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Dive into the research topics where M.J. Ulvund is active.

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Featured researches published by M.J. Ulvund.


Journal of General Virology | 2000

Distribution of prion protein in the ileal Peyer's patch of scrapie-free lambs and lambs naturally and experimentally exposed to the scrapie agent

Ragna Heggebø; Charles McL. Press; Gjermund Gunnes; Kai Inge Lie; Michael A. Tranulis; M.J. Ulvund; Martin H. Groschup; Thor Landsverk

A sensitive immunohistochemical procedure was used to investigate the presence of prion protein (PrP) in the ileal Peyers patch of PrP-genotyped lambs, including scrapie-free lambs and lambs naturally and experimentally exposed to the scrapie agent. The tyramide signal amplification system was used to enhance the sensitivity of conventional immunohistochemical procedures to show that PrP was widely distributed in the enteric nervous plexus supplying the gut wall. In scrapie-free lambs, PrP was also detected in scattered cells in the lamina propria and in the dome and interfollicular areas of the Peyers patch. In the follicles, staining for PrP was mainly confined to the capsule and cells associated with vascular structures in the light central zone. In lambs naturally exposed to the scrapie agent, staining was prominent in the dome and neck region of the follicles and was also found to be associated with the follicle-associated epithelium. Similar observations were made in lambs that had received a single oral dose of scrapie-infected brain material from sheep with a homologous and heterologous PrP genotype 1 and 5 weeks previously. These studies show that the ileal Peyers patch in young sheep may be an important site of uptake of the scrapie agent and that the biology of this major gut-associated lymphoid tissue may influence the susceptibility to oral infection in sheep. Furthermore, these studies suggest that homology or heterology between PrP genotypes or the presence of PrP genotypes seldom associated with disease does not impede uptake of PrP.


Preventive Veterinary Medicine | 2001

A case-control study on scrapie in Norwegian sheep flocks.

Petter Hopp; M.J. Ulvund; Jorun Jarp

Scrapie first was detected in indigenous sheep in Norway in 1981, and from 1995 to 1997 an increase in the number of flocks with scrapie cases was recorded. These flocks were mainly in one geographical region. A study to identify risk factors for scrapie was conducted. The study had three frequency-matched controls selected for every case within the same Veterinary District. A questionnaire was submitted to 176 sheep flocks (42 had been scrapie flocks). The data obtained by the questionnaire were linked to data collected from governmental and industry registers. After imputing missing data using single random imputation, the statistical analysis was performed using multivariable conditional logistic regression. Purchase of female sheep from scrapie flocks, sharing of rams, or sharing of pastures between different flocks were the risk factors associated with the occurrence of scrapie. Of factors potentially sustaining and promoting the infection in the flock, number of winter-fed sheep, number of buildings for housing sheep, rams and ewes shared room during mating period and increase in the flock size were associated with scrapie. We interpret these findings to show that factors involving transfer of sheep between flocks or direct contact between sheep of different flocks are important for the spread of scrapie. Management factors are important for the development of scrapie. However, it was not possible to discriminate between the different management factors in this study at the flock level. Also, factors indicating awareness and interest of the farmer (as well as willingness to contact a veterinarian for diseased sheep) were related to the detection of scrapie in the flock.


BMC Veterinary Research | 2012

Presence of an acute phase response in sheep with clinical classical scrapie

Siv Meling; Kjetil Bårdsen; M.J. Ulvund

BackgroundWork with experimental scrapie in sheep has been performed on-site for many years including studies on PrPSc dissemination and histopathology of organs and tissues both at preclinical and clinical stages. In this work serum was sampled at regular intervals from lambs which were infected immediately after birth and from parallel healthy controls, and examined for acute phase proteins. In contrast to earlier experiments, which extensively studied PrPSc dissemination and histopathology in peripheral tissues and brain, this experiment is focusing on examination of serum for non-PrPSc markers that discriminates the two groups, and give insight into other on-going processes detectable in serum samples.ResultsThere was clear evidence of an acute phase response in sheep with clinical scrapie, both experimental and natural. All the three proteins, ceruloplasmin, haptoglobin and serum amyloid A, were increased at the clinical stage of scrapie.ConclusionThere was evidence of a systemic measurable acute phase response at the clinical terminal end-stage of classical scrapie.


