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Acquisition of fungi from the environment modifies ambrosia beetle mycobiome during invasion
Microbial symbionts can play critical roles when their host attempts to colonize a new habitat. The lack of symbiont adaptation can in fact hinder the invasion process of their host. This scenario could change if the exotic species are able to acquire microorganisms from the invaded environment. Und...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6870512/ https://www.ncbi.nlm.nih.gov/pubmed/31763076 http://dx.doi.org/10.7717/peerj.8103 |
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author | Rassati, Davide Marini, Lorenzo Malacrinò, Antonino |
author_facet | Rassati, Davide Marini, Lorenzo Malacrinò, Antonino |
author_sort | Rassati, Davide |
collection | PubMed |
description | Microbial symbionts can play critical roles when their host attempts to colonize a new habitat. The lack of symbiont adaptation can in fact hinder the invasion process of their host. This scenario could change if the exotic species are able to acquire microorganisms from the invaded environment. Understanding the ecological factors that influence the take-up of new microorganisms is thus essential to clarify the mechanisms behind biological invasions. In this study, we tested whether different forest habitats influence the structure of the fungal communities associated with ambrosia beetles. We collected individuals of the most widespread exotic (Xylosandrus germanus) and native (Xyleborinus saxesenii) ambrosia beetle species in Europe in several old-growth and restored forests. We characterized the fungal communities associated with both species via metabarcoding. We showed that forest habitat shaped the community of fungi associated with both species, but the effect was stronger for the exotic X. germanus. Our results support the hypothesis that the direct contact with the mycobiome of the invaded environment might lead an exotic species to acquire native fungi. This process is likely favored by the occurrence of a bottleneck effect at the mycobiome level and/or the disruption of the mechanisms sustaining co-evolved insect-fungi symbiosis. Our study contributes to the understanding of the factors affecting insect-microbes interactions, helping to clarify the mechanisms behind biological invasions. |
format | Online Article Text |
id | pubmed-6870512 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68705122019-11-23 Acquisition of fungi from the environment modifies ambrosia beetle mycobiome during invasion Rassati, Davide Marini, Lorenzo Malacrinò, Antonino PeerJ Ecology Microbial symbionts can play critical roles when their host attempts to colonize a new habitat. The lack of symbiont adaptation can in fact hinder the invasion process of their host. This scenario could change if the exotic species are able to acquire microorganisms from the invaded environment. Understanding the ecological factors that influence the take-up of new microorganisms is thus essential to clarify the mechanisms behind biological invasions. In this study, we tested whether different forest habitats influence the structure of the fungal communities associated with ambrosia beetles. We collected individuals of the most widespread exotic (Xylosandrus germanus) and native (Xyleborinus saxesenii) ambrosia beetle species in Europe in several old-growth and restored forests. We characterized the fungal communities associated with both species via metabarcoding. We showed that forest habitat shaped the community of fungi associated with both species, but the effect was stronger for the exotic X. germanus. Our results support the hypothesis that the direct contact with the mycobiome of the invaded environment might lead an exotic species to acquire native fungi. This process is likely favored by the occurrence of a bottleneck effect at the mycobiome level and/or the disruption of the mechanisms sustaining co-evolved insect-fungi symbiosis. Our study contributes to the understanding of the factors affecting insect-microbes interactions, helping to clarify the mechanisms behind biological invasions. PeerJ Inc. 2019-11-18 /pmc/articles/PMC6870512/ /pubmed/31763076 http://dx.doi.org/10.7717/peerj.8103 Text en ©2019 Rassati et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Ecology Rassati, Davide Marini, Lorenzo Malacrinò, Antonino Acquisition of fungi from the environment modifies ambrosia beetle mycobiome during invasion |
title | Acquisition of fungi from the environment modifies ambrosia beetle mycobiome during invasion |
title_full | Acquisition of fungi from the environment modifies ambrosia beetle mycobiome during invasion |
title_fullStr | Acquisition of fungi from the environment modifies ambrosia beetle mycobiome during invasion |
title_full_unstemmed | Acquisition of fungi from the environment modifies ambrosia beetle mycobiome during invasion |
title_short | Acquisition of fungi from the environment modifies ambrosia beetle mycobiome during invasion |
title_sort | acquisition of fungi from the environment modifies ambrosia beetle mycobiome during invasion |
topic | Ecology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6870512/ https://www.ncbi.nlm.nih.gov/pubmed/31763076 http://dx.doi.org/10.7717/peerj.8103 |
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