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Seroprevalence of Rift Valley fever in cattle along the Akagera–Nyabarongo rivers, Rwanda

Rift Valley fever (RVF) virus is caused by a zoonotic arbovirus that is endemic to eastern and southern Africa. It has also been reported in West and North Africa, Madagascar and the Arabian Peninsula. The virus is transmitted by mosquitoes, but people can also become infected while handling blood o...

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Autores principales: Umuhoza, Thérèse, Berkvens, Dirk, Gafarasi, Isidore, Rukelibuga, Joseph, Mushonga, Borden, Biryomumaisho, Savino
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AOSIS 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6138214/
https://www.ncbi.nlm.nih.gov/pubmed/28240033
http://dx.doi.org/10.4102/jsava.v88i0.1379
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author Umuhoza, Thérèse
Berkvens, Dirk
Gafarasi, Isidore
Rukelibuga, Joseph
Mushonga, Borden
Biryomumaisho, Savino
author_facet Umuhoza, Thérèse
Berkvens, Dirk
Gafarasi, Isidore
Rukelibuga, Joseph
Mushonga, Borden
Biryomumaisho, Savino
author_sort Umuhoza, Thérèse
collection PubMed
description Rift Valley fever (RVF) virus is caused by a zoonotic arbovirus that is endemic to eastern and southern Africa. It has also been reported in West and North Africa, Madagascar and the Arabian Peninsula. The virus is transmitted by mosquitoes, but people can also become infected while handling blood or other body fluids of animals and humans with RVF. In 2007, there was a large outbreak of RVF in Kenya, Tanzania, Sudan and Somalia. Outbreaks were also reported in South Africa in 2008–2011. The epidemiology of RVF and factors for disease occurrence in Rwanda are neither clear nor documented. Therefore, we conducted a cross-sectional study from December 2012 to March 2013 to generate baseline information on RVF in cattle. Purposive sampling of cattle (n = 595) was done in six districts, and serum samples were screened with competitive enzyme-linked immunosorbent assay (ELISA). We performed a statistical analysis on the generated data, and risk factors associated with RVF seroprevalence were determined by a simple logistic regression. Overall, RVF seroprevalence was 16.8% (95% confidence interval [CI] [13.8% – 20.0%]). The highest seroprevalence was recorded in Kirehe district (36.9%) followed by Ngoma (22.3%), and the least was recorded in Nyagatare (7.9%). RVF was more likely to occur in adult cattle (19.9% [odds ratio {OR} = 1.88, 95% CI {0.98–3.61}]) compared to young cattle (10.5% [OR = 0.47, 95% CI {0.26–0.83}]). Pure exotic or cross-breeds were significantly exposed to RVF virus (seroprevalence 22.9% [OR = 4.26, 95% CI {1.82–9.99}]) in comparison to 14.1% (OR = 0.55, 95% CI [0.35–0.86]) in local breeds. Sex differences were not statistically significant. These findings indicated that cattle have been exposed to RVF virus in six districts in Rwanda with a significant risk in adult, exotic or cross-breeds in Kirehe district.
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spelling pubmed-61382142018-09-26 Seroprevalence of Rift Valley fever in cattle along the Akagera–Nyabarongo rivers, Rwanda Umuhoza, Thérèse Berkvens, Dirk Gafarasi, Isidore Rukelibuga, Joseph Mushonga, Borden Biryomumaisho, Savino J S Afr Vet Assoc Original Research Rift Valley fever (RVF) virus is caused by a zoonotic arbovirus that is endemic to eastern and southern Africa. It has also been reported in West and North Africa, Madagascar and the Arabian Peninsula. The virus is transmitted by mosquitoes, but people can also become infected while handling blood or other body fluids of animals and humans with RVF. In 2007, there was a large outbreak of RVF in Kenya, Tanzania, Sudan and Somalia. Outbreaks were also reported in South Africa in 2008–2011. The epidemiology of RVF and factors for disease occurrence in Rwanda are neither clear nor documented. Therefore, we conducted a cross-sectional study from December 2012 to March 2013 to generate baseline information on RVF in cattle. Purposive sampling of cattle (n = 595) was done in six districts, and serum samples were screened with competitive enzyme-linked immunosorbent assay (ELISA). We performed a statistical analysis on the generated data, and risk factors associated with RVF seroprevalence were determined by a simple logistic regression. Overall, RVF seroprevalence was 16.8% (95% confidence interval [CI] [13.8% – 20.0%]). The highest seroprevalence was recorded in Kirehe district (36.9%) followed by Ngoma (22.3%), and the least was recorded in Nyagatare (7.9%). RVF was more likely to occur in adult cattle (19.9% [odds ratio {OR} = 1.88, 95% CI {0.98–3.61}]) compared to young cattle (10.5% [OR = 0.47, 95% CI {0.26–0.83}]). Pure exotic or cross-breeds were significantly exposed to RVF virus (seroprevalence 22.9% [OR = 4.26, 95% CI {1.82–9.99}]) in comparison to 14.1% (OR = 0.55, 95% CI [0.35–0.86]) in local breeds. Sex differences were not statistically significant. These findings indicated that cattle have been exposed to RVF virus in six districts in Rwanda with a significant risk in adult, exotic or cross-breeds in Kirehe district. AOSIS 2017-01-20 /pmc/articles/PMC6138214/ /pubmed/28240033 http://dx.doi.org/10.4102/jsava.v88i0.1379 Text en © 2017. The Authors https://creativecommons.org/licenses/by/2.0/AOSIS. This work is licensed under the Creative Commons Attribution License.
spellingShingle Original Research
Umuhoza, Thérèse
Berkvens, Dirk
Gafarasi, Isidore
Rukelibuga, Joseph
Mushonga, Borden
Biryomumaisho, Savino
Seroprevalence of Rift Valley fever in cattle along the Akagera–Nyabarongo rivers, Rwanda
title Seroprevalence of Rift Valley fever in cattle along the Akagera–Nyabarongo rivers, Rwanda
title_full Seroprevalence of Rift Valley fever in cattle along the Akagera–Nyabarongo rivers, Rwanda
title_fullStr Seroprevalence of Rift Valley fever in cattle along the Akagera–Nyabarongo rivers, Rwanda
title_full_unstemmed Seroprevalence of Rift Valley fever in cattle along the Akagera–Nyabarongo rivers, Rwanda
title_short Seroprevalence of Rift Valley fever in cattle along the Akagera–Nyabarongo rivers, Rwanda
title_sort seroprevalence of rift valley fever in cattle along the akagera–nyabarongo rivers, rwanda
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6138214/
https://www.ncbi.nlm.nih.gov/pubmed/28240033
http://dx.doi.org/10.4102/jsava.v88i0.1379
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