular Growth in the Early Phase of Primary Infection, Autophagy, vol.3, issue.2, pp.117-125, 2007. ,
DOI : 10.4161/auto.3618
Recruitment of the Major Vault Protein by InlK: A Listeria monocytogenes Strategy to Avoid Autophagy, PLoS Pathogens, vol.77, issue.8, 2011. ,
DOI : 10.1371/journal.ppat.1002168.s009
Exploits Normal Host Cell Processes to Spread from Cell to Cell???, The Journal of Cell Biology, vol.266, issue.6, pp.1333-1350, 1999. ,
DOI : 10.1002/cm.970300307
URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1785326/pdf
Actin-based motility is sufficient for bacterial membrane protrusion formation and host cell uptake, Cellular Microbiology, vol.23, issue.9, pp.633-647, 2001. ,
DOI : 10.1128/jb.176.8.2362-2373.1994
Lamellipodin Is Important for Cell-to-Cell Spread and Actin-Based Motility in Listeria monocytogenes, Infection and Immunity, vol.83, issue.9, pp.3740-374800193, 2015. ,
DOI : 10.1128/IAI.00193-15
Listeria monocytogenes exploits ERM protein functions to efficiently spread from cell to cell, The EMBO Journal, vol.145, issue.6, pp.1287-1300, 2005. ,
DOI : 10.1091/mbc.6.3.247
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC556399
RNAi Screen Reveals Host Cell Kinases Specifically Involved in Listeria monocytogenes Spread from Cell to Cell, PLoS ONE, vol.5, issue.8, 2011. ,
DOI : 10.1371/journal.pone.0023399.t001
The bacterial virulence factor InlC perturbs apical cell junctions and promotes cell-to-cell spread of Listeria, Nature Cell Biology, vol.279, issue.10, pp.1212-1218, 2009. ,
DOI : 10.1046/j.1365-2958.2003.03639.x
Listeria monocytogenes exploits efferocytosis to promote cell-to-cell spread, Nature, vol.3, issue.7499, pp.1-17, 2014. ,
DOI : 10.1046/j.1462-5822.2001.00087.x
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4151619
Differential function of Listeria monocytogenes listeriolysin O and phospholipases C in vacuolar dissolution following cell-to-cell spread, Cellular Microbiology, vol.60, issue.1, pp.179-195, 2007. ,
DOI : 10.1016/0005-2736(75)90044-9
Comparative immunology, microbiology and infectious diseases, comparative immunology, Microbiol. Infect. Dis, vol.37, pp.85-96, 2014. ,
Molecular Epidemiology, Evolution, and Ecology of Francisella, Annals of the New York Academy of Sciences, vol.1105, issue.1, pp.1105-1135, 2007. ,
DOI : 10.1196/annals.1409.011
Tularemia as a Biological Weapon, JAMA, vol.285, issue.21, pp.2763-2773, 2001. ,
DOI : 10.1001/jama.285.21.2763
From the Outside-In: The Francisella tularensis Envelope and Virulence, Frontiers in Cellular and Infection Microbiology, vol.23, issue.129, 2015. ,
DOI : 10.1016/j.str.2015.03.025
Francisella tularensis travels a novel, twisted road within macrophages, Trends in Microbiology, vol.14, issue.1, pp.37-44, 2006. ,
DOI : 10.1016/j.tim.2005.11.008
into host cells, Virulence, vol.176, issue.8, pp.826-832, 2014. ,
DOI : 10.4049/jimmunol.0903790
Phagocytosis of Mycobacterium tuberculosis is mediated by human monocyte complement receptors and complement component C3, J. Immunol, pp.144-2771, 1990. ,
Francisella tularensis Enters Macrophages via a Novel Process Involving Pseudopod Loops, Infection and Immunity, vol.73, issue.9, pp.5892-5902, 2005. ,
DOI : 10.1128/IAI.73.9.5892-5902.2005
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1231130
Francisella Targets Cholesterol-Rich Host Cell Membrane Domains for Entry into Macrophages, The Journal of Immunology, vol.180, issue.12, pp.8262-8271, 2008. ,
DOI : 10.4049/jimmunol.180.12.8262
URL : http://www.jimmunol.org/content/jimmunol/180/12/8262.full.pdf
