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Metabolic Changes in Larvae of Predator Chrysopa sinica Fed on Azadirachtin-Treated Plutella xylostella Larvae

Biological control is a key component of integrated pest management (IPM). To suppress pests in a certain threshold, chemical control is used in combination with biological and other control methods. An essential premise for using pesticides in IPM is to ascertain their compatibility with beneficial...

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Autores principales: Zhang, Peiwen, Zhou, You, Qin, Deqiang, Chen, Jianjun, Zhang, Zhixiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8876581/
https://www.ncbi.nlm.nih.gov/pubmed/35208232
http://dx.doi.org/10.3390/metabo12020158
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author Zhang, Peiwen
Zhou, You
Qin, Deqiang
Chen, Jianjun
Zhang, Zhixiang
author_facet Zhang, Peiwen
Zhou, You
Qin, Deqiang
Chen, Jianjun
Zhang, Zhixiang
author_sort Zhang, Peiwen
collection PubMed
description Biological control is a key component of integrated pest management (IPM). To suppress pests in a certain threshold, chemical control is used in combination with biological and other control methods. An essential premise for using pesticides in IPM is to ascertain their compatibility with beneficial insects. Chrysopa sinica (Neuroptera: Chrysopidae) is an important predator of various pests and used for pest management. This study was intended to analyze metabolic changes in C. sinica larvae after feeding on azadirachtin-treated Plutella xylostella (Lepidoptera, Plutellidae) larvae through a non-targeted LC–MS (Liquid chromatography–mass spectrometry) based metabolomics analysis. Results showed that C. sinica larvae did not die after consuming P. xylostella larvae treated with azadirachtin. However, their pupation and eclosion were adversely affected, resulting in an impairment in the completion of their life cycle. Feeding C. sinica larvae with azadirachtin-treated P. xylostella larvae affected over 10,000 metabolites across more than 20 pathways, including the metabolism of amino acids, carbohydrates, lipid, cofactors, and vitamins in C. sinica larvae, of which changes in amnio acid metabolism were particularly pronounced. A working model was proposed to illustrate differential changes in 20 metabolites related to some amino acid metabolisms. Among them, 15 were markedly reduced and only five were elevated. Our results suggest that azadirachtin application may not be exclusively compatible with the use of the predator C. sinica for control of P. xylostella. It is recommended that the compatibility should be evaluated not only based on the survival of the predatory insects but also by the metabolic changes and the resultant detrimental effects on their development.
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spelling pubmed-88765812022-02-26 Metabolic Changes in Larvae of Predator Chrysopa sinica Fed on Azadirachtin-Treated Plutella xylostella Larvae Zhang, Peiwen Zhou, You Qin, Deqiang Chen, Jianjun Zhang, Zhixiang Metabolites Article Biological control is a key component of integrated pest management (IPM). To suppress pests in a certain threshold, chemical control is used in combination with biological and other control methods. An essential premise for using pesticides in IPM is to ascertain their compatibility with beneficial insects. Chrysopa sinica (Neuroptera: Chrysopidae) is an important predator of various pests and used for pest management. This study was intended to analyze metabolic changes in C. sinica larvae after feeding on azadirachtin-treated Plutella xylostella (Lepidoptera, Plutellidae) larvae through a non-targeted LC–MS (Liquid chromatography–mass spectrometry) based metabolomics analysis. Results showed that C. sinica larvae did not die after consuming P. xylostella larvae treated with azadirachtin. However, their pupation and eclosion were adversely affected, resulting in an impairment in the completion of their life cycle. Feeding C. sinica larvae with azadirachtin-treated P. xylostella larvae affected over 10,000 metabolites across more than 20 pathways, including the metabolism of amino acids, carbohydrates, lipid, cofactors, and vitamins in C. sinica larvae, of which changes in amnio acid metabolism were particularly pronounced. A working model was proposed to illustrate differential changes in 20 metabolites related to some amino acid metabolisms. Among them, 15 were markedly reduced and only five were elevated. Our results suggest that azadirachtin application may not be exclusively compatible with the use of the predator C. sinica for control of P. xylostella. It is recommended that the compatibility should be evaluated not only based on the survival of the predatory insects but also by the metabolic changes and the resultant detrimental effects on their development. MDPI 2022-02-08 /pmc/articles/PMC8876581/ /pubmed/35208232 http://dx.doi.org/10.3390/metabo12020158 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zhang, Peiwen
Zhou, You
Qin, Deqiang
Chen, Jianjun
Zhang, Zhixiang
Metabolic Changes in Larvae of Predator Chrysopa sinica Fed on Azadirachtin-Treated Plutella xylostella Larvae
title Metabolic Changes in Larvae of Predator Chrysopa sinica Fed on Azadirachtin-Treated Plutella xylostella Larvae
title_full Metabolic Changes in Larvae of Predator Chrysopa sinica Fed on Azadirachtin-Treated Plutella xylostella Larvae
title_fullStr Metabolic Changes in Larvae of Predator Chrysopa sinica Fed on Azadirachtin-Treated Plutella xylostella Larvae
title_full_unstemmed Metabolic Changes in Larvae of Predator Chrysopa sinica Fed on Azadirachtin-Treated Plutella xylostella Larvae
title_short Metabolic Changes in Larvae of Predator Chrysopa sinica Fed on Azadirachtin-Treated Plutella xylostella Larvae
title_sort metabolic changes in larvae of predator chrysopa sinica fed on azadirachtin-treated plutella xylostella larvae
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8876581/
https://www.ncbi.nlm.nih.gov/pubmed/35208232
http://dx.doi.org/10.3390/metabo12020158
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