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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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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. |
format | Online Article Text |
id | pubmed-6411376 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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