Cargando…
Tritrophic metabolism of plant chemical defenses and its effects on herbivore and predator performance
Insect herbivores are frequently reported to metabolize plant defense compounds, but the physiological and ecological consequences are not fully understood. It has rarely been studied whether such metabolism is genuinely beneficial to the insect, and whether there are any effects on higher trophic l...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6934381/ https://www.ncbi.nlm.nih.gov/pubmed/31841109 http://dx.doi.org/10.7554/eLife.51029 |
_version_ | 1783483375014641664 |
---|---|
author | Sun, Ruo Jiang, Xingcong Reichelt, Michael Gershenzon, Jonathan Pandit, Sagar Subhash Giddings Vassão, Daniel |
author_facet | Sun, Ruo Jiang, Xingcong Reichelt, Michael Gershenzon, Jonathan Pandit, Sagar Subhash Giddings Vassão, Daniel |
author_sort | Sun, Ruo |
collection | PubMed |
description | Insect herbivores are frequently reported to metabolize plant defense compounds, but the physiological and ecological consequences are not fully understood. It has rarely been studied whether such metabolism is genuinely beneficial to the insect, and whether there are any effects on higher trophic levels. Here, we manipulated the detoxification of plant defenses in the herbivorous pest diamondback moth (Plutella xylostella) to evaluate changes in fitness, and additionally examined the effects on a predatory lacewing (Chrysoperla carnea). Silencing glucosinolate sulfatase genes resulted in the systemic accumulation of toxic isothiocyanates in P. xylostella larvae, impairing larval development and adult reproduction. The predatory lacewing C. carnea, however, efficiently degraded ingested isothiocyanates via a general conjugation pathway, with no negative effects on survival, reproduction, or even prey preference. These results illustrate how plant defenses and their detoxification strongly influence herbivore fitness but might only subtly affect a third trophic level. |
format | Online Article Text |
id | pubmed-6934381 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-69343812019-12-30 Tritrophic metabolism of plant chemical defenses and its effects on herbivore and predator performance Sun, Ruo Jiang, Xingcong Reichelt, Michael Gershenzon, Jonathan Pandit, Sagar Subhash Giddings Vassão, Daniel eLife Ecology Insect herbivores are frequently reported to metabolize plant defense compounds, but the physiological and ecological consequences are not fully understood. It has rarely been studied whether such metabolism is genuinely beneficial to the insect, and whether there are any effects on higher trophic levels. Here, we manipulated the detoxification of plant defenses in the herbivorous pest diamondback moth (Plutella xylostella) to evaluate changes in fitness, and additionally examined the effects on a predatory lacewing (Chrysoperla carnea). Silencing glucosinolate sulfatase genes resulted in the systemic accumulation of toxic isothiocyanates in P. xylostella larvae, impairing larval development and adult reproduction. The predatory lacewing C. carnea, however, efficiently degraded ingested isothiocyanates via a general conjugation pathway, with no negative effects on survival, reproduction, or even prey preference. These results illustrate how plant defenses and their detoxification strongly influence herbivore fitness but might only subtly affect a third trophic level. eLife Sciences Publications, Ltd 2019-12-16 /pmc/articles/PMC6934381/ /pubmed/31841109 http://dx.doi.org/10.7554/eLife.51029 Text en © 2019, Sun et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Ecology Sun, Ruo Jiang, Xingcong Reichelt, Michael Gershenzon, Jonathan Pandit, Sagar Subhash Giddings Vassão, Daniel Tritrophic metabolism of plant chemical defenses and its effects on herbivore and predator performance |
title | Tritrophic metabolism of plant chemical defenses and its effects on herbivore and predator performance |
title_full | Tritrophic metabolism of plant chemical defenses and its effects on herbivore and predator performance |
title_fullStr | Tritrophic metabolism of plant chemical defenses and its effects on herbivore and predator performance |
title_full_unstemmed | Tritrophic metabolism of plant chemical defenses and its effects on herbivore and predator performance |
title_short | Tritrophic metabolism of plant chemical defenses and its effects on herbivore and predator performance |
title_sort | tritrophic metabolism of plant chemical defenses and its effects on herbivore and predator performance |
topic | Ecology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6934381/ https://www.ncbi.nlm.nih.gov/pubmed/31841109 http://dx.doi.org/10.7554/eLife.51029 |
work_keys_str_mv | AT sunruo tritrophicmetabolismofplantchemicaldefensesanditseffectsonherbivoreandpredatorperformance AT jiangxingcong tritrophicmetabolismofplantchemicaldefensesanditseffectsonherbivoreandpredatorperformance AT reicheltmichael tritrophicmetabolismofplantchemicaldefensesanditseffectsonherbivoreandpredatorperformance AT gershenzonjonathan tritrophicmetabolismofplantchemicaldefensesanditseffectsonherbivoreandpredatorperformance AT panditsagarsubhash tritrophicmetabolismofplantchemicaldefensesanditseffectsonherbivoreandpredatorperformance AT giddingsvassaodaniel tritrophicmetabolismofplantchemicaldefensesanditseffectsonherbivoreandpredatorperformance |