A homogeneous fluorescence-polarization assay (FPA) was used for the serolo
gical diagnosis of bovine brucellosis in Mexico. The assay uses O-polysacch
aride prepared from Brucella abortus Lipopolysaccharide (20-30 kDa) conjuga
ted with fluorescein isothiocyanate as a tracer. To measure the fluorescenc
e polarization, a FPM-1 fluorescence-polarization analyzer was used with th
e procedure described by Nielsen et al. (1996b). A cut-off value of 90 mill
ipolarization (mP) units was used for testing 560 bovine sera from differen
t areas of Mexico. (305 positive sera and 255 negative sera according to th
e complement fixation test; CFT.) Some were tested with the Rose Bengal pla
te (RB) test (n = 490) and some with the rivanol-agglutination (RN) test (n
= 190). Sensitivities were 98.3%, 99.3% and 99.0%, and specificities were
68.8%, 55.4% and 96.9%, respectively, for RE, RN and FPA. The FPA gave a ka
ppa coefficient of agreement with respect to CFT of 0.96, while RE and RIV
(relative to the CFT) gave coefficients of 0.70 and 0.61, respectively. Fin
ally, ROC analysis suggested a cut-off value which agreed with the one reco
mmended in the test procedure. We concluded that FPA is a suitable test to
be used instead of the CFT in Mexican conditions. (C) 1999 Elsevier Science
B.V. All rights reserved.