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A field vaccine trial in Tanzania demonstrates partial protection against malignant catarrhal fever in cattle

Malignant catarrhal fever (MCF) is a fatal lymphoproliferative disease of cattle that, in East Africa, results from transmission of the causative virus, alcelaphine herpesvirus 1 (AlHV-1), from wildebeest. A vaccine field trial involving an attenuated AlHV-1 virus vaccine was performed over two wild...

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Autores principales: Lankester, F., Russell, G.C., Lugelo, A., Ndabigaye, A., Mnyambwa, N., Keyyu, J., Kazwala, R., Grant, D., Percival, A., Deane, D., Haig, D.M., Cleaveland, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742522/
https://www.ncbi.nlm.nih.gov/pubmed/26706270
http://dx.doi.org/10.1016/j.vaccine.2015.12.009
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author Lankester, F.
Russell, G.C.
Lugelo, A.
Ndabigaye, A.
Mnyambwa, N.
Keyyu, J.
Kazwala, R.
Grant, D.
Percival, A.
Deane, D.
Haig, D.M.
Cleaveland, S.
author_facet Lankester, F.
Russell, G.C.
Lugelo, A.
Ndabigaye, A.
Mnyambwa, N.
Keyyu, J.
Kazwala, R.
Grant, D.
Percival, A.
Deane, D.
Haig, D.M.
Cleaveland, S.
author_sort Lankester, F.
collection PubMed
description Malignant catarrhal fever (MCF) is a fatal lymphoproliferative disease of cattle that, in East Africa, results from transmission of the causative virus, alcelaphine herpesvirus 1 (AlHV-1), from wildebeest. A vaccine field trial involving an attenuated AlHV-1 virus vaccine was performed over two wildebeest calving seasons on the Simanjiro Plain of northern Tanzania. Each of the two phases of the field trial consisted of groups of 50 vaccinated and unvaccinated cattle, which were subsequently exposed to AlHV-1 challenge by herding toward wildebeest. Vaccination resulted in the induction of virus-specific and virus-neutralizing antibodies. Some cattle in the unvaccinated groups also developed virus-specific antibody responses but only after the start of the challenge phase of the trial. PCR of DNA from blood samples detected AlHV-1 infection in both groups of cattle but the frequency of infection was significantly lower in the vaccinated groups. Some infected animals showed clinical signs suggestive of MCF but few animals went on to develop fatal MCF, with similar numbers in vaccinated and unvaccinated groups. This study demonstrated a baseline level of MCF-seropositivity among cattle in northern Tanzania of 1% and showed that AlHV-1 virus-neutralizing antibodies could be induced in Tanzanian zebu shorthorn cross cattle by our attenuated vaccine, a correlate of protection in previous experimental trials. The vaccine reduced infection rates by 56% in cattle exposed to wildebeest but protection from fatal MCF could not be determined due to the low number of fatal cases.
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spelling pubmed-47425222016-02-26 A field vaccine trial in Tanzania demonstrates partial protection against malignant catarrhal fever in cattle Lankester, F. Russell, G.C. Lugelo, A. Ndabigaye, A. Mnyambwa, N. Keyyu, J. Kazwala, R. Grant, D. Percival, A. Deane, D. Haig, D.M. Cleaveland, S. Vaccine Article Malignant catarrhal fever (MCF) is a fatal lymphoproliferative disease of cattle that, in East Africa, results from transmission of the causative virus, alcelaphine herpesvirus 1 (AlHV-1), from wildebeest. A vaccine field trial involving an attenuated AlHV-1 virus vaccine was performed over two wildebeest calving seasons on the Simanjiro Plain of northern Tanzania. Each of the two phases of the field trial consisted of groups of 50 vaccinated and unvaccinated cattle, which were subsequently exposed to AlHV-1 challenge by herding toward wildebeest. Vaccination resulted in the induction of virus-specific and virus-neutralizing antibodies. Some cattle in the unvaccinated groups also developed virus-specific antibody responses but only after the start of the challenge phase of the trial. PCR of DNA from blood samples detected AlHV-1 infection in both groups of cattle but the frequency of infection was significantly lower in the vaccinated groups. Some infected animals showed clinical signs suggestive of MCF but few animals went on to develop fatal MCF, with similar numbers in vaccinated and unvaccinated groups. This study demonstrated a baseline level of MCF-seropositivity among cattle in northern Tanzania of 1% and showed that AlHV-1 virus-neutralizing antibodies could be induced in Tanzanian zebu shorthorn cross cattle by our attenuated vaccine, a correlate of protection in previous experimental trials. The vaccine reduced infection rates by 56% in cattle exposed to wildebeest but protection from fatal MCF could not be determined due to the low number of fatal cases. Elsevier Science 2016-02-03 /pmc/articles/PMC4742522/ /pubmed/26706270 http://dx.doi.org/10.1016/j.vaccine.2015.12.009 Text en © 2015 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lankester, F.
Russell, G.C.
Lugelo, A.
Ndabigaye, A.
Mnyambwa, N.
Keyyu, J.
Kazwala, R.
Grant, D.
Percival, A.
Deane, D.
Haig, D.M.
Cleaveland, S.
A field vaccine trial in Tanzania demonstrates partial protection against malignant catarrhal fever in cattle
title A field vaccine trial in Tanzania demonstrates partial protection against malignant catarrhal fever in cattle
title_full A field vaccine trial in Tanzania demonstrates partial protection against malignant catarrhal fever in cattle
title_fullStr A field vaccine trial in Tanzania demonstrates partial protection against malignant catarrhal fever in cattle
title_full_unstemmed A field vaccine trial in Tanzania demonstrates partial protection against malignant catarrhal fever in cattle
title_short A field vaccine trial in Tanzania demonstrates partial protection against malignant catarrhal fever in cattle
title_sort field vaccine trial in tanzania demonstrates partial protection against malignant catarrhal fever in cattle
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742522/
https://www.ncbi.nlm.nih.gov/pubmed/26706270
http://dx.doi.org/10.1016/j.vaccine.2015.12.009
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