Genetic variability in the canker pathogen fungus, Gremmeniella abietina. 2. Fine-scale investigation of the population genetic structure

Genetic variation at 32 polymorphic random amplified polymorphic DNA loci was analysed in the ascomycete canker pathogen fungus Gremmeniella abietina (Lagerb.) Morelet collected from one plantation of Pinus contorta Dougl. ex Loud, in northern Sweden. The genetic variability maintained in the G. abi...

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Bibliographic Details
Published in:Canadian Journal of Botany
Main Authors: Wang, Xiao-Ru, Szmidt, Alfred E., Ennos, Richard A., Hansson, Per
Format: Article in Journal/Newspaper
Language:English
Published: Canadian Science Publishing 1997
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Online Access:http://dx.doi.org/10.1139/b97-860
http://www.nrcresearchpress.com/doi/pdf/10.1139/b97-860
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Summary:Genetic variation at 32 polymorphic random amplified polymorphic DNA loci was analysed in the ascomycete canker pathogen fungus Gremmeniella abietina (Lagerb.) Morelet collected from one plantation of Pinus contorta Dougl. ex Loud, in northern Sweden. The genetic variability maintained in the G. abietina population was high. Many different multilocus genotypes were found on each tree and in each sampling site within the plantation. The clonal fraction of the population was small, and identical genotypes were found either on the same tree or branch or on trees in the same sampling site. The finding of very few widely distributed clones suggests that the effective dispersal of asexual spores is limited to a few metres and resulted in small clusters of clones in local sites. Analysis of molecular variance revealed that 45.3% of the total variation was attributable to differences among isolates within trees, 22.5% to trees within sites and 32.3% to sampling sites differences. Allele frequencies at most of the loci varied significantly among the sampling sites and average total genetic diversity over the 32 loci was 0.27 indicating high population subdivision. The factors that could have contributed to the observed population structure were discussed. Key words: Gremmeniella abietina, genotype and clone distribution, population subdivision, RAPD.