Metarhizium flavoviride qc1401胁迫下的斑蝶微生物组和代谢组综合分析。

IF 2.3 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY International Microbiology Pub Date : 2024-08-15 DOI:10.1007/s10123-024-00574-y
Zhang Juefeng, Li Fang, Zhong Haiying, Liu Liwei, Chen Jianming
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引用次数: 0

摘要

Metarhizium spp.已成为保护农作物免受虫害的化学农药替代品。在这里,我们研究了在感染黄曲霉菌后三个不同时间点上的鞘翅目昆虫中肠微生物群落和代谢物。萤火虫的先天免疫系统被激活,多酚氧化酶、羧基酯酶、多功能氧化酶和谷胱甘肽 S-转移酶的活性水平显著提高。接触真菌病原体也会改变宿主中肠中细菌的丰度和多样性,这些变化因接触时间的长短而不同。与对照样本相比,我们在所有测试时间点的处理样本中发现了更多可操作的分类单元。共鉴定出 372 种代谢物,在处理后的 3 个时间点,处理组和对照组分别鉴定出 88、149 和 142 种差异累积代谢物(DAMs)。根据不同时间点DAMs对黄病毒感染的响应变化和显著富集的KEGG通路,我们推测 "酪氨酸代谢"、"半乳糖代谢"、"ATP结合盒转运体"、"神经活性配体-受体相互作用"、"嘌呤代谢"、"精氨酸和脯氨酸代谢"、"β-丙氨酸代谢"、"溶酶体 "和 "碳代谢 "可能参与了代谢水平的防御响应。对 16S-rDNA 和代谢组数据进行的综合通路分析表明了 S. litura 和中肠微生物对黄病毒感染的代谢反应之间的联系和相互依存关系。这项工作强调了综合分析昆虫与病原体相互作用的价值,为今后研究这些相互作用的关键微生物和代谢决定因素提供了一个框架,并为黄曲霉毒素的可持续利用奠定了理论基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Integrated microbiome and metabolomic analysis of Spodoptera litura under Metarhizium flavoviride qc1401 stress.

Metarhizium spp. have emerged as an alternative to chemical pesticides for protecting crops from insect pest. Here, we investigated midgut microbial community and metabolites of Spodoptera litura at three different timepoints after infection with Metarhizium flavoviride. The innate immune system of S. litura was activated with levels of polyphenol oxidase, carboxylesterase, multifunctional oxidase, and glutathione S-transferase activity significantly increasing. Exposure to the fungal pathogen also altered bacterial abundance and diversity in host's midgut, and these changes varied depending on the time elapsed since exposure. We identified more operational taxonomic units in the treated samples as compared to the control samples at all tested time points. A total of 372 metabolites were identified, and 88, 149, and 142 differentially accumulated metabolites (DAMs) were identified between the treatment and control groups at 3 timepoints after treatment, respectively. Based on the changes of DAMs in response to M. flavoviride infection at different timepoints and significantly enriched KEGG pathways, we speculated that "tyrosine metabolism," "galactose metabolism," "ATP-binding cassette transporters," "neuroactive ligand-receptor interaction," "purine metabolism," "arginine and proline metabolism," "beta-alanine metabolism," "lysosome," and "carbon metabolism" may participate in the metabolic-level defense response. An integrated pathway-level analysis of the 16S-rDNA and metabolomic data illustrated the connections and interdependencies between the metabolic responses of S. litura and the midgut microorganisms to M. flavoviride infection. This work emphasizes the value of integrated analyses of insect-pathogen interactions, provides a framework for future studies of critical microorganisms and metabolic determinants of these interactions, establishes a theoretical basis for the sustainable use of M. flavoviride.

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来源期刊
International Microbiology
International Microbiology 生物-生物工程与应用微生物
CiteScore
5.50
自引率
3.20%
发文量
67
审稿时长
3 months
期刊介绍: International Microbiology publishes information on basic and applied microbiology for a worldwide readership. The journal publishes articles and short reviews based on original research, articles about microbiologists and their work and questions related to the history and sociology of this science. Also offered are perspectives, opinion, book reviews and editorials. A distinguishing feature of International Microbiology is its broadening of the term microbiology to include eukaryotic microorganisms.
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