Brucellosis 2003 proceedings - PHIDIAS
Brucellosis 2003 proceedings - PHIDIAS
Brucellosis 2003 proceedings - PHIDIAS
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Keynote Lectures<br />
Routine biochemical and haematological laboratory tests show variable and<br />
overlapping results with many other diseases. The Brucella-specific tests are the<br />
mainstay in laboratory diagnosis of brucellosis. These include culture, slide or tube<br />
agglutination, indirect Coombs’, ELISA, IFA, and molecular techniques e.g. PCR.<br />
Different types of antigen preparations have been utilized in detecting Ig classes and<br />
subclasses seeking reliable diagnostic and prognostic assays and markers. ELISA<br />
proved to be the test of choice especially in complicated and chronic cases. So far,<br />
the key approach in determining prognosis and relapse is a sequential follow-up of<br />
patients using serological tests. Discrimination between active and inactive stages<br />
can be very difficult, however, the use of certain antigens e.g anti Brucella<br />
cytoplasmic or membranous protein antibodies in ELISA seems useful. Molecular<br />
tests were shown to have a promising role in diagnosis, however, their potential<br />
value in patient follow-up and in distinguishing among different disease forms,<br />
remains to be determined. Knowledge about the advantages, disadvantages and<br />
limitations of these tests are essential for the proper interpretation of results, in<br />
relation to the history and clinical presentation of patients under investigation.<br />
DEVELOPMENT AND VALIDATION OF DIAGNOSTIC TOOLS AND TYPING<br />
METHODS FOR THE CERTIFICATION OF THE ABSENCE OF BOVINE<br />
BRUCELLOSIS IN BELGIUM.<br />
J. Godfroid. Veterinary and Agrochemical Research Center, Brussels, Belgium.<br />
In the beginning of the nineties, the prevalence rate of bovine brucellosis was<br />
very low in Belgium, although bovine brucellosis was not eradicated. This<br />
epidemiological situation allowed us to describe a new phenomenon: the emergence<br />
of “False Positive Serological Reactions” (FPSR) in bovine brucellosis screening<br />
tests. The most likely hypothesis to explain this phenomenon (but maybe not the only<br />
one) is a Yersinia enterocolitica O:9 infection. In parallel, we described for the first<br />
time, a Brucella suis biotype 2 enzootic brucellosis in wild boars (Sus scrofa) in<br />
Western Europe.<br />
Therefore, new diagnostic tools had to be developed in order to differentiate<br />
beyond any doubt cattle infected by Brucella abortus, Brucella suis or Yersinia<br />
enterocolitica O:9. Our work allowed us to validate, under experimental conditions,<br />
the brucellosis skin test and the IFN-γ assay as bovine brucellosis diagnostic tools. A<br />
testing strategy integrating these new tools has been successfully implemented in the<br />
field in Belgium. This work has led to the incorporation of the brucellosis skin test in<br />
the new Directive 432/64/CEE that deals with living animals movements within the<br />
European Union.<br />
Recently, our knowledge of the ecological niche of Brucella has been<br />
extended to marine mammals. It has been shown that these Brucella represent a<br />
new potential source of infection for both domestic animals and humans. Studies on<br />
the molecular typing of marine mammal Brucella reinforce the proposal of adding two<br />
new species in the genus Brucella: Brucella cetaceae (infection in cetacean) and<br />
Brucella pinnipediae (infection in pinnipeds).<br />
<strong>Brucellosis</strong> <strong>2003</strong> International Research Conference<br />
39