Intersterility groups of Heterobasidion annosum and their host specificity in Bulgaria

1998 ◽  
Vol 28 (1) ◽  
pp. 1-9 ◽  
Author(s):  
N. La Porta ◽  
K. Apostolov ◽  
K. Korhonen
2001 ◽  
Vol 79 (9) ◽  
pp. 1057-1065 ◽  
Author(s):  
Paolo Gonthier ◽  
Matteo Garbelotto ◽  
Giovanna Cristina Varese ◽  
Giovanni Nicolotti

In Europe the forest pathogen Heterobasidion annosum (Fr.) Bref. includes the S, P, and F intersterility groups (ISGs), each displaying a preferential specialization on Norway spruce (Picea abies (L.) Karst.), pine, and silver fir (Abies alba Mill.), respectively. In this paper, we present data about (i) H. annosum ISGs frequency in different forest types, (ii) the degree of host specificity of each ISG, (iii) the significance of the potential movement of airborne spores among forests, and (iv) the occurrence of S–P chimeras in the northwestern Alps. Using woody spore traps, we sampled natural pure spruce and fir forests and a mixed spruce-fir forest. The ISG of 582 spores was determined by ISG-diagnostic taxon-specific competitive priming (TSCP) polymerase chain reaction (PCR) combined with PCR-mediated detection of ISG-specific introns in the ML5–ML6 DNA region of the mitochondrial large ribosomal RNA (mt LrRNA). All three ISGs were found, and a strong correlation was observed between the F ISG and fir and the S ISG and spruce. In the mixed forest, no clear relationship between tree host species and host-specialized ISGs was found. In spite of a relative dominance of fir in the overstory of the mixed stand, the fir-associated F ISG represented only 11% of the total number of spores collected. This discrepancy was explained by the recent establishment of firs at this site. No S–P nuclear-mitochondrial chimeras were found. This suggests limited gene flow between these ISGs.Key words: Heterobasidion annosum, host specificity, ISGs, gene flow, PCR, Alps.


1998 ◽  
Vol 76 (3) ◽  
pp. 397-409 ◽  
Author(s):  
Matteo Garbelotto ◽  
William J Otrosina ◽  
Fields W Cobb ◽  
Thomas D Bruns

In those regions of Europe where they coexist, the F and S intersterility groups (ISGs) of Heterobasidion annosum (Fr.) Bref. are primarily found on Abies spp. and Picea abies (L.) Karst., respectively. Eighty-three isolates of H. annosum were collected from Abies alba Mill. from 19 sites in Italy, including 10 Abies-Picea mixed conifer stands in the eastern Alps. The ISGs of a subsample of 34 isolates were determined by ISG-diagnostic arbitrary-primed (AP) PCR primers. For a subsample of 16 isolates, including two S isolates from Norway and one S isolate from California, nuclear markers generated by AP-PCR analysis, and mitochondrial markers generated by restriction fragment length polymorphisms and sequencing of the ML5-ML6 region of the mitochondrial large ribosomal RNA gene indicated that, in Europe, (i) the F and S ISGs can be found in the same forest stand but they are two genetically distinct units with restricted gene flow between them; (ii) each of the two ISGs is monophyletic and may lack strong genetic substructuring in subpopulations; and (iii) the two ISGs are closely related to each other and their nearest common close relative is the allopatric S ISG from North America. By combining these results with paleobotanical information and results from previous studies, we postulate a recent sympatric divergence of these two groups driven by differential host specificity and mating barriers.Key words: species complex, protospecies, sympatric, mating barriers, host specificity.


1992 ◽  
Vol 22 (6-7) ◽  
pp. 384-391 ◽  
Author(s):  
K. Korhonen ◽  
I. Bobko ◽  
S. Hanso ◽  
T. Piri ◽  
A. Vasiliauskas

1993 ◽  
Vol 71 (8) ◽  
pp. 1064-1071 ◽  
Author(s):  
William J. Otrosina ◽  
Thomas E. Chase ◽  
Fields W. Cobb Jr. ◽  
Kari Korhonen

Isolates of Heterobasidion annosum (Fr.) Bref. representing North American S and P and European S, P, and F intersterility groups were subjected to isozyme analysis. European S, P, and F groups had more variability than the North American S and P groups in expected hterozygosity, number of alleles per locus, and percent polymorphic loci. In contrast with the North American S and P groups, the European intersterility groups could not be distinguished from each other on the basis of individual isozyme loci, although significant differences in allele frequencies exist between European S and P groups. This suggests that evolution proceeded at different rates in the intersterility groups, or intersterility barriers appeared later in the European populations relative to the North American populations of H. annosum. Changes in climate and host species associations during the Tertiary may have been a major factor in evolution of H. annosum intersterility groups. Key words: allozymes, forest tree hosts, playnological events, evolutionary relationships, Hymenomycetes, root disease.


1995 ◽  
Vol 99 (9) ◽  
pp. 1025-1033 ◽  
Author(s):  
M.M. Müller ◽  
R. Kantola ◽  
K. Korhonen ◽  
J. Uotila

1993 ◽  
Vol 71 (4) ◽  
pp. 565-569 ◽  
Author(s):  
Matteo Garbelotto ◽  
Thomas D. Bruns ◽  
Fields W. Cobb ◽  
William J. Otrosina

Random amplified polymorphic DNAs were correlated with the intersterility group and the geographic provenance of 36 isolates of Heterobasidion annosum from North America and Europe and of one herbarium collection of basidiocarps from California. This technique is very precise and yields higher resolution than previous studies implementing techniques such as isozyme electrophoresis and restriction fragment length polymorphisms. Random amplified polymorphic DNAs revealed differentiation among the following geographic groups and intersterility groups: western North American P, eastern North American P, European P, North American S, Scandinavian S, Italian S, and Italian F. This is the first report on differentiation between eastern and western North American P isolates as well as between northern and southern European S isolates. Successful amplification of one dry basidiocarp suggests that random amplified polymorphic DNAs may be used to improve epidemiological and population studies of this pathogen. Key words: species complex, genetic variability, strain typing, forest pathology, polymerase chain reaction.


Sign in / Sign up

Export Citation Format

Share Document