FINE-LEVEL GENETIC-STRUCTURE OF WHITE-PINE BLISTER RUST POPULATIONS

Citation
Rc. Hamelin et al., FINE-LEVEL GENETIC-STRUCTURE OF WHITE-PINE BLISTER RUST POPULATIONS, Phytopathology, 88(11), 1998, pp. 1187-1191
Citations number
38
Categorie Soggetti
Plant Sciences
Journal title
ISSN journal
0031949X
Volume
88
Issue
11
Year of publication
1998
Pages
1187 - 1191
Database
ISI
SICI code
0031-949X(1998)88:11<1187:FGOWBR>2.0.ZU;2-3
Abstract
The fine-level genetic structure of the white pine blister rust agent, Cronartium ribicola, was investigated by sampling multiple monokaryot ic spermogonia directly on cankers in four eastern Canadian white pine (Pinus strobus) plantations and assessing genetic variability, using random amplified polymorphic DNA (RAPD) markers. Ninety-eight per cent of the cankers surveyed contained a single DNA haplotype, suggesting spermogonia within cankers are the result of clonal reproduction. A si ngle canker contained two haplotypes that were divided between the upp er and lower parts of the canker, suggesting it represented two conflu ent cankers. In contrast, genotypic diversity was high among cankers. Thirty-seven haplotypes were found among forty-three cankers sampled, and an analysis of molecular variance indicated that 93% (P < 0.001) o f the total genetic diversity was attributable to sampling of differen t cankers, strongly suggesting that multiple infections do not take pl ace in the white pine blister rust pathosystem, i.e., a canker is the result of infection by a single genotype. This result is in contrast w ith the high level of genetic diversity previously reported among dika ryotic aecidia within cankers and is consistent with the hypothesis th at variability in the aecidial stage is the result of outcrossing betw een resident spermogonia and alien spermatia. The genetic structure of the spermogonial stage, which is the vegetative extension of infectio n by basidiospores and, therefore, the indirect result of meiosis, was consistent with random mating; the observed genotypic diversity was n ot significantly different (P > 0.05) from the genotypic diversity exp ected under the assumption of panmixis. The results indicate that mono karyotic cankers can be genotyped by sampling a single unopened spermo gonia per canker.