Strain diversity and host specificity of the gut symbiont Gilliamella in Apis mellifera, Apis cerana and Bombus terrestris.

IF 6.1 1区 生物学 Q1 MICROBIOLOGY Microbiological research Pub Date : 2025-01-06 DOI:10.1016/j.micres.2025.128048
Nihong Zhou, Qiulan Zheng, Yao Liu, Zhichu Huang, Ye Feng, Yanping Chen, Fuliang Hu, Huoqing Zheng
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Abstract

Social bees, with their specialized gut microbiota and societal transmission between individuals, provide an ideal model for studying host-gut microbiota interactions. While the functional disparities arising from strain-level diversity of gut symbionts and their effects on host health have been studied in Apis mellifera and bumblebees, studies focusing on host-specific investigations of individual strains across different honeybee hosts remain relatively unexplored. In this study, the complete genomic sequences of 17 strains of Gilliamella from A. mellifera, Apis cerana and Bombus terrestris were analyzed. The analysis revealed that the strains of A. mellifera display a more expansive genomic and functional content compared to the strains of A. cerana and B. terrestris. Phylogenetic analysis showed a deep divergence among the Gilliamella strains from different hosts. Additionally, biochemistry tests and antibiotic susceptibility tests revealed that gut strains from A. mellifera exhibited a more extensive pathway for carbohydrate metabolism and a greater resistance to antibiotics than gut strains from A. cerana and B. terrestris. Strains from A. mellifera and A. cerana showed higher colonization efficiency and competitive ability whithin their respective host species, indicating a higher degree of host-specific adaptation of local gut microbiota. In addition, colonization by A. mellifera-derived strain triggers a stronger transcriptional response in the host than A. cerana-derived strain. The variation in the number of differentially expressed genes and the involvement of distinct signaling pathways across these two host species suggest species-specific adaptations to Gilliamella strains. These findings suggest that despite occupying similar niches in the bee gut, strain-level variations can influence microbial functions, and their impact on host physiological functions may vary across different strains.

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蜜蜂、中国蜜蜂和地蜂肠道共生体吉利菌的菌株多样性和宿主特异性。
群居蜜蜂具有特殊的肠道微生物群和个体之间的社会传播,为研究宿主-肠道微生物群相互作用提供了理想的模型。虽然已经在蜜蜂和大黄蜂中研究了肠道共生体菌株水平多样性引起的功能差异及其对宿主健康的影响,但对不同蜜蜂宿主中单个菌株的宿主特异性研究仍然相对较少。本研究分析了蜜蜂、蜜蜂和地蜂中17株吉利亚菌的全基因组序列。分析结果表明,与蜜蜂和陆地蜜蜂相比,蜜蜂蜜蜂具有更广泛的基因组和功能含量。系统发育分析表明,来自不同宿主的吉利亚菌菌株存在较深的差异。此外,生物化学试验和抗生素敏感性试验表明,蜜蜂肠道菌株比蜜蜂和地芽孢杆菌肠道菌株具有更广泛的碳水化合物代谢途径和更强的抗生素耐药性。蜜蜂和中华蜜蜂的菌株在各自的寄主物种中表现出更高的定植效率和竞争能力,表明当地肠道微生物群对寄主的适应程度更高。此外,蜜蜂a . mellifera衍生菌株的定殖在宿主体内引发的转录反应比蜜蜂a . cerana衍生菌株更强。差异表达基因数量的变化和不同信号通路在这两个宿主物种中的参与表明对吉利亚菌菌株的物种特异性适应。这些发现表明,尽管在蜜蜂肠道中占据相似的生态位,但菌株水平的变化可以影响微生物功能,并且它们对宿主生理功能的影响可能因菌株而异。
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来源期刊
Microbiological research
Microbiological research 生物-微生物学
CiteScore
10.90
自引率
6.00%
发文量
249
审稿时长
29 days
期刊介绍: Microbiological Research is devoted to publishing reports on prokaryotic and eukaryotic microorganisms such as yeasts, fungi, bacteria, archaea, and protozoa. Research on interactions between pathogenic microorganisms and their environment or hosts are also covered.
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