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Efficient dispersal and substrate acquisition traits in a marine invasive species via transient chimerism and colony mobility
Over the past three decades the colonial ascidian Didemnum vexillum has been expanding its global range, significantly impacting marine habitats and aquaculture facilities. What biological features make D. vexillum so highly invasive? Here, we show that juxtaposed allogeneic D. vexillum colony fragm...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6004106/ https://www.ncbi.nlm.nih.gov/pubmed/29915705 http://dx.doi.org/10.7717/peerj.5006 |
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author | Fidler, Andrew E. Bacq-Labreuil, Aurelie Rachmilovitz, Elad Rinkevich, Baruch |
author_facet | Fidler, Andrew E. Bacq-Labreuil, Aurelie Rachmilovitz, Elad Rinkevich, Baruch |
author_sort | Fidler, Andrew E. |
collection | PubMed |
description | Over the past three decades the colonial ascidian Didemnum vexillum has been expanding its global range, significantly impacting marine habitats and aquaculture facilities. What biological features make D. vexillum so highly invasive? Here, we show that juxtaposed allogeneic D. vexillum colony fragments (‘ramets’) may, initially, form chimeric entities. Subsequently, zooids of the differing genotypes within such chimeras coordinately retreat away from fusion zones. A few days following such post-fusion retreat movements there is further ramet fission and the formation of zooid-depauperate tunic zones. Using polymorphic microsatellite loci to distinguish between genotypes, we found that they were sectorial at the fusion zones and the subsequent ramet movements resulted in further spatial separation of the paired-genotypes indicating that the fusion events observed did not lead to formation of long-term, stable chimeras. Thus, movements of D. vexillum colony ramets from initial fusion zones lead to progressive segregation of genotypes probably minimizing potential somatic/germ-cell competition/parasitism. We speculate that relatively fast (≤10 mm/day) movement of D. vexillum colonies on substrates along with frequent, and perhaps unrestrained, transient allogeneic fusions play significant roles in this species’ striking invasiveness and capacity to colonize new substrates. |
format | Online Article Text |
id | pubmed-6004106 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60041062018-06-18 Efficient dispersal and substrate acquisition traits in a marine invasive species via transient chimerism and colony mobility Fidler, Andrew E. Bacq-Labreuil, Aurelie Rachmilovitz, Elad Rinkevich, Baruch PeerJ Conservation Biology Over the past three decades the colonial ascidian Didemnum vexillum has been expanding its global range, significantly impacting marine habitats and aquaculture facilities. What biological features make D. vexillum so highly invasive? Here, we show that juxtaposed allogeneic D. vexillum colony fragments (‘ramets’) may, initially, form chimeric entities. Subsequently, zooids of the differing genotypes within such chimeras coordinately retreat away from fusion zones. A few days following such post-fusion retreat movements there is further ramet fission and the formation of zooid-depauperate tunic zones. Using polymorphic microsatellite loci to distinguish between genotypes, we found that they were sectorial at the fusion zones and the subsequent ramet movements resulted in further spatial separation of the paired-genotypes indicating that the fusion events observed did not lead to formation of long-term, stable chimeras. Thus, movements of D. vexillum colony ramets from initial fusion zones lead to progressive segregation of genotypes probably minimizing potential somatic/germ-cell competition/parasitism. We speculate that relatively fast (≤10 mm/day) movement of D. vexillum colonies on substrates along with frequent, and perhaps unrestrained, transient allogeneic fusions play significant roles in this species’ striking invasiveness and capacity to colonize new substrates. PeerJ Inc. 2018-06-13 /pmc/articles/PMC6004106/ /pubmed/29915705 http://dx.doi.org/10.7717/peerj.5006 Text en ©2018 Fidler 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, 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 | Conservation Biology Fidler, Andrew E. Bacq-Labreuil, Aurelie Rachmilovitz, Elad Rinkevich, Baruch Efficient dispersal and substrate acquisition traits in a marine invasive species via transient chimerism and colony mobility |
title | Efficient dispersal and substrate acquisition traits in a marine invasive species via transient chimerism and colony mobility |
title_full | Efficient dispersal and substrate acquisition traits in a marine invasive species via transient chimerism and colony mobility |
title_fullStr | Efficient dispersal and substrate acquisition traits in a marine invasive species via transient chimerism and colony mobility |
title_full_unstemmed | Efficient dispersal and substrate acquisition traits in a marine invasive species via transient chimerism and colony mobility |
title_short | Efficient dispersal and substrate acquisition traits in a marine invasive species via transient chimerism and colony mobility |
title_sort | efficient dispersal and substrate acquisition traits in a marine invasive species via transient chimerism and colony mobility |
topic | Conservation Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6004106/ https://www.ncbi.nlm.nih.gov/pubmed/29915705 http://dx.doi.org/10.7717/peerj.5006 |
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