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Honeydew-associated microbes elicit defense responses against brown planthopper in rice

Feeding of sucking insects, such as the rice brown planthopper (Nilaparvata lugens; BPH), causes only limited mechanical damage on plants that is otherwise essential for injury-triggered defense responses against herbivores. In pursuit of complementary BPH elicitors perceived by plants, we examined...

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Autores principales: Wari, David, Kabir, Md Alamgir, Mujiono, Kadis, Hojo, Yuko, Shinya, Tomonori, Tani, Akio, Nakatani, Hiroko, Galis, Ivan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411376/
https://www.ncbi.nlm.nih.gov/pubmed/30715410
http://dx.doi.org/10.1093/jxb/erz041
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author Wari, David
Kabir, Md Alamgir
Mujiono, Kadis
Hojo, Yuko
Shinya, Tomonori
Tani, Akio
Nakatani, Hiroko
Galis, Ivan
author_facet Wari, David
Kabir, Md Alamgir
Mujiono, Kadis
Hojo, Yuko
Shinya, Tomonori
Tani, Akio
Nakatani, Hiroko
Galis, Ivan
author_sort Wari, David
collection PubMed
description Feeding of sucking insects, such as the rice brown planthopper (Nilaparvata lugens; BPH), causes only limited mechanical damage on plants that is otherwise essential for injury-triggered defense responses against herbivores. In pursuit of complementary BPH elicitors perceived by plants, we examined the potential effects of BPH honeydew secretions on the BPH monocot host, rice (Oryza sativa). We found that BPH honeydew strongly elicits direct and putative indirect defenses in rice, namely accumulation of phytoalexins in the leaves, and release of volatile organic compounds from the leaves that serve to attract natural enemies of herbivores, respectively. We then examined the elicitor active components in the honeydew and found that bacteria in the secretions are responsible for the activation of plant defense. Corroborating the importance of honeydew-associated microbiota for induced plant resistance, BPHs partially devoid of their microbiota via prolonged antibiotics ingestion induced significantly less defense in rice relative to antibiotic-free insects applied to similar groups of plants. Our data suggest that rice plants may additionally perceive herbivores via their honeydew-associated microbes, allowing them to discriminate between incompatible herbivores—that do not produce honeydew—and those that are compatible and therefore dangerous.
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spelling pubmed-64113762019-03-15 Honeydew-associated microbes elicit defense responses against brown planthopper in rice Wari, David Kabir, Md Alamgir Mujiono, Kadis Hojo, Yuko Shinya, Tomonori Tani, Akio Nakatani, Hiroko Galis, Ivan J Exp Bot Research Papers Feeding of sucking insects, such as the rice brown planthopper (Nilaparvata lugens; BPH), causes only limited mechanical damage on plants that is otherwise essential for injury-triggered defense responses against herbivores. In pursuit of complementary BPH elicitors perceived by plants, we examined the potential effects of BPH honeydew secretions on the BPH monocot host, rice (Oryza sativa). We found that BPH honeydew strongly elicits direct and putative indirect defenses in rice, namely accumulation of phytoalexins in the leaves, and release of volatile organic compounds from the leaves that serve to attract natural enemies of herbivores, respectively. We then examined the elicitor active components in the honeydew and found that bacteria in the secretions are responsible for the activation of plant defense. Corroborating the importance of honeydew-associated microbiota for induced plant resistance, BPHs partially devoid of their microbiota via prolonged antibiotics ingestion induced significantly less defense in rice relative to antibiotic-free insects applied to similar groups of plants. Our data suggest that rice plants may additionally perceive herbivores via their honeydew-associated microbes, allowing them to discriminate between incompatible herbivores—that do not produce honeydew—and those that are compatible and therefore dangerous. Oxford University Press 2019-02-15 2019-03-02 /pmc/articles/PMC6411376/ /pubmed/30715410 http://dx.doi.org/10.1093/jxb/erz041 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Experimental Biology. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Papers
Wari, David
Kabir, Md Alamgir
Mujiono, Kadis
Hojo, Yuko
Shinya, Tomonori
Tani, Akio
Nakatani, Hiroko
Galis, Ivan
Honeydew-associated microbes elicit defense responses against brown planthopper in rice
title Honeydew-associated microbes elicit defense responses against brown planthopper in rice
title_full Honeydew-associated microbes elicit defense responses against brown planthopper in rice
title_fullStr Honeydew-associated microbes elicit defense responses against brown planthopper in rice
title_full_unstemmed Honeydew-associated microbes elicit defense responses against brown planthopper in rice
title_short Honeydew-associated microbes elicit defense responses against brown planthopper in rice
title_sort honeydew-associated microbes elicit defense responses against brown planthopper in rice
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411376/
https://www.ncbi.nlm.nih.gov/pubmed/30715410
http://dx.doi.org/10.1093/jxb/erz041
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