昆虫学报 ›› 2025, Vol. 68 ›› Issue (3): 291-299.doi: 10.16380/j.kcxb.2025.03.005

• 研究论文 • 上一篇    下一篇

西方蜜蜂预蛹低温胁迫后恢复化蛹的转录组学分析

曹铭劼1,3, 许宏智1,3, 徐新建1,2,3, 周姝婧1,2,3, 朱晨煜1,3田园明月1,3, 周冰峰1,2,3, 姚清花3, 朱翔杰1,2,3,*   

  1. (1. 福建农林大学蜂学与生物医药学院, 福州 350002; 2. 福建农林大学蜜蜂研究所, 福州 350002; 3. 南安蜜蜂科技小院, 南安 362300)
  • 出版日期:2025-03-20 发布日期:2025-04-21

Transcriptomic insights into pupation resumption in Apis mellifera (Hymenoptera: Apidae) prepupae after low-temperature stress

CAO Ming-Jie1,3, XU Hong-Zhi1,3, XU Xin-Jian1,2,3, ZHOU Shu-Jing1,2,3, ZHU Chen-Yu1,3, TIAN Yuan-Ming-Yue1,3, ZHOU Bing-Feng1,2,3, YAO Qing-Hua3, ZHU Xiang-Jie1,2,3,*   

  1. (1. College of Bee Science and Biomedicine, Fujian Agriculture and Forestry University, Fuzhou 350002, China; 2. Honeybee Research Institute, Fujian Agriculture and Forestry University, Fuzhou 350002, China; 3. Nan′an Honeybee Science and Technology Backyard, Nan′an 362300, China)
  • Online:2025-03-20 Published:2025-04-21

摘要: 【目的】蜜蜂卵、幼虫和蛹的发育具有明显的狭温性特征,低温胁迫会导致发育停滞。本研究旨在研究西方蜜蜂Apis mellifera工蜂预蛹低温胁迫后恢复化蛹的分子机制。【方法】比较在最适温度35 ℃发育的西方蜜蜂工蜂蛹(CK)和预蛹经20 ℃低温胁迫24 h后恢复化蛹的蛹(T)的转录组测序数据,筛选CK vs T比较组的差异表达基因(differentially expressed genes, DEGs);将DEGs进行GO功能注释和KEGG通路富集;选取5个抗氧化相关的DEGs(SOD2, Tpx4, GstS1, Prdx6和Cu-Zn)进行RT-qPCR验证。【结果】CK vs T比较组检测到1 335个DEGs,其中853个DEGs上调, 482个DEGs下调; GO富集结果显示, DEGs显著富集在细胞内核糖核蛋白复合物、 NADH脱氢酶活性和抗氧化活性等GO条目上。KEGG富集结果显示,DEGs显著富集在氧化磷酸化、核糖体以及蛋白酶体通路。抗氧化相关5个DEGs (SOD2, Tpx4, GstS1, Prdx6和Cu-Zn)的RT-qPCR结果均显示上调表达,与转录组测序结果趋势一致。【结论】经低温胁迫的西方蜜蜂预蛹,当恢复正常发育温度后,通过提高能量代谢、蛋白质的合成分解以及抗氧化相关基因的表达来实现重启发育并完成化蛹。本研究有助于深入了解狭温性昆虫在经历低温胁迫后的发育恢复机制。

关键词: 西方蜜蜂, 低温胁迫; 化蛹, 抗氧化酶; 代谢, 转录组

Abstract:  【Aim】 The development of honeybee eggs, larvae and pupae is markedly stenothermic, and low-temperature stress leads to arrested development. The purpose of this study is to investigate the molecular mechanism of pupation resumption in Apis mellifera worker prepupae post lowtemperature stress. 【Methods】 Transcriptomes were compared between pupae workers developed at the optimal temperature of 35 ℃ (CK) and pupae from prepupae recovered from low-temperature stress at 20 ℃ for 24 h (T) of A. mellifera workers. The differentially expressed genes (DEGs) in the CK vs T comparison group were identified and annotated in GO and KEGG databases for enrichment. Five antioxidant-related DEGs (SOD2, Tpx4, GstS1, Prdx6 and Cu-Zn) were validated using RT-qPCR. 【Results】 A total of 1 335 DEGs were identified in the CK vs T comparison group, with 853 DEGs up-regulated and 482 DEGs down-regulated. GO enrichment result revealed that the DEGs were significantly enriched in such GO terms as intracellular ribonucleoprotein complexes, NADH dehydrogenase activity, and antioxidant activity. KEGG enrichment result showed that DEGs were significantly enriched into oxidative phosphorylation, ribosome, and proteasome pathways. The RT-qPCR results confirmed the upregulation of 5 antioxidant-related DEGs (SOD2, Tpx4, GstS1, Prdx6, and Cu-Zn), consistent with the transcriptome sequencing results.【Conclusion】 When recovered from low-temperature stress, the A. mellifera prepupae can resume development to complete pupation by increasing energy metabolism, protein synthesis and degradation, as well as the expression of antioxidant-related genes. This research provides insights into the development resumption mechanisms of stenothermic insects after experiencing low-temperature stress.

Key words: Apis mellifera, low-temperature stress, pupation, antioxidant enzyme, metabolism, transcriptome