Metabolite profiling reveals a specific response in tomato to predaceous Chrysoperla carnea larvae and herbivore(s)-predator interactions with the generalist pests Tetranychus urticae and Myzus persicae

The spider mite Tetranychus urticae Koch and the aphid Myzus persicae (Sulzer) both infest a number of economically significant crops, including tomato (Solanum lycopersicum). Although used for decades to control pests, the impact of green lacewing larvae Chrysoperla carnea (Stephens) on plant bioch...

Full description

Bibliographic Details
Main Authors: Audrey Errard, Christian Ulrichs, Stefan Kühne, Inga Mewis, Narantuya Mishig, Ronald Maul, Mario Drungowski, Pia Parolin, Monika Schreiner, Susanne Baldermann
Format: Article
Language:English
Published: Frontiers Media S.A. 2016-08-01
Series:Frontiers in Plant Science
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fpls.2016.01256/full
_version_ 1817995038649483264
author Audrey Errard
Audrey Errard
Christian Ulrichs
Stefan Kühne
Inga Mewis
Narantuya Mishig
Narantuya Mishig
Ronald Maul
Ronald Maul
Mario Drungowski
Pia Parolin
Monika Schreiner
Susanne Baldermann
Susanne Baldermann
author_facet Audrey Errard
Audrey Errard
Christian Ulrichs
Stefan Kühne
Inga Mewis
Narantuya Mishig
Narantuya Mishig
Ronald Maul
Ronald Maul
Mario Drungowski
Pia Parolin
Monika Schreiner
Susanne Baldermann
Susanne Baldermann
author_sort Audrey Errard
collection DOAJ
description The spider mite Tetranychus urticae Koch and the aphid Myzus persicae (Sulzer) both infest a number of economically significant crops, including tomato (Solanum lycopersicum). Although used for decades to control pests, the impact of green lacewing larvae Chrysoperla carnea (Stephens) on plant biochemistry was not investigated. Here we used profiling methods and targeted analyses to explore the impact of the predator and herbivore(s)-predator interactions on tomato biochemistry. Each pest and pest-predator combination induced a characteristic metabolite signature in the leaf and the fruit thus, the plant exhibited a systemic response. The treatments had a stronger impact on non-volatile metabolites including abscisic acid and amino acids in the leaves in comparison with the fruits. In contrast, the various biotic factors had a greater impact on the carotenoids in the fruits. We identified volatiles such as myrcene and α-terpinene which were induced by pest-predator interactions but not by single species, and we demonstrated the involvement of the phytohormone abscisic acid in tritrophic interactions for the first time. More importantly, C. carnea larvae alone impacted the plant metabolome, but the predator did not appear to elicit particular defense pathways on its own. Since the presence of both C. carnea larvae and pest individuals elicited volatiles which were shown to contribute to plant defense, C. carnea larvae could therefore contribute to the reduction of pest infestation, not only by its preying activity, but also by priming responses to generalist herbivores such as T. urticae and M. persicae. On the other hand, the use of C. carnea larvae alone did not impact carotenoids thus, was not prejudicial to the fruit quality. The present piece of research highlights the specific impact of predator and tritrophic interactions with green lacewing larvae, spider mites and aphids on different components of the tomato primary and secondary metabolism for the first time, and provides cues for further in-depth studies aiming to integrate entomological approaches and plant biochemistry.
