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vol.81 número2Screening for foot-and-mouth disease virus in livestock-wildlife interface areas of TanzaniaThe changing landscape of the molecular epidemiology of foot-and-mouth disease virus in southern Africa north of Limpopo and east Africa índice de autoresíndice de assuntospesquisa de artigos
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Onderstepoort Journal of Veterinary Research

versão On-line ISSN 2219-0635

Onderstepoort j. vet. res. vol.81 no.2 Cape Town Fev. 2014

 

ABSTRACTS

 

Full genome sequencing to study the evolutionary characteristics of foot-and-mouth disease virus in southern Africa

 

 

Christopher J. KasangaI; Begoña Valdazo-GonzálezII; Rahana DwarkaIII; Jemma WadsworthII; Nick J. KnowlesII; Philemon N. WamburaI; Mark M. RweyemamuI; Misheck MulumbaIV; Jimis DeveV; Donald P. KingII

ISouthern African Centre for Infectious diseases Surveillance, Sokoine University of Agriculture, Tanzania
IIWRLFMD, The Pirbright Institute, United Kingdom
IIIOnderstepoort Veterinary Institute, University of Pretoria, South Africa
IVSouthern African Development Community Secretariat, Botswana
VMinistry of Agriculture and Livestock, Mozambique

Correspondence

 

 


ABSTRACT

Foot-and-mouth disease (FMD) is endemic in most countries of southern Africa where it affects cloven-hoofed animals that include livestock and wildlife. Southern Africa relies profoundly on livestock production as a source of economic growth and livelihoods. Despite the importance of FMD in southern Africa, the epidemiology of FMD virus (FMDV) and factors contributing to the endemicity of FMD infection in susceptible animal populations are not clearly known in this region. In this study, we designed and optimised an RT-PCR strategy for amplification of the complete genome of FMDV SAT 1, and sequenced the whole genome of one isolate, designated SAT1/MOZ/BUF-B16/2010, which was isolated from an African buffalo (Syncerus caffer) in Mozambique in 2010. Preliminary analyses showed that the genome polyprotein of SAT1/MOZ/ BUF-B16/2010 consisted of 7626 nucleotides. Alignment of nucleotides and deduced amino acid sequences and phylogenetic analysis indicated that the virus is closely related to SAT 1 strains from the southern African region. Using a FASTA search, the polyprotein showed closest nucleotide identity (94%) to SAT1/RHO/5/66 isolated from cattle in Devuli ranch in southeast Zimbabwe in 1966. This RT-PCR and whole genome sequencing strategy could be deployed to study the evolutionary characteristics of viruses sampled from cattle and buffalo at different locations in time and space. A full repertoire of protocols for all of the circulating FMDV lineages is now required to conduct an in-depth genome analysis to understand the factors that impact upon FMDV endemicity in the region. This information is necessary for strategies for the control of FMD in most countries in Africa. The genome sequencing approach allows for targeted and cost-effective FMD control strategies in the endemic settings of Africa rather than application of blanket and expensive interventions - an important consideration for resource constrained countries.


 

 

Acknowledgement

This work was supported by the Wellcome Trust Grant WT087546MA to the Southern African Centre for Infectious Diseases & Surveillance (SACIDS).

 

 

Correspondence:
Christopher Kasanga
PO Box 3019, Chuo Kikuu
Morogoro, Tanzania
christopher.kasanga@sacids.org

 

 

Note: Proceedings of the 2nd One Health Conference in Africa. Jointly organised by the Southern African Centre for Infectious Disease Surveillance and the Tanzania National Institute for Medical Research, held at the Snow Crest Hotel in Arusha, Tanzania from 16th to 19th April 2013: http://www.sacids.org/kms/frontend/index.php?m=119.

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