Dear colleagues,


We have recently published a new publication in Journal of Veterinary 
Diagnostic Investigation: A protein A/G indirect enzyme-linked immunosorbent 
assay for the detection of anti-Brucella antibodies in Arctic wildlife.



Avaliable online at: 
http://vdi.sagepub.com/content/early/2013/03/28/1040638713485073.abstract



The paper validates an serological method for anti-Brucella antibodies in 
Arctic wildlife, spesifically in hooded seal, various whales, polar bear and 
reindeer. We also present seroprevalences for the different species.



Abstract:



A species-independent indirect enzyme-linked immunosorbent assay (iELISA) based 
on chimeric protein A/G was established for the detection of anti-Brucella 
antibodies in Arctic wildlife species and compared to previously established 
brucellosis serological tests for hooded seals (Cystophora cristata), minke 
whales (Balaenoptera acutorostrata), sei whales (Balaenoptera borealis), fin 
whales (Balaenoptera physalus), and polar bears (Ursus maritimus), as well as 
bacteriology results for reindeer and caribou (Rangifer tarandus sp.). The 
protein A/G iELISA results were consistent with the other serological tests 
with Cohen kappa values between 0.47 and 0.92, and the protein A/G iELISA can 
thus offer a technically simple method for these species yielding results 
consistent with established brucellosis serological tests. Receiver operator 
characteristics analysis proved that the reindeer and caribou protein A/G 
iELISA results were consistent with the bacteriological gold standard with an 
area under the curve of 0.99, and the protein A/G iELISA was thus validated as 
a sensitive and specific serological method for the detection of anti-Brucella 
antibodies in reindeer and caribou. The binding of the antibodies from the 
respective species to protein A and G were also evaluated in the iELISA. The 
antibodies from hooded seals and polar bears reacted stronger to protein A than 
to G. The sei whale, fin whale, reindeer, and caribou antibodies reacted 
stronger to protein G than to A. The minke whale antibodies reacted to both 
protein A and G. There was a strong correlation (rs = 0.88–0.98) between the 
optical density results obtained with the iELISA with protein A/G and protein A 
or G, showing that protein A/G is as well suited as protein A or G for the 
detection of anti-Brucella antibodies in these species with the iELISA.



Best wishes from the north,



Ingebjørg H. Nymo ([email protected]<mailto:[email protected]>)



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