Cargando…
An invasive insect herbivore disrupts plant volatile-mediated tritrophic signalling
Plants respond to insect attack by emission of volatile organic compounds, which recruit natural enemies of the attacking herbivore, constituting an indirect plant defence strategy. In this context, the egg parasitoid Trissolcus basalis is attracted by oviposition-induced plant volatiles emitted by...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5544816/ https://www.ncbi.nlm.nih.gov/pubmed/28824353 http://dx.doi.org/10.1007/s10340-017-0877-5 |
_version_ | 1783255312562651136 |
---|---|
author | Martorana, Letizia Foti, Maria Cristina Rondoni, Gabriele Conti, Eric Colazza, Stefano Peri, Ezio |
author_facet | Martorana, Letizia Foti, Maria Cristina Rondoni, Gabriele Conti, Eric Colazza, Stefano Peri, Ezio |
author_sort | Martorana, Letizia |
collection | PubMed |
description | Plants respond to insect attack by emission of volatile organic compounds, which recruit natural enemies of the attacking herbivore, constituting an indirect plant defence strategy. In this context, the egg parasitoid Trissolcus basalis is attracted by oviposition-induced plant volatiles emitted by Vicia faba plants as a consequence of feeding and oviposition by the pentatomid host Nezara viridula. However, this local tritrophic web could be affected by the recent invasion by the alien pentatomid bug Halyomorpha halys, an herbivore that shares the same environments as native pentatomid pests. Therefore, we investigated in laboratory conditions the possible impact of H. halys on the plant volatile-mediated signalling in the local tritrophic web V. faba–N. viridula–T. basalis. We found that T. basalis wasps were not attracted by volatiles induced in the plants by feeding and oviposition activities of H. halys, indicating specificity in the wasps’ response. However, the parasitoid attraction towards plant volatiles emitted as a consequence of feeding and oviposition by the associated host was disrupted when host, N. viridula, and non-associated host, H. halys, were concurrently present on the same plant, indicating that invasion by the alien herbivore interferes with established semiochemical webs. These outcomes are discussed in a context of multiple herbivory by evaluating the possible influences of alien insects on local parasitoid foraging behaviour. |
format | Online Article Text |
id | pubmed-5544816 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-55448162017-08-18 An invasive insect herbivore disrupts plant volatile-mediated tritrophic signalling Martorana, Letizia Foti, Maria Cristina Rondoni, Gabriele Conti, Eric Colazza, Stefano Peri, Ezio J Pest Sci (2004) Original Paper Plants respond to insect attack by emission of volatile organic compounds, which recruit natural enemies of the attacking herbivore, constituting an indirect plant defence strategy. In this context, the egg parasitoid Trissolcus basalis is attracted by oviposition-induced plant volatiles emitted by Vicia faba plants as a consequence of feeding and oviposition by the pentatomid host Nezara viridula. However, this local tritrophic web could be affected by the recent invasion by the alien pentatomid bug Halyomorpha halys, an herbivore that shares the same environments as native pentatomid pests. Therefore, we investigated in laboratory conditions the possible impact of H. halys on the plant volatile-mediated signalling in the local tritrophic web V. faba–N. viridula–T. basalis. We found that T. basalis wasps were not attracted by volatiles induced in the plants by feeding and oviposition activities of H. halys, indicating specificity in the wasps’ response. However, the parasitoid attraction towards plant volatiles emitted as a consequence of feeding and oviposition by the associated host was disrupted when host, N. viridula, and non-associated host, H. halys, were concurrently present on the same plant, indicating that invasion by the alien herbivore interferes with established semiochemical webs. These outcomes are discussed in a context of multiple herbivory by evaluating the possible influences of alien insects on local parasitoid foraging behaviour. Springer Berlin Heidelberg 2017-05-13 2017 /pmc/articles/PMC5544816/ /pubmed/28824353 http://dx.doi.org/10.1007/s10340-017-0877-5 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Paper Martorana, Letizia Foti, Maria Cristina Rondoni, Gabriele Conti, Eric Colazza, Stefano Peri, Ezio An invasive insect herbivore disrupts plant volatile-mediated tritrophic signalling |
title | An invasive insect herbivore disrupts plant volatile-mediated tritrophic signalling |
title_full | An invasive insect herbivore disrupts plant volatile-mediated tritrophic signalling |
title_fullStr | An invasive insect herbivore disrupts plant volatile-mediated tritrophic signalling |
title_full_unstemmed | An invasive insect herbivore disrupts plant volatile-mediated tritrophic signalling |
title_short | An invasive insect herbivore disrupts plant volatile-mediated tritrophic signalling |
title_sort | invasive insect herbivore disrupts plant volatile-mediated tritrophic signalling |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5544816/ https://www.ncbi.nlm.nih.gov/pubmed/28824353 http://dx.doi.org/10.1007/s10340-017-0877-5 |
work_keys_str_mv | AT martoranaletizia aninvasiveinsectherbivoredisruptsplantvolatilemediatedtritrophicsignalling AT fotimariacristina aninvasiveinsectherbivoredisruptsplantvolatilemediatedtritrophicsignalling AT rondonigabriele aninvasiveinsectherbivoredisruptsplantvolatilemediatedtritrophicsignalling AT contieric aninvasiveinsectherbivoredisruptsplantvolatilemediatedtritrophicsignalling AT colazzastefano aninvasiveinsectherbivoredisruptsplantvolatilemediatedtritrophicsignalling AT periezio aninvasiveinsectherbivoredisruptsplantvolatilemediatedtritrophicsignalling AT martoranaletizia invasiveinsectherbivoredisruptsplantvolatilemediatedtritrophicsignalling AT fotimariacristina invasiveinsectherbivoredisruptsplantvolatilemediatedtritrophicsignalling AT rondonigabriele invasiveinsectherbivoredisruptsplantvolatilemediatedtritrophicsignalling AT contieric invasiveinsectherbivoredisruptsplantvolatilemediatedtritrophicsignalling AT colazzastefano invasiveinsectherbivoredisruptsplantvolatilemediatedtritrophicsignalling AT periezio invasiveinsectherbivoredisruptsplantvolatilemediatedtritrophicsignalling |