Cargando…
Divergent immune priming responses across flour beetle life stages and populations
Growing evidence shows that low doses of pathogens may prime the immune response in many insects, conferring subsequent protection against infection in the same developmental stage (within‐life stage priming), across life stages (ontogenic priming), or to offspring (transgenerational priming). Recen...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6093166/ https://www.ncbi.nlm.nih.gov/pubmed/30128134 http://dx.doi.org/10.1002/ece3.2532 |
_version_ | 1783347663269265408 |
---|---|
author | Khan, Imroze Prakash, Arun Agashe, Deepa |
author_facet | Khan, Imroze Prakash, Arun Agashe, Deepa |
author_sort | Khan, Imroze |
collection | PubMed |
description | Growing evidence shows that low doses of pathogens may prime the immune response in many insects, conferring subsequent protection against infection in the same developmental stage (within‐life stage priming), across life stages (ontogenic priming), or to offspring (transgenerational priming). Recent work also suggests that immune priming is a costly response. Thus, depending on host and pathogen ecology and evolutionary history, tradeoffs with other fitness components may constrain the evolution of priming. However, the relative impacts of priming at different life stages and across natural populations remain unknown. We quantified immune priming responses of 10 natural populations of the red flour beetle Tribolium castaneum, primed and infected with the natural insect pathogen Bacillus thuringiensis. We found that priming responses were highly variable both across life stages and populations, ranging from no detectable response to a 13‐fold survival benefit. Comparing across stages, we found that ontogenic immune priming at the larval stage conferred maximum protection against infection. Finally, we found that various forms of priming showed sex‐specific associations that may represent tradeoffs or shared mechanisms. These results indicate the importance of sex‐, life stage‐, and population‐specific selective pressures that can cause substantial divergence in priming responses even within a species. Our work highlights the necessity of further work to understand the mechanistic basis of this variability. |
format | Online Article Text |
id | pubmed-6093166 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60931662018-08-20 Divergent immune priming responses across flour beetle life stages and populations Khan, Imroze Prakash, Arun Agashe, Deepa Ecol Evol Original Research Growing evidence shows that low doses of pathogens may prime the immune response in many insects, conferring subsequent protection against infection in the same developmental stage (within‐life stage priming), across life stages (ontogenic priming), or to offspring (transgenerational priming). Recent work also suggests that immune priming is a costly response. Thus, depending on host and pathogen ecology and evolutionary history, tradeoffs with other fitness components may constrain the evolution of priming. However, the relative impacts of priming at different life stages and across natural populations remain unknown. We quantified immune priming responses of 10 natural populations of the red flour beetle Tribolium castaneum, primed and infected with the natural insect pathogen Bacillus thuringiensis. We found that priming responses were highly variable both across life stages and populations, ranging from no detectable response to a 13‐fold survival benefit. Comparing across stages, we found that ontogenic immune priming at the larval stage conferred maximum protection against infection. Finally, we found that various forms of priming showed sex‐specific associations that may represent tradeoffs or shared mechanisms. These results indicate the importance of sex‐, life stage‐, and population‐specific selective pressures that can cause substantial divergence in priming responses even within a species. Our work highlights the necessity of further work to understand the mechanistic basis of this variability. John Wiley and Sons Inc. 2016-10-09 /pmc/articles/PMC6093166/ /pubmed/30128134 http://dx.doi.org/10.1002/ece3.2532 Text en © 2016 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Khan, Imroze Prakash, Arun Agashe, Deepa Divergent immune priming responses across flour beetle life stages and populations |
title | Divergent immune priming responses across flour beetle life stages and populations |
title_full | Divergent immune priming responses across flour beetle life stages and populations |
title_fullStr | Divergent immune priming responses across flour beetle life stages and populations |
title_full_unstemmed | Divergent immune priming responses across flour beetle life stages and populations |
title_short | Divergent immune priming responses across flour beetle life stages and populations |
title_sort | divergent immune priming responses across flour beetle life stages and populations |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6093166/ https://www.ncbi.nlm.nih.gov/pubmed/30128134 http://dx.doi.org/10.1002/ece3.2532 |
work_keys_str_mv | AT khanimroze divergentimmuneprimingresponsesacrossflourbeetlelifestagesandpopulations AT prakasharun divergentimmuneprimingresponsesacrossflourbeetlelifestagesandpopulations AT agashedeepa divergentimmuneprimingresponsesacrossflourbeetlelifestagesandpopulations |