雄性蜜蜂生殖组织相关细菌的发现和微生物群获取模式。

IF 3.7 2区 生物学 Q2 MICROBIOLOGY mSphere Pub Date : 2025-01-28 Epub Date: 2024-12-19 DOI:10.1128/msphere.00705-24
Alexis Burks, Patrick Gallagher, Kasie Raymann
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引用次数: 0

摘要

蜜蜂是世界上第三大经济上最重要的农业动物,因为它们是传粉者。蜜蜂授粉服务和所有的蜂房职责都由雌蜂完成,而雄蜂的一项工作是交配,并与来自另一个群体的处女蜂王分享他们的基因。因此,雄蜂的健康直接关系到蜂王的成功和群体的生存,但与雌蜂相比,它们的研究严重不足。在其他昆虫中,在肠道和生殖器官中发现的微生物已被证明对繁殖成功和/或整体宿主健康很重要。据我们所知,无人机生殖组织中微生物的存在从未被研究过。此外,我们对雄蜂肠道微生物群的了解非常有限,特别是与蜜蜂工蜂相比。在这里,我们从健康菌落中取样了传统的无人机,并使用16S扩增子测序来鉴定和表征未成熟和成熟无人机生殖器官中的细菌。在鉴定出无人机生殖组织中的细菌后,我们进行了一项对照实验,将新出现的无人机暴露在不同的饲养条件下,以确定它们何时以及如何获得生殖和肠道微生物群。总的来说,我们在传统饲养的无人机的生殖和肠道组织中发现了一组核心细菌,并揭示了社会互动对无人机微生物群的正常发育很重要。确定这些细菌是否在无人机繁殖力和健康中发挥作用应该是未来研究工作的目标。重要性:在过去十年中,每年的蜂群损失增加,导致迫切需要确定哪些因素有助于蜜蜂和蜂群健康。肠道微生物已被证明在不能繁殖的雌性蜜蜂工蜂的健康中起着重要作用,它们占蜜蜂群体的90%或更多。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,雄蜂只占蜂群人口的一小部分,但通过与处女蜂王交配,在未来蜂群的成功中发挥着非常关键的作用。在这里,我们发现了雄蜂生殖器官内的微生物,并说明了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。需要进一步的研究来确定微生物是否在蜜蜂的生殖健康和适应性中发挥重要作用。
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Discovery of reproductive tissue-associated bacteria and the modes of microbiota acquisition in male honey bees (drones).

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.

Importance: 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.

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来源期刊
mSphere
mSphere Immunology and Microbiology-Microbiology
CiteScore
8.50
自引率
2.10%
发文量
192
审稿时长
11 weeks
期刊介绍: mSphere™ is a multi-disciplinary open-access journal that will focus on rapid publication of fundamental contributions to our understanding of microbiology. Its scope will reflect the immense range of fields within the microbial sciences, creating new opportunities for researchers to share findings that are transforming our understanding of human health and disease, ecosystems, neuroscience, agriculture, energy production, climate change, evolution, biogeochemical cycling, and food and drug production. Submissions will be encouraged of all high-quality work that makes fundamental contributions to our understanding of microbiology. mSphere™ will provide streamlined decisions, while carrying on ASM''s tradition for rigorous peer review.
期刊最新文献
Prospective comparison of the digestive tract resistome and microbiota in cattle raised in grass-fed versus grain-fed production systems. Prophages are infrequently associated with antibiotic resistance in Pseudomonas aeruginosa clinical isolates. Virus-induced perturbations in the mouse microbiome are impacted by microbial experience. Abundance of clinically relevant antimicrobial resistance genes in the golden jackal (Canis aureus) gut. Characterization of diet-linked amino acid pool influence on Fusobacterium spp. growth and metabolism.
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