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Evolutionary analysis of foot-and-mouth disease virus serotype SAT 1 isolates from east africa suggests two independent introductions from southern africa

BACKGROUND: In East Africa, foot-and-mouth disease virus serotype SAT 1 is responsible for occasional severe outbreaks in livestock and is known to be maintained within the buffalo populations. Little is known about the evolutionary forces underlying its epidemiology in the region. To enhance our ap...

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Autores principales: Sangula, Abraham K, Belsham, Graham J, Muwanika, Vincent B, Heller, Rasmus, Balinda, Sheila N, Masembe, Charles, Siegismund, Hans R
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3004922/
https://www.ncbi.nlm.nih.gov/pubmed/21118525
http://dx.doi.org/10.1186/1471-2148-10-371
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author Sangula, Abraham K
Belsham, Graham J
Muwanika, Vincent B
Heller, Rasmus
Balinda, Sheila N
Masembe, Charles
Siegismund, Hans R
author_facet Sangula, Abraham K
Belsham, Graham J
Muwanika, Vincent B
Heller, Rasmus
Balinda, Sheila N
Masembe, Charles
Siegismund, Hans R
author_sort Sangula, Abraham K
collection PubMed
description BACKGROUND: In East Africa, foot-and-mouth disease virus serotype SAT 1 is responsible for occasional severe outbreaks in livestock and is known to be maintained within the buffalo populations. Little is known about the evolutionary forces underlying its epidemiology in the region. To enhance our appreciation of the epidemiological status of serotype SAT 1 virus in the region, we inferred its evolutionary and phylogeographic history by means of genealogy-based coalescent methods using 53 VP1 coding sequences covering a sampling period from 1948-2007. RESULTS: The VP1 coding sequence of 11 serotype SAT 1 FMD viruses from East Africa has been determined and compared with known sequences derived from other SAT 1 viruses from sub-Saharan Africa. Purifying (negative) selection and low substitution rates characterized the SAT 1 virus isolates in East Africa. Two virus groups with probable independent introductions from southern Africa were identified from a maximum clade credibility tree. One group was exclusive to Uganda while the other was present within Kenya and Tanzania. CONCLUSIONS: Our results provide a baseline characterization of the inter-regional spread of SAT 1 in sub-Saharan Africa and highlight the importance of a regional approach to trans-boundary animal disease control in order to monitor circulating strains and apply appropriate vaccines.
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spelling pubmed-30049222010-12-21 Evolutionary analysis of foot-and-mouth disease virus serotype SAT 1 isolates from east africa suggests two independent introductions from southern africa Sangula, Abraham K Belsham, Graham J Muwanika, Vincent B Heller, Rasmus Balinda, Sheila N Masembe, Charles Siegismund, Hans R BMC Evol Biol Research Article BACKGROUND: In East Africa, foot-and-mouth disease virus serotype SAT 1 is responsible for occasional severe outbreaks in livestock and is known to be maintained within the buffalo populations. Little is known about the evolutionary forces underlying its epidemiology in the region. To enhance our appreciation of the epidemiological status of serotype SAT 1 virus in the region, we inferred its evolutionary and phylogeographic history by means of genealogy-based coalescent methods using 53 VP1 coding sequences covering a sampling period from 1948-2007. RESULTS: The VP1 coding sequence of 11 serotype SAT 1 FMD viruses from East Africa has been determined and compared with known sequences derived from other SAT 1 viruses from sub-Saharan Africa. Purifying (negative) selection and low substitution rates characterized the SAT 1 virus isolates in East Africa. Two virus groups with probable independent introductions from southern Africa were identified from a maximum clade credibility tree. One group was exclusive to Uganda while the other was present within Kenya and Tanzania. CONCLUSIONS: Our results provide a baseline characterization of the inter-regional spread of SAT 1 in sub-Saharan Africa and highlight the importance of a regional approach to trans-boundary animal disease control in order to monitor circulating strains and apply appropriate vaccines. BioMed Central 2010-11-30 /pmc/articles/PMC3004922/ /pubmed/21118525 http://dx.doi.org/10.1186/1471-2148-10-371 Text en Copyright ©2010 Sangula et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Sangula, Abraham K
Belsham, Graham J
Muwanika, Vincent B
Heller, Rasmus
Balinda, Sheila N
Masembe, Charles
Siegismund, Hans R
Evolutionary analysis of foot-and-mouth disease virus serotype SAT 1 isolates from east africa suggests two independent introductions from southern africa
title Evolutionary analysis of foot-and-mouth disease virus serotype SAT 1 isolates from east africa suggests two independent introductions from southern africa
title_full Evolutionary analysis of foot-and-mouth disease virus serotype SAT 1 isolates from east africa suggests two independent introductions from southern africa
title_fullStr Evolutionary analysis of foot-and-mouth disease virus serotype SAT 1 isolates from east africa suggests two independent introductions from southern africa
title_full_unstemmed Evolutionary analysis of foot-and-mouth disease virus serotype SAT 1 isolates from east africa suggests two independent introductions from southern africa
title_short Evolutionary analysis of foot-and-mouth disease virus serotype SAT 1 isolates from east africa suggests two independent introductions from southern africa
title_sort evolutionary analysis of foot-and-mouth disease virus serotype sat 1 isolates from east africa suggests two independent introductions from southern africa
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3004922/
https://www.ncbi.nlm.nih.gov/pubmed/21118525
http://dx.doi.org/10.1186/1471-2148-10-371
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