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布鲁氏菌属omp - 31基因座的DNA多态性:流产布鲁氏菌存在大片段缺失的证据及其他种特异性标记

DNA polymorphism at the omp-31 locus of Brucella spp.: evidence for a large deletion in Brucella abortus, and other species-specific markers.

作者信息

Vizcaíno Nieves, Verger Jean-Michel, Grayon Maggy, Zygmunt Michel S, Cloeckaert Axel

机构信息

Laboratoire de Pathologie Infectieuse et Immunologie, Centre de Recherches de Tours, Institut National de la Recherche Agronomique, 37380 Nouzilly, France.

出版信息

Microbiology (Reading). 1997 Sep;143 ( Pt 9):2913-2921. doi: 10.1099/00221287-143-9-2913.

Abstract

The omp-31 gene, encoding a major outer-membrane protein in Brucella melitensis, was PCR-amplified from Brucella strains representing all species and known biovars by using primers selected according to the B. melitensis 16M omp-31 published sequence. Amplification of omp-31 was achieved from DNA of all Brucella species with the exception of Brucella abortus, the only Brucella species where expression of omp-31 was not detected by reactivity with an mAb specific for an epitope located in Omp-31. Southern blot hybridization of plasmid probes, bearing inserts (4.4-17 kb) containing B. melitensis 16M omp-31 and adjacent DNA of different sizes, with HindIII-digested total DNA showed that a large fragment, comprising the entire omp-31 gene and flanking DNA, was actually absent in B. abortus strains. The size of this DNA fragment has been determined to be about 10 kb. Southern blot hybridization with the different plasmid probes identified species-specific markers for B. abortus and B. melitensis. At the biovar level, a specific marker for B. melitensis bv. 1 was also identified. Additionally, PCR-RFLP studies of omp-31 revealed specific markers for Brucella ovis, Brucella canis and Brucella suis bv. 2. Using a combination of omp-31 PCR-RFLP patterns and Southern blot hybridization profiles Brucella species were differentiated with the sole exception of Brucella neotomae which was not differentiated from B. suis bv. 1, 3, 4 and 5. Results presented in this paper demonstrate the potential of omp-31 for differentiating the brucellae and show that B. abortus lacks a large DNA fragment of about 10 kb containing omp-31 and flanking DNA. In such a large deletion, other genes in addition to omp-31 are probably involved. Sequencing of this DNA fragment will help to identify the missing genes in B. abortus which could possibly be involved in the differences of pathogenicity and host preference seen in Brucella species.

摘要

编码羊种布鲁氏菌主要外膜蛋白的omp - 31基因,通过使用根据羊种布鲁氏菌16M的omp - 31公布序列选择的引物,从代表所有种和已知生物型的布鲁氏菌菌株中进行PCR扩增。除流产布鲁氏菌外,所有布鲁氏菌物种的DNA均可扩增出omp - 31,流产布鲁氏菌是唯一一种不能通过与针对位于Omp - 31中一个表位的单克隆抗体反应来检测到omp - 31表达的布鲁氏菌物种。携带含有羊种布鲁氏菌16M的omp - 31和不同大小相邻DNA的插入片段(4.4 - 17 kb)的质粒探针与经HindIII消化的总DNA进行Southern印迹杂交,结果表明流产布鲁氏菌菌株中实际上不存在包含整个omp - 31基因和侧翼DNA的大片段。已确定该DNA片段大小约为10 kb。与不同质粒探针的Southern印迹杂交鉴定出了流产布鲁氏菌和羊种布鲁氏菌的种特异性标记。在生物型水平上,还鉴定出了羊种布鲁氏菌生物型1的特异性标记。此外,omp - 31的PCR - RFLP研究揭示了绵羊布鲁氏菌、犬布鲁氏菌和猪种布鲁氏菌生物型2的特异性标记。结合使用omp - 31的PCR - RFLP模式和Southern印迹杂交图谱,除了新墨西哥布鲁氏菌与猪种布鲁氏菌生物型1、3、4和5无法区分外,其他布鲁氏菌物种均可被区分。本文给出的结果证明了omp - 31在区分布鲁氏菌方面的潜力,并表明流产布鲁氏菌缺乏一个约10 kb包含omp - 31和侧翼DNA的大DNA片段。在如此大的缺失中,除了omp - 31外可能还涉及其他基因。对该DNA片段进行测序将有助于鉴定流产布鲁氏菌中缺失的基因,这些基因可能与布鲁氏菌物种中观察到的致病性和宿主偏好差异有关。

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