Expression of maedi-visna virus major core protein, p25: development of a sensitive p25 antigen detection assay

1992 ◽  
Vol 37 (3) ◽  
pp. 305-320 ◽  
Author(s):  
H.T. Reyburn ◽  
D.J. Roy ◽  
B.A. Blacklaws ◽  
D.R. Sargan ◽  
I. McConnell
10.4081/849 ◽  
2009 ◽  
Vol 47 (4) ◽  
pp. 373 ◽  
Author(s):  
S Preziuso ◽  
E Taccini ◽  
G Rossi ◽  
G Renzoni ◽  
G Braca

A morphological, immunohistochemical and polymerase chain reaction (PCR) study was performed on eight ewes experimentally infected with an Italian strain of Maedi-Visna Virus (MVV) in order to evaluate the lesions and the viral distribution after three years of infection. At the moment of euthanasia, seven sheep were seropositive for MVV, while one sheep in poor body conditions was seronegative since one year. Lungs, pulmonary lymph nodes, udder, supramammary lymph nodes, carpal joints, the CNS, spleen and bone marrow of the eight infected sheep were collected for histology, for immunohistochemical detection of the MVV core protein p28 and for PCR amplification of a 218 bp viral DNA sequence of the pol region. The most common histological findings consisted of interstitial lymphoproliferative pneumonia and lymphoproliferative mastitis of different severity, while no lesions were observed in the CNS. MVV p28 antigen was immunohistochemically labelled in lungs, udder, pulmonary lymph nodes, spleen and bone marrow but not in the CNS of all the eight infected sheep. A 218 bp sequence of MVV pol region was detected in lung of a seropositive and of the seroconverted negative sheep. The results suggest that (i) MVV causes heterogeneous lesions in homogeneously reared ewes, (ii) MVV p28 antigen is detectable not only in inflammed target organs, but also in pulmonary lymph nodes, spleen and bone marrow, and (iii) immunohistochemistry and PCR are useful methods for Maedi-Visna diagnosis in suspected cases, also when serological tests are negative.


1987 ◽  
Vol 64 (3) ◽  
pp. 76-78 ◽  
Author(s):  
D M VANKAN ◽  
R B ATWELL ◽  
A S BLAKE ◽  
P G BUNDESEN ◽  
D B RYLATT ◽  
...  

2002 ◽  
Vol 83 (12) ◽  
pp. 3153-3161 ◽  
Author(s):  
R. Duval ◽  
V. Bellet ◽  
S. Delebassée ◽  
C. Bosgiraud

Maedi–visna virus (MVV) causes encephalitis, pneumonia and arthritis in sheep. In vitro, MVV infection and replication lead to strong cytopathic effects characterized by syncytia formation and subsequent cellular lysis. It was demonstrated previously that MVV infection in vitro induces cell death of sheep choroid plexus cells (SCPC) by a mechanism that can be associated with apoptotic cell death. Here, the relative implication of several caspases during acute infection with MVV is investigated by employing diverse in vitro and in situ strategies. It was demonstrated using specific pairs of caspase substrates and inhibitors that, during in vitro infection of SCPC by MVV, the two major pathways of caspase activation (i.e. intrinsic and extrinsic pathways) were stimulated: significant caspase-9 and -8 activities, as well as caspase-3 activity, were detected. To study the role of caspases during MVV infection in vitro, specific, cell-permeable, caspase inhibitors were used. First, these results showed that both z-DEVD-FMK (a potent inhibitor of caspase-3-like activities) and z-VAD-FMK (a broad spectrum caspase inhibitor) inhibit caspase-9, -8 and -3 activities. Second, both irreversible caspase inhibitors, z-DEVD-FMK and z-VAD-FMK, delayed MVV-induced cellular lysis as well as virus growth. Third, during SCPC in vitro infection by MVV, cells were positively stained with FITC-VAD-FMK, a probe that specifically stains cells containing active caspases. In conclusion, these data suggest that MVV infection in vitro induces SCPC cell death by a mechanism that is strongly dependent on active caspases.


2007 ◽  
Vol 119 (3-4) ◽  
pp. 222-232 ◽  
Author(s):  
Ana M. Henriques ◽  
Miguel Fevereiro ◽  
Duarte M.F. Prazeres ◽  
Gabriel A. Monteiro

2015 ◽  
Vol 64 (8) ◽  
pp. 845-848 ◽  
Author(s):  
Gemma Robertson ◽  
Alanna Sorenson ◽  
Brenda Govan ◽  
Natkunam Ketheesan ◽  
Raymond Houghton ◽  
...  

Author(s):  
Hallgrímur Arnarson ◽  
Arnar Pálsson ◽  
Margrét Gudnadóttir ◽  
Valgerdur Andrésdóttir

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