Development of a multiplex PCR assay for polymorphism analysis of Brucella suis biovars causing brucellosis in swine

被引:22
作者
Ferrao-Beck, Lenia
Cardoso, Regina
Munoz, Pilar Maria
de Miguel, Maria Jesus
Albert, David
Ferreira, Ana Cristina
Marin, Clara Maria
Thiebaud, Martine
Jacques, Isabelle
Grayon, Maggy
Zygmunt, Michel S.
Garin-Bastuji, Bruno
Blasco, Jose Maria
Sa, Maria Inacia
机构
[1] Lab Nacl Invest Vet, Dept Bacteriol & Virol, P-4485655 Vairao, Portugal
[2] Lab Nacl Invest Vet, P-1459011 Lisbon, Portugal
[3] Ctr Invest & Tecnol Agroalimentaria Aragon, Zaragoza 50059, Spain
[4] Agence Francaise Secur Sanit Aliments, FAO, OIE, Brucellosis Reference Lab, F-94706 Maisons Alfort, France
[5] INRA, Unite Pathol Infect & Immunol, UR918, F-37380 Nouzilly, France
[6] Univ Tours, Inst Technol, F-37082 Tours 2, France
关键词
Brucella suis; multiplex PCR; polymorphism; omp2b gene;
D O I
10.1016/j.vetmic.2006.02.002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Swine brucellosis is caused by the biovars 1, 2 and 3 of Brucella suis the identification of which up to now relies on microbiological tests lacking adequate specificity together with time consuming and expensive molecular procedures. Based on sequence variation of the omp2b gene, we have developed a four primer set multiplex PCR assay that was tested for polymorphism analysis of B. suis biovars causing brucellosis in swine. The assay exploits the single nucleotide polymorphisms found in omp2b gene of B. suis reference biovars which are conserved in 43 B. suis field isolates from different geographic origins and hosts. Three specific amplification patterns (S1, S2 and S3) were obtained for reference strains of B. suis biovars 1, 2 and 3, respectively. However, some B. suis field isolates identified as biovars 2 or 3 according AMOS-PCR, PCR-RFLP of omp31 and omp2 genes and classical bacteriological methods, resulted also in S I patterns, limiting the typing usefulness of the method. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:269 / 277
页数:9
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