Cargando…
Caterpillar saliva interferes with induced Arabidopsis thaliana defence responses via the systemic acquired resistance pathway
Arabidopsis thaliana (L.) Heynh. genotypes limited in their ability to mount either octadecanoid-dependent induced resistance (IR(–)) or systemic acquired resistance (SAR(–)) were used to characterize the roles of these pathways in plant–herbivore interactions. Molecular and biochemical markers of I...
Autores principales: | , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2008
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2423655/ https://www.ncbi.nlm.nih.gov/pubmed/18487634 http://dx.doi.org/10.1093/jxb/ern108 |
_version_ | 1782156154919452672 |
---|---|
author | Weech, Marie-Hélène Chapleau, Mélanie Pan, Li Ide, Christine Bede, Jacqueline C. |
author_facet | Weech, Marie-Hélène Chapleau, Mélanie Pan, Li Ide, Christine Bede, Jacqueline C. |
author_sort | Weech, Marie-Hélène |
collection | PubMed |
description | Arabidopsis thaliana (L.) Heynh. genotypes limited in their ability to mount either octadecanoid-dependent induced resistance (IR(–)) or systemic acquired resistance (SAR(–)) were used to characterize the roles of these pathways in plant–herbivore interactions. Molecular and biochemical markers of IR were analysed in plants subject to herbivory by caterpillars of the beet armyworm, Spodoptera exigua Hübner, which had either intact or impaired salivary secretions since salivary enzymes, such as glucose oxidase, have been implicated in the ability of caterpillars to circumvent induced plant defences. Transcript expression of genes encoding laccase-like multicopper oxidase [AtLMCO4 (polyphenol oxidase)] and defensin (AtPDF1.2) showed salivary-specific patterns which were disrupted in the SAR(–) mutant plants. The activity of octadecanoid-associated anti-nutritive proteins, such as LMCO and trypsin inhibitor, showed similar patterns. Gene and protein changes parallel plant hormone levels where elevated jasmonic acid was observed in wild-type plants fed upon by caterpillars with impaired salivary secretions compared with plants subject to herbivory by normal caterpillars. This salivary-specific difference in jasmonic acid levels was alleviated in SAR(–) mutants. These results support the model that caterpillar saliva interferes with jasmonate-dependent plant defences by activating the SAR pathway. |
format | Text |
id | pubmed-2423655 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-24236552009-02-25 Caterpillar saliva interferes with induced Arabidopsis thaliana defence responses via the systemic acquired resistance pathway Weech, Marie-Hélène Chapleau, Mélanie Pan, Li Ide, Christine Bede, Jacqueline C. J Exp Bot Research Papers Arabidopsis thaliana (L.) Heynh. genotypes limited in their ability to mount either octadecanoid-dependent induced resistance (IR(–)) or systemic acquired resistance (SAR(–)) were used to characterize the roles of these pathways in plant–herbivore interactions. Molecular and biochemical markers of IR were analysed in plants subject to herbivory by caterpillars of the beet armyworm, Spodoptera exigua Hübner, which had either intact or impaired salivary secretions since salivary enzymes, such as glucose oxidase, have been implicated in the ability of caterpillars to circumvent induced plant defences. Transcript expression of genes encoding laccase-like multicopper oxidase [AtLMCO4 (polyphenol oxidase)] and defensin (AtPDF1.2) showed salivary-specific patterns which were disrupted in the SAR(–) mutant plants. The activity of octadecanoid-associated anti-nutritive proteins, such as LMCO and trypsin inhibitor, showed similar patterns. Gene and protein changes parallel plant hormone levels where elevated jasmonic acid was observed in wild-type plants fed upon by caterpillars with impaired salivary secretions compared with plants subject to herbivory by normal caterpillars. This salivary-specific difference in jasmonic acid levels was alleviated in SAR(–) mutants. These results support the model that caterpillar saliva interferes with jasmonate-dependent plant defences by activating the SAR pathway. Oxford University Press 2008-06 2008-05-17 /pmc/articles/PMC2423655/ /pubmed/18487634 http://dx.doi.org/10.1093/jxb/ern108 Text en © 2008 The Author(s). This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. This paper is available online free of all access charges (see http://jxb.oxfordjournals.org/open_access.html for further details) |
spellingShingle | Research Papers Weech, Marie-Hélène Chapleau, Mélanie Pan, Li Ide, Christine Bede, Jacqueline C. Caterpillar saliva interferes with induced Arabidopsis thaliana defence responses via the systemic acquired resistance pathway |
title | Caterpillar saliva interferes with induced Arabidopsis thaliana defence responses via the systemic acquired resistance pathway |
title_full | Caterpillar saliva interferes with induced Arabidopsis thaliana defence responses via the systemic acquired resistance pathway |
title_fullStr | Caterpillar saliva interferes with induced Arabidopsis thaliana defence responses via the systemic acquired resistance pathway |
title_full_unstemmed | Caterpillar saliva interferes with induced Arabidopsis thaliana defence responses via the systemic acquired resistance pathway |
title_short | Caterpillar saliva interferes with induced Arabidopsis thaliana defence responses via the systemic acquired resistance pathway |
title_sort | caterpillar saliva interferes with induced arabidopsis thaliana defence responses via the systemic acquired resistance pathway |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2423655/ https://www.ncbi.nlm.nih.gov/pubmed/18487634 http://dx.doi.org/10.1093/jxb/ern108 |
work_keys_str_mv | AT weechmariehelene caterpillarsalivainterfereswithinducedarabidopsisthalianadefenceresponsesviathesystemicacquiredresistancepathway AT chapleaumelanie caterpillarsalivainterfereswithinducedarabidopsisthalianadefenceresponsesviathesystemicacquiredresistancepathway AT panli caterpillarsalivainterfereswithinducedarabidopsisthalianadefenceresponsesviathesystemicacquiredresistancepathway AT idechristine caterpillarsalivainterfereswithinducedarabidopsisthalianadefenceresponsesviathesystemicacquiredresistancepathway AT bedejacquelinec caterpillarsalivainterfereswithinducedarabidopsisthalianadefenceresponsesviathesystemicacquiredresistancepathway |