Burks Alexis, Gallagher Patrick, Raymann Kasie
Department of Biology, University of North Carolina, Greensboro, North Carolina, USA.
Department of Plant and Microbial Biology, North Carolina State University, Raleigh, North Carolina, USA.
mSphere. 2025 Jan 28;10(1):e0070524. doi: 10.1128/msphere.00705-24. Epub 2024 Dec 19.
Honey bees are the third most economically important agricultural animal in the world due to their role as pollinators. Honey bee pollination services and all hive duties are performed by female workers, while the male drones have one job to mate and share their genetics with a virgin queen from another colony. Thus, drone fitness is directly tied to queen success and colony survival, yet they have been severely understudied compared to their female counterparts. In other insects, microbes discovered in the gut and reproductive organs have been shown to be important for reproductive success and/or overall host health. To our knowledge, the existence of microbes in drone reproductive tissues has never been investigated. Moreover, our understanding of the gut microbiota of drones is severely limited, especially when compared to honey bee workers. Here, we sampled conventional drones from healthy colonies and used 16S amplicon sequencing to identify and characterize bacteria in the reproductive organs of immature and mature drones. After identifying bacteria in drone reproductive tissues, we performed a controlled experiment in which newly emerged drones were exposed to different rearing conditions in order to determine when and how they acquire their reproductive and gut microbiota. Overall, we discovered a set of core bacteria in the reproductive and gut tissues of conventionally reared drones and revealed that social interactions are important for the proper development of the drone microbiota. Determining if these bacteria play a role in drone fecundity and health should be a goal of future research efforts.
Over the last decade, annual honey bee colony loss has increased, resulting in a critical need to determine what factors contribute to honey bee and colony health. Gut microbes have been shown to play important roles in the health of the nonreproductive female honey bee workers, which make up 90% or more of a honey bee colony. However, we currently know very little about the impact of microbes on the health of male honey bees (drones), who only make up a small portion of the colony population but play a very key role in the success of future colonies by mating with virgin queens. Here, we discovered microbes within the reproductive organs of drones and illustrated that social interactions with worker bees are necessary for the proper development of the gut and reproductive tissue microbial communities in drones. Further studies are needed to determine if microbes play an important role in honey bee reproductive health and fitness.
蜜蜂作为传粉者,是世界上第三大具有重要经济意义的农业动物。蜜蜂的授粉服务和所有蜂巢职责均由雌性工蜂执行,而雄性雄蜂只有一项任务,即与来自另一个蜂群的处女蜂王交配并分享其基因。因此,雄蜂的健康状况直接关系到蜂王的成功和蜂群的生存,但与雌蜂相比,对它们的研究严重不足。在其他昆虫中,已发现肠道和生殖器官中的微生物对生殖成功和/或宿主整体健康很重要。据我们所知,从未对雄蜂生殖组织中的微生物存在情况进行过研究。此外,我们对雄蜂肠道微生物群的了解非常有限,尤其是与蜜蜂工蜂相比。在这里,我们从健康蜂群中采集了传统饲养的雄蜂样本,并使用16S扩增子测序来鉴定和表征未成熟和成熟雄蜂生殖器官中的细菌。在确定了雄蜂生殖组织中的细菌后,我们进行了一项对照实验,让新出现的雄蜂暴露于不同的饲养条件下,以确定它们何时以及如何获得生殖和肠道微生物群。总体而言,我们在传统饲养的雄蜂的生殖和肠道组织中发现了一组核心细菌,并揭示社会互动对雄蜂微生物群的正常发育很重要。确定这些细菌是否在雄蜂繁殖力和健康中发挥作用应该是未来研究工作的目标。
在过去十年中,蜜蜂蜂群的年度损失有所增加,因此迫切需要确定哪些因素有助于蜜蜂和蜂群的健康。肠道微生物已被证明在构成蜜蜂蜂群90%或更多的非生殖雌性蜜蜂工蜂的健康中发挥重要作用。然而,我们目前对微生物对雄性蜜蜂(雄蜂)健康的影响知之甚少,雄蜂只占蜂群数量的一小部分,但通过与处女蜂王交配,对未来蜂群的成功起着非常关键的作用。在这里,我们在雄蜂的生殖器官中发现了微生物,并表明与工蜂的社会互动对于雄蜂肠道和生殖组织微生物群落的正常发育是必要的。需要进一步研究以确定微生物是否在蜜蜂生殖健康和适应性中发挥重要作用。