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蜜蜂(西方蜜蜂)蜂王质量:宿主-微生物转录组学探究年龄和后肠共生菌梅丽莎共生杆菌的影响

Honey bee (Apis mellifera) queen quality: host-microbial transcriptomes exploring the influence of age and hindgut symbiont Commensalibacter melissae.

作者信息

Copeland Duan C, Kortenkamp Oliver L, Mott Brendon M, Mason Charles J, Anderson Kirk E

机构信息

USDA-ARS Carl Hayden Bee Research Center, 2000 E. Allen Rd, Tucson, AZ, 85719, USA.

Department of Entomology and Center for Insect Science, University of Arizona, Tucson, AZ, 85721, USA.

出版信息

Anim Microbiome. 2025 May 2;7(1):41. doi: 10.1186/s42523-025-00408-w.

Abstract

Understanding the biological mechanisms underlying extreme lifespan variation within species remains a fundamental challenge in aging research. Here, we investigated the role of gut microbiota and age in honey bee (Apis mellifera) queens combining 16S rRNA gene sequencing and transcriptomics. Analysis of 40 queen hindguts revealed that Commensalibacter melissae (Alpha 2.1) relative abundance was significantly higher in young queens compared to old queens. Using queens with the highest and lowest C. melissae relative abundance, RNA sequencing identified 1451 differentially expressed genes associated with C. melissae abundance, twice the number associated with age alone (719 genes). Queens with high C. melissae abundance showed distinct transcriptional profiles related to stress response, protein homeostasis, and longevity-regulating pathways, particularly genes involved in oxidative stress response and cellular maintenance. Our analysis revealed complex relationships between age, C. melissae abundance, and gene expression patterns, suggesting that multiple interacting factors contribute to queen quality. These findings contribute to our understanding of host-microbe interactions in honey bee queens and highlight the intricate relationship between gut microbiota composition and host physiology in honey bees.

摘要

了解物种内极端寿命差异背后的生物学机制仍然是衰老研究中的一项基本挑战。在此,我们结合16S rRNA基因测序和转录组学,研究了肠道微生物群和年龄在蜜蜂(西方蜜蜂)蜂王中的作用。对40只蜂王的后肠分析表明,与老年蜂王相比,年轻蜂王中梅氏共生杆菌(Alpha 2.1)的相对丰度显著更高。利用梅氏共生杆菌相对丰度最高和最低的蜂王,RNA测序确定了1451个与梅氏共生杆菌丰度相关的差异表达基因,这一数量是仅与年龄相关的差异表达基因数量(719个基因)的两倍。梅氏共生杆菌丰度高的蜂王表现出与应激反应、蛋白质稳态和长寿调节途径相关的独特转录谱,特别是参与氧化应激反应和细胞维持的基因。我们的分析揭示了年龄、梅氏共生杆菌丰度和基因表达模式之间的复杂关系,表明多种相互作用的因素影响蜂王质量。这些发现有助于我们理解蜜蜂蜂王中宿主与微生物的相互作用,并突出了蜜蜂肠道微生物群组成与宿主生理之间的复杂关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0afc/12046910/5057fde86764/42523_2025_408_Fig1_HTML.jpg

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