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The inflammatory response and neuronal injury in Streptococcus suis meningitis

BACKGROUND: Many of the currently used models of bacterial meningitis have limitations due to direct inoculation of pathogens into the cerebrospinal fluid or brain and a relatively insensitive assessment of long-term sequelae. The present study evaluates the utility of a Streptococcus (S.) suis intr...

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Autores principales: Seele, Jana, Tauber, Simone C., Bunkowski, Stephanie, Baums, Christoph G., Valentin-Weigand, Peter, de Buhr, Nicole, Beineke, Andreas, Iliev, Asparouh I., Brück, Wolfgang, Nau, Roland
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029386/
https://www.ncbi.nlm.nih.gov/pubmed/29970011
http://dx.doi.org/10.1186/s12879-018-3206-6
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author Seele, Jana
Tauber, Simone C.
Bunkowski, Stephanie
Baums, Christoph G.
Valentin-Weigand, Peter
de Buhr, Nicole
Beineke, Andreas
Iliev, Asparouh I.
Brück, Wolfgang
Nau, Roland
author_facet Seele, Jana
Tauber, Simone C.
Bunkowski, Stephanie
Baums, Christoph G.
Valentin-Weigand, Peter
de Buhr, Nicole
Beineke, Andreas
Iliev, Asparouh I.
Brück, Wolfgang
Nau, Roland
author_sort Seele, Jana
collection PubMed
description BACKGROUND: Many of the currently used models of bacterial meningitis have limitations due to direct inoculation of pathogens into the cerebrospinal fluid or brain and a relatively insensitive assessment of long-term sequelae. The present study evaluates the utility of a Streptococcus (S.) suis intranasal infection model for the investigation of experimental therapies in meningitis. METHODS: We examined the brains of 10 piglets with S. suis meningitis as well as 14 control piglets by histology, immunohistochemistry and in-situ tailing for morphological alterations in the hippocampal dentate gyrus and microglial activation in the neocortex. RESULTS: In piglets with meningitis, the density of apoptotic neurons was significantly higher than in control piglets. Moreover, scoring of microglial morphology revealed a significant activation of these cells during meningitis. The slight increase in the density of dividing cells, young neurons and microglia observed in piglets suffering from meningitis was not statistically significant, probably because of the short time frame between onset of clinical signs and organ sampling. CONCLUSIONS: The morphological changes found during S. suis meningitis are in accordance with abnormalities in other animal models and human autopsy cases. Therefore, the pig should be considered as a model for evaluating effects of experimental therapeutic approaches on neurological function in bacterial meningitis.
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spelling pubmed-60293862018-07-09 The inflammatory response and neuronal injury in Streptococcus suis meningitis Seele, Jana Tauber, Simone C. Bunkowski, Stephanie Baums, Christoph G. Valentin-Weigand, Peter de Buhr, Nicole Beineke, Andreas Iliev, Asparouh I. Brück, Wolfgang Nau, Roland BMC Infect Dis Research Article BACKGROUND: Many of the currently used models of bacterial meningitis have limitations due to direct inoculation of pathogens into the cerebrospinal fluid or brain and a relatively insensitive assessment of long-term sequelae. The present study evaluates the utility of a Streptococcus (S.) suis intranasal infection model for the investigation of experimental therapies in meningitis. METHODS: We examined the brains of 10 piglets with S. suis meningitis as well as 14 control piglets by histology, immunohistochemistry and in-situ tailing for morphological alterations in the hippocampal dentate gyrus and microglial activation in the neocortex. RESULTS: In piglets with meningitis, the density of apoptotic neurons was significantly higher than in control piglets. Moreover, scoring of microglial morphology revealed a significant activation of these cells during meningitis. The slight increase in the density of dividing cells, young neurons and microglia observed in piglets suffering from meningitis was not statistically significant, probably because of the short time frame between onset of clinical signs and organ sampling. CONCLUSIONS: The morphological changes found during S. suis meningitis are in accordance with abnormalities in other animal models and human autopsy cases. Therefore, the pig should be considered as a model for evaluating effects of experimental therapeutic approaches on neurological function in bacterial meningitis. BioMed Central 2018-07-03 /pmc/articles/PMC6029386/ /pubmed/29970011 http://dx.doi.org/10.1186/s12879-018-3206-6 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Seele, Jana
Tauber, Simone C.
Bunkowski, Stephanie
Baums, Christoph G.
Valentin-Weigand, Peter
de Buhr, Nicole
Beineke, Andreas
Iliev, Asparouh I.
Brück, Wolfgang
Nau, Roland
The inflammatory response and neuronal injury in Streptococcus suis meningitis
title The inflammatory response and neuronal injury in Streptococcus suis meningitis
title_full The inflammatory response and neuronal injury in Streptococcus suis meningitis
title_fullStr The inflammatory response and neuronal injury in Streptococcus suis meningitis
title_full_unstemmed The inflammatory response and neuronal injury in Streptococcus suis meningitis
title_short The inflammatory response and neuronal injury in Streptococcus suis meningitis
title_sort inflammatory response and neuronal injury in streptococcus suis meningitis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029386/
https://www.ncbi.nlm.nih.gov/pubmed/29970011
http://dx.doi.org/10.1186/s12879-018-3206-6
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