first_indexed 2024-04-14T02:01:27Z
format Article
id doaj.art-5e4a52898e034081a13fbceaeef0ac38
institution Directory Open Access Journal
issn 1664-462X
language English
last_indexed 2024-04-14T02:01:27Z
publishDate 2016-08-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Plant Science
spelling doaj.art-5e4a52898e034081a13fbceaeef0ac382022-12-22T02:18:50ZengFrontiers Media S.A.Frontiers in Plant Science1664-462X2016-08-01710.3389/fpls.2016.01256209689Metabolite profiling reveals a specific response in tomato to predaceous Chrysoperla carnea larvae and herbivore(s)-predator interactions with the generalist pests Tetranychus urticae and Myzus persicaeAudrey Errard0Audrey Errard1Christian Ulrichs2Stefan Kühne3Inga Mewis4Narantuya Mishig5Narantuya Mishig6Ronald Maul7Ronald Maul8Mario Drungowski9Pia Parolin10Monika Schreiner11Susanne Baldermann12Susanne Baldermann13(IGZ) Leibniz Institute of Vegetable and Ornamental CropsUniversity of PotsdamHumboldt-Universität zu BerlinJulius Kühn-Institut (JKI), Federal Research Centre for Cultivated PlantsJulius Kühn-Institut (JKI), Federal Research Centre for Cultivated Plants(IGZ) Leibniz Institute of Vegetable and Ornamental CropsUniversity of Potsdam(IGZ) Leibniz Institute of Vegetable and Ornamental CropsUniversity of Hamburg(IGZ) Leibniz Institute of Vegetable and Ornamental CropsINRA-CNRS-Université de Nice Sophia Antipolis(IGZ) Leibniz Institute of Vegetable and Ornamental Crops(IGZ) Leibniz Institute of Vegetable and Ornamental CropsUniversity of PotsdamThe spider mite Tetranychus urticae Koch and the aphid Myzus persicae (Sulzer) both infest a number of economically significant crops, including tomato (Solanum lycopersicum). Although used for decades to control pests, the impact of green lacewing larvae Chrysoperla carnea (Stephens) on plant biochemistry was not investigated. Here we used profiling methods and targeted analyses to explore the impact of the predator and herbivore(s)-predator interactions on tomato biochemistry. Each pest and pest-predator combination induced a characteristic metabolite signature in the leaf and the fruit thus, the plant exhibited a systemic response. The treatments had a stronger impact on non-volatile metabolites including abscisic acid and amino acids in the leaves in comparison with the fruits. In contrast, the various biotic factors had a greater impact on the carotenoids in the fruits. We identified volatiles such as myrcene and α-terpinene which were induced by pest-predator interactions but not by single species, and we demonstrated the involvement of the phytohormone abscisic acid in tritrophic interactions for the first time. More importantly, C. carnea larvae alone impacted the plant metabolome, but the predator did not appear to elicit particular defense pathways on its own. Since the presence of both C. carnea larvae and pest individuals elicited volatiles which were shown to contribute to plant defense, C. carnea larvae could therefore contribute to the reduction of pest infestation, not only by its preying activity, but also by priming responses to generalist herbivores such as T. urticae and M. persicae. On the other hand, the use of C. carnea larvae alone did not impact carotenoids thus, was not prejudicial to the fruit quality. The present piece of research highlights the specific impact of predator and tritrophic interactions with green lacewing larvae, spider mites and aphids on different components of the tomato primary and secondary metabolism for the first time, and provides cues for further in-depth studies aiming to integrate entomological approaches and plant biochemistry.http://journal.frontiersin.org/Journal/10.3389/fpls.2016.01256/fullCarotenoidsSolanaceaeplant volatilesBiological pest controltritrophic systemChrysopidae
spellingShingle Audrey Errard
Audrey Errard
Christian Ulrichs
Stefan Kühne
Inga Mewis
Narantuya Mishig
Narantuya Mishig
Ronald Maul
Ronald Maul
Mario Drungowski
Pia Parolin
Monika Schreiner
Susanne Baldermann
Susanne Baldermann
Metabolite profiling reveals a specific response in tomato to predaceous Chrysoperla carnea larvae and herbivore(s)-predator interactions with the generalist pests Tetranychus urticae and Myzus persicae
Frontiers in Plant Science
Carotenoids
