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Nippostrongylus brasiliensis infection leads to impaired reference memory and myeloid cell interference
Hookworm infection is endemic in developing countries, leading to poor cognitive function—among other disruptions. In this study, the effects of Nippostrongylus brasiliensis infection (a murine model of Necator Americanus) on cognitive function were investigated. Though impaired cognition has been e...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5811425/ https://www.ncbi.nlm.nih.gov/pubmed/29440657 http://dx.doi.org/10.1038/s41598-018-20770-x |
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author | Brombacher, T. M. De Gouveia, K. S. Cruywagen, L. Makena, N. Booley, F. Tamgue, O. Brombacher, F. |
author_facet | Brombacher, T. M. De Gouveia, K. S. Cruywagen, L. Makena, N. Booley, F. Tamgue, O. Brombacher, F. |
author_sort | Brombacher, T. M. |
collection | PubMed |
description | Hookworm infection is endemic in developing countries, leading to poor cognitive function—among other disruptions. In this study, the effects of Nippostrongylus brasiliensis infection (a murine model of Necator Americanus) on cognitive function were investigated. Though impaired cognition has been extensively reported, the exact domain of cognition affected is still unknown, hence requiring investigation. The objective of this study was to identify possible cognitive changes during Nippostrongylus brasiliensis infection in mice, using the Morris water maze. Here, we show for the first time that mice infected with Nippostrongylus brasiliensis were able to learn the Morris water maze task, but demonstrated impaired reference memory. Anxiety measured by thigmotaxis in the maze, did not play a role for the observed cognitive impairment. Of further interest, an increase in the number of hippocampal macrophages and microglia with training and/or infection suggested a significant role of these cell types during spatial learning. Together, these experimental mouse studies suggest that helminth infections do have an impact on cognition. Further experimental animal studies on cognition and infection might open new approaches for a better understanding and impact of pathogen infections. |
format | Online Article Text |
id | pubmed-5811425 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58114252018-02-16 Nippostrongylus brasiliensis infection leads to impaired reference memory and myeloid cell interference Brombacher, T. M. De Gouveia, K. S. Cruywagen, L. Makena, N. Booley, F. Tamgue, O. Brombacher, F. Sci Rep Article Hookworm infection is endemic in developing countries, leading to poor cognitive function—among other disruptions. In this study, the effects of Nippostrongylus brasiliensis infection (a murine model of Necator Americanus) on cognitive function were investigated. Though impaired cognition has been extensively reported, the exact domain of cognition affected is still unknown, hence requiring investigation. The objective of this study was to identify possible cognitive changes during Nippostrongylus brasiliensis infection in mice, using the Morris water maze. Here, we show for the first time that mice infected with Nippostrongylus brasiliensis were able to learn the Morris water maze task, but demonstrated impaired reference memory. Anxiety measured by thigmotaxis in the maze, did not play a role for the observed cognitive impairment. Of further interest, an increase in the number of hippocampal macrophages and microglia with training and/or infection suggested a significant role of these cell types during spatial learning. Together, these experimental mouse studies suggest that helminth infections do have an impact on cognition. Further experimental animal studies on cognition and infection might open new approaches for a better understanding and impact of pathogen infections. Nature Publishing Group UK 2018-02-13 /pmc/articles/PMC5811425/ /pubmed/29440657 http://dx.doi.org/10.1038/s41598-018-20770-x Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Brombacher, T. M. De Gouveia, K. S. Cruywagen, L. Makena, N. Booley, F. Tamgue, O. Brombacher, F. Nippostrongylus brasiliensis infection leads to impaired reference memory and myeloid cell interference |
title | Nippostrongylus brasiliensis infection leads to impaired reference memory and myeloid cell interference |
title_full | Nippostrongylus brasiliensis infection leads to impaired reference memory and myeloid cell interference |
title_fullStr | Nippostrongylus brasiliensis infection leads to impaired reference memory and myeloid cell interference |
title_full_unstemmed | Nippostrongylus brasiliensis infection leads to impaired reference memory and myeloid cell interference |
title_short | Nippostrongylus brasiliensis infection leads to impaired reference memory and myeloid cell interference |
title_sort | nippostrongylus brasiliensis infection leads to impaired reference memory and myeloid cell interference |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5811425/ https://www.ncbi.nlm.nih.gov/pubmed/29440657 http://dx.doi.org/10.1038/s41598-018-20770-x |
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