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Larval nutrition-induced plasticity affects reproduction and gene expression of the ladybeetle, Cryptolaemus montrouzieri

BACKGROUND: Organisms may develop into multiple phenotypes under different nutritional environments by developmental plasticity, whereas the potential costs and mechanisms of such plasticity are poorly understood. Here we examined the fitness and gene expression of nutrition-induced phenotypes in th...

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Autores principales: Xie, Jiaqin, De Clercq, Patrick, Pan, Chang, Li, Haosen, Zhang, Yuhong, Pang, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4672569/
https://www.ncbi.nlm.nih.gov/pubmed/26643316
http://dx.doi.org/10.1186/s12862-015-0549-0
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author Xie, Jiaqin
De Clercq, Patrick
Pan, Chang
Li, Haosen
Zhang, Yuhong
Pang, Hong
author_facet Xie, Jiaqin
De Clercq, Patrick
Pan, Chang
Li, Haosen
Zhang, Yuhong
Pang, Hong
author_sort Xie, Jiaqin
collection PubMed
description BACKGROUND: Organisms may develop into multiple phenotypes under different nutritional environments by developmental plasticity, whereas the potential costs and mechanisms of such plasticity are poorly understood. Here we examined the fitness and gene expression of nutrition-induced phenotypes in the ladybeetle, Cryptolaemus montrouzieri after having experienced varying larval food regimes. RESULTS: We found that C. montrouzieri adults undergoing a variable larval food regime achieved a similar developmental time, survival, body mass and egg production as those undergoing a high larval food regime. The survival, developmental time, body mass and fecundity of the adults from a restricted larval food regime were inferior to those from the high and variable larval food regimes. However, the adults from this restricted larval food regime had a higher expression level of genes encoding immune- and antioxidant-related enzymes than those from the high and variable larval food regimes when exposed to starvation and pesticide conditions in adult life. CONCLUSIONS: These results suggest that larval food availability in C. montrouzieri not only triggers adult phenotypic differences but also affects reproduction and expression level of genes in adult life, indicating that the larval nutritional conditions can affect adult fitness and resistance to stressful conditions through developmental plasticity.
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spelling pubmed-46725692015-12-09 Larval nutrition-induced plasticity affects reproduction and gene expression of the ladybeetle, Cryptolaemus montrouzieri Xie, Jiaqin De Clercq, Patrick Pan, Chang Li, Haosen Zhang, Yuhong Pang, Hong BMC Evol Biol Research Article BACKGROUND: Organisms may develop into multiple phenotypes under different nutritional environments by developmental plasticity, whereas the potential costs and mechanisms of such plasticity are poorly understood. Here we examined the fitness and gene expression of nutrition-induced phenotypes in the ladybeetle, Cryptolaemus montrouzieri after having experienced varying larval food regimes. RESULTS: We found that C. montrouzieri adults undergoing a variable larval food regime achieved a similar developmental time, survival, body mass and egg production as those undergoing a high larval food regime. The survival, developmental time, body mass and fecundity of the adults from a restricted larval food regime were inferior to those from the high and variable larval food regimes. However, the adults from this restricted larval food regime had a higher expression level of genes encoding immune- and antioxidant-related enzymes than those from the high and variable larval food regimes when exposed to starvation and pesticide conditions in adult life. CONCLUSIONS: These results suggest that larval food availability in C. montrouzieri not only triggers adult phenotypic differences but also affects reproduction and expression level of genes in adult life, indicating that the larval nutritional conditions can affect adult fitness and resistance to stressful conditions through developmental plasticity. BioMed Central 2015-12-08 /pmc/articles/PMC4672569/ /pubmed/26643316 http://dx.doi.org/10.1186/s12862-015-0549-0 Text en © Xie et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Xie, Jiaqin
De Clercq, Patrick
Pan, Chang
Li, Haosen
Zhang, Yuhong
Pang, Hong
Larval nutrition-induced plasticity affects reproduction and gene expression of the ladybeetle, Cryptolaemus montrouzieri
title Larval nutrition-induced plasticity affects reproduction and gene expression of the ladybeetle, Cryptolaemus montrouzieri
title_full Larval nutrition-induced plasticity affects reproduction and gene expression of the ladybeetle, Cryptolaemus montrouzieri
title_fullStr Larval nutrition-induced plasticity affects reproduction and gene expression of the ladybeetle, Cryptolaemus montrouzieri
title_full_unstemmed Larval nutrition-induced plasticity affects reproduction and gene expression of the ladybeetle, Cryptolaemus montrouzieri
title_short Larval nutrition-induced plasticity affects reproduction and gene expression of the ladybeetle, Cryptolaemus montrouzieri
title_sort larval nutrition-induced plasticity affects reproduction and gene expression of the ladybeetle, cryptolaemus montrouzieri
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4672569/
https://www.ncbi.nlm.nih.gov/pubmed/26643316
http://dx.doi.org/10.1186/s12862-015-0549-0
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