代谢组学为沃尔巴克氏体诱导的棉螨植物防御机制提供了新的见解。

IF 4.1 2区 生物学 Q2 MICROBIOLOGY
Xinlei Wang, Sha Wang, Ali Basit, Qianchen Wei, Kedi Zhao, Feng Liu, Yiying Zhao
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引用次数: 0

摘要

内共生细菌在昆虫和植物的共同进化中起着重要的作用。然而,它们是否诱导或抑制寄主植物的防御反应尚不清楚。本研究采用单性回交和抗生素处理方法,对感染沃尔巴克氏体和未感染沃尔巴克氏体的蜘蛛螨饲养的棉花叶片进行非靶向代谢组学测序。共鉴定出55种差异代谢物,包括脂质、苯丙素和聚酮。KEGG通路富集分析显示有7条代谢通路显著富集。其中,类黄酮和黄酮醇生物合成、甘油磷脂代谢、醚类脂质代谢差异极显著。沃尔巴克氏体感染棉花叶片中,槲皮素、杨梅素等类黄酮生物合成途径被显著上调,表明植物产生了更多的次生代谢物,增强了防御能力。甘油酸胆碱(GPC)和森-甘油酸-3-磷酸乙醇胺(PE)显著下调,表明沃尔巴克氏菌可能破坏植物细胞膜的完整性和功能。赖氨酸的下调和l -苹果酸的上调表明沃尔巴克氏体感染可能缩短了蜘蛛螨的寿命。在蜘蛛螨的各个发育阶段,沃尔巴克氏体感染增加了解毒代谢相关基因的表达,包括细胞色素P450、谷胱甘肽s -转移酶、羧酸酯酶和ABC转运蛋白等基因家族,从而增强了宿主蜘蛛螨的解毒能力。本研究为进一步阐明内共生细菌诱导植物防御反应的机制提供了理论基础,拓展了虫植物协同进化的理论框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metabolomics Provides New Insights into the Mechanisms of Wolbachia-Induced Plant Defense in Cotton Mites.

Endosymbiotic bacteria play a significant role in the co-evolution of insects and plants. However, whether they induce or inhibit host plant defense responses remains unclear. In this study, non-targeted metabolomic sequencing was performed on cotton leaves fed with Wolbachia-infected and uninfected spider mites using parthenogenetic backcrossing and antibiotic treatment methods. A total of 55 differential metabolites were identified, which involved lipids, phenylpropanoids, and polyketides. KEGG pathway enrichment analysis revealed seven significantly enriched metabolic pathways. Among them, flavonoid and flavonol biosynthesis, glycerophospholipid metabolism, and ether lipid metabolism showed extremely significant differences. In Wolbachia-infected cotton leaves, the flavonoid biosynthesis pathway was significantly up-regulated, including quercetin and myricetin, suggesting that the plant produces more secondary metabolites to enhance its defense capability. Glycerophosphocholine (GPC) and sn-glycerol-3-phosphoethanolamine (PE) were significantly down-regulated, suggesting that Wolbachia may impair the integrity and function of plant cell membranes. The downregulation of lysine and the upregulation of L-malic acid indicated that Wolbachia infection may shorten the lifespan of spider mites. At various developmental stages of the spider mites, Wolbachia infection increased the expression of detoxification metabolism-related genes, including gene families such as cytochrome P450, glutathione S-transferase, carboxylesterase, and ABC transporters, thereby enhancing the detoxification capability of the host spider mites. This study provides a theoretical basis for further elucidating the mechanisms by which endosymbiotic bacteria induce plant defense responses and expands the theoretical framework of insect-plant co-evolution.

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来源期刊
Microorganisms
Microorganisms Medicine-Microbiology (medical)
CiteScore
7.40
自引率
6.70%
发文量
2168
审稿时长
20.03 days
期刊介绍: Microorganisms (ISSN 2076-2607) is an international, peer-reviewed open access journal which provides an advanced forum for studies related to prokaryotic and eukaryotic microorganisms, viruses and prions. It publishes reviews, research papers and communications. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Electronic files and software regarding the full details of the calculation or experimental procedure, if unable to be published in a normal way, can be deposited as supplementary electronic material.
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