2009 Annual Report
1a.Objectives (from AD-416)
1) Develop rapid detection/diagnostic procedures for identifying new Pgt races in plant tissues and urediniospores;.
2)Organize and conduct training courses for National Plant Diagnostic Network (NDPN);.
3)Use new detection/diagnostic procedures to monitor for wheat rust urediniospores, including new Pgt races in rain samples across central and southern U.S.; and.
4)Improve resistance in wheat germplasm to new races of Pgt through marker selected selection.
1b.Approach (from AD-416)
There is an urgent need to develop a rapid PCR procedure for the diagnosis of Ug99. The present diagnostic method is based on infecting a set of wheat differential lines and evaluating avirulence/virulence phenotypes. A TaqMan PCR will be developed based on the current genome sequence of P. graminis f. sp. tritici and the resequencing of several isolates (including Ug99 and two variants). Comparison of genomic sequences will identify potential DNA targets for assay development. A suite of real-time assays will be combined to identify individual variants within the Ug99 genetic lineage. Plant Diagnostic Center technicians will be trained to implement the new combination assay for detecting Ug99 in wheat and barley. A second more sensitive assay will be developed to detect low concentrations of Ug99 spores in rainwater. The increased sensitivity will be achieved by integrating TaqMan assays in a nested design. This sensitive nested assay design will be used to detect Ug99 spores in rain samples collected from the nationwide NADP/NTN network. This detection will help monitor long distance transport of Ug99 spores and validate stem rust aerobiological model predictions. In addition, rain samples will be monitored for P. graminis and P. triticina to better understand the movement of rust spores through the central and southern U.S. Finally, marker-selected-selection will be used to facilitate movement of known stem rust resistance genes into advanced lines of wheat.
DNA sequence data was analyzed and candidate target regions for developing Ug99 specific assay were identified. One hundred and fifty-two primers were designed and tested. Twenty-five probes were developed and testing has begun.
Regular e-mails, telephone calls and meetings were used to plan and coordinate the project.