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A field study evaluating the humoral immune response in Mongolian sheep vaccinated against sheeppox virus.
Fay, Petra; Limon, Georgina; Ulziibat, Gerelmaa; Khanui, Buyantogtokh; Myagmarsuren, Odonchimeg; Tore, Gessica; Khishgee, Bodisaikhan; Flannery, John; Sandag, Batkhuyag; Damdinjav, Batchuluun; Beard, Philippa M.
Affiliation
  • Fay P; The Pirbright Institute, Pirbright, UK.
  • Limon G; The Pirbright Institute, Pirbright, UK.
  • Ulziibat G; State Central Veterinary Laboratory, Zaisan, Khan-Uul District, Ulaanbaatar, Mongolia.
  • Khanui B; State Central Veterinary Laboratory, Zaisan, Khan-Uul District, Ulaanbaatar, Mongolia.
  • Myagmarsuren O; State Central Veterinary Laboratory, Zaisan, Khan-Uul District, Ulaanbaatar, Mongolia.
  • Tore G; The Pirbright Institute, Pirbright, UK.
  • Khishgee B; State Central Veterinary Laboratory, Zaisan, Khan-Uul District, Ulaanbaatar, Mongolia.
  • Flannery J; The Pirbright Institute, Pirbright, UK.
  • Sandag B; The Mongolian General Authority for Veterinary Services, Ulaanbaatar, Mongolia.
  • Damdinjav B; State Central Veterinary Laboratory, Zaisan, Khan-Uul District, Ulaanbaatar, Mongolia.
  • Beard PM; The Pirbright Institute, Pirbright, UK.
Transbound Emerg Dis ; 69(4): 1837-1846, 2022 Jul.
Article de En | MEDLINE | ID: mdl-34033248
Sheeppox is a transboundary disease of small ruminants caused by infection with the capripoxvirus sheeppox virus. Sheeppox is found in Africa, the Middle East and Asia and is characterized by fever, multifocal cutaneous raised lesions and death. Vaccination with live attenuated capripoxvirus (CPPV) strains is an effective and widely used strategy to contol sheeppox outbreaks; however, there are few reports of post-vaccination field surveillance studies. This study used a commercially available enzyme-linked immunosorbent assay (ELISA) to examine quantitative and temporal features of the humoral response of sheep vaccinated with a live-attenuated CPPV strain in Mongolia. Four hundred samples were tested using the ELISA commercial kit, and a subset of 45 samples were also tested with a virus neutralization test (VNT). There was substantial agreement between the VNT and ELISA tests. Antibodies to CPPV were detected between 40 and 262 days post-vaccination. There was no significant difference between serological status (positive/negative) and sex or age; however, an inverse correlation was found between the length of time since vaccination and serological status. Animals between 90 and 180 days post-vaccination were more likely to be positive than animals greater than 180 days post-vaccination. Our results show that a commercial CPPV ELISA kit is a robust and reliable assay for post-CPPV vaccination surveillance in resource-restricted settings and provide temporal parameters to be considered when planning sheeppox post-vaccination monitoring programmes.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Maladies des ovins / Capripoxvirus / Infections à Poxviridae Type d'étude: Diagnostic_studies Limites: Animals Langue: En Journal: Transbound Emerg Dis Sujet du journal: MEDICINA VETERINARIA Année: 2022 Type de document: Article Pays de publication: Allemagne

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Maladies des ovins / Capripoxvirus / Infections à Poxviridae Type d'étude: Diagnostic_studies Limites: Animals Langue: En Journal: Transbound Emerg Dis Sujet du journal: MEDICINA VETERINARIA Année: 2022 Type de document: Article Pays de publication: Allemagne