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Comparative transcriptome and metabolome analysis of Ostrinia furnacalis female adults under UV-A exposure

Ultraviolet A (UV-A) radiation is a significant environmental factor that causes photoreceptor damage, apoptosis, and oxidative stress in insects. Ostrinia furnacalis is an important pest of corn. To understand the adaptation mechanisms of insect response to UV-A exposure, this study revealed differ...

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Autores principales: Su, Li, Yang, Changli, Meng, Jianyu, Zhou, Lv, Zhang, Changyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7990960/
https://www.ncbi.nlm.nih.gov/pubmed/33762675
http://dx.doi.org/10.1038/s41598-021-86269-0
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author Su, Li
Yang, Changli
Meng, Jianyu
Zhou, Lv
Zhang, Changyu
author_facet Su, Li
Yang, Changli
Meng, Jianyu
Zhou, Lv
Zhang, Changyu
author_sort Su, Li
collection PubMed
description Ultraviolet A (UV-A) radiation is a significant environmental factor that causes photoreceptor damage, apoptosis, and oxidative stress in insects. Ostrinia furnacalis is an important pest of corn. To understand the adaptation mechanisms of insect response to UV-A exposure, this study revealed differentially expressed genes (DEGs) and differently expressed metabolites (DEMs) in O. furnacalis under UV-A exposure. Three complementary DNA libraries were constructed from O. furnacalis adult females (CK, UV1h, and UV2h), and 50,106 expressed genes were obtained through Illumina sequencing. Of these, 157 and 637 DEGs were detected in UV1h and UV2h after UV-A exposure for 1 and 2 h, respectively, compared to CK, with 103 and 444 upregulated and 54 and 193 downregulated genes, respectively. Forty four DEGs were detected in UV2h compared to UV1h. Comparative transcriptome analysis between UV-treated and control groups revealed signal transduction, detoxification and stress response, immune defense, and antioxidative system involvement. Metabolomics analysis showed that 181 (UV1h vs. CK), 111 (UV2h vs. CK), and 34 (UV2h vs. UV1h) DEMs were obtained in positive ion mode, while 135 (UV1h vs. CK), 93 (UV2h vs. CK), and 36 (UV2h vs. UV1h) DEMs were obtained in negative ion mode. Moreover, UV-A exposure disturbed amino acid, sugar, and lipid metabolism. These findings provide insight for further studies on how insects protect themselves under UV-A stress.
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spelling pubmed-79909602021-03-26 Comparative transcriptome and metabolome analysis of Ostrinia furnacalis female adults under UV-A exposure Su, Li Yang, Changli Meng, Jianyu Zhou, Lv Zhang, Changyu Sci Rep Article Ultraviolet A (UV-A) radiation is a significant environmental factor that causes photoreceptor damage, apoptosis, and oxidative stress in insects. Ostrinia furnacalis is an important pest of corn. To understand the adaptation mechanisms of insect response to UV-A exposure, this study revealed differentially expressed genes (DEGs) and differently expressed metabolites (DEMs) in O. furnacalis under UV-A exposure. Three complementary DNA libraries were constructed from O. furnacalis adult females (CK, UV1h, and UV2h), and 50,106 expressed genes were obtained through Illumina sequencing. Of these, 157 and 637 DEGs were detected in UV1h and UV2h after UV-A exposure for 1 and 2 h, respectively, compared to CK, with 103 and 444 upregulated and 54 and 193 downregulated genes, respectively. Forty four DEGs were detected in UV2h compared to UV1h. Comparative transcriptome analysis between UV-treated and control groups revealed signal transduction, detoxification and stress response, immune defense, and antioxidative system involvement. Metabolomics analysis showed that 181 (UV1h vs. CK), 111 (UV2h vs. CK), and 34 (UV2h vs. UV1h) DEMs were obtained in positive ion mode, while 135 (UV1h vs. CK), 93 (UV2h vs. CK), and 36 (UV2h vs. UV1h) DEMs were obtained in negative ion mode. Moreover, UV-A exposure disturbed amino acid, sugar, and lipid metabolism. These findings provide insight for further studies on how insects protect themselves under UV-A stress. Nature Publishing Group UK 2021-03-24 /pmc/articles/PMC7990960/ /pubmed/33762675 http://dx.doi.org/10.1038/s41598-021-86269-0 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Su, Li
Yang, Changli
Meng, Jianyu
Zhou, Lv
Zhang, Changyu
Comparative transcriptome and metabolome analysis of Ostrinia furnacalis female adults under UV-A exposure
title Comparative transcriptome and metabolome analysis of Ostrinia furnacalis female adults under UV-A exposure
title_full Comparative transcriptome and metabolome analysis of Ostrinia furnacalis female adults under UV-A exposure
title_fullStr Comparative transcriptome and metabolome analysis of Ostrinia furnacalis female adults under UV-A exposure
title_full_unstemmed Comparative transcriptome and metabolome analysis of Ostrinia furnacalis female adults under UV-A exposure
title_short Comparative transcriptome and metabolome analysis of Ostrinia furnacalis female adults under UV-A exposure
title_sort comparative transcriptome and metabolome analysis of ostrinia furnacalis female adults under uv-a exposure
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7990960/
https://www.ncbi.nlm.nih.gov/pubmed/33762675
http://dx.doi.org/10.1038/s41598-021-86269-0
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