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.