Diagnosis of bovine brucellosis using a homogeneous fluorescence polarization assay

被引:31
作者
Nielsen, K
Gall, D
Lin, M
Massangill, C
Samartino, L
Perez, B
Coats, M
Hennager, S
Dajer, A
Nicoletti, P
Thomas, F
机构
[1] Anim Dis Res Inst, Canadian Food Inspect Agcy, Nepean, ON K2H 8P9, Canada
[2] Jefferson City Diagnost Lab, Div Anim Hlth, Dept Agr, Jefferson City, MO 65102 USA
[3] Inst Nacl Tecnol Agropecuaria, Ctr Invest Ciencias Vet, Inst Bacteriol, RA-1708 Moron, Buenos Aires, Argentina
[4] Lab Reg Osorno, Serv Agricola & Ganadero, Osorno, Chile
[5] Texas Anim Hlth Commiss, Austin, TX USA
[6] USDA, Natl Vet Serv Labs, Ames, IA 50010 USA
[7] Univ Autonoma Yucatan, Fac Med Vet & Zootecn, Merida, Yucatan, Mexico
[8] Univ Florida, Coll Vet Med, Gainesville, FL USA
关键词
homogeneous assay; fluorescence polarization; serology; brucellosis;
D O I
10.1016/S0165-2427(98)00195-0
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To evaluate the fluorescence polarization assay (FPA) for the serological diagnosis of bovine brucellosis, 118 sera from cattle which were culture positive for Brucella abortus, 1751 sera from cattle from premises containing cattle infected with B. abortus, 1222 sera from cattle vaccinated with B. abortus strain 19 and 1199 sera from cattle with no evidence of brucellosis were tested in Argentina, Chile, Mexico and in the American states of Iowa, Missouri and Texas. Initial determination of serological positivity and negativity was based upon reactivity in currently used serological tests, consisting of a rapid screening test, the rose-bengal or the buffered plate antigen tests, followed by a second serological test, the complement fixation test, Sensitivity of the FPA (sera from culture positive animals) ranged from 87.5% to 100%. Serological positivity of cattle from infected premises ranged from 65.5% to 99.0% while the % negative cattle in herds without evidence of brucellosis was between 94.9 and 100%. Of B. abortus strain 19 vaccinated cattle which were positive in at least one in-use serological tests, 88.2% were negative in the FPA. In contrast, previous Canadian studies, sensitivity values were 99.0% and 100% and the specificity in both cases was 100%. This discrepancy was probably due to the use of less well characterized sera in the current study. (C) 1998 Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:321 / 329
页数:9
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