Skip to main content Accessibility help
×
Hostname: page-component-cd9895bd7-fscjk Total loading time: 0 Render date: 2024-12-29T13:33:36.203Z Has data issue: false hasContentIssue false

Chapter 17 - Transolfactory Spread in the Pathogenesis of Meningoencephalitis

Published online by Cambridge University Press:  27 July 2023

Robert Laureno
Affiliation:
Georgetown University, Washington DC
Get access

Summary

Various infectious agents invade brain and spinal fluid through the olfactory nerves and bulbs. The best example is the amoeba Naegleria which usually enters the nose during recreation in fresh water. Strong epidemiologic, pathologic, and experimental evidence support this transolfactory route of neurologic infection. Viruses can also cause meningioencephalitis via transolfactory spread.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2023

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Patras, D., Andujar, J. J.. Meningoencephalitis due to Hartmannella (Acanthamoeba). Am J Clin Pathol 1966; 46: 226233.Google ScholarPubMed
Culbertson, C. G., Smith, J. W., Cohen, H. K. et al. Experimental infection of mice and monkeys by Acanthamoeba. Am J Pathol 1959; 35: 185197.Google ScholarPubMed
Carter, R. F.. Primary amoebic meningo-encephalitis: clinical, pathological and epidemiological features of six fatal cases. J Pathol Bacteriol 1968; 96: 125.CrossRefGoogle ScholarPubMed
Gharpure, R., Bliton, J. H., Goodman, A. et al. Epidemiology and clinical characteristics of primary amebic meningoencephalitis caused by Naegleria fowleri: a global review. Clin Infect Dis 2021; 73: e1927.CrossRefGoogle ScholarPubMed
Mori, I.. Transolfactory neuroinvasion by viruses threatens the human brain. Acta Virol 2015; 59: 338349.CrossRefGoogle ScholarPubMed
Butt, C. G., Baro, C., Knorr, R. W.. Naegleria (sp.) identified in amebic encephalitis. Am J Clin Pathol 1968; 50: 568574.CrossRefGoogle ScholarPubMed
Callicott, J. H., Nelson, E. C., Jones, M. M. et al. Meningoencephalitis due to pathogenic free-living amoebae. Report of two cases. JAMA 1968; 206: 579582.CrossRefGoogle ScholarPubMed
Jarolim, K. L., McCosh, J. K., Howard, M. J. et al. A light microscopy study of the migration of Naegleria fowleri from the nasal submucosa to the central nervous system during the early stage of primary amebic meningoencephalitis in mice. J Parasitol 2000; 86: 5055.CrossRefGoogle Scholar
Tomlinson, A. H., Esiri, M. M.. Herpes simplex encephalitis. Immunohistological demonstration of spread of virus via olfactory pathways in mice. J Neurol Sci 1983; 60: 473484.CrossRefGoogle ScholarPubMed
Ojeda, V. J., Archer, M., Robertson, T. A. et al. Necropsy study of the olfactory portal of entry in herpes simplex encephalitis. Med J Aust 1983; 1: 7981.CrossRefGoogle ScholarPubMed
Twomey, J. A., Barker, C. M., Robinson, G. et al. Olfactory mucosa in herpes simplex encephalitis. J Neurol Neurosurg Psychiatry 1979; 42: 983987.CrossRefGoogle ScholarPubMed
Dinn, J. J.. Transolfactory spread of virus in herpes simplex encephalitis. Br Med J 1980; 281: 1392.CrossRefGoogle ScholarPubMed
Mori, I., Nishiyama, Y., Yokochi, T. et al. Olfactory transmission of neurotropic viruses. J Neurovirol 2005; 11: 129137.CrossRefGoogle ScholarPubMed
Davis, L. E., Johnson, R. T.. An explanation for the localization of herpes simplex encephalitis? Ann Neurol 1979; 5: 25.CrossRefGoogle ScholarPubMed
Damasio, A. R., Van Hoesen, G. W.. The limbic system and the localisation of herpes simplex encephalitis. J Neurol Neurosurg Psychiatry 1985; 48: 297301.CrossRefGoogle ScholarPubMed
Menendez, C. M., Carr, D. J.. Herpes simplex virus-1 infects the olfactory bulb shortly following ocular infection and exhibits a long-term inflammatory profile in the form of effector and HSV-1-specific T cells. J Neuroinflammation 2017; 14: 124.CrossRefGoogle ScholarPubMed
Conomy, J. P., Leibovitz, A., McCombs, W. et al. Airborne rabies encephalitis: demonstration of rabies virus in the human central nervous system. Neurology 1977; 27: 6769.CrossRefGoogle ScholarPubMed
Perlman, S., Evans, G., Afifi, A.. Effect of olfactory bulb ablation on spread of a neurotropic coronavirus into the mouse brain. J Exp Med 1990; 172: 11271132.CrossRefGoogle ScholarPubMed
Barnett, E. M., Perlman, S.. The olfactory nerve and not the trigeminal nerve is the major site of CNS entry for mouse hepatitis virus, strain JHM. Virology 1993; 194: 185191.CrossRefGoogle Scholar
Johnson, R. T.. Viral Infections of the Nervous System. New York, Raven Press, 1982.Google Scholar

Save book to Kindle

To save this book to your Kindle, first ensure [email protected] is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×