A new study from Rothamsted Research has developed a pipeline to help expedite the discovery of microbial compounds with the potential to become future fungicide leads.
The work uses a high-throughput in vitro bioassay to identify environmental bacterial isolates that antagonise septoria tritici, before combining this with genome mining, mutagenesis and analytical chemistry to pinpoint the compounds responsible.
The pipeline was developed within Rothamsted’s Growing Health Institute Strategic Programme and supported by UKRI through the Biotechnology and Biological Sciences Research Council (BBSRC).
In the study, the team screened a library of 534 environmental Pseudomonas isolates and identified 52 that could suppress a standard septoria tritici strain. They then tested selected promising bacterial isolates against a genetically diverse septoria tritici panel of 12 isolates collected from across Europe.
This revealed significant differences in how strongly different fungal isolates were inhibited, showing that activity against a single reference strain may not tell the whole story. The findings make a clear case for testing future antifungal leads against genetically diverse pathogen panels earlier in discovery, rather than assuming that one strain can stand in for the wider pathogen population.
The team then began to uncover the biology behind the effect. Their analysis pointed to bacterial genes linked to the production of antifungal molecules, including the known antifungal compound 2,4-diacetylphloroglucinol (2,4-DAPG). In a proof-of-concept experiment, disruption of a key gene involved in 2,4-DAPG production caused the bacterial mutant to lose both 2,4-DAPG production and its ability to visibly inhibit septoria tritici the assay.
Crucially, the study also identified antagonistic isolates whose activity could not be readily explained by similarity to known reference gene clusters. That suggests some strains may produce previously unknown antifungal molecules, giving researchers a practical route to prioritise the most promising candidates for further investigation.
Dr George Lund, lead author of the study at Rothamsted Research, said:
“Septoria tritici remains a major challenge for wheat production, and new solutions are urgently needed for farmers. What this pipeline gives us is a practical way to search for future fungicide leads from bacteria in a much more informed way. It also allows us to test candidates against genetically diverse septoria isolates early in the process. That matters because activity seen against one strain may not always translate across the wider pathogen population, so this gives us a better way to decide which microbial metabolites are most worth pursuing.”
Dr Tim Mauchline, senior author at Rothamsted Research, said: “The development of microbiome facilitated agriculture relies on researchers understanding microbial function to enhance agricultural production. The work in this study allows us to mine and fast-track the deployment of candidate fungicidal bacteria for biological control as well as to identify novel chemistry for the next generation of synthetic fungicides.”
Although the work was carried out in vitro and does not yet demonstrate field performance, it establishes a scalable and cost-effective route for finding and prioritising candidate antifungal metabolites against septoria tritici. The same platform could also help researchers test whether promising molecules have activity against other fungal pathogens in future studies.
