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12 - Type III protein secretion and inhibition of NF-κB

from Part III - Evasion of cellular immunity

Published online by Cambridge University Press:  13 August 2009

Klaus Ruckdeschel
Affiliation:
INSERM U431, Universite Montpelier II, CC100, F34095, Montpelier, Cedex 05, France
Bruno Rouot
Affiliation:
INSERM U-432, Montpellier, France
Jürgen Heesemann
Affiliation:
Max von Pettenkofer-Institut for Hygiene and Medical Microbiology, Pettenkofestr.9a, 80336 Munich, Germany
Brian Henderson
Affiliation:
University College London
Petra C. F. Oyston
Affiliation:
Defence Science and Technology Laboratory, Salisbury
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Summary

INTRODUCTION

When faced with a bacterial pathogen, the multicellular organism raises a series of defense responses involving both the innate and adaptive immune systems. The innate immune system refers to the first-line host defense, which confers immediate antimicrobial activities. Professional phagocytes, such as neutrophils and resident macrophages, largely constitute the cellular components of innate immunity. These cells directly attack the invading pathogen, mediate secretion of proinflammatory cytokines (see Chapter 10), and mount a protective inflammatory response. In addition to these early defense responses, the innate immune system facilitates the maturation of subsequent adaptive immunity. Both the innate and adaptive immune responses serve to eliminate the infectious challenge. However, to prevail within the host, pathogenic bacteria have evolved sophisticated strategies for evasion or neutralization of host defense mechanisms. A broad range of pathogenic Gram-negative bacteria, including phytopathogens, utilize the type III protein secretion system as a powerful tool to modulate immune responses of the host, which first enables disease.

The type III protein secretion systems are complex weapons that specifically mediate polarized delivery of bacterial virulence proteins directly inside eukaryotic cells (Galan and Collmer, 1999; Donnenberg, 2000). These secretion machineries are composed of approximately twenty proteins, which form a needle complex that protrudes from the inner bacterial membrane to the attached eukaryotic cell. The type III protein secretion systems are first activated when the bacteria come into contact with the host cell.

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Publisher: Cambridge University Press
Print publication year: 2003

