Publikasjoner
NIBIOs ansatte publiserer flere hundre vitenskapelige artikler og forskningsrapporter hvert år. Her finner du referanser og lenker til publikasjoner og andre forsknings- og formidlingsaktiviteter. Samlingen oppdateres løpende med både nytt og historisk materiale. For mer informasjon om NIBIOs publikasjoner, besøk NIBIOs bibliotek.
2004
Forfattere
Ingerd Skow Hofgaard Birgitte Henriksen Åshild Ergon Hilde Kolstad Helge Skinnes Yalew Tarkegne Anne-Marte TronsmoSammendrag
Development of Fusarium head blight (FHB) was studied in winter wheat pre-treated with potential defence activators. Several chemicals were pre-screened for their capacity to reduce development of Microdochium nivale in a detached leaf assay. Selected compounds were further tested for their capacity to reduce Fusarium culmorum development in heads of winter wheat in greenhouse and field experiments. In the detached leaf assay, leaves from plants pre-treated with a foliar fertilizer displayed reduced disease development compared to untreated control. A significantly reduced disease development of FHB in plants pre-treated with the foliar fertilizer was also registered in the greenhouse and field experiments. In the field experiment, harvested grainsfrom plants treated with the foliar fertilizer had up to 75% reduction in Fusarium infected seeds compared to grains from non-treated plants.
Sammendrag
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Sammendrag
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Forfattere
Risto Kasanen Jarkko Hantula M. Vourinen Jan Stenlid Halvor Solheim Timo KurkelaSammendrag
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.
Sammendrag
Border cells from the seedling root tips were added to the conidium suspensions of two soilborne rootpathogens, Fusarium sp. and Cylindrocarpon sp. The presence of border cells in the suspension clearly stimulated germination of fungal conidia. Conidia of Fusarium sp. and Cylindrocarpon sp.started to germinate within 3 hours after inoculation.When border cells were washed off, the stimulating effect disappeared. Addition of malt extract caused similar stimulation as border cells. Germination of conidia was suppressed in Al-treated plants.
Sammendrag
When conifers such as Picea abies (Norway spruce) are attacked by insects or pathogens, they often produce increased quantities of terpenoid oleoresin. This response can be mimicked in young P. abies seedlings by treatment with methyl jasmonate. In this study, we determined the effect of methyl jasmonate on the terpenoids and other chemical defenses of mature P. abies, and investigated if this treatment protected trees against attack by the blue-stain fungus Ceratocystis polonica, the most important fungal associate of the bark beetle Ips typographus. Methyl jasmonate treatment induced the formation of traumatic resin ducts in the developing xylem, enhanced resin flow, and stimulated increased accumulation of monoterpenes, sesquiterpenes, and diterpene resin acids. However, almost no significant changes in terpene composition were detected. In addition, no changes in soluble phenolic content were observed. There was a very high variability both among and within clones in the timing and degree of response to methyl jasmonate. These chemical and anatomical changes were correlated with increased resistance to C. polonica, suggesting that terpenoid oleoresin may function in defense against this pathogen.
Sammendrag
Utvalgt Forelesning/Selected Talk: Survival and competitive successes of boreal forest trees depend on a balance between exploiting the full growing season and minimising frost injury through proper timing of hardening in autumn and dehardening in spring. Our research has shown that the female parents of Norway spruce adjust these timing events in their progeny according to the prevailing temperature conditions during sexual reproduction. Reproduction in a cold environment advances bud-set and cold acclimation in the autumn and dehardening and flushing in spring, whereas a warm reproductive environment delays these progeny traits by an unknown non-Mendelian mechanism. We have performed identical crosses in combination with timed temperature treatments during shorter and longer periods from female meiosis, pollen tube growth, syngamy and embryogenesis, tested the progenies for bud-set and frost hardiness, and concluded that the effect of temperature most likely is a response to accumulated heat during embryogenesis and seed maturation. Our first attempt to look for a molecular mechanism has revealed that transcription of PHYO, PHYP and PHYN and the class IV chitinase PaChi4 (using RealTime PCR) all show higher transcription levels in progenies born under cold conditions than their full-sibs born under warmer conditions. This result is consistent with preliminary findings that methylation of cytosine in total DNA is higher in progenies reproduce under warm conditions than their colder full-sib counterparts. If these observations are related to methylation, we may explain why progenies with a memory of a past time cold embryogenesis are more sensitive to short days than their full-sibs with a warmer embryonic history.
Sammendrag
Pathogen colonization and transcript levels of three host chitinases,putatively representing classes I, II, and IV, were monitored with real-time PCR after wounding and bark infection by Heterobasidion annosum in 32-year-old trees of Norway spruce (Picea abies) with low (clone 409) or high (clone 589) resistance to this pathogen. Three days after inoculation, comparable colonization levels were observed in both clones in the area immediately adjacent to inoculation. At 14 days after infection, pathogen colonization was restricted to the area immediately adjacent to the site of inoculation for clone 589 but had progressed further into the host tissue in clone 409. Transcript levels of the class II and IV chitinases increased after wounding or inoculation, but the transcript level of the class I chitinase declined after these treatments. Transcript levels of the class II and class IV chitinases were higher in areas immediately adjacent to the inoculation site in clone 589 than in similar sites in clone 409 3 days after inoculation. This difference was even more pronounced 2 to 6 mm away from the inoculation point, where no infection was yet established, and suggests that the clones differ in the rate of chitinase-related signal perception or transduction. At 14 days after inoculation, these transcript levels were higher in clone 409 than in clone 589, suggesting that the massive upregulation of class II and IV chitinases after the establishment of infection comes too late to reduce or prevent pathogen colonization.
Sammendrag
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.
Forfattere
Axel Schmidt K. Witzel Gazmend Zeneli D. Martin J. Bohlmann Paal Krokene Trygve Krekling Ari M. Hietala Carl Gunnar Fossdal Erik Christiansen Jonathan GershenzonSammendrag
The study of conifer chemical defense has been dominated by investigations of oleoresin and its components. However, the actual function of resin components in plant defense and their mode of action is still uncertain, and the role of other defense compounds is relatively unexplored.We are studying the biochemical and molecular bases of chemical defenses, including terpenes, phenolics and chitinases, in Norway spruce (Picea abies) to learn more about how the accumulation of defense compounds is regulated, with the long-term goal of manipulating defense levels to test their function.Manipulation can be crudely accomplished by treatment with methyl jasmonate, which often mimics the general increases in defenses seen following herbivore or pathogen attack. Such treatment was shown to increase resistance to a fungal associate of bark beetles.To more conclusively test function, isolated genes of defense biosynthetic pathways are being transformed into Norway spruce to produce plants whose defense profiles are altered more precisely.