暴露于克氏原螯虾(Procambarus clarkii)的pinoxaden会破坏肝脏转录组、肠道微生物组和氧化还原稳态

IF 2.2 2区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Ruichun Li , Wenqi Qian , Chenhui Li , Boxuan Yao , Aimin Wang , Tao Guan , Zhicen Liu , Lei Gao , Dongli Qin
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引用次数: 0

摘要

随着农药的广泛使用,吡诺菌登已成为水稻-小龙虾共养殖田中常用的除草剂。然而,对水生生物的毒性机制尚不清楚。本研究探讨了皮诺沙登对小龙虾的急性毒性作用。生化分析显示丙二醛含量、谷胱甘肽过氧化物酶、超氧化物歧化酶和过氧化氢酶活性在暴露后肝胰腺组织中发生了显著变化。组织学检查显示小龙虾肝胰腺和肠道组织损伤。转录组学分析检测了皮诺登处理后差异表达的基因,包括溶酶体、抗原加工呈递、吞噬体等途径的显著富集。此外,暴露于皮诺沙登改变了暴露组肠道微生物群中放线菌群和丹毒弧菌群等细菌家族的丰度。本研究为研究吡诺菌登对小龙虾的毒性提供了重要依据,为水稻-小龙虾共养系统中农药的科学合理使用提供了实践指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Exposure of crayfish (Procambarus clarkii) to pinoxaden disrupts hepatic transcriptome, gut microbiome, and redox homeostasis

Exposure of crayfish (Procambarus clarkii) to pinoxaden disrupts hepatic transcriptome, gut microbiome, and redox homeostasis
With the widespread use of pesticides, pinoxaden has become a commonly used herbicide in rice-crayfish co-culture fields. However, the mechanism of toxicity to aquatic organisms is unclear. This study investigated the acute toxicity effects of pinoxaden on crayfish. Biochemical analysis revealed significant alterations in malondialdehyde content, as well as glutathione peroxidase, superoxide dismutase and catalase activities in hepatopancreas tissues following pinoxaden exposure. Histological examination revealed pinoxaden-induced impairment in the hepatopancreas and gut tissues of crayfish. Transcriptomic profiling detected genes with differential expression following pinoxaden treatment, significant enrichment of pathways including lysosome, antigen processing presentation, phagosome. Furthermore, pinoxaden exposure altered the abundance of bacterial families such as Actinobacteriota and Erysipelatoclostridium in the gut microbiota of exposed groups. This study provides important insights into the toxicity of pinoxaden to crayfish, offering practical guidance for the scientifically based and rational use of pesticides in rice-crayfish co-culture systems.
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来源期刊
CiteScore
5.10
自引率
3.30%
发文量
69
审稿时长
33 days
期刊介绍: Comparative Biochemistry & Physiology (CBP) publishes papers in comparative, environmental and evolutionary physiology. Part D: Genomics and Proteomics (CBPD), focuses on “omics” approaches to physiology, including comparative and functional genomics, metagenomics, transcriptomics, proteomics, metabolomics, and lipidomics. Most studies employ “omics” and/or system biology to test specific hypotheses about molecular and biochemical mechanisms underlying physiological responses to the environment. We encourage papers that address fundamental questions in comparative physiology and biochemistry rather than studies with a focus that is purely technical, methodological or descriptive in nature.
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