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Applied and Environmental Microbiology, March 1999, p. 903-909, Vol. 65, No. 3
Laboratoire d'Ecologie Microbienne (UMR CNRS
5557), Université Claude Bernard Lyon 1, F-69622 Villeurbanne
Cedex, France,1 and Dipartimento di
Scienze e Tecnologie Alimentari e Microbiologiche, Sezione di
Microbiologia Applicata, Università degli Studi di Firenze, 50144 Florence, Italy2
Received 27 July 1998/Accepted 1 December 1998
Polymorphism of the nuclear ribosomal DNA intergenic spacer (IGS)
of the ectomycorrhizal basidiomycete Hebeloma
cylindrosporum was studied to evaluate whether this sequence
could be used in field studies to estimate the diversity of strains
forming mycorrhizas on individual Pinus pinaster root
systems. This sequence was amplified by PCR from 125 haploid
homokaryotic strains collected in 14 P. pinaster stands
along the Atlantic coast of France by using conserved oligonucleotide
primers. Restriction enzyme digestion of the amplified 3.4-kbp-long IGS
allowed us to characterize 24 alleles whose frequencies differed. Nine
of these alleles were found only once, whereas about 60% of the
strains contained four of the alleles. Local populations could be
almost as diverse as the entire population along a 150-km stretch of
coastline that was examined; for example, 13 alleles were found in a
single forest stand. The IGS from one strain was partially sequenced,
and the sequence data were used to design oligonucleotides which
allowed separate PCR amplification of three different segments of the
IGS. Most polymorphisms observed among the full-length IGS regions
resulted from polymorphisms in an internal ca. 1,500-bp-long sequence
characterized by length variations that may have resulted from variable
numbers of a T2AG3 motif. This internal
polymorphic sequence could not be amplified from the genomes of nine
other Hebeloma species. Analysis of this internal sequence
amplified from the haploid progenies of 10 fruiting bodies collected in
a 70-m2 area resulted in identification of six allelic
forms and seven distinct diplotypes out of the 21 possible different
combinations. Moreover, optimization of the PCR conditions resulted in
amplification of this sequence from more than 80% of the DNA samples
extracted from individual H. cylindrosporum infected
P. pinaster mycorrhizal root tips, thus demonstrating the
usefulness of this sequence for studying the below-ground diversity of
mycorrhizas formed by genets belonging to the same fungal species.
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
The Nuclear Ribosomal DNA Intergenic Spacer as a
Target Sequence To Study Intraspecific Diversity of the Ectomycorrhizal
Basidiomycete Hebeloma cylindrosporum Directly on
Pinus Root Systems
*
Corresponding author. Mailing address: Laboratoire
d'Ecologie Microbienne (UMR CNRS 5557), Université Claude
Bernard Lyon 1, Bât. 405, 43 Bd. du 11 Novembre 1918, F-69622
Villeurbanne Cedex, France. Phone: 33 472448047. Fax: 33 472431643. E-mail: gay{at}cismsun.univ-lyon1.fr.
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