Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/51916
Title: A transversal study on antibodies against selected pathogens in dromedary camels in the Canary Islands, Spain
Authors: Mentaberre, Gregorio
Gutierrez, Carlos 
Rodríguez, Noé F.
Joseph, Sunitha
González-Barrio, David
Cabezón, Oscar
de la Fuente, José
Gortazar, Christian
Boadella, Mariana
Keywords: Toxoplasma-Gondii Antibodies
West Nile Virus
Neospora-Caninum
Detecting Antibodies
Mycobacterium-Bovis, et al
Issue Date: 2013
Publisher: 0378-1135
Journal: Veterinary Microbiology 
Abstract: The Canary Islands contain the most important dromedary camel (Camelus dromedarius) population in the European Union and are the main export point of dromedaries to continental Europe and Latin America. We investigated the presence of antibodies against relevant disease agents in 100 Canarian camel sera. Selected blood samples of the same animals were also tested by PCR. Sera were tested for antibodies against Bluetongue virus (BTV; 0%), Bovine Viral Diarrhoea virus (BVDV; 0%), Camelpox virus (CPV; 8% by serum neutralization, 16% by ELISA), Peste des Petits Ruminants virus (PPRV, 0%), Rift Valley Fever virus (RVFV; 0%) and West Nile Fever virus (WNV; 3%), the bacterial pathogens Anaplasma sp. (3%), Brucella sp. (1%), Coxiella burnetii (19%), Mycobacterium avium paratuberculosis (MAP; 22%), Mycobacterium tuberculosis complex (MTC; 10%) and Rickettsia sp. (83%), and the parasites Toxoplasma gondii (36%) and Neospora caninum (86%). The most remarkable findings were the detection of antibodies against CPV and the high antibody prevalence against C burnetii, Rickettsia sp., T. gondii and N. caninum. By PCR, we found no C burnetii, N. caninum and Anaplasma sp. DNA in the tested samples. However, Rickettsia sp. DNA was detected in six antibody positive tested samples. These results should be taken into consideration in order to implement adequate control measures and avoid a potential dissemination of infections to other territories. (C) 2013 Elsevier B.V. All rights reserved.
URI: http://hdl.handle.net/10553/51916
ISSN: 0378-1135
DOI: 10.1016/j.vetmic.2013.07.029
Source: Veterinary Microbiology[ISSN 0378-1135],v. 167 (3-4), p. 468-473
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