Comparative transcriptomic and metabolomics analysis of modified atmosphere responses in Tribolium castaneum (Coleoptera: Tenebrionidae).

IF 2.1 3区 农林科学 Q1 ENTOMOLOGY Journal of Insect Science Pub Date : 2024-03-01 DOI:10.1093/jisesa/ieae015
Min Zhou, Biying Pan, Liwen Guan, Yuanyuan Wang, Kangkang Xu, Shigui Wang, Bin Tang, Can Li
{"title":"Comparative transcriptomic and metabolomics analysis of modified atmosphere responses in Tribolium castaneum (Coleoptera: Tenebrionidae).","authors":"Min Zhou, Biying Pan, Liwen Guan, Yuanyuan Wang, Kangkang Xu, Shigui Wang, Bin Tang, Can Li","doi":"10.1093/jisesa/ieae015","DOIUrl":null,"url":null,"abstract":"<p><p>Modified atmosphere is effective in controlling Tribolium castaneum Herbst, but it has adaptations. Comprehending the potential mechanism of resistance to T. castaneum in a modified atmosphere will help advance related management methods. This study conducted a comparative transcriptomic and metabolomic analysis to understand the physiological mechanism of T. castaneum in adapting to CO2 stress. Results showed that there were a large number of differentially expressed genes (DEGs) in T. castaneum treated with different concentrations of CO2. Gene ontology (GO) analysis revealed significant enrichment of DEGs mainly in binding, catalytic activity, cell, membrane, membrane part, protein-containing complex, biological regulation, and cellular and metabolic process. Kyoto Encyclopedia of Genes and Genomes analysis showed that different treatments had different effects on the metabolic pathways of T. castaneum. DEGs induced by 25% CO2 were involved in arginine and proline metabolism, and 50% air + 50% CO2 treatment affected most kinds of metabolic pathways, mainly the signal transduction pathway, including PI3K-Akt signaling pathway, AMPK signaling pathway, neurotrophin signaling pathway, insulin signaling pathway, and thyroid hormone signaling. Ribosome and DNA replication were enriched under high CO2 stress (75% and 95%). The metabolomics revealed that different concentrations of CO2 treatments might inhibit the growth of T. castaneum through acidosis, or they may adapt to anoxic conditions through histamine and N-acetylhistamine. Multiple analyses have shown significant changes in histamine and N-acetylhistamine levels, as well as their associated genes, with increasing CO2 concentration. In conclusion, this study comprehensively revealed the molecular mechanism of T. castaneum responding to CO2 stress and provided the basis for an effectively modified atmosphere in the T. castaneum.</p>","PeriodicalId":16156,"journal":{"name":"Journal of Insect Science","volume":"24 2","pages":""},"PeriodicalIF":2.1000,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10944018/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Insect Science","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1093/jisesa/ieae015","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENTOMOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Modified atmosphere is effective in controlling Tribolium castaneum Herbst, but it has adaptations. Comprehending the potential mechanism of resistance to T. castaneum in a modified atmosphere will help advance related management methods. This study conducted a comparative transcriptomic and metabolomic analysis to understand the physiological mechanism of T. castaneum in adapting to CO2 stress. Results showed that there were a large number of differentially expressed genes (DEGs) in T. castaneum treated with different concentrations of CO2. Gene ontology (GO) analysis revealed significant enrichment of DEGs mainly in binding, catalytic activity, cell, membrane, membrane part, protein-containing complex, biological regulation, and cellular and metabolic process. Kyoto Encyclopedia of Genes and Genomes analysis showed that different treatments had different effects on the metabolic pathways of T. castaneum. DEGs induced by 25% CO2 were involved in arginine and proline metabolism, and 50% air + 50% CO2 treatment affected most kinds of metabolic pathways, mainly the signal transduction pathway, including PI3K-Akt signaling pathway, AMPK signaling pathway, neurotrophin signaling pathway, insulin signaling pathway, and thyroid hormone signaling. Ribosome and DNA replication were enriched under high CO2 stress (75% and 95%). The metabolomics revealed that different concentrations of CO2 treatments might inhibit the growth of T. castaneum through acidosis, or they may adapt to anoxic conditions through histamine and N-acetylhistamine. Multiple analyses have shown significant changes in histamine and N-acetylhistamine levels, as well as their associated genes, with increasing CO2 concentration. In conclusion, this study comprehensively revealed the molecular mechanism of T. castaneum responding to CO2 stress and provided the basis for an effectively modified atmosphere in the T. castaneum.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
鞘翅目:天牛科)对改良大气反应的转录组学和代谢组学比较分析
改良大气能有效控制蓖麻毛虫,但蓖麻毛虫也有适应性。了解蓖麻在改良大气中的潜在抗性机制将有助于推进相关的管理方法。本研究通过转录组和代谢组的比较分析,了解蓖麻鳞叶虫适应二氧化碳胁迫的生理机制。结果表明,在不同浓度的 CO2 处理下,T. castaneum 存在大量差异表达基因(DEGs)。基因本体(GO)分析显示,DEGs主要在结合、催化活性、细胞、膜、膜部分、含蛋白复合物、生物调控、细胞和代谢过程等方面有显著富集。京都基因组百科全书》分析表明,不同的处理对蓖麻的代谢途径有不同的影响。25%CO2诱导的DEGs参与精氨酸和脯氨酸代谢,50%空气+50%CO2处理影响大部分代谢途径,主要是信号转导途径,包括PI3K-Akt信号转导途径、AMPK信号转导途径、神经营养素信号转导途径、胰岛素信号转导途径和甲状腺激素信号转导途径。在高二氧化碳胁迫下(75% 和 95%),核糖体和 DNA 复制被富集。代谢组学研究发现,不同浓度的二氧化碳处理可能通过酸中毒抑制蓖麻菌的生长,也可能通过组胺和N-乙酰组胺适应缺氧条件。多项分析表明,随着二氧化碳浓度的增加,组胺和 N-乙酰组胺的水平及其相关基因都会发生显著变化。总之,本研究全面揭示了T. castaneum应对二氧化碳胁迫的分子机制,为有效改变T. castaneum的大气环境提供了依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Journal of Insect Science
Journal of Insect Science 生物-昆虫学
CiteScore
3.70
自引率
0.00%
发文量
80
审稿时长
7.5 months
期刊介绍: The Journal of Insect Science was founded with support from the University of Arizona library in 2001 by Dr. Henry Hagedorn, who served as editor-in-chief until his death in January 2014. The Entomological Society of America was very pleased to add the Journal of Insect Science to its publishing portfolio in 2014. The fully open access journal publishes papers in all aspects of the biology of insects and other arthropods from the molecular to the ecological, and their agricultural and medical impact.
期刊最新文献
Bee cups 2.0: P-cups as single-use cages for honey bee (Hymenoptera: Apidae) experiments. Direct and indirect effects of selective insecticides on 2 generalist predators of Bemisia tabaci (Hemiptera: Aleyrodidae). Low-density migratory beekeeping induces intermediate disturbance effects on native bee communities in Tibetan Plateau alpine meadows. Population records reveal expanded habitat preference for the endemic, predaceous Jamaican fungus gnat Neoditomyia farri (Diptera, Keroplatidae). Cellulose degradation in Glenea cantor (Fabricius) (Coleoptera: Cerambycidae): functional characterization of GcEGaseZ7 and Cellulase reveals a novel enzymatic activity.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1