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Invasion of the Central Nervous System by Neisseria meningitidis

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Meningococcal Disease

Part of the book series: Methods in Molecular Medicine™ ((MIMM,volume 67))

Abstract

Neisseria meningitidis is an extracellular pathogen responsible for septicemia and meningitis. The occurrence of meningitis requires that bacteria cross the blood-brain barrier (BBB) and induce an inflammatory response within the sub arachnoid space. The mechanisms that lead to the development of cerebrospinal fluid (CSF) pleocytosis once bacteria have reached the CSF have been studied using several animal models. These mechanisms are similar among extracellular pathogens responsible for meningitis (i.e., Haemophilus influenzae type b, Streptococcuspneumoniae, and N. meningitidis). The in situ production of cytokines is the primary event leading to transmigration of leucocytes through the BBB (14).

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References

  1. Saukkonen K., Sande S., Cioffe C., Wolpe S., Sherry B., Cerami A., and Tuomanen E. (1990) The role of cytokines in the generation of inflammation and tissue damage in experimental gram-positive meningitis. J. Exp. Med. 171,439–448.

    Article  CAS  PubMed  Google Scholar 

  2. Quagliarello V. J., Wispelwey B., Long Jr. W. J., and Scheld W. M. (1991) Recombinant human interleukin-1 induces meningitis and blood-brain barrier injury in the rat. J. Clin. Invest. 87, 1360–1366.

    Article  CAS  PubMed  Google Scholar 

  3. Tuomanen E., Tomasz A., Hengstler B., and Zak O. (1985) The relative role of bacterial cell wall and capsule in the induction of inflammation in pneumococcal meningitis. J. Infect. Dis. 151, 535–540.

    CAS  PubMed  Google Scholar 

  4. Burroughs M., Prasad S., and Tuomanen E. (1991) Peptidoglycan derived from lysis of Haemophilus influenzae induces blood-barrier permeability independant leukocytosis, in Programs and Abstracts of the 31st Interscience Conference on Antimicrobial Agents and Chemotherapy, American Society for Microbiology Washington, D.C.

    Google Scholar 

  5. Reese T. S. and Karnovsky M. J. (1967) Fine strutural localization of a bloodbrain barrier to exogenous peroxidase. J. Cell. Biol. 34, 207–217.

    Article  CAS  PubMed  Google Scholar 

  6. Butt A. M., Jones H. C., and Abbott N. J. (1990) Electrical resistance across the blood-brain barrier in anaesthetized rats: a developmental study. J. Physiol. 429, 47–62.

    CAS  PubMed  Google Scholar 

  7. Janzer R. C. and Raff M. C. (1987) Astrocytes induce blood-brain barrier barrier properties in endothelial cells. Nature 325, 253–256.

    Article  CAS  PubMed  Google Scholar 

  8. Levine S. (1987) Choroid plexus: target for systemic disease and pathway to the brain. Lab. Invest. 56,231–233.

    CAS  PubMed  Google Scholar 

  9. Saukkonen K., Abdillahi H., Poolman J. T., and Leinonen M. (1987) Protective efficacy of monoclonal antibodies to class 1 and class 3 oter membrane proteins of Neisseria meningitidis B:15:P1.16 in infant rat infection model: new prospects for vaccine development. Microb. Path. 3, 261–267.

    Article  CAS  Google Scholar 

  10. Pron B., Taha M. K., Rambaud C., Fournet J. C., Pattey N., Monnet J. P., et al. (1997) Interaction of Neisseria meningitidis with the components of the bloodbrain barrier correlates with an increased expression of PilC. J. Infect. Dis. 176, 1285–1292.

    Article  CAS  PubMed  Google Scholar 

  11. Durieu-Trautmann O., Bourdoulous S., Roux F., Bourre J. M., Strosberg A. D., and Couraud P. O. (1993) Immortalized rat brain microvessel endothelial cells: II. Pharmacological characterization. Adv. Exp. Med. Biol. 331, 205–210.

    CAS  PubMed  Google Scholar 

  12. Prud’homme J. G., Sherman I. W., Kirkwood M. L., Moses A. V., Stenglein S., and Nelson J. A. (1996) Studies of Plasmodium falciparum (human Malaria) cytoadherence using immortalized human brain endothelial cells. Int. J. Parasitol. 26,647–655.

    Article  CAS  PubMed  Google Scholar 

  13. Tuomanen E. (1996) Entry of pathogens into the central nervous system. FEMS Microbiol. Rev. 18, 289–299.

    Article  CAS  PubMed  Google Scholar 

  14. Merz A. J., Rifenbery D. B., Grove Arvidson C., and So M. (1996) Traversal of a polarized epithelium by pathogenic Neisseriae: facilitation by type IV pili and maintenance of epithelial barrier function. Mol. Med. 2, 745–754.

    CAS  PubMed  Google Scholar 

  15. Pujol C., Eugene E., de Saint Martin L., and Nassif X. (1997) Interaction of Neisseria meningitidis with a polarised monolayer of epithelial cells. Infect. Immun. 65,4836–4842.

    CAS  PubMed  Google Scholar 

  16. Pujol C., Eugene E., Marceau M., and Nassif X. (1999) The meningococcal PilT protein is required for induction of intimate attachment to epithelial cells following pilus-mediated adhesion. Proc. Natl. Acad. Sci. USA 96,4017–4022.

    CAS  Google Scholar 

  17. Bortulossi R., Ferrieri P., and Wannamaker L. W. (1978) Dynamics of Escherichia coli infection and meningitis in infant rats. Infect. Immun. 22,480–486.

    Google Scholar 

  18. Saukkonen K. (1988) Experimental meningococcal meningitis in the infant rat. Microb. Pathog. 4, 203–211.

    Article  CAS  PubMed  Google Scholar 

  19. Kellogg D. S. J., Peacock W. L., Deacon W. E., Brown L., and Pirkle C. I. (1963) Neisseria gonorrhoeae. I. Virulence genetically linked to clonal variation. J. Bacteriol. 85, 1274–1279.

    PubMed  Google Scholar 

  20. Madara J. L. and Dharmsathaphorn K. (1985) Occluding junctions structurefunction relationships in a cultured epithelial monolayer. J. Cell. Biol. 101,2124–2133.

    Article  CAS  PubMed  Google Scholar 

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© 2001 Humana Press Inc., Totowa, NJ

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Tinsley, C., Nassif, X. (2001). Invasion of the Central Nervous System by Neisseria meningitidis . In: Walker, J.M., Pollard, A.J., Maiden, M.C.J. (eds) Meningococcal Disease. Methods in Molecular Medicine™, vol 67. Humana Press. https://doi.org/10.1385/1-59259-149-3:635

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  • DOI: https://doi.org/10.1385/1-59259-149-3:635

  • Publisher Name: Humana Press

  • Print ISBN: 978-0-89603-849-3

  • Online ISBN: 978-1-59259-149-7

  • eBook Packages: Springer Protocols

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