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dc.contributor.authorTefula Dhikusooka, Moses
dc.contributor.authorAyebazibwe, Chrisostom
dc.contributor.authorNamatovu, Alice
dc.contributor.authorBelsham, Graham J.
dc.contributor.authorRedlef Siegismund, Hans
dc.contributor.authorNabalayo Wekesa, Sabenzia
dc.contributor.authorNina Balinda, Sheila
dc.contributor.authorMuwanika, Vincent B.
dc.contributor.authorTjørnehøj, Kirsten
dc.date.accessioned2023-01-24T17:21:09Z
dc.date.available2023-01-24T17:21:09Z
dc.date.issued2016
dc.identifier.citationDhikusooka, M. T., Ayebazibwe, C., Namatovu, A., Belsham, G. J., Siegismund, H. R., Wekesa, S. N., ... & Tjørnehøj, K. (2016). Unrecognized circulation of SAT 1 foot-and-mouth disease virus in cattle herds around Queen Elizabeth National Park in Uganda. BMC veterinary research, 12(1), 1-13. DOI 10.1186/s12917-015-0616-1en_US
dc.identifier.other10.1186/s12917-015-0616-1
dc.identifier.urihttps://nru.uncst.go.ug/handle/123456789/7171
dc.description.abstractFoot-and-mouth disease (FMD) is endemic in Uganda in spite of the control measures used. Various aspects of the maintenance and circulation of FMD viruses (FMDV) in Uganda are not well understood; these include the role of the African buffalo (Syncerus caffer) as a reservoir for FMDV. To better understand the epidemiology of FMD at the livestock-wildlife-interface, samples were collected from young, unvaccinated cattle from 24 pastoral herds that closely interact with wildlife around Queen Elizabeth National Park in Uganda, and analysed for evidence of FMDV infection. Results: In total, 37 (15 %) of 247 serum samples had detectable antibodies against FMDV non-structural proteins (NSPs) using a pan-serotypic assay. Within these 37 sera, antibody titres ≥ 80 against the structural proteins of serotypes O, SAT 1, SAT 2 and SAT 3 were detected by ELISA in 5, 7, 4 and 3 samples, respectively, while neutralizing antibodies were only detected against serotype O in 3 samples. Two FMDV isolates, with identical VP1 coding sequences, were obtained from probang samples from clinically healthy calves from the same herd and are serotype SAT 1 (topotype IV (EA-I)). Based on the VP1 coding sequences, these viruses are distinct from previous cattle and buffalo SAT 1 FMDV isolates obtained from the same area (19–30 % nucleotide difference) and from the vaccine strain (TAN/155/71) used within Uganda (26 % nucleotide difference). Eight herds had only one or a few animals with antibodies against FMDV NSPs while six herds had more substantial evidence of prior infection with FMDV. There was no evidence for exposure to FMDV in the other ten herds. Conclusions: The two identical SAT 1 FMDV VP1 sequences are distinct from former buffalo and cattle isolates from the same area, thus, transmission between buffalo and cattle was not demonstrated. These new SAT 1 FMDV isolates differed significantly from the vaccine strain used to control Ugandan FMD outbreaks, indicating a need for vaccine matching studies. Only six herds had clear serological evidence for exposure to O and SAT 1 FMDV. Scattered presence of antibodies against FMDV in other herds may be due to the occasional introduction of animals to the area or maternal antibodies from past infection and/or vaccination. The evidence for asymptomatic FMDV infection has implications for disease control strategies in the area since this obstructs early disease detection that is based on clinical signs in FMDV infected animals.en_US
dc.language.isoenen_US
dc.publisherBMC veterinary researchen_US
dc.subjectLivestock-wildlife interfaceen_US
dc.subjectFoot-and-mouth disease virusen_US
dc.subjectSAT 1en_US
dc.subjectYoung cattleen_US
dc.titleUnrecognized circulation of SAT 1 foot-andmouth disease virus in cattle herds around Queen Elizabeth National Park in Ugandaen_US
dc.typeArticleen_US


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