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Parental investment matters for maternal and offspring immune defense in the mouthbrooding cichlid Astatotilapia burtoni
BACKGROUND: Parental care, while increasing parental fitness through offspring survival, also bears cost to the care-giving parent. Consequentially, trade offs between parental care and other vitally important traits, such as the immune system seem evident. In co-occurring phases of parental care an...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5738712/ https://www.ncbi.nlm.nih.gov/pubmed/29262789 http://dx.doi.org/10.1186/s12862-017-1109-6 |
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author | Keller, Isabel S. Salzburger, Walter Roth, Olivia |
author_facet | Keller, Isabel S. Salzburger, Walter Roth, Olivia |
author_sort | Keller, Isabel S. |
collection | PubMed |
description | BACKGROUND: Parental care, while increasing parental fitness through offspring survival, also bears cost to the care-giving parent. Consequentially, trade offs between parental care and other vitally important traits, such as the immune system seem evident. In co-occurring phases of parental care and immunological challenges negative consequences through a resource allocation trade off on both the parental and the offspring conditions can be predicted. While the immune system reflects parental stress conditions, parental immunological investments also boost offspring survival via the transfer of immunological substances (trans-generational immune priming). We investigated this relationship in the mouthbrooding East African cichlid Astotatilapia burtoni. Prior to mating, females were exposed to an immunological activation, while others remained immunologically naïve. Correspondingly, the immunological status of females was either examined directly after reproduction or after mouthbrooding had ceased. Offspring from both groups were exposed to immunological challenges to assess the extent of trans-generational immune priming. As proxy for immune status, cellular immunological activity and gene expression were determined. RESULTS: Both reproducing and mouthbrooding females allocate their resources towards reproduction. While upon reproduction the innate immune system was impeded, mouthbrooding females showed an attenuation of inflammatory components. Juveniles from immune challenged mouthbrooding females showed downregulation of immune and life history candidate genes, implying a limitation of trans-generational plasticity when parents experience stress during the costly reproductive phase. CONCLUSION: Our results provide evidence that both parental investment via mouthbrooding and the rise of the immunological activity upon an immune challenge are costly traits. If applied simultaneously, not only mothers seem to be impacted in their performance, but also offspring are impeded in their ability to react upon a potentially virulent pathogen exposure. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12862-017-1109-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5738712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57387122017-12-21 Parental investment matters for maternal and offspring immune defense in the mouthbrooding cichlid Astatotilapia burtoni Keller, Isabel S. Salzburger, Walter Roth, Olivia BMC Evol Biol Research Article BACKGROUND: Parental care, while increasing parental fitness through offspring survival, also bears cost to the care-giving parent. Consequentially, trade offs between parental care and other vitally important traits, such as the immune system seem evident. In co-occurring phases of parental care and immunological challenges negative consequences through a resource allocation trade off on both the parental and the offspring conditions can be predicted. While the immune system reflects parental stress conditions, parental immunological investments also boost offspring survival via the transfer of immunological substances (trans-generational immune priming). We investigated this relationship in the mouthbrooding East African cichlid Astotatilapia burtoni. Prior to mating, females were exposed to an immunological activation, while others remained immunologically naïve. Correspondingly, the immunological status of females was either examined directly after reproduction or after mouthbrooding had ceased. Offspring from both groups were exposed to immunological challenges to assess the extent of trans-generational immune priming. As proxy for immune status, cellular immunological activity and gene expression were determined. RESULTS: Both reproducing and mouthbrooding females allocate their resources towards reproduction. While upon reproduction the innate immune system was impeded, mouthbrooding females showed an attenuation of inflammatory components. Juveniles from immune challenged mouthbrooding females showed downregulation of immune and life history candidate genes, implying a limitation of trans-generational plasticity when parents experience stress during the costly reproductive phase. CONCLUSION: Our results provide evidence that both parental investment via mouthbrooding and the rise of the immunological activity upon an immune challenge are costly traits. If applied simultaneously, not only mothers seem to be impacted in their performance, but also offspring are impeded in their ability to react upon a potentially virulent pathogen exposure. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12862-017-1109-6) contains supplementary material, which is available to authorized users. BioMed Central 2017-12-20 /pmc/articles/PMC5738712/ /pubmed/29262789 http://dx.doi.org/10.1186/s12862-017-1109-6 Text en © The Author(s). 2017 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 Keller, Isabel S. Salzburger, Walter Roth, Olivia Parental investment matters for maternal and offspring immune defense in the mouthbrooding cichlid Astatotilapia burtoni |
title | Parental investment matters for maternal and offspring immune defense in the mouthbrooding cichlid Astatotilapia burtoni |
title_full | Parental investment matters for maternal and offspring immune defense in the mouthbrooding cichlid Astatotilapia burtoni |
title_fullStr | Parental investment matters for maternal and offspring immune defense in the mouthbrooding cichlid Astatotilapia burtoni |
title_full_unstemmed | Parental investment matters for maternal and offspring immune defense in the mouthbrooding cichlid Astatotilapia burtoni |
title_short | Parental investment matters for maternal and offspring immune defense in the mouthbrooding cichlid Astatotilapia burtoni |
title_sort | parental investment matters for maternal and offspring immune defense in the mouthbrooding cichlid astatotilapia burtoni |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5738712/ https://www.ncbi.nlm.nih.gov/pubmed/29262789 http://dx.doi.org/10.1186/s12862-017-1109-6 |
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