Bacterial pathogens are diverse and important enemies of plants. In agriculture, these pathogens cause significant destruction of crops and necessitate costly applications of antibiotics. How is it that wild plants are able to resist infection by these same bacteria? If the resistance mechanisms of wild plants can be identified, they can be used to improve the resistance of crops. Towards this goal, this research team has discovered that some wild collected plants of Arabidopsis thaliana are dramatically more resistant to infection by the virulent bacterial pathogen, Pseudomonas syringae pv. tomato DC3000. The focus of the current project is to understand how elevated resistance in these plants is accomplished. For this purpose, the researchers use a powerful new approach, genome-wide association mapping, combined with mining of microarray data on gene expression, to identify focal candidate genes. RNAi knockdown lines will be created for these focal genes in the Stewart Lab and characterized in the Traw Lab for defects in plant resistance. In addition, plants lacking functional copies of these genes will be complemented with resistance allele candidates in both labs and tested in the Traw Lab to determine whether resistance is restored to those lines. Finally, given suspected roles of several candidates in membrane transport, broad and focused metabolite screening will be conducted by the Traw Lab using a subset of the experimental lines. One of the novel candidate genes is involved in the downstream response to abscisic acid. Allelic variation at that locus may therefore help explain how this bacterial pathogen is able to hijack the abscisic acid pathway in some plants. Thus, the project will provide strong insights into the mechanisms of natural plant resistance to bacteria. The findings are likely to contribute to the improvement of crop yields and reduction of exogenous antibiotic use in agriculture. The research may also contribute to improved treatment of bacterial diseases in humans. The project will advance the training of two postdocs and a graduate student, and will be used to create a series of laboratories that can be used in the teaching of introductory biology.

Project Report

Bacterial pathogens are diverse and important enemies of plants. In agriculture, these pathogens cause significant destruction of crops and necessitate costly applications of antibiotics. However, certain plants of natural variation have been found to be able to resist infection by these same bacteria. If the resistance mechanisms of wild plants can be identified, they can be used to improve the resistance of crops. Towards this goal, this research team has discovered that some wild collected plants of Arabidopsis thaliana are dramatically more resistant to infection by the virulent bacterial pathogen, Pseudomonas syringae pv. tomato DC3000. The project greatly increased our understanding about how elevated resistance in these plants is accomplished. For this purpose, by used a powerful new approach, genome-wide association mapping, combined with mining of microarray data on gene expression, focal candidate genes have been identified. RNAi knockdown lines had been created for these focal genes in the Stewart Lab and been characterized for defects in plant resistance. In addition, plants lacking functional copies of these genes had been complemented with resistance allele candidates in Stewart Lab and tested in the Traw Lab (Pitt) to determine whether resistance is restored to those lines. One of the novel candidate genes, AtABCG16 has been shown to be involved in the downstream response to abscisic acid. Transgenic plants having overexpression or RNAi knockdown of this gene, were generated. The membrane localization and expression profiles of the gene were studied using GFP and GUS transgenic plants. Allelic variation at that locus may therefore help explain how this bacterial pathogen is able to hijack the abscisic acid pathway in some plants. Thus, the project has provided strong insights into the mechanisms of natural plant resistance to bacteria. The findings are likely to contribute to the improvement of crop yields and reduction of exogenous antibiotic use in agriculture. The research may also contribute to improved treatment of bacterial diseases in humans.

Agency
National Science Foundation (NSF)
Institute
Division of Integrative Organismal Systems (IOS)
Application #
1051581
Program Officer
Michael Mishkind
Project Start
Project End
Budget Start
2011-05-01
Budget End
2014-04-30
Support Year
Fiscal Year
2010
Total Cost
$222,740
Indirect Cost
Name
University of Tennessee Institute of Agriculture
Department
Type
DUNS #
City
Knoxville
State
TN
Country
United States
Zip Code
37996