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Distinct Signatures of Host Defense Suppression by Plant-Feeding Mites
Tomato plants are attacked by diverse herbivorous arthropods, including by cell-content-feeding mites, such as the extreme generalist Tetranychus urticae and specialists like Tetranychus evansi and Aculops lycopersici. Mite feeding induces plant defense responses that reduce mite performance. Howeve...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6214137/ https://www.ncbi.nlm.nih.gov/pubmed/30347842 http://dx.doi.org/10.3390/ijms19103265 |
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author | Schimmel, Bernardus C. J. Alba, Juan M. Wybouw, Nicky Glas, Joris J. Meijer, Tomas T. Schuurink, Robert C. Kant, Merijn R. |
author_facet | Schimmel, Bernardus C. J. Alba, Juan M. Wybouw, Nicky Glas, Joris J. Meijer, Tomas T. Schuurink, Robert C. Kant, Merijn R. |
author_sort | Schimmel, Bernardus C. J. |
collection | PubMed |
description | Tomato plants are attacked by diverse herbivorous arthropods, including by cell-content-feeding mites, such as the extreme generalist Tetranychus urticae and specialists like Tetranychus evansi and Aculops lycopersici. Mite feeding induces plant defense responses that reduce mite performance. However, T. evansi and A. lycopersici suppress plant defenses via poorly understood mechanisms and, consequently, maintain a high performance on tomato. On a shared host, T. urticae can be facilitated by either of the specialist mites, likely due to the suppression of plant defenses. To better understand defense suppression and indirect plant-mediated interactions between herbivorous mites, we used gene-expression microarrays to analyze the transcriptomic changes in tomato after attack by either a single mite species (T. urticae, T. evansi, A. lycopersici) or two species simultaneously (T. urticae plus T. evansi or T. urticae plus A. lycopersici). Additionally, we assessed mite-induced changes in defense-associated phytohormones using LC-MS/MS. Compared to non-infested controls, jasmonates (JAs) and salicylate (SA) accumulated to higher amounts upon all mite-infestation treatments, but the response was attenuated after single infestations with defense-suppressors. Strikingly, whereas 8 to 10% of tomato genes were differentially expressed upon single infestations with T. urticae or A. lycopersici, respectively, only 0.1% was altered in T. evansi-infested plants. Transcriptome analysis of dual-infested leaves revealed that A. lycopersici primarily suppressed T. urticae-induced JA defenses, while T. evansi dampened T. urticae-triggered host responses on a transcriptome-wide scale. The latter suggests that T. evansi not solely down-regulates plant gene expression, but rather directs it back towards housekeeping levels. Our results provide valuable new insights into the mechanisms underlying host defense suppression and the plant-mediated facilitation of competing herbivores. |
format | Online Article Text |
id | pubmed-6214137 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62141372018-11-14 Distinct Signatures of Host Defense Suppression by Plant-Feeding Mites Schimmel, Bernardus C. J. Alba, Juan M. Wybouw, Nicky Glas, Joris J. Meijer, Tomas T. Schuurink, Robert C. Kant, Merijn R. Int J Mol Sci Article Tomato plants are attacked by diverse herbivorous arthropods, including by cell-content-feeding mites, such as the extreme generalist Tetranychus urticae and specialists like Tetranychus evansi and Aculops lycopersici. Mite feeding induces plant defense responses that reduce mite performance. However, T. evansi and A. lycopersici suppress plant defenses via poorly understood mechanisms and, consequently, maintain a high performance on tomato. On a shared host, T. urticae can be facilitated by either of the specialist mites, likely due to the suppression of plant defenses. To better understand defense suppression and indirect plant-mediated interactions between herbivorous mites, we used gene-expression microarrays to analyze the transcriptomic changes in tomato after attack by either a single mite species (T. urticae, T. evansi, A. lycopersici) or two species simultaneously (T. urticae plus T. evansi or T. urticae plus A. lycopersici). Additionally, we assessed mite-induced changes in defense-associated phytohormones using LC-MS/MS. Compared to non-infested controls, jasmonates (JAs) and salicylate (SA) accumulated to higher amounts upon all mite-infestation treatments, but the response was attenuated after single infestations with defense-suppressors. Strikingly, whereas 8 to 10% of tomato genes were differentially expressed upon single infestations with T. urticae or A. lycopersici, respectively, only 0.1% was altered in T. evansi-infested plants. Transcriptome analysis of dual-infested leaves revealed that A. lycopersici primarily suppressed T. urticae-induced JA defenses, while T. evansi dampened T. urticae-triggered host responses on a transcriptome-wide scale. The latter suggests that T. evansi not solely down-regulates plant gene expression, but rather directs it back towards housekeeping levels. Our results provide valuable new insights into the mechanisms underlying host defense suppression and the plant-mediated facilitation of competing herbivores. MDPI 2018-10-20 /pmc/articles/PMC6214137/ /pubmed/30347842 http://dx.doi.org/10.3390/ijms19103265 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Schimmel, Bernardus C. J. Alba, Juan M. Wybouw, Nicky Glas, Joris J. Meijer, Tomas T. Schuurink, Robert C. Kant, Merijn R. Distinct Signatures of Host Defense Suppression by Plant-Feeding Mites |
title | Distinct Signatures of Host Defense Suppression by Plant-Feeding Mites |
title_full | Distinct Signatures of Host Defense Suppression by Plant-Feeding Mites |
title_fullStr | Distinct Signatures of Host Defense Suppression by Plant-Feeding Mites |
title_full_unstemmed | Distinct Signatures of Host Defense Suppression by Plant-Feeding Mites |
title_short | Distinct Signatures of Host Defense Suppression by Plant-Feeding Mites |
title_sort | distinct signatures of host defense suppression by plant-feeding mites |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6214137/ https://www.ncbi.nlm.nih.gov/pubmed/30347842 http://dx.doi.org/10.3390/ijms19103265 |
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