Haoran Xiao , Ye Tian , Zitong Wang , Weiyan Li , Jiayi Zhang , Lingshu Han , Chong Zhao , Jun Ding
{"title":"亚硝酸盐胁迫对刺参代谢产物及基因表达的影响","authors":"Haoran Xiao , Ye Tian , Zitong Wang , Weiyan Li , Jiayi Zhang , Lingshu Han , Chong Zhao , Jun Ding","doi":"10.1016/j.marenvres.2025.107203","DOIUrl":null,"url":null,"abstract":"<div><div>Chronic nitrite accumulation in intensive aquaculture poses a significant threat to the sustainability of sea cucumbers (<em>Apostichopus japonicus)</em>, a key species in marine aquaculture. This study investigated the molecular and metabolic responses of <em>A. japonicus</em> to 21-day nitrite stress (4.88 mg/L) through transcriptomic and metabolomic analyses. At the end of the experiment, the weight gain rate of the Cg group was 11 %, while that of the Nc group was −9 %. Nitrite exposure significantly impaired growth performance of <em>A. japonicus</em> (<em>p</em> < 0.05).</div><div>Metabolomic profiling identified 36 differential metabolites, revealing activation of the TCA cycle and amino acid metabolism to prioritize energy production and nitrogen reallocation. Transcriptomic data highlighted 226 differentially expressed genes. Notably, <em>Zimp10</em>, a key regulator of TCA cycle activity in echinoderms, was upregulated, while <em>FALDH</em>, a glycolysis-related gene, was downregulated, indicating a shift toward energy-efficient aerobic respiration.</div><div>Antioxidant capacity was compromised through suppression of glutathione metabolism genes (<em>MGST1</em>, <em>GST</em>), exacerbating oxidative damage. Stress signaling pathways were dynamically regulated. Downregulation of <em>Ras1-X2</em> suppressed mTOR activity, activating autophagy and mitophagy for cellular repair. Additionally, enrichment of NOD-like receptor pathways and upregulation of <em>vGTPase1-like</em> signaled immune engagement. Prolonged nitrite exposure overwhelmed adaptive mechanisms, leading to physiological decline.</div><div>These results demonstrate <em>A. japonicus</em> of reliance on metabolic reprogramming and stress signaling to mitigate nitrite toxicity, while highlighting vulnerabilities in antioxidant defenses. The study provides critical insights for optimizing aquaculture environments through targeted management of nitrite exposure and metabolic resilience strategies.</div></div>","PeriodicalId":18204,"journal":{"name":"Marine environmental research","volume":"209 ","pages":"Article 107203"},"PeriodicalIF":3.0000,"publicationDate":"2025-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The effects of nitrite stress on metabolites and gene expression in sea Cucumbers (Apostichopus japonicus)\",\"authors\":\"Haoran Xiao , Ye Tian , Zitong Wang , Weiyan Li , Jiayi Zhang , Lingshu Han , Chong Zhao , Jun Ding\",\"doi\":\"10.1016/j.marenvres.2025.107203\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Chronic nitrite accumulation in intensive aquaculture poses a significant threat to the sustainability of sea cucumbers (<em>Apostichopus japonicus)</em>, a key species in marine aquaculture. This study investigated the molecular and metabolic responses of <em>A. japonicus</em> to 21-day nitrite stress (4.88 mg/L) through transcriptomic and metabolomic analyses. At the end of the experiment, the weight gain rate of the Cg group was 11 %, while that of the Nc group was −9 %. Nitrite exposure significantly impaired growth performance of <em>A. japonicus</em> (<em>p</em> < 0.05).</div><div>Metabolomic profiling identified 36 differential metabolites, revealing activation of the TCA cycle and amino acid metabolism to prioritize energy production and nitrogen reallocation. Transcriptomic data highlighted 226 differentially expressed genes. Notably, <em>Zimp10</em>, a key regulator of TCA cycle activity in echinoderms, was upregulated, while <em>FALDH</em>, a glycolysis-related gene, was downregulated, indicating a shift toward energy-efficient aerobic respiration.</div><div>Antioxidant capacity was compromised through suppression of glutathione metabolism genes (<em>MGST1</em>, <em>GST</em>), exacerbating oxidative damage. Stress signaling pathways were dynamically regulated. Downregulation of <em>Ras1-X2</em> suppressed mTOR activity, activating autophagy and mitophagy for cellular repair. Additionally, enrichment of NOD-like receptor pathways and upregulation of <em>vGTPase1-like</em> signaled immune engagement. Prolonged nitrite exposure overwhelmed adaptive mechanisms, leading to physiological decline.