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References

Aderem, A. and Ulevitch, R. J. (2000). Toll-like receptors in the induction of the innate immune response. Nature 406, 782–787CrossRefGoogle ScholarPubMed
Aliprantis, A. O., Yang, R. B., Mark, M. R., Suggett, S., Devaux, B., Radolf, J. D., Klimpel, G. R., Godowski, P., and Zychlinsky, A. (1999). Cell activation and apoptosis by bacterial lipoproteins through toll-like receptor-2. Science 285, 736–739CrossRefGoogle ScholarPubMed
Aliprantis, A. O., Yang, R. B., Weiss, D. S., Godowski, P., and Zychlinsky, A. (2000). The apoptotic signaling pathway activated by Toll-like receptor-2. European Molecular Biology Organisation Journal 19, 3325–3336CrossRefGoogle ScholarPubMed
Anderson, K. V. (2000). Toll signaling pathways in the innate immune response. Current Opinion in Immunology 12, 13–19CrossRefGoogle Scholar
Autenrieth, I. B. and Heesemann, J. (1992). In vivo neutralization of tumor necrosis factor-alpha and interferon-gamma abrogates resistance to Yersinia enterocolitica infection in mice. Medical Microbiology and Immunology 181, 333–338CrossRefGoogle ScholarPubMed
Baichwal, V. R. and Baeuerle, P. A. (1997). Apoptosis: activate NF-κB or die?Current Biology 7, R94-R96CrossRefGoogle ScholarPubMed
Baker, B., Zambryski, P., Staskawicz, B., and Dinesh-Kumar, S. P. (1997). Signaling in plant-microbe interactions. Science 276, 726–733CrossRefGoogle ScholarPubMed
Baldwin, A. S. Jr. (2001). The transcription factor NF-κB and human disease. Journal of Clinical Investigation 107, 3–6CrossRefGoogle Scholar
Boland, A. and Cornelis, G. R. (1998). Role of YopP in suppression of tumor necrosis factor alpha release by macrophages during Yersinia infection. Infection and Immunity 66, 1878–1884Google ScholarPubMed
Brightbill, H. D. and Modlin, R. L. (2000). Toll-like receptors: molecular mechanisms of the mammalian immune response. Immunology 101, 1–10CrossRefGoogle ScholarPubMed
Cornelis, G. R., Boland, A., Boyd, A. P., Geuijen, C., Iriarte, M., Neyt, C., Sory, M. P., and Stainier, I. (1998). The virulence plasmid of Yersinia, an antihost genome. Microbiology and Molecular Biology Reviews 62, 1315–1352Google ScholarPubMed
DiMango, E., Ratner, A. J., Bryan, R., Tabibi, S., and Prince, A. (1998). Activation of NF-κB by adherent Pseudomonas aeruginosa in normal and cystic fibrosis respiratory epithelial cells. Journal of Clinical Investigation 101, 2598–2605CrossRefGoogle ScholarPubMed
Donnenberg, M. S. (2000). Pathogenic strategies of enteric bacteria. Nature 406, 768–774CrossRefGoogle ScholarPubMed
Dyer, R. B., Collaco, C. R., Niesel, D. W., and Herzog, N. K. (1993). Shigella flexneri invasion of HeLa cells induces NF-κB DNA-binding activity. Infection and Immunity 61, 4427–4443Google Scholar
Ebnet, K., Brown, K. D., Siebenlist, U. K., Simon, M. M., and Shaw, S. (1997). Borrelia burgdorferi activates nuclear factor-kappa B and is a potent inducer of chemokine and adhesion molecule gene expression in endothelial cells and fibroblasts. Journal of Immunology 158, 3285–3292Google ScholarPubMed
Galan, J. E. (1999). Interaction of Salmonella with host cells through the centisome 63 type III secretion system. Current Opinion in Microbiology 2, 46–50CrossRefGoogle ScholarPubMed
Galan, J. E. and Collmer, A. (1999). Type III secretion machines: bacterial devices for protein delivery into host cells. Science 284, 1322–1328Google ScholarPubMed
Hardt, W. D., Chen, L. M., Schuebel, K. E., Bustelo, X. R., and Galan, J. E. (1998). S. typhimurium encodes an activator of Rho GTPases that induces membrane ruffling and nuclear responses in host cells. Cell 93, 815–826CrossRefGoogle ScholarPubMed
Hatada, E. N., Krappmann, D., and Scheidereit, C. (2000). NF-κB and the innate immune response. Current Opinion in Immunology 12, 52–58CrossRefGoogle ScholarPubMed
Hauf, N., Goebel, W., Fiedler, F., Sokolovic, Z., and Kuhn, M. (1997). Listeria monocytogenes infection of P388D1 macrophages results in a biphasic NF-κB (RelA/p50) activation induced by lipoteichoic acid and bacterial phospholipases and mediated by IκBα and IκBβ degradation. Proceedings of the National Academy of Sciences USA 94, 9394–9399CrossRefGoogle Scholar