Mechanisms of Francisella tularensis intracellular pathogenesis, Cold Spring Harb ,
The Early Phagosomal Stage of Francisella tularensis Determines Optimal Phagosomal Escape and Francisella Pathogenicity Island Protein Expression, Infection and Immunity, vol.76, issue.12, pp.5488-549900682, 2008. ,
DOI : 10.1128/IAI.00682-08
Acquisition of the Vacuolar ATPase Proton Pump and Phagosome Acidification Are Essential for Escape of Francisella tularensis into the Macrophage Cytosol, Infection and Immunity, vol.76, issue.6, pp.2671-267700185, 2008. ,
DOI : 10.1128/IAI.00185-08
Virulent and Avirulent Strains of Francisella tularensis Prevent Acidification and Maturation of Their Phagosomes and Escape into the Cytoplasm in Human Macrophages, Infection and Immunity, vol.72, issue.6, pp.3204-3217, 2004. ,
DOI : 10.1128/IAI.72.6.3204-3217.2004
Multiple mechanisms of NADPH oxidase inhibition by type A and type B Francisella tularensis, Journal of Leukocyte Biology, vol.88, issue.4, pp.791-805, 2010. ,
DOI : 10.1189/jlb.1209811
Phagocytic Receptors Dictate Phagosomal Escape and Intracellular Proliferation of Francisella tularensis, Infection and Immunity, vol.79, issue.6, pp.2204-2214, 2011. ,
DOI : 10.1128/IAI.01382-10
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3125850
Pathogenesis, Molecular & Cellular Proteomics, vol.787, issue.8, pp.2278-2292, 2013. ,
DOI : 10.1016/j.chom.2011.06.004
The Francisella tularensis pathogenicity island protein IglC and its regulator MglA are essential for modulating phagosome biogenesis and subsequent bacterial escape into the cytoplasm, Cellular Microbiology, vol.70, issue.7, pp.969-979, 2005. ,
DOI : 10.1001/jama.1925.02660430001001
Identification of fevR, a Novel Regulator of Virulence Gene Expression in Francisella novicida, Infection and Immunity, vol.76, issue.8, pp.3473-3480, 2008. ,
DOI : 10.1128/IAI.00430-08
Atomic Structure of T6SS Reveals Interlaced Array Essential to Function, Cell, vol.160, issue.5, pp.940-951, 2015. ,
DOI : 10.1016/j.cell.2015.02.005
The complex amino acid diet of Francisella in infected macrophages, Frontiers in Cellular and Infection Microbiology, vol.104, issue.86, pp.1-5, 2015. ,
DOI : 10.1073/pnas.0609675104
Francisella tularensis Harvests Nutrients Derived via ATG5-Independent Autophagy to Support Intracellular Growth, PLoS Pathogens, vol.452, issue.(2), 2013. ,
DOI : 10.1371/journal.ppat.1003562.s007
URL : http://doi.org/10.1371/journal.ppat.1003562
Autophagy-mediated reentry of Francisella tularensis into the endocytic compartment after cytoplasmic replication, Proceedings of the National Academy of Sciences, vol.64, issue.10, pp.14578-14583, 2006. ,
DOI : 10.1128/AEM.70.12.7511-7519.2004
Guanylate-binding proteins promote activation of the AIM2 inflammasome during infection with Francisella novicida, Nature Immunology, vol.16, issue.5, pp.476-484, 2015. ,
DOI : 10.1371/journal.ppat.1003414
Author response, eLife, vol.3, 2016. ,
DOI : 10.7554/eLife.10625.019
Global burden of Shigella infections: implications for vaccine development and implementation of control strategies, Bull. World Health Org, pp.77-651, 1999. ,
Shigella???s ways of manipulating the host intestinal innate and adaptive immune system: a tool box for survival?, Immunology and Cell Biology, vol.3, issue.2, pp.119-129, 2007. ,
DOI : 10.1038/ni1102-1033
The virulence plasmid pWR100 and the repertoire of proteins secreted by the type III secretion apparatus of Shigella flexneri, Molecular Microbiology, vol.11, issue.4, pp.38-760, 2000. ,
DOI : 10.1038/358167a0
