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Microb Ecol. 2023 Nov;86(4):3013-3026. doi: 10.1007/s00248-023-02304-9. Epub 2023 Oct 5.
2
The gut microbiome of solitary bees is mainly affected by pathogen assemblage and partially by land use.独居蜂的肠道微生物群主要受病原体组合的影响,部分受土地利用的影响。
Environ Microbiome. 2023 Apr 26;18(1):38. doi: 10.1186/s40793-023-00494-w.
3
Solitary bee larvae modify bacterial diversity of pollen provisions in the stem-nesting bee, (Megachilidae).独居蜜蜂幼虫改变了茎巢蜂(切叶蜂科)花粉储备的细菌多样性。
Front Microbiol. 2023 Jan 9;13:1057626. doi: 10.3389/fmicb.2022.1057626. eCollection 2022.
4
Floral nectar microbial communities exhibit seasonal shifts associated with extreme heat: Potential implications for climate change and plant-pollinator interactions.花蜜微生物群落呈现出与酷热相关的季节性变化:对气候变化和植物 - 传粉者相互作用的潜在影响。
Front Microbiol. 2022 Aug 25;13:931291. doi: 10.3389/fmicb.2022.931291. eCollection 2022.
5
Composition and acquisition of the microbiome in solitary, ground-nesting alkali bees.独居、地面筑巢碱蜂的微生物组组成和获取。
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6
(More than) Hitchhikers through the network: the shared microbiome of bees and flowers.(超)过路人在网络中:蜜蜂和花的共享微生物组。
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Susceptibility of Red Mason Bee Larvae to Bacterial Threats Due to Microbiome Exchange with Imported Pollen Provisions.由于与进口花粉供应进行微生物群落交换,红壁蜂幼虫对细菌威胁的易感性。
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Division of labor in honey bee gut microbiota for plant polysaccharide digestion.蜜蜂肠道微生物群的分工用于植物多糖消化。
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9
Linking pollen foraging of megachilid bees to their nest bacterial microbiota.将切叶蜂科蜜蜂的花粉采集行为与其巢穴细菌微生物群联系起来。
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10
Drivers, Diversity, and Functions of the Solitary-Bee Microbiota.独居蜂微生物组的驱动因素、多样性和功能。
Trends Microbiol. 2019 Dec;27(12):1034-1044. doi: 10.1016/j.tim.2019.07.011. Epub 2019 Aug 23.

在独居蜜蜂中,从环境中获得的肠道相关细菌对于其生长和存活并不是至关重要的。

Environmentally acquired gut-associated bacteria are not critical for growth and survival in a solitary bee, .

机构信息

Department of Biological Sciences, North Dakota State University, Fargo, North Dakota, USA.

Department of Entomology, University of California, Riverside, California, USA.

出版信息

Appl Environ Microbiol. 2024 Sep 18;90(9):e0207623. doi: 10.1128/aem.02076-23. Epub 2024 Aug 13.

DOI:10.1128/aem.02076-23
PMID:39136489
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11409666/
Abstract

Social bees have been extensively studied for their gut microbial functions, but the significance of the gut microbiota in solitary bees remains less explored. Solitary bee, females provision their offspring with pollen from various plant species, harboring a diverse microbial community that colonizes larvae guts. The is the most abundant microbe, but evidence concerning the effects of and other provision microbes on growth and survival are lacking. We hypothesized that the presence of in abundance would enhance larval and prepupal development, weight, and survival, while the absence of intact microbial communities was expected to have a negative impact on bee fitness. We reared larvae on pollen provisions with naturally collected microbial communities (Natural pollen) or devoid of microbial communities (Sterile pollen). We also assessed the impact of introducing by adding it to both types of pollen provisions. Feeding larvae with sterile pollen + led to the highest mortality rate, followed by natural pollen + , and sterile pollen. Larval development was significantly delayed in groups fed with sterile pollen. Interestingly, larval and prepupal weights did not significantly differ across treatments compared to natural pollen-fed larvae. 16S rRNA gene sequencing found a dominance of , when was introduced to natural pollen. The presence of with abundant ri suggests potential crosstalk between both, shaping bee nutrition and health. Hence, this study highlights that the reliance on nonhost-specific environmental bacteria may not impact fitness of .IMPORTANCEThis study investigates the impact of environmentally acquired gut microbes of solitary bee fitness with insights into the microbial ecology of bee and their health. While the symbiotic microbiome is well-studied in social bees, the role of environmental acquired microbiota in solitary bees remains unclear. Assessing this relationship in a solitary pollinator, the leaf-cutting bee, , we discovered that this bee species does not depend on the diverse environmental bacteria found in pollen for either its larval growth or survival. Surprisingly, high concentrations of the most abundant pollen bacteria did not consistently benefit bee fitness, but caused larval mortality. Our findings also suggest an interaction between and the and perhaps their role in bee nutrition. Hence, this study provides significant insights that contribute to understanding the fitness, conservation, and pollination ecology of other solitary bee species in the future.

摘要

社会性蜜蜂的肠道微生物功能已得到广泛研究,但独居蜜蜂的肠道微生物群的意义仍未得到充分探索。独居蜜蜂的雌性会用来自各种植物物种的花粉喂养后代,其幼虫的肠道中栖息着多样的微生物群落。 是最丰富的微生物,但缺乏关于 和其他供应微生物对生长和生存的影响的证据。我们假设大量存在 会促进幼虫和预蛹的发育、体重和存活率,而完整微生物群落的缺失预计会对蜜蜂的适应性产生负面影响。我们在含有自然收集的微生物群落的花粉供应物(天然花粉)或不含微生物群落的花粉供应物(无菌花粉)上饲养幼虫。我们还评估了通过向两种花粉供应物中添加 来引入 的影响。用无菌花粉+ 喂养幼虫导致死亡率最高,其次是天然花粉+ ,然后是无菌花粉。用无菌花粉喂养的幼虫的发育明显延迟。有趣的是,与用天然花粉喂养的幼虫相比,各组幼虫和预蛹的体重没有显著差异。16S rRNA 基因测序发现,当 将 引入天然花粉时, 占主导地位。 的存在伴随着丰富的 ri 表明两者之间存在潜在的相互作用,塑造了蜜蜂的营养和健康。因此,这项研究强调了对非宿主特异性环境细菌的依赖可能不会影响 的适应性。