2027-W13 How do bacteriophages shape microbial communities and ecological functions in plant environments?

PROJECT HIGHLIGHTS

  • Determines how bacteriophages reshape the diversity, composition and resilience of plant-associated microbial communities. 
  • Establishes the ecological consequences of phage-driven microbiome change for pathogen suppression and plant function. 
  • Generates fundamental knowledge of phage-microbiome interactions to support sustainable management of plant health and disease. 

Overview

The plant microbiome, particularly within the phyllosphere (above-ground surfaces) and rhizosphere (root-associated zone), plays a fundamental role in plant health, nutrient cycling, pathogen suppression and ecosystem function [1]. While bacteria and fungi within these communities have been extensively studied, much less is known about the ecological role of bacteriophages: viruses that infect bacteria and are abundant components of plant-associated microbial communities [2,3]. 

Phages can selectively reduce bacterial populations and alter competition between microbial taxa, potentially restructuring entire communities. However, we do not yet understand the extent to which phages act as ecological drivers within plant environments, whether phage-induced changes persist or communities recover following disturbance, or what these changes mean for microbial function and plant health. 

Our recent work showed that application of a phage cocktail targeting Pseudomonas syringae did not significantly alter overall microbial diversity on cherry leaves and shoots (Fig.1) [4]. However, measures of overall diversity alone cannot reveal changes in individual microbial taxa, community structure, ecological interactions or function. This raises an important question: what are the wider ecological consequences when phages exert pressure on plant-associated microbial communities? 

This project will determine how phage pressure influences the composition, diversity, structure and resilience of microbial communities within the phyllosphere and rhizosphere. Using controlled plant and microcosm experiments combined with microbiome and virome sequencing, we will track how bacterial, fungal and viral communities respond to phage disturbance over time. 

We will then determine whether phage-driven community changes alter important ecological functions, including pathogen suppression and interactions between microbial community members. Finally, metabolomics and transcriptomics will establish whether changes within the microbiome are associated with altered plant biochemical and molecular responses. 

By linking phage pressure, microbiome structure, ecological function, plant response, this project will establish the wider ecological role of bacteriophages in plant environments and provide fundamental knowledge needed to understand the consequences of natural and applied phages for sustainable plant and ecosystem management. 

Figure 1. Alpha diversity indices of bacterial and fungal communities from cherry leaves sampled 3 and 30 days after treatment (DPT). The treatments were Pseudomonas syringae pv. syringae 9097, phage cocktail 5C, Pss combined with phage cocktail 5C, and a control. Diversity was evaluated using three indices: Chao1, estimating the total number of species per sample; Shannon’s index, reflecting community diversity (higher values indicate greater diversity); and Simpson’s index, reflecting community evenness (higher values indicate a more even community) [4]. 

Six boxplots comparing bacterial (16S) and fungal (ITS) alpha diversity across four treatments and two DPT levels (3 and 30). Diversity is measured using Chao1 richness, Shannon diversity, and Simpson diversity indices. Bacterial richness and diversity generally vary among treatments, while fungal diversity shows more modest differences. Points represent individual samples and boxes show the distribution of values within each group.

This project is a CENTA Flagship Project.

Case Projects

This project offers a CASE studentship

Host

Theme

Supervisors

Project investigator

Co-investigators

How to apply

Each host has a slightly different application process.
Find out how to apply for this studentship.

All applications must include the CENTA application form.
Choose your application route

  1. How does phage pressure alter the structure and resilience of plant microbial communities? Leaf and rhizosphere samples will be collected from selected crop species and subjected to controlled phage perturbation experiments. Communities will be sampled longitudinally before and after phage exposure to determine the magnitude, persistence and recovery of microbiome responses. Metagenomic sequencing, together with virome sequencing, will characterise bacterial, fungal and phage communities. Changes in diversity, community composition, taxa and community resilience will be quantified. 
  2. What are the ecological consequences of phage-driven microbiome change? Bacteria, fungi and phages will be isolated from control and phage-perturbed communities. Their interactions and ability to suppress plant-pathogenic bacteria will be investigated individually and within microbial consortia to determine whether phage-driven changes in community composition alter ecological function. 

DRs will be awarded CENTA Training Credits (CTCs) for participation in CENTA-provided and ‘free choice’ external training. One CTC can be earned per 3 hours training, and DRs must accrue 100 CTCs across the three and a half years of their PhD.  

The doctoral researcher will receive multidisciplinary training in microbial ecology, bacteriophage biology, plant-microbe interactions, field and controlled-environment experimentation, microbiome and virome sequencing, metabolomics, transcriptomics, bioinformatics, statistics and integration of complex multi-omics datasets. 

Training at Warwick will provide expertise in experimental design, microbial and phage isolation, community profiling, functional microbiology and analysis and interpretation of large sequencing and multi-omics datasets. The CASE partnership with Carus Animal Health Ltd will complement this academic training through experience of industrial research, translation of phage science, product development and assessment of the wider environmental implications of applied biological products. 