Shigella type III secretion effectors: how, where, when, for what purposes?, Current Opinion in Microbiology, vol.12, issue.1, pp.110-116, 2009. ,
DOI : 10.1016/j.mib.2008.12.002
Secretion of type III effectors into host cells in real time, Nature Methods, vol.16, issue.12, pp.959-965, 2005. ,
DOI : 10.1038/nmeth804
ATP-Mediated Erk1/2 Activation Stimulates Bacterial Capture by Filopodia, which Precedes Shigella Invasion of Epithelial Cells, Cell Host & Microbe, vol.9, issue.6, pp.508-519, 1996. ,
DOI : 10.1016/j.chom.2011.05.005
URL : https://hal.archives-ouvertes.fr/pasteur-00685251
Shigella Effector IpaB-Induced Cholesterol Relocation Disrupts the Golgi Complex and Recycling Network to Inhibit Host Cell Secretion, Cell Host & Microbe, vol.12, issue.3, pp.381-389, 2012. ,
DOI : 10.1016/j.chom.2012.07.010
IcsA is a Shigella flexneri adhesin regulated by the type III secretion system and required for pathogenesis, Cell Host Microbe, vol.15, pp.435-445, 2014. ,
Initial steps of Shigella infection depend on the cholesterol/sphingolipid raft-mediated CD44-IpaB interaction, The EMBO Journal, vol.21, issue.17, pp.4449-4457, 2002. ,
DOI : 10.1093/emboj/cdf457
Rafts Can Trigger Contact-mediated Secretion of Bacterial Effectors via a Lipid-based Mechanism, Journal of Biological Chemistry, vol.115, issue.46, pp.47792-47798, 2004. ,
DOI : 10.1046/j.1365-2958.2003.03598.x
CD44 binds to the Shigella IpaB protein and participates in bacterial invasion of epithelial cells, Cellular Microbiology, vol.154, issue.1, pp.19-33, 2000. ,
DOI : 10.1126/science.283.5410.2092
Bacterial Invasion: The Paradigms of Enteroinvasive Pathogens, Science, vol.304, issue.5668, pp.242-248, 2004. ,
DOI : 10.1126/science.1090124
IpaA carboxyl-terminal domain, FEBS Letters, vol.175, issue.5, pp.853-857, 2007. ,
DOI : 10.1083/jcb.200605091
Entry, Journal of Biological Chemistry, vol.125, issue.51, pp.39534-39541, 2006. ,
DOI : 10.1038/ncb1262
The IpaC Carboxyterminal Effector Domain Mediates Src-Dependent Actin Polymerization during Shigella Invasion of Epithelial Cells, PLoS Pathogens, vol.581, issue.1, 2009. ,
DOI : 10.1371/journal.ppat.1000271.s009
invasion of epithelial cells, The Journal of Cell Biology, vol.11, issue.2, pp.225-235, 2004. ,
DOI : 10.1073/pnas.97.16.9076
Effector Protein Involved in Bacterial Invasion of Host Cells, Journal of Biological Chemistry, vol.4, issue.25, pp.24022-24034, 2005. ,
DOI : 10.1016/0022-2836(80)90283-1
Shigella IpgB1 promotes bacterial entry through the ELMO???Dock180 machinery, Nature Cell Biology, vol.20, issue.1, pp.121-128, 2006. ,
DOI : 10.1128/MCB.16.4.1770
Hierarchies of Host Factor Dynamics at the Entry Site of Shigella flexneri during Host Cell Invasion, Infection and Immunity, vol.80, issue.7, pp.2548-255706391, 2012. ,
DOI : 10.1128/IAI.06391-11
Identification of a Bacterial Type III Effector Family with G Protein Mimicry Functions, Cell, vol.124, issue.1, pp.133-145, 2006. ,
DOI : 10.1016/j.cell.2005.10.031
Mimicking GEFs: a common theme for bacterial pathogens, Cellular Microbiology, vol.323, issue.1, pp.10-18, 2011. ,
DOI : 10.1126/science.1166382
The versatility of Shigella effectors, Nature Reviews Microbiology, vol.68, issue.1, pp.11-16, 2008. ,
DOI : 10.4161/auto.4450
Shigella deliver an effector protein to trigger host microtubule destabilization, which promotes Rac1 activity and efficient bacterial internalization, The EMBO Journal, vol.21, issue.12, pp.2923-2935, 2002. ,
DOI : 10.1093/emboj/cdf319
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC126072
