The Keys to Controlling Wheat Rusts: Identification and Deployment of Genetic Resistance

Author:

Norman Michael12ORCID,Bariana Harbans3,Bansal Urmil1ORCID,Periyannan Sambasivam4ORCID

Affiliation:

1. School of Life and Environmental Sciences, Faculty of Science, The University of Sydney Plant Breeding Institute, 107 Cobbitty Road, Cobbitty, NSW 2570, Australia

2. Commonwealth Scientific and Industrial Research Organization Agriculture and Food, Canberra, ACT 2601, Australia

3. School of Science, Western Sydney University, Bourke Road, Richmond, NSW 2753, Australia

4. School of Agriculture and Environmental Science & Centre for Crop Health, University of Southern Queensland, Toowoomba, Qld 4350, Australia

Abstract

Rust diseases are among the major constraints for wheat production worldwide due to the emergence and spread of highly destructive races of Puccinia. The most common approach to minimize yield losses due to rust is to use cultivars that are genetically resistant. Modern wheat cultivars, landraces, and wild relatives can contain undiscovered resistance genes, which typically encode kinase or nucleotide-binding site leucine rich repeat (NLR) domain containing receptor proteins. Recent research has shown that these genes can provide either resistance in all growth stages (all-stage resistance; ASR) or specially in later growth stages (adult-plant resistance; APR). ASR genes are pathogen and race-specific, meaning can function against selected races of the Puccinia fungus due to the necessity to recognize specific avirulence molecules in the pathogen. APR genes are either pathogen-specific or multipathogen resistant but often race-nonspecific. Prediction of resistance genes through rust infection screening alone remains complex when more than one resistance gene is present. However, breakthroughs during the past half century such as the single-nucleotide polymorphism-based genotyping techniques and resistance gene isolation strategies like mutagenesis, resistance gene enrichment, and sequencing (MutRenSeq), mutagenesis and chromosome sequencing (MutChromSeq), and association genetics combined with RenSeq (AgRenSeq) enables rapid transfer of resistance from source to modern cultivars. There is a strong need for combining multiple genes for better efficacy and longer-lasting resistance. Hence, techniques like gene cassette creation speeds up the gene combination process, but their widespread adoption and commercial use is limited due to their transgenic nature.

Funder

Sydney Institute of Agriculture, University of Sydney

Commonwealth Scientific and Industrial Research Organization

Publisher

Scientific Societies

Subject

Plant Science,Agronomy and Crop Science

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