Carus Animal Health Ltd will act as the industrial CASE partner and contribute to project development, co-supervision and doctoral training. The student will undertake a placement with Carus, gaining experience in translating fundamental phage ecology into industrial research and product-development considerations. Training will include the development and application of phage-based biological products and consideration of how microbiome and ecological-impact data inform product development, environmental assessment and responsible deployment. Carus will provide industrial expertise, access to relevant facilities and resources, and financial support for the CASE placement and associated research activities. 

  • Year 1 – Establishing phage-microbiome systems Field and controlled-environment experimental design and training will be completed. Phyllosphere and rhizosphere samples will be collected from selected crop systems. Bacterial, fungal and phage communities will be characterised and controlled phage-perturbation experiments established. Longitudinal sampling will determine immediate and longer-term community responses to phage pressure. 
  • Year 2 – Microbiome structure, dynamics and resilience 16S rRNA and ITS amplicon sequencing and virome sequencing will characterise bacterial, fungal and phage communities across treatments and time points. Bioinformatic and ecological analyses will identify changes in diversity, community composition, individual taxa and community resilience. Microorganisms from control and phage-perturbed communities will be isolated for functional studies. 
  • Year 3 – Ecological function and plant response Microbial isolates and reconstructed consortia will be used to determine whether phage-driven community changes affect pathogen suppression and other microbial interactions. Plant tissues associated with contrasting microbial communities will undergo untargeted metabolomics and transcriptomic analysis to determine whether microbiome changes influence plant biochemical and molecular responses.  
  • Year 3.5 – Integration and synthesis Microbiome, virome, functional, metabolomic and transcriptomic datasets will be integrated to determine relationships between phage pressure, microbial community structure, ecological function and plant response. Final analyses, manuscripts and the PhD thesis will be completed. 
  1. Trivedi P, Leach JE, Tringe SG, Sa T, Singh BK. Plant–microbiome interactions: from community assembly to plant health. Nat Rev Microbiol. 2020;18(11):607–621. DOI: https://doi.org/10.1038/s41579-020-0412-1 
  2. Fitzpatrick CR, Copeland J, Wang PW, et al. Assembly and ecological function of the root microbiome across angiosperm plant species. Proc Natl Acad Sci USA. 2018;115(6):E1157–E1165. DOI: https://doi.org/10.1073/pnas.1717617115 
  3. Koskella B, Brockhurst MA. Bacteria–phage coevolution as a driver of ecological and evolutionary processes in microbial communities. FEMS Microbiol Rev. 2014;38(5):916–931. DOI: https://doi.org/10.1111/1574-6976.12072 
  4. Papp‑Rupar M, Grace ER, Korotania N, Ciusa ML, Jackson RW, Rabiey M. Impact of Phage Therapy on Pseudomonas syringae pv. syringae and Plant Microbiome Dynamics Through Coevolution and Field Experiments. Environ Microbiol. 2025 Mar;27(3):e70076. DOI: https://doi.org/10.1111/1462-2920.70076  
  5. Chaturongakul S, Ounjai P, Pholwat S, et al. Phage–host interaction: an ecological perspective. J Bacteriol. 2004 Jun;186(12):3677–3686. doi: 10.1128/JB.186.12.3677-3686.2004 
  6. Mazor Y, Greenberg I, Toporik H, et al. Novel phages of Pseudomonas syringae unveil numerous potential auxiliary metabolic genes. J Gen Virol. 2024;105:001990. DOI: https://doi.org/10.1099/jgv.0.001990  
  7. Morella NM, Gomez AL, Wang G, Leung MS, Koskella B. The impact of bacteriophages on phyllosphere bacterial abundance and composition. Mol Ecol. 2018;27(8):2025–2038. DOI: https://doi.org/10.1111/mec.14542  
  8. Hampton HG, Watson BNJ, Fineran PC. The arms race between bacteria and their phage foes. Nature. 2020;577(7790):327–336. DOI: https://doi.org/10.1038/s41586-019-1894-8  
  9. Warring SL, Sisson HM, Fineran PC, Rabiey M. Strategies for the biocontrol of Pseudomonas infections pre‑fruit harvest. Microb Biotechnol. 2024;17(3):700–712. DOI: https://doi.org/10.1111/1751-7915.70017  
  10. Fems Microbiol Ecol. The role of rhizosphere phages in soil health. FEMS Microbiol Ecol. 2024;100(5):fiae052. DOI: https://doi.org/10.1093/femsec/fiae052  

Further details and How to Apply

Ethical, genetic and biological risk 

We are not carrying out experiments on organisms that necessitate ethical or other types of approvals or licenses, other than necessary APHA compliance. There is no genetic or biological risk, as all bacteria are sourced directly from the UK natural environment. There are no plans to release genetically modified organisms during this project. This work is approved by the UoW under existing genetic manipulation and biological safety committee project. 

For any enquiries related to this project please contact Mojgan Rabiey ([email protected]). 

To apply to this project:  

  • You must include a CV with the names of at least two referees (preferably three) who can comment on your academic abilities.  

 Applications must be submitted by 23:59 GMT on Wednesday 6th January 2027.   

you are here:
Skip to content