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Mechanisms by which lumpy skin disease virus is shed in semen of artificially infected bulls

Dissertation (MMedVet (Theriogenology))--University of Pretoria, 2006.

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Other Authors: Irons, Pete Charles
Format: Thesis
Published: University of Pretoria 2013
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access_status_str Open Access
author2 Irons, Pete Charles
author_browse Irons, Pete Charles
author_facet Irons, Pete Charles
collection Thesis
dc_rights_str_mv © 2006, University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria.
description Dissertation (MMedVet (Theriogenology))--University of Pretoria, 2006.
format Thesis
id oai:repository.up.ac.za:2263/29168
institution University of Pretoria (South Africa)
last_indexed 2026-06-10T12:37:49.734Z
license_str Other — see source repository
provenance_str_mv Harvested via OAI-PMH from UPSpace — University of Pretoria Institutional Repository
publishDate 2013
publishDateRange 2013
publishDateSort 2013
publisher University of Pretoria
publisherStr University of Pretoria
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source_str UPSpace — University of Pretoria Institutional Repository
spelling oai:repository.up.ac.za:2263/29168 Mechanisms by which lumpy skin disease virus is shed in semen of artificially infected bulls Irons, Pete Charles Venter, Estelle Hildegard henry.annandale@up.ac.za Annandale, C.H. (Cornelius Henry) Cattle Semen Lumpy skin disease (LSD) Bulls Virus UCTD Dissertation (MMedVet (Theriogenology))--University of Pretoria, 2006. Lumpy skin disease (LSD) is a disease of significant economic importance in Africa. It causes considerable production losses and its presence in semen is a constraint to international trade. Recent findings that LSDV viral DNA can be found in the semen of artificially infected bulls for up to five months, while viable virus could be isolated 42 days after infection, indicated the need for studies into the mechanism by which this protracted shedding occurs. Six healthy, seronegative, postpubertal Dexter bulls were housed in vector-free stables and challenged with LSD virus by intravenous injection. Sheath washes, vesicular fluid and semen collection was performed every other day and subjected to PCR. On these days, blood was collected for serum neutralization tests and virus isolation, and ultrasonography of the reproductive tracts performed. Semen was centrifuged to separate cell-rich and seminal plasma fractions, and tested by PCR. Clinical parameters were recorded twice daily. Bulls shedding viral DNA 28 days after challenge were slaughtered, their reproductive tracts were harvested and diagnostic post mortem was performed. Histopathology, immunoperoxidase staining, electron microscopy, virus isolation and PCR were done on tissue samples. Of the six bulls, two showed no clinical signs, two showed mild and two showed severe clinical signs. Fever appeared five to seven days and lesions eight to ten days post challenge. Bulls were viraemic and febrile during the same time. Viral DNA was detected in all semen fractions of all bulls, but mostly from the cell-rich fraction and from the bulls showing the most severe clinical signs. Ultrasonography showed infarction in the testes and epididymides of the two bulls that were most severely affected. Necropsy of the two bulls that were still shedding after 28 days showed testicular degeneration and infarction, as well as epididymal granuloma formation. None of the accessory sex organs showed significant pathology. Histopathological changes seen were necrogranulomata in testes and peididymides. IMP staining of reproductive tissues showed that staining was restricted to areas in the testes and epididymides that were associated with necrosis. Virus could be seen on negative staining EM of sections of the testes. Our results show that LSDV is not limited to specific fractions of the ejaculate and that the testes and epididymides are most profoundly affected. Blood contamination is not responsible for the presence of viral DNA in semen, and it is unlikely that the virus is sperm-associated. Results suggest that the ejaculate is contaminated with viral DNA as it is shed from necrotic lesions in the genital tract. Further research is indicated into the ability of infected semen to produce disease as well as treatment protocols that could render semen free of viral DNA. Production Animal Studies unrestricted 2013-09-07T15:03:26Z 2007-12-17 2013-09-07T15:03:26Z 2007-04-18 2007-12-17 2007-10-31 Dissertation Annandale, CH 2006, Mechanisms by which lumpy skin disease virus is shed in semen of artificially infected bulls, MMedVet dissertation, University of Pretoria, Pretoria, viewed yymmdd < http://upetd.up.ac.za/thesis/available/etd-10312007-160900 / > http://hdl.handle.net/2263/29168 http://upetd.up.ac.za/thesis/available/etd-10312007-160900/ © 2006, University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria. application/pdf University of Pretoria
spellingShingle Cattle
Semen
Lumpy skin disease (LSD)
Bulls
Virus
UCTD
Mechanisms by which lumpy skin disease virus is shed in semen of artificially infected bulls
title Mechanisms by which lumpy skin disease virus is shed in semen of artificially infected bulls
title_full Mechanisms by which lumpy skin disease virus is shed in semen of artificially infected bulls
title_fullStr Mechanisms by which lumpy skin disease virus is shed in semen of artificially infected bulls
title_full_unstemmed Mechanisms by which lumpy skin disease virus is shed in semen of artificially infected bulls
title_short Mechanisms by which lumpy skin disease virus is shed in semen of artificially infected bulls
title_sort mechanisms by which lumpy skin disease virus is shed in semen of artificially infected bulls
topic Cattle
Semen
Lumpy skin disease (LSD)
Bulls
Virus
UCTD
url http://hdl.handle.net/2263/29168
http://upetd.up.ac.za/thesis/available/etd-10312007-160900/