Hiscott, J., Kwon, H., and Genin, P. (2001). Hostile takeovers: viral appropriation of the NF-κB pathway. Journal of Clinical Investigation 107, 143–151CrossRefGoogle ScholarPubMed
Hobbie, S., Chen, L. M., Davis, R. J., and Galan, J. E. (1997). Involvement of mitogen-activated protein kinase pathways in the nuclear responses and cytokine production induced by Salmonella typhimurium in cultured intestinal epithelial cells. Journal of Immunology 159, 5550–5559Google ScholarPubMed
Kitamura, M. (1999). NF-κB-mediated self defense of macrophages faced with bacteria. European Journal of Immunology 29, 1647–16553.0.CO;2-Y>CrossRefGoogle ScholarPubMed
Medzhitov, R. and Janeway, C. (2000). The toll receptor family and microbial recognition. Trends in Microbiology 8, 452–456CrossRefGoogle ScholarPubMed
Meijer, L. K., Schesser, K., Wolf-Watz, H., Sassone-Corsi, P., and Pettersson, S. (2000). The bacterial protein YopJ abrogates multiple signal transduction pathways that converge on the transcription factor CREB. Cellular Microbiology 2, 231–238CrossRefGoogle ScholarPubMed
Mills, S. D., Boland, A., Sory, M. P., van-der-Smissen, P., Kerbourch, C., Finlay, B. B., and Cornelis, G. R. (1997). Yersinia enterocolitica induces apoptosis in macrophages by a process requiring functional type III secretion and translocation mechanisms and involving YopP, presumably acting as an effector protein. Proceedings of the National Academy of Sciences USA 94, 12,638–12,643CrossRefGoogle ScholarPubMed
Molestina, R. E., Miller, R. D., Lentsch, A. B., Ramirez, J. A., and Summersgill, J. T. (2000). Requirement for NF-κB in transcriptional activation of monocyte chemotactic protein 1 by Chlamydia pneumoniae in human endothelial cells. Infection and Immunity 68, 4282–4288CrossRefGoogle ScholarPubMed
Monack, D. M., Mecsas, J., Ghori, N., and Falkow, S. (1997). Yersinia signals macrophages to undergo apoptosis and YopJ is necessary for this cell death. Proceedings of the National Academy of Sciences USA 94, 10,385–10,390CrossRefGoogle ScholarPubMed
Monack, D. M., Mecsas, J., Bouley, D., and Falkow, S. (1998). Yersinia-induced apoptosis in vivo aids in the establishment of a systemic infection of mice. Journal of Experimental Medicine 188, 2127–2137CrossRefGoogle ScholarPubMed
Munzenmaier, A., Lange, C., Glocker, E., Covacci, A., Moran, A., Bereswill, S., Baeuerle, P. A., Kist, M., and Pahl, H. L. (1997). A secreted/shed product of Helicobacter pylori activates transcription factor nuclear factor-kappa B. Journal of Immunology 159, 6140–6147Google ScholarPubMed
Nakajima, R. and Brubaker, R. R. (1993). Association between virulence of Yersinia pestis and suppression of gamma interferon and tumor necrosis factor alpha. Infection and Immunity 61, 23–31Google ScholarPubMed
Naumann, M., Wessler, S., Bartsch, C., Wieland, B., and Meyer, T. F. (1997). Neisseria gonorrhoeae epithelial cell interaction leads to the activation of the transcription factors nuclear factor kappaB and activator protein 1 and the induction of inflammatory cytokines. Journal of Experimental Medicine 186, 247–258CrossRefGoogle ScholarPubMed
Neish, A. S., Gewirtz, A. T., Zeng, H., Young, A. N., Hobert, M. E., Karmali, V., Rao, A. S., and Madara, J. L. (2000). Prokaryotic regulation of epithelial responses by inhibition of IκBβ ubiquitination. Science 289, 1560–1563CrossRefGoogle Scholar
O'Connell, M. A., Bennett, B. L., Mercurio, F., Manning, A. M., and Mackman, N. (1998). Role of IKK1 and IKK2 in lipopolysaccharide signaling in human monocytic cells. Journal of Biological Chemistry 273, 30,410–30,414CrossRefGoogle ScholarPubMed
Orth, K., Palmer, L. E., Bao, Z. Q., Stewart, S., Rudolph, A. E., Bliska, J. B., and Dixon, J. E. (1999). Inhibition of the mitogen-activated protein kinase kinase superfamily by a Yersinia effector. Science 285, 1920–1923CrossRefGoogle ScholarPubMed
Orth, K., Xu, Z., Mudgett, M. B., Bao, Z. Q., Palmer, L. E., Bliska, J. B., Mangel, W. F., Staskawicz, B., and Dixon, J. E. (2000). Disruption of signaling by Yersinia effector YopJ, a ubiquitin-like protein protease. Science 290, 1594–1597CrossRefGoogle ScholarPubMed
