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Deciphering the molecular mechanisms of mother-to-egg immune protection in the mealworm beetle Tenebrio molitor
In a number of species, individuals exposed to pathogens can mount an immune response and transmit this immunological experience to their offspring, thereby protecting them against persistent threats. Such vertical transfer of immunity, named trans-generational immune priming (TGIP), has been descri...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7591081/ https://www.ncbi.nlm.nih.gov/pubmed/33057453 http://dx.doi.org/10.1371/journal.ppat.1008935 |
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author | Tetreau, Guillaume Dhinaut, Julien Galinier, Richard Audant-Lacour, Pascaline Voisin, Sébastien N. Arafah, Karim Chogne, Manon Hilliou, Frédérique Bordes, Anaïs Sabarly, Camille Chan, Philippe Walet-Balieu, Marie-Laure Vaudry, David Duval, David Bulet, Philippe Coustau, Christine Moret, Yannick Gourbal, Benjamin |
author_facet | Tetreau, Guillaume Dhinaut, Julien Galinier, Richard Audant-Lacour, Pascaline Voisin, Sébastien N. Arafah, Karim Chogne, Manon Hilliou, Frédérique Bordes, Anaïs Sabarly, Camille Chan, Philippe Walet-Balieu, Marie-Laure Vaudry, David Duval, David Bulet, Philippe Coustau, Christine Moret, Yannick Gourbal, Benjamin |
author_sort | Tetreau, Guillaume |
collection | PubMed |
description | In a number of species, individuals exposed to pathogens can mount an immune response and transmit this immunological experience to their offspring, thereby protecting them against persistent threats. Such vertical transfer of immunity, named trans-generational immune priming (TGIP), has been described in both vertebrates and invertebrates. Although increasingly studied during the last decade, the mechanisms underlying TGIP in invertebrates are still elusive, especially those protecting the earliest offspring life stage, i.e. the embryo developing in the egg. In the present study, we combined different proteomic and transcriptomic approaches to determine whether mothers transfer a “signal” (such as fragments of infecting bacteria), mRNA and/or protein/peptide effectors to protect their eggs against two natural bacterial pathogens, namely the Gram-positive Bacillus thuringiensis and the Gram-negative Serratia entomophila. By taking the mealworm beetle Tenebrio molitor as a biological model, our results suggest that eggs are mainly protected by an active direct transfer of a restricted number of immune proteins and of antimicrobial peptides. In contrast, the present data do not support the involvement of mRNA transfer while the transmission of a “signal”, if it happens, is marginal and only occurs within 24h after maternal exposure to bacteria. This work exemplifies how combining global approaches helps to disentangle the different scenarios of a complex trait, providing a comprehensive characterization of TGIP mechanisms in T. molitor. It also paves the way for future alike studies focusing on TGIP in a wide range of invertebrates and vertebrates to identify additional candidates that could be specific to TGIP and to investigate whether the TGIP mechanisms found herein are specific or common to all insect species. |
format | Online Article Text |
id | pubmed-7591081 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-75910812020-10-30 Deciphering the molecular mechanisms of mother-to-egg immune protection in the mealworm beetle Tenebrio molitor Tetreau, Guillaume Dhinaut, Julien Galinier, Richard Audant-Lacour, Pascaline Voisin, Sébastien N. Arafah, Karim Chogne, Manon Hilliou, Frédérique Bordes, Anaïs Sabarly, Camille Chan, Philippe Walet-Balieu, Marie-Laure Vaudry, David Duval, David Bulet, Philippe Coustau, Christine Moret, Yannick Gourbal, Benjamin PLoS Pathog Research Article In a number of species, individuals exposed to pathogens can mount an immune response and transmit this immunological experience to their offspring, thereby protecting them against persistent threats. Such vertical transfer of immunity, named trans-generational immune priming (TGIP), has been described in both vertebrates and invertebrates. Although increasingly studied during the last decade, the mechanisms underlying TGIP in invertebrates are still elusive, especially those protecting the earliest offspring life stage, i.e. the embryo developing in the egg. In the present study, we combined different proteomic and transcriptomic approaches to determine whether mothers transfer a “signal” (such as fragments of infecting bacteria), mRNA and/or protein/peptide effectors to protect their eggs against two natural bacterial pathogens, namely the Gram-positive Bacillus thuringiensis and the Gram-negative Serratia entomophila. By taking the mealworm beetle Tenebrio molitor as a biological model, our results suggest that eggs are mainly protected by an active direct transfer of a restricted number of immune proteins and of antimicrobial peptides. In contrast, the present data do not support the involvement of mRNA transfer while the transmission of a “signal”, if it happens, is marginal and only occurs within 24h after maternal exposure to bacteria. This work exemplifies how combining global approaches helps to disentangle the different scenarios of a complex trait, providing a comprehensive characterization of TGIP mechanisms in T. molitor. It also paves the way for future alike studies focusing on TGIP in a wide range of invertebrates and vertebrates to identify additional candidates that could be specific to TGIP and to investigate whether the TGIP mechanisms found herein are specific or common to all insect species. Public Library of Science 2020-10-15 /pmc/articles/PMC7591081/ /pubmed/33057453 http://dx.doi.org/10.1371/journal.ppat.1008935 Text en © 2020 Tetreau 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Tetreau, Guillaume Dhinaut, Julien Galinier, Richard Audant-Lacour, Pascaline Voisin, Sébastien N. Arafah, Karim Chogne, Manon Hilliou, Frédérique Bordes, Anaïs Sabarly, Camille Chan, Philippe Walet-Balieu, Marie-Laure Vaudry, David Duval, David Bulet, Philippe Coustau, Christine Moret, Yannick Gourbal, Benjamin Deciphering the molecular mechanisms of mother-to-egg immune protection in the mealworm beetle Tenebrio molitor |
title | Deciphering the molecular mechanisms of mother-to-egg immune protection in the mealworm beetle Tenebrio molitor |
title_full | Deciphering the molecular mechanisms of mother-to-egg immune protection in the mealworm beetle Tenebrio molitor |
title_fullStr | Deciphering the molecular mechanisms of mother-to-egg immune protection in the mealworm beetle Tenebrio molitor |
title_full_unstemmed | Deciphering the molecular mechanisms of mother-to-egg immune protection in the mealworm beetle Tenebrio molitor |
title_short | Deciphering the molecular mechanisms of mother-to-egg immune protection in the mealworm beetle Tenebrio molitor |
title_sort | deciphering the molecular mechanisms of mother-to-egg immune protection in the mealworm beetle tenebrio molitor |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7591081/ https://www.ncbi.nlm.nih.gov/pubmed/33057453 http://dx.doi.org/10.1371/journal.ppat.1008935 |
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