Publications
NIBIOs employees contribute to several hundred scientific articles and research reports every year. You can browse or search in our collection which contains references and links to these publications as well as other research and dissemination activities. The collection is continously updated with new and historical material.
2004
Abstract
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Authors
Guro BrodalAbstract
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Authors
Guro BrodalAbstract
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Authors
Karl Thunes John Skartveit Ivar Gjerde Josef Stary Torstein Solhøy Arne Fjellberg Sverre Kobro Sueo Nakahara R. Zur Strassen Gijsbertus Vierbergen Ryszard Szadziewski Daniel V. Hagan William. L. Grogan Jr Terje Jonassen Kjetil Aakra Johannes Anonby Lita Greve Berend Aukema Kai Heller Verner Michelsen Jean-Paul Haenni Alexandr F. Emeljanov Per Douwes Kai Berggren Jutta Franzen R. Henry L. Disney Sabine Prescher Kjell Arne Johanson Boris Mamaev Sigitas Podenas Stig Andersen Stephen D. Gaimari Emilia Narchuk Geir Einar Ellefsen Søli Laszlo Papp Fred Midtgaard Arild Andersen Michael von Tschirnhaus Gerhard Bächli Kjell Magne Olsen Hans A. Olsvik Mihaly Földvari Jan Emil Raastad Lars Ove Hansen Per DjursvollAbstract
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Abstract
Genetic variation in three multiallelic loci was analysed with Temperature Gradient Gel Electrophoresis in order to assess the genetic population structure of Venturia tremulae var. tremulae in order to understand the evolutionary potential of the pathogen against resistance breeding. Also the identification of the fungus was verified with molecular analysis of reference isolates. The Fst and Gst values were very low indicating no substructuring or restrictions to gene flow between Fennoscandian populations of V. tremulae. The results imply high epidemiological efficiency of the fungus and therefore continuous breeding programme should be implemented for Venturia resistance of aspen.
Authors
Paivi Liisa Rinne Carl Gunnar Fossdal Sissel Torre Heather Danforth Aksel Granhus Gunnhild Søgaard John Einset Harald Kvaalen Øystein Johnsen Christiaan van der SchootAbstract
No abstract has been registered
Abstract
Introduction: The objectives of the present study were to monitor H. annosum colonization rate (Hietala et al., 2003) and expression of host chitinases in clonal Norway spruce material with differing resistances. Transcript levels of three chitinases, representing classes I, II and IV, were monitored with real-time PCR.Material and MethodsInoculation experiment: Ramets of two 32 -year-old clones differing in resistance were employed as host material. Inoculation and wounding was performed. A rectangular strip containing phloem and cambium, with the inoculation site in the middle, was removed 3, 7 and 14 days after inoculation.Quantification of fungal colonizationMultiplex real-time PCR detection of host and pathogen DNA was performed (Hietala et al., 2003). Quantification of gene expression: Chitinase levels were monitored with Singleplex real-time PCR.Results and ConclusionsThe colonization profiles provided by the quantitative multiplex real-time PCR procedure (Hietala et al., 2003), when combined with spatial and temporal transcript profiling of 3 chitinases, provide a useful basis for identifying defense related genes, and for assessing their impact on pathogen colonization rates.Three days after inoculation, comparable colonization levels were observed in both clones in the area immediately adjacent to inoculation. Fourteen days after infection, pathogen colonization was restricted to the area immediately adjacent to the site of inoculation for the strong clone (589), but had progressed further into the host tissue in the weak (409) clone.Transcript levels of the class II and IV chitinases increased following wounding or inoculation, while the transcript level of the class I chitinase declined following these treatments. Transcript levels of the class II and class IV chitinases were higher in areas immediately adjacent to the inoculation site in 589 than in similar sites in 409 three days after inoculation, suggesting that the clones differ in the rate of chitinase-related signalperception.
Abstract
We have monitored the H. annosum colonization rate and expression of host chitinases in Norway spruce material with differing resistances. Transcript levels of three chitinases, representing classes I, II and IV, were monitored with real-time PCR. Ramets of two 32 -year-old clones differing in resistance were employed as host material and inoculation and wounding was performed. Quantification of fungal colonization: Multiplex real-time PCR detection of host and pathogen DNA was performed. Chitinase transcript levels were also monitored with real-time PCR. Three days after inoculation, comparable colonization levels were observed in both clones in the area immediately adjacent to inoculation. Fourteen days after infection, pathogen colonization was restricted to the area immediately adjacent to the site of inoculation for the strong clone (589), but had progressed further into the host tissue in the weak clone (409). Transcript levels of the class II and IV chitinases increased following wounding or inoculation, while the transcript level of the class I chitinase declined following these treatments. Transcript levels of the class II and class IV chitinases were higher in areas immediately adjacent to the inoculation site in 589 than in similar sites in 409 three days after inoculation, suggesting that the clones differ in the rate of chitinase-related signal perception. The spatiotemporal accumulation patterns obtained for the two clones used are consistent with their resistance classifications, these warranting further and more detailed studies on these chitinases.
Authors
Tore Skrøppa Øystein Johnsen Carl Gunnar Fossdal Rudiger Baumann Jørgen A. Mølmann Ola G Dæhlen Nina Elisabeth Nagy G Müller-StarckAbstract
No abstract has been registered