Susanne DiSalvo, Negar Maness, Andrew Braun, My Tran, Andrew Hofferkamp
{"title":"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。","authors":"Susanne DiSalvo, Negar Maness, Andrew Braun, My Tran, Andrew Hofferkamp","doi":"10.3389/fmicb.2025.1537073","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>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.</p><p><strong>Methods: </strong>To better elucidate tripartite phage-bacteria-host interactions in real-time, we expanded the <i>Dictyostelium discoideum-Paraburkholderia</i> symbiosis system to include <i>Paraburkholderia</i>-specific phages. We isolated six environmental <i>Paraburkholderia</i> phages from soil samples using a multi-host enrichment approach. We also identified a functional prophage from monocultures of one of the <i>Paraburkholderia</i> symbiont strains implemented in the enrichment approach. These phages were evaluated across all three amoeba-associated <i>Paraburkholderia</i> symbiont species. Finally, we treated <i>Paraburkholderia</i> infected amoeba lines with select phage isolates and assessed their effects on symbiont prevalence and host fitness.</p><p><strong>Results: </strong>The isolated phages exhibited diverse plaquing characteristics and virion morphologies, collectively targeting <i>Paraburkholderia</i> 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.</p><p><strong>Discussion: </strong>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.</p>","PeriodicalId":12466,"journal":{"name":"Frontiers in Microbiology","volume":"16 ","pages":"1537073"},"PeriodicalIF":4.0000,"publicationDate":"2025-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12081417/pdf/","citationCount":"0","resultStr":"{\"title\":\"Tracking tripartite interaction dynamics: isolation, integration, and influence of bacteriophages in the <i>Paraburkholderia-Dictyostelium discoideum</i> symbiosis system.\",\"authors\":\"Susanne DiSalvo, Negar Maness, Andrew Braun, My Tran, Andrew Hofferkamp\",\"doi\":\"10.3389/fmicb.2025.1537073\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>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.</p><p><strong>Methods: </strong>To better elucidate tripartite phage-bacteria-host interactions in real-time, we expanded the <i>Dictyostelium discoideum-Paraburkholderia</i> symbiosis system to include <i>Paraburkholderia</i>-specific phages. We isolated six environmental <i>Paraburkholderia</i> phages from soil samples using a multi-host enrichment approach. We also identified a functional prophage from monocultures of one of the <i>Paraburkholderia</i> symbiont strains implemented in the enrichment approach. These phages were evaluated across all three amoeba-associated <i>Paraburkholderia</i> symbiont species. Finally, we treated <i>Paraburkholderia</i> infected amoeba lines with select phage isolates and assessed their effects on symbiont prevalence and host fitness.</p><p><strong>Results: </strong>The isolated phages exhibited diverse plaquing characteristics and virion morphologies, collectively targeting <i>Paraburkholderia</i> 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.</p><p><strong>Discussion: </strong>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.</p>\",\"PeriodicalId\":12466,\"journal\":{\"name\":\"Frontiers in Microbiology\",\"volume\":\"16 \",\"pages\":\"1537073\"},\"PeriodicalIF\":4.0000,\"publicationDate\":\"2025-05-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12081417/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Frontiers in Microbiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.3389/fmicb.2025.1537073\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Microbiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3389/fmicb.2025.1537073","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
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.
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.