</div><div>These results demonstrate <em>A. japonicus</em> of reliance on metabolic reprogramming and stress signaling to mitigate nitrite toxicity, while highlighting vulnerabilities in antioxidant defenses. The study provides critical insights for optimizing aquaculture environments through targeted management of nitrite exposure and metabolic resilience strategies.</div></div>\",\"PeriodicalId\":18204,\"journal\":{\"name\":\"Marine environmental research\",\"volume\":\"209 \",\"pages\":\"Article 107203\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2025-05-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Marine environmental research\",\"FirstCategoryId\":\"93\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0141113625002600\",\"RegionNum\":3,\"RegionCategory\":\"环境科学与生态学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENVIRONMENTAL SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Marine environmental research","FirstCategoryId":"93","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0141113625002600","RegionNum":3,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
The effects of nitrite stress on metabolites and gene expression in sea Cucumbers (Apostichopus japonicus)
Chronic nitrite accumulation in intensive aquaculture poses a significant threat to the sustainability of sea cucumbers (Apostichopus japonicus), a key species in marine aquaculture. This study investigated the molecular and metabolic responses of A. japonicus to 21-day nitrite stress (4.88 mg/L) through transcriptomic and metabolomic analyses. At the end of the experiment, the weight gain rate of the Cg group was 11 %, while that of the Nc group was −9 %. Nitrite exposure significantly impaired growth performance of A. japonicus (p < 0.05).
Metabolomic profiling identified 36 differential metabolites, revealing activation of the TCA cycle and amino acid metabolism to prioritize energy production and nitrogen reallocation. Transcriptomic data highlighted 226 differentially expressed genes. Notably, Zimp10, a key regulator of TCA cycle activity in echinoderms, was upregulated, while FALDH, a glycolysis-related gene, was downregulated, indicating a shift toward energy-efficient aerobic respiration.
Antioxidant capacity was compromised through suppression of glutathione metabolism genes (MGST1, GST), exacerbating oxidative damage. Stress signaling pathways were dynamically regulated. Downregulation of Ras1-X2 suppressed mTOR activity, activating autophagy and mitophagy for cellular repair. Additionally, enrichment of NOD-like receptor pathways and upregulation of vGTPase1-like signaled immune engagement. Prolonged nitrite exposure overwhelmed adaptive mechanisms, leading to physiological decline.
These results demonstrate A. japonicus of reliance on metabolic reprogramming and stress signaling to mitigate nitrite toxicity, while highlighting vulnerabilities in antioxidant defenses. The study provides critical insights for optimizing aquaculture environments through targeted management of nitrite exposure and metabolic resilience strategies.
期刊介绍:
Marine Environmental Research publishes original research papers on chemical, physical, and biological interactions in the oceans and coastal waters. The journal serves as a forum for new information on biology, chemistry, and toxicology and syntheses that advance understanding of marine environmental processes.
Submission of multidisciplinary studies is encouraged. Studies that utilize experimental approaches to clarify the roles of anthropogenic and natural causes of changes in marine ecosystems are especially welcome, as are those studies that represent new developments of a theoretical or conceptual aspect of marine science. All papers published in this journal are reviewed by qualified peers prior to acceptance and publication. Examples of topics considered to be appropriate for the journal include, but are not limited to, the following:
– The extent, persistence, and consequences of change and the recovery from such change in natural marine systems
– The biochemical, physiological, and ecological consequences of contaminants to marine organisms and ecosystems
– The biogeochemistry of naturally occurring and anthropogenic substances
– Models that describe and predict the above processes
– Monitoring studies, to the extent that their results provide new information on functional processes
– Methodological papers describing improved quantitative techniques for the marine sciences.