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A PCR-Based Identification Method for Species of Armillaria
T. C. Harrington and B. D. Wingfield
Vol. 87, No. 2 (Mar. - Apr., 1995), pp. 280-288
Published by: Mycological Society of America
Stable URL: http://www.jstor.org/stable/3760915
Page Count: 9
You can always find the topics here!Topics: Armillaria, Species, Mycology, Enzymes, Biological taxonomies, Polymerase chain reaction, Mycelium, DNA, Taxa, Gels
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A portion of the Intergenic Spacer (IGS) of the ribosomal RNA operon of 74 isolates of 11 Armillaria species from Europe and North America was amplified using the polymerase chain reaction. Amplifications were made from scrapes of living mycelium without DNA extraction. Alu I digests of the amplified product were electrophoresed in agarose and stained with ethidium bromide. With few exceptions, each taxon had a unique combination of restriction fragments. Most taxa had a single Alu I pattern, but two restriction patterns were seen among isolates of A. borealis, A. cepistipes, A. gallica, A. tabescens, and A. mellea. Armillaria ostoyae, A. gemina, one of the A. borealis types, and one of the A. cepistipes types had identical sizes of Alu I fragments, but each of these taxa could be distinguished by their polymorphisms after restriction with the enzymes Nde I, Bsm I, or Hind II. European isolates of A. gallica had a distinct Alu I restriction pattern, but North American isolates of this species had a restriction pattern identical to A. calvescens. IGS amplification products were obtained from 8-year-old spore prints and dried basidiomes, as well as fresh wood decay without DNA extraction. The technique allows for identification from decayed wood, basidiomes or mycelia of these Armillaria species in a single day.
Mycologia © 1995 Mycological Society of America