跟踪三方相互作用动力学:副叶氏菌-盘状盘齿钢菌共生系统中噬菌体的分离、整合和影响。

IF 4 2区 生物学 Q2 MICROBIOLOGY
Frontiers in Microbiology Pub Date : 2025-05-02 eCollection Date: 2025-01-01 DOI:10.3389/fmicb.2025.1537073
Susanne DiSalvo, Negar Maness, Andrew Braun, My Tran, Andrew Hofferkamp
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引用次数: 0

摘要

噬菌体通过对共生群体施加寄生压力,并通过选择、基因交换和噬菌体整合促进细菌进化,从而影响细菌与宿主之间的相互作用。宿主生物也调节噬菌体与细菌的相互作用,宿主特异性环境可能限制或促进噬菌体进入细菌共生体或驱动替代表型或进化结果。方法:为了更好地实时阐明噬菌体-细菌-宿主三方相互作用,我们扩展了盘状盘基骨菌-副aburkholderia共生系统,纳入了副aburkholderia特异性噬菌体。我们使用多宿主富集方法从土壤样品中分离出六种环境副aburkholderia噬菌体。我们还从富集方法中实现的副aburkholderia共生菌株之一的单一培养中鉴定了一个功能性的前噬菌体。这些噬菌体在所有三种与变形虫相关的拟乌氏菌共生物种中进行了评估。最后,我们选择噬菌体分离物处理副阿布霍尔德菌感染的阿米巴原虫系,并评估其对共生体流行率和宿主适应性的影响。结果:分离的噬菌体表现出不同的斑块特征和病毒粒子形态,共同靶向属于每一种阿米巴共生物种的拟aburkholderia菌株。在阿米巴原虫处理实验中,我们观察到噬菌体在某些情况下降低了共生体感染的患病率,减轻了宿主的适应性影响,而在其他情况下,没有显著的影响。值得注意的是,噬菌体能够在多次培养转移中持续存在于共生体感染的阿米巴原虫种群中,这表明潜在的长期相互作用。讨论:这些发现突出了宿主环境中噬菌体-共生体相互作用的可变性,并强调了噬菌体治疗结果的复杂性。观察到的变异性为未来研究三方系统的长期动态奠定了基础,提示了可能形成不同噬菌体治疗结果的潜在机制,并为未来的研究提供了有价值的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tracking tripartite interaction dynamics: isolation, integration, and influence of bacteriophages in the Paraburkholderia-Dictyostelium discoideum symbiosis system.

Introduction: Bacteriophages influence interactions between bacterial symbionts and their hosts by exerting parasitic pressure on symbiont populations and facilitating bacterial evolution through selection, gene exchange, and prophage integration. Host organisms also modulate phage-bacteria interactions, with host-specific contexts potentially limiting or promoting phage access to bacterial symbionts or driving alternative phenotypic or evolutionary outcomes.

Methods: To better elucidate tripartite phage-bacteria-host interactions in real-time, we expanded the Dictyostelium discoideum-Paraburkholderia symbiosis system to include Paraburkholderia-specific phages. We isolated six environmental Paraburkholderia phages from soil samples using a multi-host enrichment approach. We also identified a functional prophage from monocultures of one of the Paraburkholderia symbiont strains implemented in the enrichment approach. These phages were evaluated across all three amoeba-associated Paraburkholderia symbiont species. Finally, we treated Paraburkholderia infected amoeba lines with select phage isolates and assessed their effects on symbiont prevalence and host fitness.

Results: The isolated phages exhibited diverse plaquing characteristics and virion morphologies, collectively targeting Paraburkholderia strains belonging to each of the amoeba-symbiotic species. Following amoeba treatment experiments, we observed that phage application in some cases reduced symbiont infection prevalence and alleviated host fitness impacts, while in others, no significant effects were noted. Notably, phages were able to persist within the symbiont-infected amoeba populations over multiple culture transfers, indicating potential long-term interactions.

Discussion: These findings highlight the variability of phage-symbiont interactions within a host environment and underscore the complex nature of phage treatment outcomes. The observed variability lays the foundation for future studies exploring the long-term dynamics of tripartite systems, suggesting potential mechanisms that may shape differential phage treatment outcomes and presenting valuable avenues for future investigation.

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来源期刊
CiteScore
7.70
自引率
9.60%
发文量
4837
审稿时长
14 weeks
期刊介绍: Frontiers in Microbiology is a leading journal in its field, publishing rigorously peer-reviewed research across the entire spectrum of microbiology. Field Chief Editor Martin G. Klotz at Washington State University is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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