Ruichun Li , Wenqi Qian , Chenhui Li , Boxuan Yao , Aimin Wang , Tao Guan , Zhicen Liu , Lei Gao , Dongli Qin
{"title":"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","authors":"Ruichun Li , Wenqi Qian , Chenhui Li , Boxuan Yao , Aimin Wang , Tao Guan , Zhicen Liu , Lei Gao , Dongli Qin","doi":"10.1016/j.cbd.2025.101627","DOIUrl":null,"url":null,"abstract":"<div><div>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 <em>Erysipelatoclostridium</em> 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.</div></div>","PeriodicalId":55235,"journal":{"name":"Comparative Biochemistry and Physiology D-Genomics & Proteomics","volume":"56 ","pages":"Article 101627"},"PeriodicalIF":2.2000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Exposure of crayfish (Procambarus clarkii) to pinoxaden disrupts hepatic transcriptome, gut microbiome, and redox homeostasis\",\"authors\":\"Ruichun Li , Wenqi Qian , Chenhui Li , Boxuan Yao , Aimin Wang , Tao Guan , Zhicen Liu , Lei Gao , Dongli Qin\",\"doi\":\"10.1016/j.cbd.2025.101627\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>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 <em>Erysipelatoclostridium</em> 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.</div></div>\",\"PeriodicalId\":55235,\"journal\":{\"name\":\"Comparative Biochemistry and Physiology D-Genomics & Proteomics\",\"volume\":\"56 \",\"pages\":\"Article 101627\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2025-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Comparative Biochemistry and Physiology D-Genomics & Proteomics\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1744117X25002163\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Comparative Biochemistry and Physiology D-Genomics & Proteomics","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1744117X25002163","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
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.
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.