Developmental and Comparative Immunology | 1999

Increased γδ T-cell populations in draining lymph nodes of lambs during the elicitation phase of dinitrochlorobenzene-induced contact hypersensitivity

Gjermund Gunnes; Einar Jörundsson; Charles McL. Press; Eystein Skjerve; M.J. Ulvund; Thor Landsverk

Ten lambs were sensitised with the hapten DNCB in an acetone/olive oil vehicle. The hapten/vehicle solution was applied onto the skin on the shaved ventral surface of the right ear. Two weeks later these lambs were rechallenged with the DNCB/vehicle solution. Simultaneously, ten non-sensitised lambs were treated with vehicle only, serving as vehicle controls. The 20 lambs were slaughtered 48 h after challenge/vehicle treatment, along with ten untreated animals serving as normal controls. Specimens of draining lymph nodes were collected from the 30 animals. All lambs were between 149 and 187 days old. Lymph node cryosections were stained for several leukocyte markers using monoclonal antibodies with the ABC immunohistochemical method. The stained sections were subsequently assessed in three different cortical compartments in each section, using an image analysis system. The resulting measurements from the three groups were compared. A marked increase of gammadelta T cells was detected in the DNCB group. The number of CD4+ T helper cells was decreased in the DNCB group compared with the normal control group, but not with the vehicle control group. No differences were revealed for CD8+ T cytotoxic cells or B cells. These findings were interpreted to be the consequences of possible downregulatory mechanisms protecting the lymphoid tissue from hypersensitivity. The prominence of gammadelta T-cells could indicate that these cells are involved in downregulation.


BMC Research Notes | 2013

Investigation of serum protein profiles in scrapie infected sheep by means of SELDI-TOF-MS and multivariate data analysis.

Siv Meling; Olav M. Kvalheim; Reidar Arneberg; Kjetil Bårdsen; Anne Hjelle; M.J. Ulvund

BackgroundClassical scrapie in sheep is a fatal neurodegenerative disease associated with the conversion PrPC to PrPSc. Much is known about genetic susceptibility, uptake and dissemination of PrPSc in the body, but many aspects of prion diseases are still unknown. Different proteomic techniques have been used during the last decade to investigate differences in protein profiles between affected animals and healthy controls. We have investigated the protein profiles in serum of sheep with scrapie and healthy controls by SELDI-TOF-MS and LC-MS/MS. Latent Variable methods such as Principal Component Analysis, Partial Least Squares-Discriminant Analysis and Target Projection methods were used to describe the MS data.ResultsThe serum proteomic profiles showed variable differences between the groups both throughout the incubation period and at the clinical end stage of scrapie. At the end stage, the target projection model separated the two groups with a sensitivity of 97.8%, and serum amyloid A was identified as one of the protein peaks that differed significantly between the groups.ConclusionsAt the clinical end stage of classical scrapie, ten SELDI peaks significantly discriminated the scrapie group from the healthy controls. During the non-clinical incubation period, individual SELDI peaks were differently expressed between the groups at different time points. Investigations of differences in -omic profiles can contribute to new insights into the underlying disease processes and pathways, and advance our understanding of prion diseases, but comparison and validation across laboratories is difficult and challenging.


Journal of Comparative Pathology | 2006

Detection of PrPSc in rectal biopsy and necropsy samples from sheep with experimental scrapie

Arild Espenes; C.McL. Press; Thor Landsverk; Michael A. Tranulis; Mona Aleksandersen; Gjermund Gunnes; S.L. Benestad; R. Fuglestveit; M.J. Ulvund


Journal of Comparative Pathology | 2003

Detection of PrPSc in Lymphoid Tissues of Lambs Experimentally Exposed to the Scrapie Agent

Ragna Heggebø; C.McL. Press; Gjermund Gunnes; M.J. Ulvund; Michael A. Tranulis; T Lsverk


Biochemical and Biophysical Research Communications | 2004

cDNA representational difference analysis of ileal Peyer's patches in lambs after oral inoculation with scrapie.

Grethe Skretting; Arild Espenes; M.J. Ulvund; Ingrid Olsaker


Small Ruminant Research | 2008

Ovine Scrapie disease: Do we have to live with it?

M.J. Ulvund


Small Ruminant Research | 2014

Experimental infection of sheep with ovine and bovine Dichelobacter nodosus isolates

Maren Knappe-Poindecker; Hannah J. Jørgensen; Tim Kåre Jensen; Bereket Tesfamichael; M.J. Ulvund; Synnøve Vatn; T. Fjeldaas

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Gjermund Gunnes

Norwegian University of Life Sciences

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E. Brundtland

Norwegian University of Life Sciences

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K. Bårdsen

Norwegian University of Life Sciences

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Kjetil Bårdsen

Norwegian University of Life Sciences

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Michael A. Tranulis

Norwegian University of Life Sciences

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Siv Meling

Norwegian University of Life Sciences

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Thor Landsverk

Norwegian University of Life Sciences

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Arild Espenes

Norwegian University of Life Sciences

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C.McL. Press

Norwegian University of Life Sciences

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Charles McL. Press

Norwegian University of Life Sciences

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