Microbiome diversity and composition across development stages of the Blue Orchard Bee, Osmia lignaria (Megachilidae)

IF 2.1 3区 生物学 Q3 MICROBIOLOGY
Bailey L. Crowley, Robert N. Schaeffer
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Abstract

Host-associated microbes are increasingly recognized as important drivers of bee health. Surveys of bee microbiomes have primarily sampled social bees, yet non-social bees constitute the majority of species. We employed 16S and ITS amplicon sequencing to describe the diversity and composition of bacterial and fungal communities across multiple developmental stages of Osmia lignaria, an important native and managed solitary mason bee. Bacterial and fungal diversity were not significantly different across bee development. However, the composition of bacteria and fungi significantly changed between larval and fully pigmented adult stages, in agreement with dramatic changes in host morphology during metamorphosis. Many of the microbial taxa found in provisions were also present in larvae, indicating that immature bees likely acquire their microbiome from food. Notably, the most prevalent bacterial genus was Arsenophonus, a symbiont with many recorded phenotypes, ranging from reproductive parasitism to beneficial endosymbiont. Arsenophonus was found in samples from provisions and eggs, yet reached higher read counts in larvae and fully pigmented adults. The Arsenophonus amplicon sequencing variants (ASVs) detected in this study had high sequence similarity with a symbiont that displays the son-killing phenotype, suggesting that the ASVs in O. lignaria are also reproductive parasites. The causative agent of chalkbrood disease in bees, Ascosphaera, was also detected in provisions and larvae. Most other taxa present were plant pathogens or commonly found in soil. This study highlights that O. lignaria may harbor horizontally and vertically transmitted microbial taxa with diverse consequences for bee fitness.

Abstract Image

蓝色果园蜂茭白(Megachilidae)各发育阶段微生物组的多样性和组成
宿主相关微生物越来越被认为是影响蜜蜂健康的重要因素。对蜜蜂微生物组的调查主要以社会性蜜蜂为取样对象,但非社会性蜜蜂却占蜜蜂物种的大多数。我们采用 16S 和 ITS 扩增片段测序技术,描述了一种重要的本地和管理独居石匠蜂 Osmia lignaria 在多个发育阶段中细菌和真菌群落的多样性和组成。在蜜蜂的不同发育阶段,细菌和真菌的多样性没有显著差异。然而,细菌和真菌的组成在幼虫期和完全色素化的成虫期之间发生了显著变化,这与变态过程中宿主形态的巨大变化是一致的。在饲料中发现的许多微生物类群也存在于幼虫体内,这表明未成熟蜜蜂很可能从食物中获得微生物群。值得注意的是,最常见的细菌属是Arsenophonus,这种共生体有许多表型记录,从生殖寄生到有益的内共生。在食物和卵的样本中都发现了 Arsenophonus,但在幼虫和完全色素化的成虫中读数更高。本研究中检测到的胂虫扩增子测序变体(ASVs)与具有杀子表型的共生体序列相似度很高,这表明木犀属褐藻中的ASVs也是生殖寄生虫。蜜蜂垩病的病原体 Ascosphaera 也在蜂粮和幼虫中被检测到。其他分类群大多是植物病原体或土壤中常见的病原体。这项研究表明,木质素树可能藏有横向和纵向传播的微生物类群,对蜜蜂的健康产生不同的影响。
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来源期刊
Symbiosis
Symbiosis 生物-微生物学
CiteScore
4.80
自引率
8.00%
发文量
56
审稿时长
>12 weeks
期刊介绍: Since 1985, Symbiosis publishes original research that contributes to the understanding of symbiotic interactions in a wide range of associations at the molecular, cellular and organismic level. Reviews and short communications on well-known or new symbioses are welcomed as are book reviews and obituaries. This spectrum of papers aims to encourage and enhance interactions among researchers in this rapidly expanding field. Topics of interest include nutritional interactions; mutual regulatory and morphogenetic effects; structural co-adaptations; interspecific recognition; specificity; ecological adaptations; evolutionary consequences of symbiosis; and methods used for symbiotic research.
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