VIEW ARTICLE

Genetics

Virulence and Molecular Polymorphism in Puccinia recondita f. sp. tritici in Canada. J. A. Kolmer, Research scientist, National Science and Engineering Research Council, Agriculture and Agri-Food Canada, Research Centre, 195 Dafoe Rd, Winnipeg, MB R3T 2M9; J. Q. Liu(2), and M. Sies(3). (2)Postdoctoral fellow, National Science and Engineering Research Council, Agriculture and Agri-Food Canada, Research Centre, 195 Dafoe Rd, Winnipeg, MB R3T 2M9; (3)Visiting student, Department of Phytopathology, Wageningen Agricultural University, P.O. Box 8025, 6700 EE, Wageningen, Netherlands. Phytopathology 85:276-285. Accepted for publication 20 October 1994. 1995 Department of Agriculture and Agri-Food, Government of Canada. DOI: 10.1094/Phyto-85-276.

Sixty-four representative single-uredinial isolates of Puccinia recondita f. sp. tritici collected from wheat in the eastern (Ontario and Quebec), prairie (Manitoba and Saskatchewan), and Pacific (Alberta and British Columbia) regions of Canada were analyzed for virulence polymorphism on 19 near-isogenic wheat differential lines and for randomly amplified polymorphic DNA (RAPD) using 10 arbitrary decamer primers. Thirty-seven phenotypes of P. r. tritici were distinguished by the 19 host differential lines. Fifteen molecular phenotypes were distinguished by the 10 primers in the RAPD analysis. Forty-five unique phenotypes of P. r. tritici were distinguished by combined virulence and RAPD data. Molecular variation was greatest between isolates of different virulence phenotypes. There was some molecular variation among isolates with identical virulences. Virulence and RAPD data were used separately and combined in cluster analyses. Two major clusters were distinguished with the combined data sets. The first cluster consisted of isolates virulent or avirulent to both resistance genes Lr2a and Lr2c, and the second cluster consisted of isolates avirulent to Lr2a and virulent to Lr2c. The molecular polymorphisms were more effective in distinguishing between the major clusters of P. r. tritici compared to the virulence polymorphisms. However, virulence polymorphisms were more effective in distinguishing between isolates within the major clusters compared to the molecular polymorphisms. There was a correlation of 0.58 between the virulence and molecular dissimilarity matrices. The cluster analyses indicated a general relationship between virulence and molecular polymorphism in P. r. tritici in Canada. There are currently two major groups of P. r. tritici in Canada. One group consists of isolates found in the prairie and eastern regions. Isolates in this group have limited molecular polymorphisms and consist of many virulence phenotypes that are either virulent or avirulent to both Lr2a and Lr2c. Isolates in the second group are found in eastern Canada and in the Pacific region. These isolates are avirulent to Lr2a and virulent to Lr2c and have molecular phenotypes distinct from isolates in the first group. The molecular data support conclusions from virulence survey data that distinct geographic populations of P. r. tritici exist in Canada and that new virulences arise and increase in the prairie population by mutations from preexisting phenotypes.