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Parasite Presence Induces Gene Expression Changes in an Ant Host Related to Immunity and Longevity

Most species are either parasites or exploited by parasites, making parasite–host interactions a driver of evolution. Parasites with complex life cycles often evolve strategies to facilitate transmission to the definitive host by manipulating their intermediate host. Such manipulations could explain...

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Autores principales: Stoldt, Marah, Klein, Linda, Beros, Sara, Butter, Falk, Jongepier, Evelien, Feldmeyer, Barbara, Foitzik, Susanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7828512/
https://www.ncbi.nlm.nih.gov/pubmed/33451085
http://dx.doi.org/10.3390/genes12010095
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author Stoldt, Marah
Klein, Linda
Beros, Sara
Butter, Falk
Jongepier, Evelien
Feldmeyer, Barbara
Foitzik, Susanne
author_facet Stoldt, Marah
Klein, Linda
Beros, Sara
Butter, Falk
Jongepier, Evelien
Feldmeyer, Barbara
Foitzik, Susanne
author_sort Stoldt, Marah
collection PubMed
description Most species are either parasites or exploited by parasites, making parasite–host interactions a driver of evolution. Parasites with complex life cycles often evolve strategies to facilitate transmission to the definitive host by manipulating their intermediate host. Such manipulations could explain phenotypic changes in the ant Temnothorax nylanderi, the intermediate host of the cestode Anomotaenia brevis. In addition to behavioral and morphological alterations, infected workers exhibit prolonged lifespans, comparable to that of queens, which live up to two decades. We used transcriptomic data from cestodes and ants of different castes and infection status to investigate the molecular underpinnings of phenotypic alterations in infected workers and explored whether the extended lifespan of queens and infected workers has a common molecular basis. Infected workers and queens commonly upregulated only six genes, one of them with a known anti-aging function. Both groups overexpressed immune genes, although not the same ones. Our findings suggest that the lifespan extension of infected workers is not achieved via the expression of queen-specific genes. The analysis of the cestodes’ transcriptome revealed dominant expression of genes of the mitochondrial respiratory transport chain, which indicates an active metabolism and shedding light on the physiology of the parasite in its cysticercoid stage.
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spelling pubmed-78285122021-01-25 Parasite Presence Induces Gene Expression Changes in an Ant Host Related to Immunity and Longevity Stoldt, Marah Klein, Linda Beros, Sara Butter, Falk Jongepier, Evelien Feldmeyer, Barbara Foitzik, Susanne Genes (Basel) Article Most species are either parasites or exploited by parasites, making parasite–host interactions a driver of evolution. Parasites with complex life cycles often evolve strategies to facilitate transmission to the definitive host by manipulating their intermediate host. Such manipulations could explain phenotypic changes in the ant Temnothorax nylanderi, the intermediate host of the cestode Anomotaenia brevis. In addition to behavioral and morphological alterations, infected workers exhibit prolonged lifespans, comparable to that of queens, which live up to two decades. We used transcriptomic data from cestodes and ants of different castes and infection status to investigate the molecular underpinnings of phenotypic alterations in infected workers and explored whether the extended lifespan of queens and infected workers has a common molecular basis. Infected workers and queens commonly upregulated only six genes, one of them with a known anti-aging function. Both groups overexpressed immune genes, although not the same ones. Our findings suggest that the lifespan extension of infected workers is not achieved via the expression of queen-specific genes. The analysis of the cestodes’ transcriptome revealed dominant expression of genes of the mitochondrial respiratory transport chain, which indicates an active metabolism and shedding light on the physiology of the parasite in its cysticercoid stage. MDPI 2021-01-13 /pmc/articles/PMC7828512/ /pubmed/33451085 http://dx.doi.org/10.3390/genes12010095 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Stoldt, Marah
Klein, Linda
Beros, Sara
Butter, Falk
Jongepier, Evelien
Feldmeyer, Barbara
Foitzik, Susanne
Parasite Presence Induces Gene Expression Changes in an Ant Host Related to Immunity and Longevity
title Parasite Presence Induces Gene Expression Changes in an Ant Host Related to Immunity and Longevity
title_full Parasite Presence Induces Gene Expression Changes in an Ant Host Related to Immunity and Longevity
title_fullStr Parasite Presence Induces Gene Expression Changes in an Ant Host Related to Immunity and Longevity
title_full_unstemmed Parasite Presence Induces Gene Expression Changes in an Ant Host Related to Immunity and Longevity
title_short Parasite Presence Induces Gene Expression Changes in an Ant Host Related to Immunity and Longevity
title_sort parasite presence induces gene expression changes in an ant host related to immunity and longevity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7828512/
https://www.ncbi.nlm.nih.gov/pubmed/33451085
http://dx.doi.org/10.3390/genes12010095
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