Solanaceae
plant volatiles
Biological pest control
tritrophic system
Chrysopidae
title Metabolite profiling reveals a specific response in tomato to predaceous Chrysoperla carnea larvae and herbivore(s)-predator interactions with the generalist pests Tetranychus urticae and Myzus persicae
title_full Metabolite profiling reveals a specific response in tomato to predaceous Chrysoperla carnea larvae and herbivore(s)-predator interactions with the generalist pests Tetranychus urticae and Myzus persicae
title_fullStr Metabolite profiling reveals a specific response in tomato to predaceous Chrysoperla carnea larvae and herbivore(s)-predator interactions with the generalist pests Tetranychus urticae and Myzus persicae
title_full_unstemmed Metabolite profiling reveals a specific response in tomato to predaceous Chrysoperla carnea larvae and herbivore(s)-predator interactions with the generalist pests Tetranychus urticae and Myzus persicae
title_short Metabolite profiling reveals a specific response in tomato to predaceous Chrysoperla carnea larvae and herbivore(s)-predator interactions with the generalist pests Tetranychus urticae and Myzus persicae
title_sort metabolite profiling reveals a specific response in tomato to predaceous chrysoperla carnea larvae and herbivore s predator interactions with the generalist pests tetranychus urticae and myzus persicae
topic Carotenoids
Solanaceae
plant volatiles
Biological pest control
tritrophic system
Chrysopidae
url http://journal.frontiersin.org/Journal/10.3389/fpls.2016.01256/full
work_keys_str_mv AT audreyerrard metaboliteprofilingrevealsaspecificresponseintomatotopredaceouschrysoperlacarnealarvaeandherbivorespredatorinteractionswiththegeneralistpeststetranychusurticaeandmyzuspersicae
AT audreyerrard metaboliteprofilingrevealsaspecificresponseintomatotopredaceouschrysoperlacarnealarvaeandherbivorespredatorinteractionswiththegeneralistpeststetranychusurticaeandmyzuspersicae
AT christianulrichs metaboliteprofilingrevealsaspecificresponseintomatotopredaceouschrysoperlacarnealarvaeandherbivorespredatorinteractionswiththegeneralistpeststetranychusurticaeandmyzuspersicae
AT stefankuhne metaboliteprofilingrevealsaspecificresponseintomatotopredaceouschrysoperlacarnealarvaeandherbivorespredatorinteractionswiththegeneralistpeststetranychusurticaeandmyzuspersicae
AT ingamewis metaboliteprofilingrevealsaspecificresponseintomatotopredaceouschrysoperlacarnealarvaeandherbivorespredatorinteractionswiththegeneralistpeststetranychusurticaeandmyzuspersicae
AT narantuyamishig metaboliteprofilingrevealsaspecificresponseintomatotopredaceouschrysoperlacarnealarvaeandherbivorespredatorinteractionswiththegeneralistpeststetranychusurticaeandmyzuspersicae
AT narantuyamishig metaboliteprofilingrevealsaspecificresponseintomatotopredaceouschrysoperlacarnealarvaeandherbivorespredatorinteractionswiththegeneralistpeststetranychusurticaeandmyzuspersicae
AT ronaldmaul metaboliteprofilingrevealsaspecificresponseintomatotopredaceouschrysoperlacarnealarvaeandherbivorespredatorinteractionswiththegeneralistpeststetranychusurticaeandmyzuspersicae
AT ronaldmaul metaboliteprofilingrevealsaspecificresponseintomatotopredaceouschrysoperlacarnealarvaeandherbivorespredatorinteractionswiththegeneralistpeststetranychusurticaeandmyzuspersicae
AT mariodrungowski metaboliteprofilingrevealsaspecificresponseintomatotopredaceouschrysoperlacarnealarvaeandherbivorespredatorinteractionswiththegeneralistpeststetranychusurticaeandmyzuspersicae
AT piaparolin metaboliteprofilingrevealsaspecificresponseintomatotopredaceouschrysoperlacarnealarvaeandherbivorespredatorinteractionswiththegeneralistpeststetranychusurticaeandmyzuspersicae
AT monikaschreiner metaboliteprofilingrevealsaspecificresponseintomatotopredaceouschrysoperlacarnealarvaeandherbivorespredatorinteractionswiththegeneralistpeststetranychusurticaeandmyzuspersicae
AT susannebaldermann metaboliteprofilingrevealsaspecificresponseintomatotopredaceouschrysoperlacarnealarvaeandherbivorespredatorinteractionswiththegeneralistpeststetranychusurticaeandmyzuspersicae
AT susannebaldermann metaboliteprofilingrevealsaspecificresponseintomatotopredaceouschrysoperlacarnealarvaeandherbivorespredatorinteractionswiththegeneralistpeststetranychusurticaeandmyzuspersicae