Gu H W, Lu C P
Key Lab Animal Disease Diagnostic & Immunology, Ministry of Agriculture, Nanjing Agricultural University, Nanjing 210095, PR China.
Vet Microbiol. 2006 Jul 20;115(4):339-48. doi: 10.1016/j.vetmic.2006.02.020. Epub 2006 Apr 11.
A random 12-peptide library was used to screen immunodominant mimics of 99kDa iron-regulated outer membrane protein (IROMP-99) of rabbit Pasteurella multocida. In the present study, expression of IROMPs of rabbit P. multocida strain C51-12 were analyzed by SDS-PAGE, and Western blot to determine the specificity of rat antiserum antibodies against IROMP-99. Only IROMP-99 whose expression was induced under iron-restricted conditions was detected on nitrocellulose paper. The phage display library was screened with rat normal and IROMP-99-specific antiserum. The positive phage clones were identified using enzyme-linked immunoadsorbent assay (ELISA) and inhibition assays for their reactivity to the antiserum. Out of the 18 randomly selected positive clones that showed higher reactivity to rat antiserum, only ten clones efficaciously inhibited binding of rat antisera to IROMPs and their displayed peptides were determined. Alignment using DNAStar-MegAlign software, results showed that motif WHxTxP was highly conserved among nine clones, only clone A7 had no obvious linear homology with either. Our findings suggest that the motif WHxTxP could be an immunodominant mimic epitope of IROMP-99 of rabbit P. multocida strain C51-12.
利用一个随机的12肽文库筛选兔多杀性巴氏杆菌99kDa铁调节外膜蛋白(IROMP-99)的免疫显性模拟表位。在本研究中,通过SDS-PAGE和蛋白质印迹分析兔多杀性巴氏杆菌C51-12菌株IROMPs的表达,以确定大鼠抗血清抗体针对IROMP-99的特异性。在硝酸纤维素膜上仅检测到在铁限制条件下诱导表达的IROMP-99。用大鼠正常血清和IROMP-99特异性抗血清筛选噬菌体展示文库。使用酶联免疫吸附测定(ELISA)和抑制试验鉴定阳性噬菌体克隆与抗血清的反应性。在18个随机选择的对大鼠抗血清显示出较高反应性的阳性克隆中,只有10个克隆有效抑制大鼠抗血清与IROMPs的结合,并确定了它们展示的肽段。使用DNAStar-MegAlign软件进行比对,结果显示基序WHxTxP在9个克隆中高度保守,只有克隆A7与两者均无明显的线性同源性。我们的研究结果表明,基序WHxTxP可能是兔多杀性巴氏杆菌C51-12菌株IROMP-99的免疫显性模拟表位。