Cholesterol binding by the bacterial type III translocon is essential for virulence effector delivery into mammalian cells, Molecular Microbiology, vol.115, issue.3, pp.590-603, 2005. ,
DOI : 10.1021/bi982497j
IpaB of Shigella flexneri causes entry into epithelial cells and escape from the phagocytic vacuole, EMBO J, vol.11, pp.1991-1999, 1992. ,
Inserts Ipab and Ipac into Host Membranes, The Journal of Cell Biology, vol.11, issue.3, pp.683-693, 1999. ,
DOI : 10.1111/j.1365-2958.1994.tb00341.x
URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2151192/pdf
The type III secretion system apparatus determines the intracellular niche of bacterial pathogens, Proceedings of the National Academy of Sciences, vol.88, issue.5, pp.1-6, 2016. ,
DOI : 10.1111/j.1365-2958.2010.07248.x
Shigella flexneri Phagosomal Escape Is Independent of Invasion, Infection and Immunity, vol.75, issue.10, pp.4826-4830, 2007. ,
DOI : 10.1128/IAI.00454-07
Galectin-3, a marker for vacuole lysis by invasive pathogens, Cellular Microbiology, vol.358, issue.2, pp.530-544, 2010. ,
DOI : 10.4049/jimmunol.166.12.7309
URL : https://hal.archives-ouvertes.fr/hal-00486248
Tracking the dynamic interplay between bacterial and host factors during pathogen-induced vacuole rupture in real time, Cellular Microbiology, vol.279, issue.11, pp.545-556, 2010. ,
DOI : 10.1016/j.tim.2007.10.002
Shigella Subverts the Host Recycling Compartment to Rupture Its Vacuole, Cell Host & Microbe, vol.16, issue.4, pp.517-530, 2014. ,
DOI : 10.1016/j.chom.2014.09.005
URL : https://hal.archives-ouvertes.fr/pasteur-01113365
Macropinosomes are Key Players in Early Shigella Invasion and Vacuolar Escape in Epithelial Cells, PLOS Pathogens, vol.4, issue.5, 2016. ,
DOI : 10.1371/journal.ppat.1005602.s014
URL : http://doi.org/10.1371/journal.ppat.1005602
Shigella Phagocytic Vacuolar Membrane Remnants Participate in the Cellular Response to Pathogen Invasion and Are Regulated by Autophagy, Cell Host & Microbe, vol.6, issue.2, pp.137-149, 2009. ,
DOI : 10.1016/j.chom.2009.07.005
Actin-dependent movement of bacterial pathogens, Nature Reviews Microbiology, vol.63, issue.2, pp.91-101, 2006. ,
DOI : 10.1038/nrmicro1320
Life on the inside: the intracellular lifestyle of cytosolic bacteria, Nature Reviews Microbiology, vol.46, issue.5, pp.333-340, 2009. ,
DOI : 10.4161/auto.6246
Entrapment of Intracytosolic Bacteria by Septin Cage-like Structures, Cell Host & Microbe, vol.8, issue.5, pp.433-444, 2010. ,
DOI : 10.1016/j.chom.2010.10.009
URL : https://hal.archives-ouvertes.fr/pasteur-01376115
'Add, stir and reduce': Yersinia spp. as model bacteria for pathogen evolution, Nature Reviews Microbiology, vol.49, issue.3, pp.177-190, 2016. ,
DOI : 10.1128/JCM.00064-11
Involvement of M cells in the bacterial invasion of Peyer's patches: a common mechanism shared by Yersinia enterocolitica and other enteroinvasive bacteria., Gut, vol.31, issue.9, pp.31-1011, 1990. ,
DOI : 10.1136/gut.31.9.1011
Yersinia enterocolitica invasin: a primary role in the initiation of infection., Proceedings of the National Academy of Sciences, vol.90, issue.14, pp.90-6473, 1993. ,
DOI : 10.1073/pnas.90.14.6473
M-cell surface beta1 integrin expression and invasin-mediated targeting of Yersinia pseudotuberculosis to mouse Peyer's patch M cells, Infect. Immun, pp.66-1237, 1998. ,
Identification of invasin: A protein that allows enteric bacteria to penetrate cultured mammalian cells, Cell, vol.50, issue.5, pp.769-778, 1987. ,
DOI : 10.1016/0092-8674(87)90335-7
Involvement of focal adhesion kinase in invasin-mediated uptake, Proceedings of the National Academy of Sciences, vol.140, issue.1, pp.95-13658, 1998. ,
