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Identification of new Corynebacterium pseudotuberculosis antigens by immunoscreening of gene expression library

机译:通过基因表达文库的免疫筛选鉴定新的假杆菌棒状杆菌抗原

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Caseous lymphadenitis (CLA) is a disease that affects sheep, goats and occasionally humans. The etiologic agent is the Corynebacterium pseudotuberculosis bacillus. The objective of this study was to build a gene expression library from C. pseudotuberculosis and use immunoscreening to identify genes that encode potential antigenic proteins for the development of DNA and subunit vaccines against CLA. A wild strain of C. pseudotuberculosis was used for extraction and partial digestion of genomic DNA. Sequences between 1000 and 5000 base pairs (bp) were excised from the gel, purified, and the digested DNA fragments were joined to bacteriophage vector ZAP Express, packaged into phage and transfected into Escherichia coli. For immunoscreening a positive sheep sera pool and a negative sera pool for CLA were used. Four clones were identified that strongly reacted to sera. The clones were confirmed by polymerase chain reaction (PCR) followed by sequencing for genomic comparison of C. pseudotuberculosis in GenBank. The genes identified were dak2, fagA, fagB, NlpC/P60 protein family and LPxTG putative protein family. Proteins of this type can be antigenic which could aid in the development of subunit or DNA vaccines against CLA as well as in the development of serological tests for diagnosis. Immunoscreening of the gene expression library was shown to be a sensitive and efficient technique to identify probable immunodominant genes.
机译:干酪性淋巴结炎(CLA)是一种会影响绵羊,山羊以及人类的疾病。病原体是假结核杆菌。这项研究的目的是从假结核杆菌建立一个基因表达文库,并使用免疫筛选来鉴定编码潜在抗原蛋白的基因,这些抗原蛋白可用于开发抗CLA的DNA和亚单位疫苗。使用野生假单胞菌菌株来提取和部分消化基因组DNA。从凝胶上切下1000至5000个碱基对(bp)的序列,进行纯化,然后将消化的DNA片段连接到噬菌体载体ZAP Express,包装入噬菌体并转染到大肠杆菌中。为了免疫筛选使用CLA的阳性绵羊血清库和阴性血清库。鉴定出四个与血清强烈反应的克隆。通过聚合酶链反应(PCR)确认克隆,然后通过测序对GenBank中的假结核假单胞菌进行基因组比较。鉴定的基因为dak2,fagA,fagB,NlpC / P60蛋白家族和LPxTG推定蛋白家族。这种类型的蛋白质可以是抗原性的,可以帮助开发抗CLA的亚基或DNA疫苗以及开发用于诊断的血清学检测。基因表达文库的免疫筛选显示是识别可能的免疫优势基因的灵敏和有效的技术。

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