DiSalvo Susanne, Maness Negar, Braun Andrew, Tran My, Hofferkamp Andrew
Department of Biological Sciences, Southern Illinois University Edwardsville, Edwardsville, IL, United States.
Front Microbiol. 2025 May 2;16:1537073. doi: 10.3389/fmicb.2025.1537073. eCollection 2025.
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.
To better elucidate tripartite phage-bacteria-host interactions in real-time, we expanded the symbiosis system to include -specific phages. We isolated six environmental phages from soil samples using a multi-host enrichment approach. We also identified a functional prophage from monocultures of one of the symbiont strains implemented in the enrichment approach. These phages were evaluated across all three amoeba-associated symbiont species. Finally, we treated infected amoeba lines with select phage isolates and assessed their effects on symbiont prevalence and host fitness.
The isolated phages exhibited diverse plaquing characteristics and virion morphologies, collectively targeting 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.
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.
噬菌体通过对共生菌种群施加寄生压力,并通过选择、基因交换和原噬菌体整合促进细菌进化,从而影响细菌共生体与其宿主之间的相互作用。宿主生物也会调节噬菌体与细菌的相互作用,特定宿主环境可能会限制或促进噬菌体接触细菌共生体,或驱动其他表型或进化结果。
为了更好地实时阐明噬菌体-细菌-宿主三方相互作用,我们扩展了共生系统,使其包括特定噬菌体。我们使用多宿主富集方法从土壤样本中分离出六种环境噬菌体。我们还从富集方法中使用的一种共生菌菌株的单培养物中鉴定出一种功能性原噬菌体。对所有三种与变形虫相关的共生菌物种评估了这些噬菌体。最后,我们用选定的噬菌体分离株处理感染变形虫的细胞系,并评估它们对共生菌流行率和宿主适应性的影响。
分离出的噬菌体表现出不同的噬菌斑特征和病毒粒子形态,共同靶向属于每种变形虫共生菌物种的菌株。在变形虫处理实验之后,我们观察到在某些情况下应用噬菌体降低了共生菌感染流行率并减轻了对宿主适应性的影响,而在其他情况下,则未观察到显著影响。值得注意的是,噬菌体能够在多次传代培养中在感染共生菌的变形虫群体中持续存在,表明存在潜在的长期相互作用。
这些发现突出了宿主环境中噬菌体-共生菌相互作用的可变性,并强调了噬菌体治疗结果的复杂性。观察到的可变性为未来探索三方系统长期动态的研究奠定了基础,提示了可能塑造不同噬菌体治疗结果的潜在机制,并为未来研究提供了有价值的途径。