首页|克氏原螯虾响应高温胁迫的生理代谢机制

克氏原螯虾响应高温胁迫的生理代谢机制

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[目的]研究克氏原螯虾响应高温胁迫的生理代谢机制,为改善其养殖管理和品种选育提供参考.[方法]以 26℃为对照组,对克氏原螯虾进行 32℃和 37℃的高温胁迫实验,分别在胁迫后 24 h和 72 h收集鳃丝样品.通过组织学观察、生化指标测定(丙二醛、活性氧、总抗氧化能力、丙酮酸激酶、己糖激酶、碱性磷酸酶、磷酸烯醇式丙酮酸羧激酶、溶菌酶、酸性磷酸酶)和转录组学分析,综合探讨克氏原螯虾响应高温胁迫的生理代谢机制.[结果]高温导致鳃丝组织损伤,生化指标总体上随着温度的升高而下降.与对照组相比,32℃胁迫组在 24 和 72 h分别鉴定出 226 和 6 937 个差异表达基因(DEGs);37℃胁迫组则有高达2 928 和 9 449 个DEGs.GO和KEGG富集分析表明,DEGs显著富集在O-聚糖生物合成、细胞外基质-受体相互作用、花生四烯酸代谢、鞘脂代谢以及淀粉和蔗糖代谢等过程.此外,加权基因表达网络分析发现DEGs聚类在免疫和能量代谢等模块上,并筛选出组蛋白(H2A)、线粒体(ND6)等核心基因.选取 10 个DEGs进行RT-qPCR验证,结果和测序结果一致,验证了转录组结果的准确性.[结论]在 32℃和 37℃的温度下,克氏原螯虾的鳃丝受到损伤并降低了葡萄糖的利用率,迫使其通过调整热休克蛋白、抗氧化能力和代谢等途径维持细胞功能.
Physiological and Metabolic Mechanisms of Procambarus clarkii in Response to High Temperature Stress
[Objective]To understand the physiological and metabolic mechanisms of Procambarus clarkii in response to high temperature stress,and to provide references for improving P.clarkii culture management and variety breeding.[Method]The P.clarkii were exposed to 32℃and 37℃,and 26℃serving as the control condition.Gill samples were collected at 24 and 72 h post-exposure.The study employed a comprehensive analysis of histological observation,biochemical indicators(malondialdehyde,reactive oxygen species,total antioxidant capacity,pyruvate kinase,hexokinase,alkaline phosphatase,phosphoenolpyruvate carboxykinase,lysozyme,and acid phosphatase),and transcriptome to comprehensively explore the physiological and metabolic responses of P.clarkii to high temperature stress.[Result]High temperature damaged the gill tissues and the biochemical indicators overall decreased with the increasing of temperature.When compared to the control group,a total of 226 and 6 937 differentially expressed genes(DEGs)were identified at 24 and 72 h in 32℃group,and a total of 2 928 and 9 449 DEGs were identified at 24 and 72 h in 37℃group.GO and KEGG enrichment analyses indicate that DEGs were significantly enriched in O-glycan biosynthesis,extracellular matrix-receptor interaction,arachidonic acid metabolism,sphingolipid metabolism,as well as starch and sucrose metabolism processes.Additionally,the DEGs were found to cluster in modules pertinent to immune and energy metabolism based on weighted gene co-expression network analysis(WGCNA),hub genes like histones(H2A)and mitochondrial components(ND6)were identified.Ten DEGs were randomly selected to validate the RNA-seq results using reverse transcription-quantitative polymerase chain reaction(RT-qPCR),and the results and the expression profiles of these DEGs were of a well consistent with the high-throughput data,which confirmed the reliability of transcriptome results.[Conclusion]At temperatures of 32℃and 37℃,the gills of P.clarkii are damaged.The glucose utilization rate of P.clarkii is reduced in high temperature environments,causing cellular function to be maintained through the adjustments of heat shock proteins,antioxidant capacity,and metabolism.

Procambarus clarkiihigh temperaturegillphysiological metabolismmechanism

邹永烽、包志明、曹攀辉、张嘉媛、郭介宇、苏现斌、徐宇、许志强、郭慧

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广东海洋大学水产学院,湛江 524000

湛江市海洋生态与养殖环境重点实验室,湛江 524088

江苏省淡水水产研究所 农业农村部淡水虾蟹遗传育种与养殖重点实验室,南京 210017

克氏原螯虾 高温 生理代谢 机制

2024

生物技术通报
中国农业科学院农业信息研究所

生物技术通报

CSTPCD北大核心
影响因子:0.505
ISSN:1002-5464
年,卷(期):2024.40(11)