Comparison of vegetative compatibility types in Italian and Swiss subpopulations of Cryphonectria parasitica

Summary Tester isolates of 20 vegetative compatibility (vc) types from 11 Italian subpopulations and tester isolates of 26 vc types from five Swiss subpopulations of Cryphonectria parasitica were compared by two different vc test methods. A total of 31 different vc types was identified; 15 vc types were common to both countries, five Italian vc types were not found in Switzerland and 11 Swiss vc types were not found in Italy. These 31 vc types were labelled with the acronym EU, followed by progressive numbers and may constitute the base for a common European nomenclature. The vc type EU-2 was the most common vc type in both countries and dominated in all Swiss and in seven Italian subpopulations. The vc types EU-1 and EU-5 were found primarily in northern Italy and Switzerland, while EU-10 and EU-12 were most common in southern Italy. The diversity of vc types was greater in the subpopulations of Switzerland and northern Italy than in the subpopulations of southern Italy. The geographical distribution of vc types in Europe should therefore be taken into consideration for biological control measures of chestnut blight and quarantine regulations.

[1]  P. Cortesi,et al.  Distribution and diversity of vegetative compatibility types in subpopulations of Cryphonectria parasitica in Italy , 1996 .

[2]  W. Powell Vegetative incompatibility and mycelial death of Cryphonectria parasitica detected with a pH indicator , 1995 .

[3]  L. Montecchio,et al.  Vegetative compatibility and conversion to hypovirulence among Italian isolates of Cryphonectria parasitica , 1995 .

[4]  D. Seemann,et al.  Rindenkrebs der Eßkastanie (Cryphonectria parasitica) in Südwestdeutschland , 1994 .

[5]  M. Garbelotto,et al.  Vegetative compatibility and conversion to hypovirulence among isolates of Cryphonectria parasitica from northern Italy , 1992 .

[6]  G. Choi,et al.  Hypovirulence of chestnut blight fungus conferred by an infectious viral cDNA. , 1992, Science.

[7]  U. Heiniger,et al.  Chestnut blight (Cryphonectria parasitica) north of the Swiss alps , 1991 .

[8]  G. Maresi,et al.  Inoculation trials with hypovirulent strains of Cryphonectria parasitica , 1991 .

[9]  G. Bazzigher,et al.  Long‐term conservation of living fungal pathogens , 1985 .

[10]  G. Bazzigher,et al.  Irreversible Pathogenitätsverminderung bei Endothia parasitica durch übertragbare Hypovirulenz , 1981 .

[11]  S. Anagnostakis Vegetative incompatibility in Endothia parasitica , 1977 .

[12]  S. L. Anagnostakis,et al.  Chestnut Blight: Biological Control by Transmissible Hypovirulence in Endothia parasitica , 1975, Science.

[13]  M Bissegger,et al.  Population Structure and Disease Development of Cryphonectria parasitica in European Chestnut Forests in the Presence of Natural Hypovirulence. , 1997, Phytopathology.

[14]  P. Cortesi,et al.  Diversity and multilocus genetic structure in populations of Cryphonectria parasitica , 1996 .

[15]  Michael G. Milgroom,et al.  Correlation between hypovirus transmission and the number of vegetative incompatibility (vic) genes different among isolates from a natural population of Cryphonectria parasitica. , 1996 .

[16]  D. Rigling,et al.  Biological Control of Chestnut Blight in Europe , 1994 .

[17]  S. Anagnostakis,et al.  Diversity of vegetative compatibility groups of Cryphonectria parasitica in Connecticut and Europe , 1986 .

[18]  W. Macdonald,et al.  Identifying Hypovirulent Isolates of Cryphonectria parasitica with Broad Conversion Capacity , 1984 .

[19]  E. Kuhlman Vegetative compatibility and hypovirulence conversion among naturally occurring isolates of Cryphonectria parasitica , 1984 .