Award details

Impact of mutations in the target-encoding CYP51 gene in Mycosphaerella graminicola populations developing resistance to triazole fungicides.

Reference	BB/E021832/1
Principal Investigator / Supervisor	Professor Steven Kelly
Co-Investigators / Co-Supervisors	Professor Diane Kelly
Institution	Swansea University
Department	Institute of Life Science Medical School
Funding type	Research
Value (£)	291,703
Status	Completed
Type	Research Grant
Start date	01/02/2008
End date	31/01/2011
Duration	36 months

Abstract

The emergence of resistance to antifungal drugs and fungicides is an increasing challenge in the management of fungal diseases in agriculture and medicine. Human pathogenic fungi such as Candida have already developed resistance to triazole drugs and the mechanisms involved have been characterised, but not exhaustively. Less is known about the development of resistance in plant pathogens. Septoria leaf blotch, caused by Mycosphaerella graminicola, is the most important foliar disease of wheat in the UK and Europe. Almost all wheat crops (around 2 million hectares in the UK) receive one or more fungicide treatments to control Septoria, and triazoles are the most widely used compounds. There is evidence that the efficacy of triazoles in controlling M. graminicola has declined over the past 10 years, due to the emergence of strains with reduced sensitivity. The project aims to determine the exact contribution of mutations, individually and in combination, in the CYP51 gene encoding the sterol 14a-demethylase target for triazole fungicides, to reduced sensitivity of M. graminicola isolates, thereby clarifying the current status of evolution to resistance to triazoles in field populations. Sequencing of the CYP51 genes of recently characterised isolates of M. graminicola from fungicide-selected populations will identify which encoded amino acid alterations are most closely correlated with a reduced sensitivity phenotype. The emergence of these changes in the pathogen population in relation to triazole use will also be tracked by Pyrosequencing the CYP51 gene from M. graminicola DNA in historical wheat samples from the Broadbalk archive. Candidate mutations will be introduced into a 'sensitive' CYP51 M. graminicola gene, both as individual changes and in combination, by site directed mutagenesis. The effect of candidate mutations, and additional mutations not predicted to directly impact on triazole binding, but identified in the native CYP51 genes of M. graminicola.

Summary

The emergence of resistance to antifungal compounds is an increasing problem for the management of fungal diseases in agriculture and medicine. One of the most important groups of fungicides is the triazoles, used for the treatment of fungal infections of both crop plants and humans. Unfortunately, when fungi are exposed to these chemicals, the treatment can select for strains of the fungus that are less sensitive to the chemical. Over time, resistant strains of the fungus can develop and the chemical no longer controls the disease. This has happened with the human pathogenic yeast Candida, and there is now evidence that some plant pathogenic fungi are also becoming less sensitive to triazoles. The aim of this project is to understand the mechanisms responsible for these changes in sensitivity to triazoles in Mycosphaerella graminicola, the causal agent of Septoria leaf blotch, the most important foliar disease of wheat in the UK. This pathogen has already adapted to many of the fungicides used to control it. Resistance to the strobilurin fungicides, first detected in 2002, is now widespread in UK and European M. graminicola populations, so control of the disease now relies heavily on triazoles. Over the past decade there has been a gradual change in the sensitivity of the fungus to these fungicides so that higher doses are now required to achieve disease control. There is a growing concern, amongst both the agricultural and agrochemical industries, that further shifts in triazole sensitivity will reduce our ability to manage this important disease. There are few new Septoria fungicides available, and the older chemicals used for Septoria control are more damaging to the environment. Several mechanisms are known to contribute to resistance to triazoles. These include changes in the target site protein, as well as participation of other proteins, known as transporters, that are able to pump the fungicide out of the fungus. Therefore, to understand how changes inthe target protein may affect triazole sensitivity, the altered forms of the protein must be expressed and studied in isolation. The proposed project aims to determine the effect on sensitivity of mutations in the triazole target protein, a cytochrome P450 called CYP51 involved in sterol 14a-demethylation. The research will assess how such mutations affect interactions between the fungicide and the protein, as well as the activity of the enzyme itself, using several approaches. The mutant proteins will be expressed in another fungus, the yeast Saccharomyces cerevisiae, to see how sensitivity to different triazoles is affected, and to make pure samples of the protein to measure enzyme activity, altered properties and inhibition. In particular the project will concentrate on several mutations that have occurred quite recently in M. graminicola populations exposed to triazole fungicides. We also intend to introduce further changes identified in Candida to the protein by targeted mutation to assess their effects on sensitivity and protein function. The project will provide key information on the contribution of target site mutations to the current status of M. graminicola azole sensitivity in the field and the potential for future resistance development. Information gained from these studies will be used to design novel molecular diagnostics to detect target site changes and monitor the occurrence of such changes in field populations of the fungus. This will show how the fungus evolves in response to treatment by different triazoles and help to devise control strategies to maintain the effectiveness of this group of chemicals against M. graminicola. Results should also aid the design of more effective triazole compounds. Furthermore, determining the relationship between target site changes, fungicide sensitivity and enzyme activity will improve understanding ofr the molecular evolution of the CYP51 protein in plant pathogenic fungi in response to selection.

Committee	Closed Committee - Agri-food (AF)
Research Topics	Crop Science, Microbiology, Plant Science
Research Priority	X – Research Priority information not available
Research Initiative	X - not in an Initiative
Funding Scheme	X – not Funded via a specific Funding Scheme

Associated awards:

BB/E02257X/1 Impact of mutations in the target-encoding CYP51 gene in Mycosphaerella graminicola populations developing resistance to triazole fungicides

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