Palmer, L. E., Hobbie, S., Galan, J. E., and Bliska, J. B. (1998). YopJ of Yersinia pseudotuberculosis is required for the inhibition of macrophage TNF-alpha production and downregulation of the MAP kinases p38 and JNK. Molecular Microbiology 27, 953–965CrossRefGoogle ScholarPubMed
Perkins, N. D. (2000). The Rel/NF-κB family: friends and foe. Trends in Biochemical Sciences 25, 434–440CrossRefGoogle Scholar
Philpott, D. J., Yamaoka, S., Israel, A., and Sansonetti, P. J. (2000). Invasive Shigella flexneri activates NF-κB through a lipopolysaccharide-dependent innate intracellular response and leads to IL-8 expression in epithelial cells. Journal of Immunology 165, 903–914CrossRefGoogle ScholarPubMed
Ruckdeschel, K., Machold, J., Roggenkamp, A., Schubert, S., Pierre, J., Zumbihl, R., Liautard, J. P., Heesemann, J., and Rouot, B. (1997a). Yersinia enterocolitica promotes deactivation of macrophage mitogen-activated protein kinases extracellular signal-regulated kinase-1/2, p38, and c-Jun NH2-terminal kinase: Correlation with its inhibitory effect on tumor necrosis factor-alpha production. Journal of Biological Chemistry 272, 15,920–15,927CrossRefGoogle Scholar
Ruckdeschel, K., Roggenkamp, A., Lafont, V., Mangeat, P., Heesemann, J., and Rouot, B. (1997b). Interaction of Yersinia enterocolitica with macrophages leads to macrophage cell death through apoptosis. Infection and Immunity 65, 4813–4821Google Scholar
Ruckdeschel, K., Harb, S., Roggenkamp, A., Hornef, M., Zumbihl, R., Kohler, S., Heesemann, J., and Rouot, B. (1998). Yersinia enterocolitica impairs activation of transcription factor NF-κB: involvement in the induction of programmed cell death and in the suppression of the macrophage tumor necrosis factor alpha production. Journal of Experimental Medicine 187, 1069–1079CrossRefGoogle ScholarPubMed
Ruckdeschel, K., Mannel, O., Richter, K., Jacobi, C. A., Trulzsch, K., Rouot, B., and Heesemann, J. (2001). Yersinia outer protein P of Yersinia enterocolitica simultaneously blocks the nuclear factor-kappaB pathway and exploits lipopolysaccharide signaling to trigger apoptosis in macrophages. Journal of Immunology 166, 1823–1831CrossRefGoogle Scholar
Savkovic, S. D., Koutsouris, A., and Hecht, G. (1997). Activation of NF-κB in intestinal epithelial cells by enteropathogenic Escherichia coli. American Journal of Physiology 273, 1160–1167CrossRefGoogle ScholarPubMed
Schesser, K., Spiik, A. K., Dukuzumuremyi, J. M., Neurath, M. F., Pettersson, S., and Wolf-Watz, H. (1998). The YopJ locus is required for Yersinia-mediated inhibition of NF-κB activation and cytokine expression: YopJ contains a eukaryotic SH2-like domain that is essential for its repressive activity. Molecular Microbiology 28, 1067–1079CrossRefGoogle ScholarPubMed
Schesser, K., Dukuzumuremyi, J. M., Cilio, C., Borg, S., Wallis, T. S., Pettersson, S., and Galyov, E. E. (2000). The Salmonella YopJ-homologue AvrA does not possess YopJ-like activity. Microbial Pathogenesis 28, 59–70CrossRefGoogle Scholar
Vallejo, J. G., Knuefermann, P., Mann, D. L., and Sivasubramanian, N. (2000). Group B Streptococcus induces TNF-α gene expression and activation of the transcription factors NF-κB and activator protein-1 in human cord blood monocytes. Journal of Immunology 165, 419–425CrossRefGoogle ScholarPubMed
Yao, J., Mackman, N., Edgington, T. S., and Fan, S. T. (1997). Lipopolysaccharide induction of the tumor necrosis factor-alpha promoter in human monocytic cells. Regulation by Egr-1, c-Jun, and NF-κB transcription factors. Journal of Biological Chemistry 272, 17,795–17,801CrossRefGoogle ScholarPubMed
Yuk, M. H., Harvill, E. T., Cotter, P. A., and Miller, J. F. (2000). Modulation of host immune responses, induction of apoptosis and inhibition of NF-κB activation by the Bordetella type III secretion system. Molecular Microbiology 35, 991–1004CrossRefGoogle ScholarPubMed
Zhang, G. and Ghosh, S. (2001). Toll-like receptor-mediated NF-kappaB activation: A phylogenetically conserved paradigm in innate immunity. Journal of Clinical Investigation 107, 13–19CrossRefGoogle ScholarPubMed

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