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Note: An IS711 Element Downstream of the bp26 Gene Is a Specific Marker of Brucella spp. Isolated from Marine Mammals

机译:注意:bp26基因下游的IS711元素是布鲁氏菌属的特异性标记。与海洋哺乳动物隔离

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摘要

DNA polymorphism of the bp26 gene, coding for a diagnostic protein antigen for brucellosis, was assessed by PCR and restriction fragment length polymorphism analysis using primers to amplify the bp26 gene with its flanking regions. Surprisingly, whereas PCR performed on DNA of the reference strains of the six recognized Brucella species produced a product of the expected size (1,029 bp), PCR performed on DNA of three representative strains from marine mammals (from a seal, a dolphin, and a porpoise) produced a larger product, of about 1,900 bp. Nucleotide sequencing of the 1,900-bp PCR products revealed the presence of an insertion sequence, IS711, downstream of the bp26 gene and adjacent to a Bru-RS1 element previously described as being a hot spot for IS711 insertion. PCR performed on a large number of field strains from different geographic origins and from marine mammal isolates indicated that the occurrence of an IS711 element downstream of the bp26 gene was a feature specific to the marine mammal Brucella strains. Thus, this PCR assay is able to differentiate Brucella terrestrial isolates from marine mammal isolates and could be applied for diagnostic purposes.
机译:通过PCR和限制性片段长度多态性分析,使用引物扩增bp26基因及其侧翼区域,评估bp26基因的DNA多态性,该基因编码布鲁氏菌病诊断蛋白抗原。出乎意料的是,虽然对六个公认布鲁氏菌物种的参考菌株的DNA进行PCR产生了预期大小(1,029 bp)的产物,但是对三种来自海洋哺乳动物的代表性菌株的DNA进行了PCR(来自海豹,海豚和海豚)。 porpoise)产生了一个更大的产物,大约1,900 bp。 1,900 bp PCR产物的核苷酸测序表明,在bp26基因的下游且与先前描述为IS711插入热点的Bru-RS1元件相邻,存在插入序列IS711。对来自不同地理起源和海洋哺乳动物分离株的大量野外菌株进行的PCR表明,bp26基因下游的IS711元件的出现是海洋哺乳动物布鲁氏菌菌株特有的特征。因此,该PCR测定法能够将陆生布鲁氏菌分离株与海洋哺乳动物分离株区分开,并可用于诊断目的。

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