昆虫学报 ›› 2025, Vol. 68 ›› Issue (8): 1057-1066.doi: 10.16380/j.kcxb.2025.08.004

• 研究论文 • 上一篇    下一篇

蜜蜂慢性麻痹病毒侵染对中华蜜蜂免疫和肠道菌群的影响

邹德馨1,3,#, 袁春颖2,#, 金红梅1,3, 杨扬4, 杨喜爱3马鸣潇1, 侯春生3, 费东亮1,*, 邓炎春3,*   

  1. (1.锦州医科大学畜牧兽医学院, 锦州 121000; 2. 辽宁省农业发展服务中心, 兴城 125100; 3. 中国农业科学院麻类研究所, 长沙 410205; 4. 内蒙古自治区农牧业科学院综合试验示范中心, 呼和浩特 010000)
  • 出版日期:2025-08-20 发布日期:2025-09-30

Effects of chronic bee paralysis virus infection on the immune and gut microbiota in Apis cerana cerana(Hymenoptera: Apidae)

ZOU De-Xin1,3,#, YUAN Chun-Ying2,#, JIN Hong-Mei1,3, YANG Yang4, YANG Xi-Ai3, MA Ming-Xiao1, HOU Chun-Sheng3, FEI Dong-Liang1,*, DENG Yan-Chun3,*   

  1. (1. College of Animal Husbandry and Veterinary Medicine, Jinzhou Medical University, Jinzhou 121000, China; 2. Liaoning Agricultural Development Service Center, Xingcheng 125100, China; 3. Institute of Bast Fiber Crops, Chinese Academy of Agricultural Sciences, Changsha 410205, China; 4. Center for Comprehensive Test and Demonstration, Inner Mongolia Academy of Agricultural and Animal Husbandry Sciences, Hohhot 010000, China)
  • Online:2025-08-20 Published:2025-09-30

摘要: 【目的】本研究旨在探究蜜蜂慢性麻痹病毒(chronic bee paralysis virus, CBPV)侵染对中华蜜蜂Apis cerana cerana免疫和肠道菌群的影响。【方法】采用注射CBPV RNA的方式使中华蜜蜂新出房成年工蜂感染CBPV,统计存活率; qRT-PCR检测CBPV侵染后中华蜜蜂工蜂体内CBPV基因组拷贝数和15个免疫相关基因(PGRP-S2, Cactus1, Toll, PGRPLC-like, Relish, Defensin1, Hymenoptaecin,  SP14, PPO, Dicer, HSP70, HSP90, Stat, StamPISA3)的表达量;利用宏基因组测序检测中华蜜蜂工蜂感染CBPV后的肠道菌群结构的变化,并对肠道菌群进行alpha多样性分析和beta多样性分析。【结果】相对于注射1×PBS的对照组,感染CBPV的中华蜜蜂成年工蜂存活率逐渐降低,在感染第7天时的累计存活率降低到了27%;感染第1-4天CBPV基因组拷贝数急剧稳步增加,第4天时CBPV基因组拷贝数增加了106倍。同时,CBPV显著激活中华蜜蜂Toll免疫通路基因,尤其抗菌肽基因Defensin1和Hymenoptaecin的表达量在CBPV侵染的第1-5天均显著上调,在侵染第5天,上调倍数超过10倍。宏基因组测序结果显示CBPV侵染影响中华蜜蜂工蜂肠道菌群结构,显著改变肠道菌群多样性,尤其蜜蜂乳杆菌Lactobacillus apisSnodgrassella alvi的相对丰度在CBPV侵染后较对照显著下调。【结论】CBPV侵染能引起中华蜜蜂工蜂死亡,激活抗菌肽基因的表达,显著减少其肠道中有益菌的相对丰度,研究结果为也为建立蜜蜂新的健康管理策略和防控措施提供重要的理论基础。

关键词: 中华蜜蜂, 蜜蜂慢性麻痹病毒, 免疫, 抗菌肽, 肠道菌群

Abstract: 【Aim】 The objective of this study is to explore the effects of chronic bee paralysis virus (CBPV) infection on the immunity and gut microbiota of Apis cerana cerana. 【Methods】 The newly emerged adult workers of A. c. cerana were infected with CBPV by injecting CBPV RNA, and the survival rate was recorded. qRT-PCR was used to detect the genomic copy number of CBPV and the expression levels of 15 immune-related genes (PGRP-S2, Cactus1, Toll, PGRPLC-like, Relish, Defensin1, Hymenoptaecin, SP14, PPO, Dicer, HSP70, HSP90, Stat, Stam and PISA3) in the CBPV-infected A. c. cerana workers. Metagenomic sequencing was used to detect the change of the gut microbiota structure in the CSBV-infected A. c. cerana workers, and alpha- and beta- diversity analyses of gut microbiota were performed. 【Results】The survival rate of A. c. cerana adult workers infected with CBPV gradually decreased as compared with that of the control group injected with 1×PBS, and the cumulative survival rate decreased to 27% on the 7th day after infection. The overall trend of the genomic copy number of CBPV increased sharply and steadily from the 1st-4th day, with a 106-fold increase of genomic copy number on the 4th day after infection. Meanwhile, CBPV infection significantly activated the Toll immune pathway genes, especially the antimicrobial peptide genes Defensin1 and Hymenoptaecin, with their expression levels significantly up-regulated on the 1st-5th day after CBPV infection and more than 10-fold on the 5th day. Metagenomic sequencing result showed that CBPV infection affected the gut microbiota structure, and significantly changed the gut microbiota diversity of A. c. cerana workers, especially the relative abundance of Lactobacillus apis and Snodgrassella alvi was significantly down-regulated in the CBPV-infected A. c. cerana as compared with that in the control. 【Conclusion】 CBPV infection can cause the death of A. c. cerana workers, activate the expression of antimicrobial peptide genes and significantly reduce the relative abundance of beneficial bacteria in the gut. The results provide an important theoretical basis for developing bees’ new health management strategies and prevention and control measures.

Key words: Apis cerana cerana, chronic bee paralysis virus, immunity, antimicrobial peptides, gut microbiota