Fan Yuanchan, Wang Jie, Yu Kejun, Zhang Wende, Cai Zongbing, Sun Minghui, Hu Ying, Zhao Xiao, Xiong Cuiling, Niu Qingsheng, Chen Dafu, Guo Rui
College of Animal Sciences (College of Bee Science), Fujian Agriculture and Forestry University, Fuzhou 350002, China.
Jilin Province Institute of Apicultural Science, Jilin 132000, China.
Insects. 2022 Feb 28;13(3):241. doi: 10.3390/insects13030241.
is the original host for , a widespread fungal parasite resulting in honey bee nosemosis, which leads to severe losses to the apiculture industry throughout the world. However, knowledge of infecting eastern honey bees is extremely limited. Currently, the mechanism underlying infection is still largely unknown. Based on our previously gained high-quality transcriptome datasets derived from spores (NcCK group), infecting workers at seven days post inoculation (dpi) and 10 dpi (NcT1 and NcT2 groups), comparative transcriptomic investigation was conducted in this work, with a focus on virulence factor-associated differentially expressed genes (DEGs). Microscopic observation showed that the midguts of workers were effectively infected after inoculation with clean spores of . In total, 1411, 604, and 38 DEGs were identified from NcCK vs. NcT1, NcCK vs. NcT2, and NcT1 vs. NcT2 comparison groups. Venn analysis showed that 10 upregulated genes and nine downregulated ones were shared by the aforementioned comparison groups. The GO category indicated that these DEGs were involved in a series of functional terms relevant to biological process, cellular component, and molecular function such as metabolic process, cell part, and catalytic activity. Additionally, KEGG pathway analysis suggested that the DEGs were engaged in an array of pathways of great importance such as metabolic pathway, glycolysis, and the biosynthesis of secondary metabolites. Furthermore, expression clustering analysis demonstrated that the majority of genes encoding virulence factors such as ricin B lectins and polar tube proteins displayed apparent upregulation, whereas a few virulence factor-associated genes such as hexokinase gene and 6-phosphofructokinase gene presented downregulation during the fungal infection. Finally, the expression trend of 14 DEGs was confirmed by RT-qPCR, validating the reliability of our transcriptome datasets. These results together demonstrated that an overall alteration of the transcriptome of occurred during the infection of workers, and most of the virulence factor-related genes were induced to activation to promote the fungal invasion. Our findings not only lay a foundation for clarifying the molecular mechanism underlying infection of eastern honey bee workers and microsporidian-host interaction.
是一种广泛传播的真菌寄生虫的原始宿主,这种寄生虫会导致蜜蜂微孢子虫病,给全球养蜂业造成严重损失。然而,关于感染东方蜜蜂的相关知识极其有限。目前,感染的潜在机制在很大程度上仍然未知。基于我们之前获得的来自孢子(NcCK组)、接种后7天(dpi)和10 dpi感染中华蜜蜂工蜂的(NcT1和NcT2组)的高质量转录组数据集,本研究进行了比较转录组学调查,重点关注与毒力因子相关的差异表达基因(DEGs)。显微镜观察表明,用的干净孢子接种后,中华蜜蜂工蜂的中肠被有效感染。总共从NcCK与NcT1、NcCK与NcT2以及NcT1与NcT2比较组中鉴定出1411个、604个和38个DEGs。维恩分析表明,上述比较组共有10个上调基因和9个下调基因。基因本体(GO)类别表明,这些DEGs涉及一系列与生物过程、细胞成分和分子功能相关的功能术语,如代谢过程、细胞部分和催化活性。此外,京都基因与基因组百科全书(KEGG)通路分析表明,这些DEGs参与了一系列重要的通路,如代谢通路、糖酵解和次生代谢物的生物合成。此外,表达聚类分析表明,大多数编码毒力因子的基因,如蓖麻毒蛋白B凝集素和极管蛋白,表现出明显上调,而一些与毒力因子相关的基因,如己糖激酶基因和6-磷酸果糖激酶基因,在真菌感染期间呈现下调。最后,通过逆转录定量聚合酶链反应(RT-qPCR)证实了14个DEGs的表达趋势,验证了我们转录组数据集的可靠性。这些结果共同表明,在中华蜜蜂工蜂感染期间,的转录组发生了整体变化,并且大多数与毒力因子相关的基因被诱导激活以促进真菌入侵。我们的研究结果不仅为阐明东方蜜蜂工蜂感染和微孢子虫-宿主相互作用的分子机制奠定了基础。