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作 者:刘俊琦[1] 余兴龙[1] 蒋大良[1] 朱小宁[1] 李润成[1] 肖利军[1] 刘春红[1] 罗维[1] 葛猛[1]
机构地区:[1]湖南农业大学动物医学院,湖南长沙410128
出 处:《中国兽医科学》2010年第8期822-826,共5页Chinese Veterinary Science
基 金:国家科技支撑计划项目(2006BAD06A00);长沙市科技计划重大专项(K0902007-21)
摘 要:为研究副猪嗜血杆菌(HPS)基因工程疫苗,以HPS5型毒株为模板,通过PCR扩增获得副猪嗜血杆菌神经氨酸酶(Neu)全基因,将其克隆至pMD18-T载体并对其进行测定和分析。结果表明,Neu全基因含一个2187bp的开放阅读框,编码一含729个氨基酸的蛋白,与Neu基因参考序列(登录号:NZ-ABKM01000006)的同源性为99.0%。以pMD-Neu基因为模板,重新设计引物,扩增得到HPSNeu蛋白的部分编码区,将其克隆至原核表达载体pET-28a(+)中,构建得到重组原核表达质粒pET-Neu。将pET-Neu在大肠杆菌Rosetta(DE3)中进行优化表达,经SDS-PAGE分析,重组蛋白Neu主要以包涵体形式表达,分子质量为52ku;Western-blot分析表明,重组蛋白Neu能与阳性血清发生特异性抗原反应。将纯化重组蛋白Neu试验性注射免疫昆明小鼠,攻毒试验结果显示,氢氧化铝佐剂组的保护性较低,仅有10%;而弗氏佐剂组具有较高的保护性,保护率高达60%。The full-length Neu gene was amplified from Haemophilus parasuis(HPS) serotype 5 SP strain by PCR with a pair of primers based on the whole genome shotgun sequence(Accession No.:NZ-ABKM01000005) in GenBank.Sequencing showed that the amplified Neu gene was successfully cloned into pMD18-T vector and the complete open reading frame with an ATG initiation codon comprised 2187 nucleotides and encoded a protein of 805 amino acids.It shared 99.0% identity with that of the reference sequence.The HPS Neu gene fragment was amplified by PCR from pMD-Neu,and cloned into the prokaryotic expression vector pET-28a(+) to obtain the recombinant prokaryotic expression vector pET-Neu.The pET-Neu was transformed into Escherichia coli Rosetta(DE3) and expressed optimally.The recombinant protein Neu of approximately 52ku was detected by SDS-PAGE and existed mainly in the form of inclusion bodies.Western-blotting showed that the recombinant protein Neu could specifically react with the antibodies in positive sera well.Kunming mice were immunized with the purified recombinant protein Neu,and challenged with HPS post-immunization.The results showed that the Al(OH)3 group got a poor protective(10%),but the Freund's had a higher protection(60%).
分 类 号:S852.612[农业科学—基础兽医学] Q786[农业科学—兽医学]
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