Use of polymerase chain reaction to detect Brucella abortus biovar 1 in infected goats

被引:52
作者
Leal-Klevezas, DS
Martínez-Vázquez, IO
García-Cantú, J
López-Merino, A
Martínez-Soriano, JP
机构
[1] Inst Politecn Nacl, Ctr Invest & Estudios Avanzados, Unidad Biotecnol & Ingn Genet Plantas, Irapuato 36500, Gto, Mexico
[2] Inst Politecn Nacl, Escuela Nacl Ciencias Biol, Mexico City 11340, DF, Mexico
[3] Univ Autonoma Nuevo Leon, Fac Agron, San Nicolas De Los Garza 64000, NL, Mexico
[4] Univ Autonoma Nuevo Leon, Fac Ciencias Biol, San Nicolas De Los Garza 64000, NL, Mexico
[5] Inst Mexicano Seguro Social, Ctr Invest Biomed Occidente, Guadalajara 44340, Jalisco, Mexico
关键词
goat; polymerase chain reaction (PCR); diagnosis-Brucella abortus; bacteria; blood; milk;
D O I
10.1016/S0378-1135(00)00200-5
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The polymerase chain reaction (PCR) was used to diagnose goat brucellosis and compare its sensitivity against some of the most commonly used serological and bacteriological techniques. Twenty two female and one male out of 300 clinically healthy, mixed-breed goats were randomly chosen from a ranch located at Marin, Nuevo Leon, Mexico. Milk and blood samples were taken from each animal and used to obtain both microbiological cultures and DNA of the pathogen, and sera was tested against Rose Bengal antigen (RBT). Results showed that 86% of the blood samples were positive on the PCR test, while 60% were positive on the serological test. The pathogen was isolated from only one blood culture, Sixty four percent of the milk samples were positive on PCR tests, but failed to yield bacteria in culture, Biochemical and PCR specific assay demonstrated that Brucella abortus biovar 1 was associated with the infection. This study demonstrates the higher sensitivity of PCR over RBT and blood culture and its potential towards a rapid identification of Brucella strains, (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:91 / 97
页数:7
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