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Bacterial phytopathogen infection disrupts belowground plant indirect defense mediated by tritrophic cascade

Plants can defend themselves against herbivores through activation of defensive pathways and attraction of third‐trophic‐level predators and parasites. Trophic cascades that mediate interactions in the phytobiome are part of a larger dynamic including the pathogens of the plant itself, which are kno...

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Autores principales: Rivera, Monique J., Pelz‐Stelinski, Kirsten S., Martini, Xavier, Stelinski, Lukasz L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5496533/
https://www.ncbi.nlm.nih.gov/pubmed/28690813
http://dx.doi.org/10.1002/ece3.3052
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author Rivera, Monique J.
Pelz‐Stelinski, Kirsten S.
Martini, Xavier
Stelinski, Lukasz L.
author_facet Rivera, Monique J.
Pelz‐Stelinski, Kirsten S.
Martini, Xavier
Stelinski, Lukasz L.
author_sort Rivera, Monique J.
collection PubMed
description Plants can defend themselves against herbivores through activation of defensive pathways and attraction of third‐trophic‐level predators and parasites. Trophic cascades that mediate interactions in the phytobiome are part of a larger dynamic including the pathogens of the plant itself, which are known to greatly influence plant defenses. As such, we investigated the impact of a phloem‐limited bacterial pathogen, Candidatus Liberibacter asiaticus (CLas), in cultivated citrus rootstock on a well‐studied belowground tritrophic interaction involving the attraction of an entomopathogenic nematode (EPN), Steinernema diaprepesi, to their root‐feeding insect hosts, Diaprepes abbreviatus larvae. Using belowground olfactometers, we show how CLas infection interferes with this belowground interaction by similarly inducing the release of a C12 terpene, pregeijerene, and disconnecting the association of the terpene with insect presence. D. abbreviatus larvae that were not feeding but in the presence of a CLas‐infected plant were more likely to be infected by EPN than those near uninfected plants. Furthermore, nonfeeding larvae associated with CLas‐infected plants were just as likely to be infected by EPN as those near noninfected plants with D. abbreviatus larval damage. Larvae of two weevil species, D. abbreviatus and Pachnaeus litus, were also more attracted to plants with infection than to uninfected plants. D. abbreviatus larvae were most active when exposed to pregeijerene at a concentration of 0.1 μg/μl. We attribute this attraction to CLas‐infected plants to the same signal previously thought to be a herbivore‐induced plant volatile specifically induced by root‐feeding insects, pregeijerene, by assessing volatiles collected from the roots of infected plants and uninfected plants with and without feeding D. abbreviatus. Synthesis. Phytopathogens can influence the structuring of soil communities extending to the third trophic level. Field populations of EPN may be less effective at host‐finding using pregeijerene as a cue in citrus grove agroecosystems with high presence of CLas infection.
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spelling pubmed-54965332017-07-07 Bacterial phytopathogen infection disrupts belowground plant indirect defense mediated by tritrophic cascade Rivera, Monique J. Pelz‐Stelinski, Kirsten S. Martini, Xavier Stelinski, Lukasz L. Ecol Evol Original Research Plants can defend themselves against herbivores through activation of defensive pathways and attraction of third‐trophic‐level predators and parasites. Trophic cascades that mediate interactions in the phytobiome are part of a larger dynamic including the pathogens of the plant itself, which are known to greatly influence plant defenses. As such, we investigated the impact of a phloem‐limited bacterial pathogen, Candidatus Liberibacter asiaticus (CLas), in cultivated citrus rootstock on a well‐studied belowground tritrophic interaction involving the attraction of an entomopathogenic nematode (EPN), Steinernema diaprepesi, to their root‐feeding insect hosts, Diaprepes abbreviatus larvae. Using belowground olfactometers, we show how CLas infection interferes with this belowground interaction by similarly inducing the release of a C12 terpene, pregeijerene, and disconnecting the association of the terpene with insect presence. D. abbreviatus larvae that were not feeding but in the presence of a CLas‐infected plant were more likely to be infected by EPN than those near uninfected plants. Furthermore, nonfeeding larvae associated with CLas‐infected plants were just as likely to be infected by EPN as those near noninfected plants with D. abbreviatus larval damage. Larvae of two weevil species, D. abbreviatus and Pachnaeus litus, were also more attracted to plants with infection than to uninfected plants. D. abbreviatus larvae were most active when exposed to pregeijerene at a concentration of 0.1 μg/μl. We attribute this attraction to CLas‐infected plants to the same signal previously thought to be a herbivore‐induced plant volatile specifically induced by root‐feeding insects, pregeijerene, by assessing volatiles collected from the roots of infected plants and uninfected plants with and without feeding D. abbreviatus. Synthesis. Phytopathogens can influence the structuring of soil communities extending to the third trophic level. Field populations of EPN may be less effective at host‐finding using pregeijerene as a cue in citrus grove agroecosystems with high presence of CLas infection. John Wiley and Sons Inc. 2017-05-26 /pmc/articles/PMC5496533/ /pubmed/28690813 http://dx.doi.org/10.1002/ece3.3052 Text en © 2017 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Rivera, Monique J.
Pelz‐Stelinski, Kirsten S.
Martini, Xavier
Stelinski, Lukasz L.
Bacterial phytopathogen infection disrupts belowground plant indirect defense mediated by tritrophic cascade
title Bacterial phytopathogen infection disrupts belowground plant indirect defense mediated by tritrophic cascade
title_full Bacterial phytopathogen infection disrupts belowground plant indirect defense mediated by tritrophic cascade
title_fullStr Bacterial phytopathogen infection disrupts belowground plant indirect defense mediated by tritrophic cascade
title_full_unstemmed Bacterial phytopathogen infection disrupts belowground plant indirect defense mediated by tritrophic cascade
title_short Bacterial phytopathogen infection disrupts belowground plant indirect defense mediated by tritrophic cascade
title_sort bacterial phytopathogen infection disrupts belowground plant indirect defense mediated by tritrophic cascade
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5496533/
https://www.ncbi.nlm.nih.gov/pubmed/28690813
http://dx.doi.org/10.1002/ece3.3052
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