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Molecular Evidence that Lysiphlebia japonica Regulates the Development and Physiological Metabolism of Aphis gossypii

Lysiphlebia japonica Ashmead (Hymenoptera, Braconidae) is an endophagous parasitoid and Aphis gossypii Glover (Hemiptera, Aphididae) is a major pest in cotton. The relationship between insect host-parasitoids and their hosts involves complex physiological, biochemical and genetic interactions. This...

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Autores principales: Gao, Xueke, Xue, Hui, Luo, Junyu, Ji, Jichao, Zhang, Lijuan, Niu, Lin, Zhu, Xiangzhen, Wang, Li, Zhang, Shuai, Cui, Jinjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7370083/
https://www.ncbi.nlm.nih.gov/pubmed/32610524
http://dx.doi.org/10.3390/ijms21134610
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author Gao, Xueke
Xue, Hui
Luo, Junyu
Ji, Jichao
Zhang, Lijuan
Niu, Lin
Zhu, Xiangzhen
Wang, Li
Zhang, Shuai
Cui, Jinjie
author_facet Gao, Xueke
Xue, Hui
Luo, Junyu
Ji, Jichao
Zhang, Lijuan
Niu, Lin
Zhu, Xiangzhen
Wang, Li
Zhang, Shuai
Cui, Jinjie
author_sort Gao, Xueke
collection PubMed
description Lysiphlebia japonica Ashmead (Hymenoptera, Braconidae) is an endophagous parasitoid and Aphis gossypii Glover (Hemiptera, Aphididae) is a major pest in cotton. The relationship between insect host-parasitoids and their hosts involves complex physiological, biochemical and genetic interactions. This study examines changes in the development and physiological metabolism of A. gossypii regulated by L. japonica. Our results demonstrated that both the body length and width increased compared to non-parasitized aphids. We detected significantly increases in the developmental period as well as severe reproductive castration following parasitization by L. japonica. We then used proteomics to characterize these biological changes, and when combined with transcriptomes, this analysis demonstrated that the differential expression of mRNA (up or downregulation) captured a maximum of 48.7% of the variations of protein expression. We assigned these proteins to functional categories that included immunity, energy metabolism and transport, lipid metabolism, and reproduction. We then verified the contents of glycogen and 6-phosphate glucose, which demonstrated that these important energy sources were significantly altered following parasitization. These results uncover the effects on A. gossypii following parasitization by L. japonica, additional insight into the mechanisms behind insect-insect parasitism, and a better understanding of host-parasite interactions.
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spelling pubmed-73700832020-07-21 Molecular Evidence that Lysiphlebia japonica Regulates the Development and Physiological Metabolism of Aphis gossypii Gao, Xueke Xue, Hui Luo, Junyu Ji, Jichao Zhang, Lijuan Niu, Lin Zhu, Xiangzhen Wang, Li Zhang, Shuai Cui, Jinjie Int J Mol Sci Article Lysiphlebia japonica Ashmead (Hymenoptera, Braconidae) is an endophagous parasitoid and Aphis gossypii Glover (Hemiptera, Aphididae) is a major pest in cotton. The relationship between insect host-parasitoids and their hosts involves complex physiological, biochemical and genetic interactions. This study examines changes in the development and physiological metabolism of A. gossypii regulated by L. japonica. Our results demonstrated that both the body length and width increased compared to non-parasitized aphids. We detected significantly increases in the developmental period as well as severe reproductive castration following parasitization by L. japonica. We then used proteomics to characterize these biological changes, and when combined with transcriptomes, this analysis demonstrated that the differential expression of mRNA (up or downregulation) captured a maximum of 48.7% of the variations of protein expression. We assigned these proteins to functional categories that included immunity, energy metabolism and transport, lipid metabolism, and reproduction. We then verified the contents of glycogen and 6-phosphate glucose, which demonstrated that these important energy sources were significantly altered following parasitization. These results uncover the effects on A. gossypii following parasitization by L. japonica, additional insight into the mechanisms behind insect-insect parasitism, and a better understanding of host-parasite interactions. MDPI 2020-06-29 /pmc/articles/PMC7370083/ /pubmed/32610524 http://dx.doi.org/10.3390/ijms21134610 Text en © 2020 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
Gao, Xueke
Xue, Hui
Luo, Junyu
Ji, Jichao
Zhang, Lijuan
Niu, Lin
Zhu, Xiangzhen
Wang, Li
Zhang, Shuai
Cui, Jinjie
Molecular Evidence that Lysiphlebia japonica Regulates the Development and Physiological Metabolism of Aphis gossypii
title Molecular Evidence that Lysiphlebia japonica Regulates the Development and Physiological Metabolism of Aphis gossypii
title_full Molecular Evidence that Lysiphlebia japonica Regulates the Development and Physiological Metabolism of Aphis gossypii
title_fullStr Molecular Evidence that Lysiphlebia japonica Regulates the Development and Physiological Metabolism of Aphis gossypii
title_full_unstemmed Molecular Evidence that Lysiphlebia japonica Regulates the Development and Physiological Metabolism of Aphis gossypii
title_short Molecular Evidence that Lysiphlebia japonica Regulates the Development and Physiological Metabolism of Aphis gossypii
title_sort molecular evidence that lysiphlebia japonica regulates the development and physiological metabolism of aphis gossypii
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7370083/
https://www.ncbi.nlm.nih.gov/pubmed/32610524
http://dx.doi.org/10.3390/ijms21134610
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