DOI : 10.1083/jcb.140.1.211
Cas Fak and Pyk2 function in diverse signaling cascades to promote Yersinia uptake, J. Cell Sci, vol.115, pp.2689-2700, 2002. ,
Efficient uptake of Yersinia pseudotuberculosis via integrin receptors involves a Rac1-Arp 2/3 pathway that bypasses N-WASP function, Molecular Microbiology, vol.9, issue.3, pp.42-689, 2001. ,
DOI : 10.1128/jb.169.12.5708-5714.1987
Integrin???mediated Bacterial Uptake, The Journal of Experimental Medicine, vol.115, issue.4, pp.603-614, 2003. ,
DOI : 10.1074/jbc.M104917200
Yersinia Entry into Host Cells Requires Rab5-Dependent Dephosphorylation of PI(4,5)P2 and Membrane Scission, Cell Host & Microbe, vol.11, issue.2, pp.117-128, 2012. ,
DOI : 10.1016/j.chom.2012.01.010
??1 Integrin-Dependent Engulfment of Yersinia enterocolitica by Macrophages Is Coupled to the Activation of Autophagy and Suppressed by Type III Protein Secretion, The Journal of Immunology, vol.183, issue.9, pp.5847-5860, 2009. ,
DOI : 10.4049/jimmunol.0804242
Yersinia pestis Can Reside in Autophagosomes and Avoid Xenophagy in Murine Macrophages by Preventing Vacuole Acidification, Infection and Immunity, vol.77, issue.6, pp.2251-226100068, 2009. ,
DOI : 10.1128/IAI.00068-09
URL : http://iai.asm.org/content/77/6/2251.full.pdf
Yersinia pestis Requires Host Rab1b for Survival in Macrophages, PLOS Pathogens, vol.101, issue.38, 2015. ,
DOI : 10.1371/journal.ppat.1005241.s004
URL : http://doi.org/10.1371/journal.ppat.1005241
Autophagosomes can support Yersinia pseudotuberculosis replication in macrophages, Cellular Microbiology, vol.23, issue.2, pp.1108-1123, 2010. ,
DOI : 10.4161/auto.2829
URL : http://onlinelibrary.wiley.com/doi/10.1111/j.1462-5822.2010.01456.x/pdf
to LC3-associated pathways involving single- or double-membrane vacuoles, Autophagy, vol.58, issue.9, pp.1588-1602, 2014. ,
DOI : 10.1242/jcs.00467
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4206537
Interactions of Yersinia enterocolitica with polarized human intestinal Caco-2 cells, Medical Microbiology and Immunology, vol.184, issue.3, pp.123-127, 1995. ,
DOI : 10.1007/BF00224348
The Yersinia Ysc???Yop 'Type III' weaponry, Nature Reviews Molecular Cell Biology, vol.8, issue.10, pp.742-754, 2002. ,
DOI : 10.1038/nsb1101-974
and FAK, and the associated accumulation of these proteins in peripheral focal adhesions, The EMBO Journal, vol.267, issue.9, pp.2307-2318, 1997. ,
DOI : 10.1083/jcb.116.1.197
GAP activity of the Yersinia YopE cytotoxin specifically targets the Rho pathway: a mechanism for disruption of actin microfilament structure, Mol. Microbiol, pp.36-737, 2000. ,
Comparison of YopE and YopT activities in counteracting host signalling responses to Yersinia pseudotuberculosis infection, Cellular Microbiology, vol.174, issue.9, pp.1504-1515, 2006. ,
DOI : 10.1074/jbc.274.41.29289
Effector YopO Blocks Fc?? Receptor-mediated Phagocytosis, Journal of Biological Chemistry, vol.173, issue.6, pp.4087-4098, 2010. ,
DOI : 10.1083/jcb.119.3.617
protein kinase A phosphorylates vasodilator-stimulated phosphoprotein to modify the host cytoskeleton, Cellular Microbiology, vol.38, issue.4, pp.473-485, 2014. ,
DOI : 10.1093/nar/gkq536
Biochemical characterization of the Yersinia YopT protease: Cleavage site and recognition elements in Rho GTPases, Proc. Natl. Acad. Sci, pp.904-909, 2003. ,
DOI : 10.1074/jbc.M101763200
Regulation of focal adhesion formation by a vinculin-Arp2/3 hybrid complex, Nature Communications, vol.40, pp.1-11, 2014. ,
DOI : 10.1021/ac035406j