Cargando…
Sex-Specific Routes To Immune Senescence In Drosophila melanogaster
Animal immune systems change dramatically during the ageing process, often accompanied by major increases in pathogen susceptibility. However, the extent to which senescent elevations in infection mortality are causally driven by deteriorations in canonical systemic immune processes is unclear. We s...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5585412/ https://www.ncbi.nlm.nih.gov/pubmed/28874758 http://dx.doi.org/10.1038/s41598-017-11021-6 |
_version_ | 1783261620071301120 |
---|---|
author | Kubiak, Marco Tinsley, Matthew C. |
author_facet | Kubiak, Marco Tinsley, Matthew C. |
author_sort | Kubiak, Marco |
collection | PubMed |
description | Animal immune systems change dramatically during the ageing process, often accompanied by major increases in pathogen susceptibility. However, the extent to which senescent elevations in infection mortality are causally driven by deteriorations in canonical systemic immune processes is unclear. We studied Drosophila melanogaster and compared the relative contributions of impaired systemic immune defences and deteriorating barrier defences to increased pathogen susceptibility in aged flies. To assess senescent changes in systemic immune response efficacy we injected one and four-week old flies with the entomopathogenic fungus Beauveria bassiana and studied subsequent mortality; whereas to include the role of barrier defences we infected flies by dusting the cuticle with fungal spores. We show that the processes underlying pathogen defence senescence differ between males and females. Both sexes became more susceptible to infection as they aged. However, we conclude that for males, this was principally due to deterioration in barrier defences, whereas for females systemic immune defence senescence was mainly responsible. We discuss the potential roles of sex-specific selection on the immune system and behavioural variation between males and females in driving these different senescent trends. |
format | Online Article Text |
id | pubmed-5585412 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55854122017-09-13 Sex-Specific Routes To Immune Senescence In Drosophila melanogaster Kubiak, Marco Tinsley, Matthew C. Sci Rep Article Animal immune systems change dramatically during the ageing process, often accompanied by major increases in pathogen susceptibility. However, the extent to which senescent elevations in infection mortality are causally driven by deteriorations in canonical systemic immune processes is unclear. We studied Drosophila melanogaster and compared the relative contributions of impaired systemic immune defences and deteriorating barrier defences to increased pathogen susceptibility in aged flies. To assess senescent changes in systemic immune response efficacy we injected one and four-week old flies with the entomopathogenic fungus Beauveria bassiana and studied subsequent mortality; whereas to include the role of barrier defences we infected flies by dusting the cuticle with fungal spores. We show that the processes underlying pathogen defence senescence differ between males and females. Both sexes became more susceptible to infection as they aged. However, we conclude that for males, this was principally due to deterioration in barrier defences, whereas for females systemic immune defence senescence was mainly responsible. We discuss the potential roles of sex-specific selection on the immune system and behavioural variation between males and females in driving these different senescent trends. Nature Publishing Group UK 2017-09-05 /pmc/articles/PMC5585412/ /pubmed/28874758 http://dx.doi.org/10.1038/s41598-017-11021-6 Text en © The Author(s) 2017 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 Kubiak, Marco Tinsley, Matthew C. Sex-Specific Routes To Immune Senescence In Drosophila melanogaster |
title | Sex-Specific Routes To Immune Senescence In Drosophila melanogaster |
title_full | Sex-Specific Routes To Immune Senescence In Drosophila melanogaster |
title_fullStr | Sex-Specific Routes To Immune Senescence In Drosophila melanogaster |
title_full_unstemmed | Sex-Specific Routes To Immune Senescence In Drosophila melanogaster |
title_short | Sex-Specific Routes To Immune Senescence In Drosophila melanogaster |
title_sort | sex-specific routes to immune senescence in drosophila melanogaster |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5585412/ https://www.ncbi.nlm.nih.gov/pubmed/28874758 http://dx.doi.org/10.1038/s41598-017-11021-6 |
work_keys_str_mv | AT kubiakmarco sexspecificroutestoimmunesenescenceindrosophilamelanogaster AT tinsleymatthewc sexspecificroutestoimmunesenescenceindrosophilamelanogaster |