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Trans-generational Immune Priming Protects the Eggs Only against Gram-Positive Bacteria in the Mealworm Beetle

In many vertebrates and invertebrates, offspring whose mothers have been exposed to pathogens can exhibit increased levels of immune activity and/or increased survival to infection. Such phenomena, called “Trans-generational immune priming” (TGIP) are expected to provide immune protection to the off...

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Autores principales: Dubuffet, Aurore, Zanchi, Caroline, Boutet, Gwendoline, Moreau, Jérôme, Teixeira, Maria, Moret, Yannick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4592268/
https://www.ncbi.nlm.nih.gov/pubmed/26430786
http://dx.doi.org/10.1371/journal.ppat.1005178
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author Dubuffet, Aurore
Zanchi, Caroline
Boutet, Gwendoline
Moreau, Jérôme
Teixeira, Maria
Moret, Yannick
author_facet Dubuffet, Aurore
Zanchi, Caroline
Boutet, Gwendoline
Moreau, Jérôme
Teixeira, Maria
Moret, Yannick
author_sort Dubuffet, Aurore
collection PubMed
description In many vertebrates and invertebrates, offspring whose mothers have been exposed to pathogens can exhibit increased levels of immune activity and/or increased survival to infection. Such phenomena, called “Trans-generational immune priming” (TGIP) are expected to provide immune protection to the offspring. As the offspring and their mother may share the same environment, and consequently similar microbial threats, we expect the immune molecules present in the progeny to be specific to the microbes that immune challenged the mother. We provide evidence in the mealworm beetle Tenebrio molitor that the antimicrobial activity found in the eggs is only active against Gram-positive bacteria, even when females were exposed to Gram-negative bacteria or fungi. Fungi were weak inducers of TGIP while we obtained similar levels of anti-Gram-positive activity using different bacteria for the maternal challenge. Furthermore, we have identified an antibacterial peptide from the defensin family, the tenecin 1, which spectrum of activity is exclusively directed toward Gram-positive bacteria as potential contributor to this antimicrobial activity. We conclude that maternal transfer of antimicrobial activity in the eggs of T. molitor might have evolved from persistent Gram-positive bacterial pathogens between insect generations.
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spelling pubmed-45922682015-10-09 Trans-generational Immune Priming Protects the Eggs Only against Gram-Positive Bacteria in the Mealworm Beetle Dubuffet, Aurore Zanchi, Caroline Boutet, Gwendoline Moreau, Jérôme Teixeira, Maria Moret, Yannick PLoS Pathog Research Article In many vertebrates and invertebrates, offspring whose mothers have been exposed to pathogens can exhibit increased levels of immune activity and/or increased survival to infection. Such phenomena, called “Trans-generational immune priming” (TGIP) are expected to provide immune protection to the offspring. As the offspring and their mother may share the same environment, and consequently similar microbial threats, we expect the immune molecules present in the progeny to be specific to the microbes that immune challenged the mother. We provide evidence in the mealworm beetle Tenebrio molitor that the antimicrobial activity found in the eggs is only active against Gram-positive bacteria, even when females were exposed to Gram-negative bacteria or fungi. Fungi were weak inducers of TGIP while we obtained similar levels of anti-Gram-positive activity using different bacteria for the maternal challenge. Furthermore, we have identified an antibacterial peptide from the defensin family, the tenecin 1, which spectrum of activity is exclusively directed toward Gram-positive bacteria as potential contributor to this antimicrobial activity. We conclude that maternal transfer of antimicrobial activity in the eggs of T. molitor might have evolved from persistent Gram-positive bacterial pathogens between insect generations. Public Library of Science 2015-10-02 /pmc/articles/PMC4592268/ /pubmed/26430786 http://dx.doi.org/10.1371/journal.ppat.1005178 Text en © 2015 Dubuffet et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Dubuffet, Aurore
Zanchi, Caroline
Boutet, Gwendoline
Moreau, Jérôme
Teixeira, Maria
Moret, Yannick
Trans-generational Immune Priming Protects the Eggs Only against Gram-Positive Bacteria in the Mealworm Beetle
title Trans-generational Immune Priming Protects the Eggs Only against Gram-Positive Bacteria in the Mealworm Beetle
title_full Trans-generational Immune Priming Protects the Eggs Only against Gram-Positive Bacteria in the Mealworm Beetle
title_fullStr Trans-generational Immune Priming Protects the Eggs Only against Gram-Positive Bacteria in the Mealworm Beetle
title_full_unstemmed Trans-generational Immune Priming Protects the Eggs Only against Gram-Positive Bacteria in the Mealworm Beetle
title_short Trans-generational Immune Priming Protects the Eggs Only against Gram-Positive Bacteria in the Mealworm Beetle
title_sort trans-generational immune priming protects the eggs only against gram-positive bacteria in the mealworm beetle
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4592268/
https://www.ncbi.nlm.nih.gov/pubmed/26430786
http://dx.doi.org/10.1371/journal.ppat.1005178
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