Symbiont loss and gain, rather than co-diversification shapes honeybee gut microbiota diversity and function

Aiswarya Prasad, Asha Devi Pallujam, Rajath Siddaganga, Ashwin Suryanarayanan, Florent Mazel, Axel Brockmann, Sze Huei Yek, Philipp Engel
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Abstract

Studying gut microbiota evolution across animals is crucial for understanding symbiotic interactions but is hampered by the lack of high-resolution genomic data. Honeybees, with their specialized gut microbiota and well-known ecology, offer an ideal system to study this evolution. Using shotgun metagenomics on 200 honeybee workers from five species, we recovered thousands of metagenome-assembled genomes, identifying several novel bacterial species. While microbial communities were mostly host-specific, we found both specialist and generalist bacteria, even among closely related species, with notable variation between host species. Some generalists emerged host-specific only at the strain level, suggesting recent host switches. Unexpectedly, we found no evidence of codiversification between hosts and symbionts. Instead, symbiont gains, losses, and replacements led to functional differences, such as the ability to degrade pollen-derived pectin. Our results provide new insights into gut microbiota evolution and uncover the functional potential of the previously underexplored gut microbiota of these important pollinators.
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影响蜜蜂肠道微生物群多样性和功能的是共生菌的损耗和增殖,而非共同多样化
研究动物肠道微生物群的进化对于了解共生互动至关重要,但由于缺乏高分辨率的基因组数据而受到阻碍。蜜蜂拥有专门的肠道微生物群和著名的生态学,为研究这种进化提供了一个理想的系统。通过对来自五个物种的200只蜜蜂工蜂进行猎枪元基因组学研究,我们恢复了数以千计的元基因组组装基因组,并确定了几个新的细菌物种。虽然微生物群落大多具有宿主特异性,但我们发现既有专性细菌,也有通性细菌,即使在亲缘关系很近的物种之间也是如此。一些通性细菌仅在菌株水平出现了宿主特异性,这表明宿主最近发生了转换。出乎意料的是,我们没有发现宿主和共生体之间有代码共享的迹象。相反,共生体的增减和替换导致了功能上的差异,例如降解花粉衍生果胶的能力。我们的研究结果为肠道微生物群的进化提供了新的见解,并揭示了这些重要传粉昆虫的肠道微生物群以前未被充分探索的功能潜力。
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