Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Rassati, Davide, Marini, Lorenzo, Malacrinò, Antonino
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2019
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
_version_ 1783472400825843712
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
work_keys_str_mv AT rassatidavide acquisitionoffungifromtheenvironmentmodifiesambrosiabeetlemycobiomeduringinvasion
AT marinilorenzo acquisitionoffungifromtheenvironmentmodifiesambrosiabeetlemycobiomeduringinvasion
AT malacrinoantonino acquisitionoffungifromtheenvironmentmodifiesambrosiabeetlemycobiomeduringinvasion