Human brucellosis poses a significant public health problem in many develop
ing countries and requires fast and accurate diagnosis. A PCR assay amplify
ing part of the 31-kDa Brucella abortus antigenic protein gene sequence was
developed and applied to whole-blood and serum samples from 31 brucellosis
patients and 45 healthy individuals. All patients except one had detectabl
e Brucella DNA in either whole blood or serum (combined sensitivity, 97%),
but, the assay sensitivity was higher with serum samples (94%) than with wh
ole-blood samples (61%). The assay specificity was excellent (100%). A conf
irmatory PCR assay targeting another Brucella gene region (omp-2) was also
developed but lacked sensitivity. Serum is the optimal specimen for the dia
gnosis of brucellosis by PCR, a choice that leads to assay simplification a
nd shortens turnaround time.