INRA, UR 406 Abeilles et Environnement, Site Agroparc, Avignon, France.
PLoS One. 2012;7(5):e37017. doi: 10.1371/journal.pone.0037017. Epub 2012 May 18.
The microsporidium Nosema ceranae is a newly prevalent parasite of the European honey bee (Apis mellifera). Although this parasite is presently spreading across the world into its novel host, the mechanisms by it which affects the bees and how bees respond are not well understood. We therefore performed an extensive characterization of the parasite effects at the molecular level by using genetic and biochemical tools. The transcriptome modifications at the midgut level were characterized seven days post-infection with tiling microarrays. Then we tested the bee midgut response to infection by measuring activity of antioxidant and detoxification enzymes (superoxide dismutases, glutathione peroxidases, glutathione reductase, and glutathione-S-transferase). At the gene-expression level, the bee midgut responded to N. ceranae infection by an increase in oxidative stress concurrent with the generation of antioxidant enzymes, defense and protective response specifically observed in the gut of mammals and insects. However, at the enzymatic level, the protective response was not confirmed, with only glutathione-S-transferase exhibiting a higher activity in infected bees. The oxidative stress was associated with a higher transcription of sugar transporter in the gut. Finally, a dramatic effect of the microsporidia infection was the inhibition of genes involved in the homeostasis and renewal of intestinal tissues (Wnt signaling pathway), a phenomenon that was confirmed at the histological level. This tissue degeneration and prevention of gut epithelium renewal may explain early bee death. In conclusion, our integrated approach not only gives new insights into the pathological effects of N. ceranae and the bee gut response, but also demonstrate that the honey bee gut is an interesting model system for studying host defense responses.
微孢子虫 Nosema ceranae 是欧洲蜜蜂(Apis mellifera)的一种新流行寄生虫。尽管这种寄生虫目前正在向其新宿主传播,但它影响蜜蜂的机制以及蜜蜂如何做出反应还不是很清楚。因此,我们使用遗传和生化工具在分子水平上对寄生虫的影响进行了广泛的描述。通过使用 tiling 微阵列,我们在感染后 7 天对中肠水平的转录组修饰进行了特征描述。然后,我们通过测量抗氧化和解毒酶(超氧化物歧化酶、谷胱甘肽过氧化物酶、谷胱甘肽还原酶和谷胱甘肽-S-转移酶)的活性来测试蜜蜂中肠对感染的反应。在基因表达水平上,蜜蜂中肠通过增加抗氧化应激来响应 N. ceranae 感染,同时还会产生抗氧化酶,这种防御和保护反应在哺乳动物和昆虫的肠道中特异性观察到。然而,在酶水平上,没有确认保护反应,只有谷胱甘肽-S-转移酶在感染蜜蜂中表现出更高的活性。氧化应激与肠道中糖转运蛋白的转录增加有关。最后,微孢子虫感染的一个显著影响是抑制与肠道组织稳态和更新相关的基因(Wnt 信号通路),这一现象在组织学水平上得到了证实。这种组织退化和阻止肠道上皮细胞更新可能解释了早期蜜蜂死亡的原因。总之,我们的综合方法不仅深入了解了 N. ceranae 的病理影响和蜜蜂肠道的反应,还证明了蜜蜂肠道是研究宿主防御反应的一个有趣的模型系统。