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Reactions of sera from laboratory, domestic and wild animals in Africa with Protein a and a recombinant chimeric Protein AG
Authors:Patrick J. Kelly   Margaret Tagwira   Linda Matthewman   Peter R. Mason  E.Pamela Wright  
Affiliation:

a Department of Clinical Veterinary Studies, University of Zimbabwe, Harare, Zimbabwe

b Department of Medical Microbiology, University of Zimbabwe, Harare, Zimbabwe

c Department of Health Care Training, Royal Tropical Institute, Mauritskade 63, 1092 AD, Amsterdam, The Netherlands

Abstract:An ELISA was developed to determine the reactivity of peroxidase labelled Protein A and a recombinant Protein A + Protein G construct, to sera from a variety of laboratory, domestic and wild animals from Africa. There was variability in the binding capacity of sera from individuals of the same species, but four groups could be recognized. Sera from birds and crocodiles were at most weakly reactive with either Protein A or the chimeric construct. Sera from some domestic animals such as horse, goat and cat, and sera from some wild ungulates including buffalo, wildebeest, waterbuck and impala were reactive with Protein A, but reacted to a much greater degree with the chimeric construct. Sera from larger wild animals such as elephant, rhinoceros and giraffe were strongly reactive with the chimeric protein and moderately reactive with Protein A. Sera from primates and dog, pig, guinea pig and rabbit reacted strongly with both proteins. Chimeric proteins that combine the IgG binding capacities of Protein A and Protein G can be used to detect immunoglobulin from a wide variety of African wild animal species. They may thus be of great value in seroepidemiological investigations of these animal populations.
Keywords:Protein A   Protein G   wildlife   serology   epidemiologyAuthor Keywords: Protéine A   Protéine G   animaux sauvages   sérologie   épidémiologie
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