Björkman, Camilla
- Department of Clinical Sciences, Swedish University of Agricultural Sciences
Research article2004Peer reviewed
von Blumroder D, Schares G, Norton R, Williams DJL, Esteban-Redondo I, Wright S, Bjorkman C, Frossling J, Risco-Castillo V, Fernandez-Garcia A, Ortega-Mora LM, Sager H, Hemphill A, van Maanen C, Wouda W, Conraths FJ
Various existing serological tests were compared with a standard panel of 523 sera in a multicentred study across Europe. Well characterised sera from animals that were experimentally or naturally infected with Neospora caninum as well as sera from cattle deemed uninfected with N. caninum were provided by the participants of the study and analysed in several commercial (CHEKIT(R) Dr. Bommeli/Intervet, CIVTESTTM BOVIS NEOSPORA Hipra, Cypress Diagnostics C.V., Herd Check((R)) IDEXX, Mastazyme(TM) MAST Diagnostics, P38-ELISA Animal Welfare and Food Safety GmbH (AFOSA)) as well as in-house assays (five ELISAs and one IFAT). Most tests showed a high level of agreement in the interpretation of the test results (positive or negative). A further distinct increase in agreement between tests was obtained after the application of standardised cut-offs offered by a two-graph receiver operating characteristic analysis. This procedure allows a standardised interpretation of results obtained with different tests used in independent, parallel seroepidemiological studies. (C) 2004 Elsevier B.V. All rights reserved
Veterinary Parasitology
2004, Volume: 120, number: 1-2, pages: 11-22
Publisher: ELSEVIER SCIENCE BV
DOI: https://doi.org/10.1016/j.vetpar.2003.12.010
https://res.slu.se/id/publ/2726