Handbook Part 2 - International Mycological Association
Handbook Part 2 - International Mycological Association
Handbook Part 2 - International Mycological Association
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PS8-458-0267<br />
Population Biology Of The Sapstain Fungus, Ophiostoma ips, Reflects Global Movement Of Its Bark Beetle<br />
Vectors<br />
X.D. Zhou 1, T. Burgess 2, Z.W. de beer 3, F. Lieutier 4, A. Yart 5, K. Klepzig 6, A. Carnegie 7, J.M. Portales 8, B.D. Wingfield<br />
9, M.J. Wingfield 10<br />
1 Forestry and Agricultural Biotechnology Institute (FABI); University of Pretoria, Pretoria, South Africa, 2 Department of<br />
Biological Sciences and Biotechnology, Murdoch University, Perth, Australia, 3 Department of Microbiology and Plant<br />
Pathology, University of Pretoria, Pretoria, South Africa, 4 Laboratoire de Biologie des Ligneux et des Grandes Cultures,<br />
Université d’Orléans, Rue de Chartres, B.P. 6759, 45067 Orleans Cedex 2, Orléans, France, 5 Institut National de la<br />
Recherche Agronomique (INRA), Pathologie Forestiere, Champenoux, F-54280, Champenoux, France, 6 USDA Forest<br />
Service, Southern Research Station, 2500 Shreveport Hwy, Pineville, 71360, LA, United States, 7 Forest Research<br />
Development Division, State Forest of NSW, NSW, Australia, 8 Instituto de Ecología y Sistemática (IES), Agencia de<br />
Medio Ambiente (AMA), Carretera de Varona km. 31/2, Capdevila, Boyeros, A.P.8029, C.P. 10800, Ciudad de La<br />
Habana, Cuba, 9 Department of Genetics, University of Pretoria, Pretoria, South Africa, 10 Forestry and Agricultural<br />
Biotechnology Institute (FABI); University of Pretoria, Pretoria, South Africa<br />
Bark beetles commonly infest conifers and live in a close association with fungi, especially Ophiostoma species and<br />
their anamorphs. Ophiostoma ips is a common fungal associate of various bark beetle species in their native ranges<br />
and has been introduced into non-native pine plantations in the Southern Hemisphere. In this study, we consider the<br />
population biology of O. ips in native and non-native areas to characterize host specificity, reproductive behavior, the<br />
potential origin, and spread patterns of this fungus, together with its insect vectors. Ten pairs of Single Short Repeat<br />
(SSR) markers were used to examine the structure of seven populations of O. ips including four native populations from<br />
Cuba, France, Morocco and USA, and three introduced populations from Australia, Chile and South Africa. The SSR<br />
markers across 10 loci examined resolved a total of 41 alleles and 93 genotypes across all populations. Higher genetic<br />
diversity was found in the native populations than in the introduced populations. Most alleles were present in all native<br />
populations although allele frequencies among populations varied. There was no evidence of specificity of the<br />
fungus to particular bark beetle vectors and hosts. Although O. ips is homothallic, recombination occurred in the four<br />
native populations surveyed. Genetic relatedness of the fungal isolates both from native and exotic environments<br />
confirmed the origins of the fungus and its insect vectors. Most alleles observed in the native European population<br />
were also found in the native North American population, and this could be due to multiple introductions of European<br />
vectors to North America. The higher genetic diversity in the North American population than in the European<br />
population suggests that North America would be the most probable source region of O. ips.<br />
PS8-459-0275<br />
Phylogeography, cryptic speciation and hybridization in the cellar fungus Coniophora puteana<br />
I Bjorvand Svegården 1, N Hallenberg 3, C DeCock 2, H Kauserud 1<br />
1 Department of Biology, University of Oslo, Oslo, Norway, 2 Mycothèque de l’Université Catholique de Louvain,<br />
Faculté des Sciences Agronomiques, Louvain-la-Neuve, Belgium, 3 Systematic Botany, Botanical Institute, Göteborg<br />
University, Göteborg, Sweden<br />
Fungi often have complex and unpredictable population structures and phylogeographic patterns due to their highly<br />
variable life history characteristics. The occurrence of unknown biological mating barriers adds an extra layer of<br />
complexity to the analysis of genetic variation in fungi. In this study, we explored the genetic variation and<br />
phylogeographic structure in a global sample of the cellar fungus Coniophora putana, which is an important<br />
destroyer of wooden constructions indoor. DNA sequences were obtained from three independent nuclear DNA loci<br />
(beta tubulin, nrDNA ITS and translation elongation factor). The genealogies revealed the occurrence of three<br />
separate lineages in the morphotaxon C. puteana, apparently representing three cryptic species (PS1-PS3). One of<br />
the lineages (PS3) seems to be restricted to North America while the other two have wider distributions, occurring on<br />
different continents. In these two lineages (PS1 and PS2), there was little correspondence between genetic and<br />
geographic separation, apparently reflecting high gene flow at intercontinental scales. Our data demonstrate that<br />
the three lineages reproduce mainly by outcrossing. All three lineages occur in sympatry in North America and our<br />
data indicate that hybridization and subsequent intralocus recombination, leading to mosaic sequences, have<br />
occurred among two of the lineages in this region (PS1 and PS3). We hypothesize that these two lineages evolved in<br />
allopatry earlier, succeeded by a more recent reoccurrence in sympatry, enabling reticulate evolution. Thus,<br />
biological barriers to gene flow have apparently not yet evolved between two of the lineages. This study supports the<br />
view that cryptic speciation is a very common phenomenon in fungi.<br />
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