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Susceptibility of Red Mason Bee Larvae to Bacterial Threats Due to Microbiome Exchange with Imported Pollen Provisions

机译:由于进口花粉规定,红梅森蜂幼虫对细菌威胁的易感性

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Solitary bees are subject to a variety of pressures that cause severe population declines. Currently, habitat loss, temperature shifts, agrochemical exposure, and new parasites are identified as major threats. However, knowledge about detrimental bacteria is scarce, although they may disturb natural microbiomes, disturb nest environments, or harm the larvae directly. To address this gap, we investigated 12 Osmia bicornis nests with deceased larvae and 31 nests with healthy larvae from the same localities in a 16S ribosomal RNA (rRNA) gene metabarcoding study. We sampled larvae, pollen provisions, and nest material and then contrasted bacterial community composition and diversity in healthy and deceased nests. Microbiomes of pollen provisions and larvae showed similarities for healthy larvae, whilst this was not the case for deceased individuals. We identified three bacterial taxa assigned to Paenibacillus sp. (closely related to P. pabuli/amylolyticus/xylanexedens ), Sporosarcina sp., and Bacillus sp. as indicative for bacterial communities of deceased larvae, as well as Lactobacillus for corresponding pollen provisions. Furthermore, we performed a provisioning experiment, where we fed larvae with untreated and sterilized pollens, as well as sterilized pollens inoculated with a Bacillus sp. isolate from a deceased larva. Untreated larval microbiomes were consistent with that of the pollen provided. Sterilized pollen alone did not lead to acute mortality, while no microbiome was recoverable from the larvae. In the inoculation treatment, we observed that larval microbiomes were dominated by the seeded bacterium, which resulted in enhanced mortality. These results support that larval microbiomes are strongly determined by the pollen provisions. Further, they underline the need for further investigation of the impact of detrimental bacterial acquired via pollens and potential buffering by a diverse pollen provision microbiome in solitary bees.
机译:孤独的蜜蜂受到造成严重人口下降的各种压力。目前,栖息地损失,温度变化,农用化学曝光和新寄生虫被确定为主要威胁。然而,关于有害细菌的知识是稀缺的,尽管它们可能会扰乱自然微生物,干扰巢环境,或直接伤害幼虫。为了解决这一差距,我们调查了12个Osmia Bicornis与死者的幼虫和31名巢穴,来自16S核糖体RNA(rRNA)基因成立研究的相同地区的健康幼虫。我们采样幼虫,花粉条款和巢材料,然后对比细菌群落组成和健康和已故巢穴的多样性。花粉条款和幼虫的微生物均显示出健康幼虫的相似之处,而死者个体则不为此。我们确定了三种分配给Paenibacillus sp的细菌征集。 (与P. pabuli / amylolyticus / Xylanexedens密切相关),SporoSarcina Sp。和芽孢杆菌。作为死亡的幼虫的细菌群落以及相应的花粉条款的细菌群落。此外,我们进行了一个休养实验,其中我们用未处理和灭菌的花粉喂养幼虫,以及用芽孢杆菌接种的灭菌花粉。孤立于死者的幼虫。未经处理的幼虫微生物酶与所提供的花粉的幼虫一致。仅杀菌的花粉不会导致急性死亡率,而幼虫没有微生物组。在接种治疗中,我们观察到幼虫微生物体由种子细菌支配,导致死亡率提高。这些结果支持幼虫微生物体强烈地由花粉条款确定。此外,它们强调了进一步调查通过在孤立蜜蜂中的各种花粉供应微生物组织的有害细菌的影响。

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