牛乳腺炎金黄色葡萄球菌肠毒素A基因的克隆及序列分析

摘要

A pair of primers were designed by biological software primer 5.0 and oligo 6.0 and synthesized according to SEA gene sequences of bovine mastitis Staphylococcus aureus published on Genbank. SEA gene fragment was amplified by PCR.Sequencing result showed that SEA gene had 101 bp in length. Isolated strain from Jinzhou and the standard strain had 100% of homology in genes sequence. The SEA Gene sequence of the two strains and published Staphylococcus aureus strain (EF520720.1) on Genbank were homology reach 99.14%. The result of a high degree of homology had laid a consult and experimental basis for further research and established Molecular Diagnostic Techniques.%根据Genbank上公布的金黄色葡萄球菌肠毒素A的全序列,利用生物学软件Primer 5.0和oligo 6.0设计了一对特异性引物来扩增靶序列片段,经克隆预测序,结果表明扩增片段长度为101 bp,锦州分离株与标准菌株的基因片段序列相似性为100％,与Genbank上公布的金黄色葡萄球菌菌株(EF520720.1)SEA基因相似性达到99.14％.高度相似性结果为进一步研究建立分子检测技术奠定了实验基础.