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Effect of co-infection with a small intestine-restricted helminth pathogen on oral prion disease pathogenesis in mice
The early replication of some orally-acquired prion strains upon stromal-derived follicular dendritic cells (FDC) within the small intestinal Peyer’s patches is essential to establish host infection, and for the disease to efficiently spread to the brain. Factors that influence the early accumulatio...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6491469/ https://www.ncbi.nlm.nih.gov/pubmed/31040320 http://dx.doi.org/10.1038/s41598-019-42900-9 |
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author | Sánchez-Quintero, Alejandra Bradford, Barry M. Maizels, Rick Donaldson, David S. Mabbott, Neil A. |
author_facet | Sánchez-Quintero, Alejandra Bradford, Barry M. Maizels, Rick Donaldson, David S. Mabbott, Neil A. |
author_sort | Sánchez-Quintero, Alejandra |
collection | PubMed |
description | The early replication of some orally-acquired prion strains upon stromal-derived follicular dendritic cells (FDC) within the small intestinal Peyer’s patches is essential to establish host infection, and for the disease to efficiently spread to the brain. Factors that influence the early accumulation of prions in Peyer’s patches can directly influence disease pathogenesis. The host’s immune response to a gastrointestinal helminth infection can alter susceptibility to co-infection with certain pathogenic bacteria and viruses. Here we used the natural mouse small intestine-restricted helminth pathogen Heligmosomoides polygyrus to test the hypothesis that pathology specifically within the small intestine caused by a helminth co-infection would influence oral prion disease pathogenesis. When mice were co-infected with prions on d 8 after H. polygyrus infection the early accumulation of prions within Peyer’s patches was reduced and survival times significantly extended. Natural prion susceptible hosts such as sheep, deer and cattle are regularly exposed to gastrointestinal helminth parasites. Our data suggest that co-infections with small intestine-restricted helminth pathogens may be important factors that influence oral prion disease pathogenesis. |
format | Online Article Text |
id | pubmed-6491469 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64914692019-05-17 Effect of co-infection with a small intestine-restricted helminth pathogen on oral prion disease pathogenesis in mice Sánchez-Quintero, Alejandra Bradford, Barry M. Maizels, Rick Donaldson, David S. Mabbott, Neil A. Sci Rep Article The early replication of some orally-acquired prion strains upon stromal-derived follicular dendritic cells (FDC) within the small intestinal Peyer’s patches is essential to establish host infection, and for the disease to efficiently spread to the brain. Factors that influence the early accumulation of prions in Peyer’s patches can directly influence disease pathogenesis. The host’s immune response to a gastrointestinal helminth infection can alter susceptibility to co-infection with certain pathogenic bacteria and viruses. Here we used the natural mouse small intestine-restricted helminth pathogen Heligmosomoides polygyrus to test the hypothesis that pathology specifically within the small intestine caused by a helminth co-infection would influence oral prion disease pathogenesis. When mice were co-infected with prions on d 8 after H. polygyrus infection the early accumulation of prions within Peyer’s patches was reduced and survival times significantly extended. Natural prion susceptible hosts such as sheep, deer and cattle are regularly exposed to gastrointestinal helminth parasites. Our data suggest that co-infections with small intestine-restricted helminth pathogens may be important factors that influence oral prion disease pathogenesis. Nature Publishing Group UK 2019-04-30 /pmc/articles/PMC6491469/ /pubmed/31040320 http://dx.doi.org/10.1038/s41598-019-42900-9 Text en © The Author(s) 2019 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 Sánchez-Quintero, Alejandra Bradford, Barry M. Maizels, Rick Donaldson, David S. Mabbott, Neil A. Effect of co-infection with a small intestine-restricted helminth pathogen on oral prion disease pathogenesis in mice |
title | Effect of co-infection with a small intestine-restricted helminth pathogen on oral prion disease pathogenesis in mice |
title_full | Effect of co-infection with a small intestine-restricted helminth pathogen on oral prion disease pathogenesis in mice |
title_fullStr | Effect of co-infection with a small intestine-restricted helminth pathogen on oral prion disease pathogenesis in mice |
title_full_unstemmed | Effect of co-infection with a small intestine-restricted helminth pathogen on oral prion disease pathogenesis in mice |
title_short | Effect of co-infection with a small intestine-restricted helminth pathogen on oral prion disease pathogenesis in mice |
title_sort | effect of co-infection with a small intestine-restricted helminth pathogen on oral prion disease pathogenesis in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6491469/ https://www.ncbi.nlm.nih.gov/pubmed/31040320 http://dx.doi.org/10.1038/s41598-019-42900-9 |
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