花粉饮食,超过地理距离,形状提供微生物组组成的两种腔巢蜜蜂。

IF 3.2 3区 生物学 Q2 MICROBIOLOGY
Rachel L Vannette, Neal M Williams, Stephen S Peterson, Alexia N Martin
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引用次数: 0

摘要

储存食物的微生物组成可以影响其稳定性,并决定以其为食的生物所消耗的微生物种类。许多蜜蜂将花蜜和花粉储存在喂养发育中的后代的容器中。然而,微生物组成是否由食物中的花粉类型、同一筑巢地点的蜜蜂种类之间的差异或地理距离决定尚不清楚。在这里,我们在加利福尼亚的13个地点取样了两种共存的Osmia属的洞巢蜜蜂,并研究了它们的花粉、真菌和细菌的组成。花粉组成解释了细菌组成变异的15%和真菌组成变异的30%,而位点之间的空间距离解释了最小的额外变异。共生微生物属Ascosphaera、Sodalis和Wolbachia与花粉组成的关联模式截然不同,表明每种微生物的获取和传播途径不同。比较由相同花粉组成的两种蜜蜂物种的供给,指出环境获取而不是蜜蜂物种是塑造Osmia蜜蜂微生物组早期阶段的关键因素。我们观察到的模式也与其他独居蜜蜂物种中以芽胞杆菌为主的供应微生物组形成对比,表明蜜蜂物种之间储存食物中微生物组装的不同机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Pollen diet, more than geographic distance, shapes provision microbiome composition in two species of cavity-nesting bees.

Pollen diet, more than geographic distance, shapes provision microbiome composition in two species of cavity-nesting bees.

Pollen diet, more than geographic distance, shapes provision microbiome composition in two species of cavity-nesting bees.

Pollen diet, more than geographic distance, shapes provision microbiome composition in two species of cavity-nesting bees.

The microbial composition of stored food can influence its stability and the microbial species consumed by the organism feeding on it. Many bee species store nectar and pollen in provisions constructed to feed developing offspring. Yet, whether microbial composition is determined by the pollen types within provisions, variation between bee species at the same nesting sites, or geographic distance was unclear. Here, we sampled two species of cooccurring cavity nesting bees in the genus Osmia at 13 sites in California and examined the composition of pollen, fungi, and bacteria in provisions. Pollen composition explained 15% of variation in bacterial composition and ∼30% of variation in fungal composition, whereas spatial distance among sites explained minimal additional variation. Symbiotic microbe genera Ascosphaera, Sodalis, and Wolbachia showed contrasting patterns of association with pollen composition, suggesting distinct acquisition and transmission routes for each. Comparing provisions from both bee species comprised of the same pollens points to environmental acquisition rather than bee species as a key factor shaping the early stages of the bee microbiome in Osmia. The patterns we observed also contrast with Apilactobacillus-dominated provision microbiome in other solitary bee species, suggesting variable mechanisms of microbial assembly in stored food among bee species.

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来源期刊
FEMS microbiology ecology
FEMS microbiology ecology 生物-微生物学
CiteScore
7.50
自引率
2.40%
发文量
132
审稿时长
3 months
期刊介绍: FEMS Microbiology Ecology aims to ensure efficient publication of high-quality papers that are original and provide a significant contribution to the understanding of microbial ecology. The journal contains Research Articles and MiniReviews on fundamental aspects of the ecology of microorganisms in natural soil, aquatic and atmospheric habitats, including extreme environments, and in artificial or managed environments. Research papers on pure cultures and in the areas of plant pathology and medical, food or veterinary microbiology will be published where they provide valuable generic information on microbial ecology. Papers can deal with culturable and non-culturable forms of any type of microorganism: bacteria, archaea, filamentous fungi, yeasts, protozoa, cyanobacteria, algae or viruses. In addition, the journal will publish Perspectives, Current Opinion and Controversy Articles, Commentaries and Letters to the Editor on topical issues in microbial ecology. - Application of ecological theory to microbial ecology - Interactions and signalling between microorganisms and with plants and animals - Interactions between microorganisms and their physicochemical enviornment - Microbial aspects of biogeochemical cycles and processes - Microbial community ecology - Phylogenetic and functional diversity of microbial communities - Evolutionary biology of microorganisms
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