Wang Hongjun, Gao Yaping, Gong Yumei, Chen Xiaoling, Liu Chuan, Zhou Xuemei, Blackall P J, Zhang Peijun, Yang Hanchun
Key Laboratory of Preventive Veterinary Medicine of Ministry of Agriculture, College of Veterinary Medicine, China Agricultural University, Beijing 100094, China.
Vet Microbiol. 2007 Jan 31;119(2-4):231-9. doi: 10.1016/j.vetmic.2006.08.034. Epub 2006 Sep 17.
Avibacterium paragallinarum is the causative agent of infectious coryza. The protective antigens of this important pathogen have not yet been clearly identified. In this paper, we applied phage display technique to screen the immunodominant mimotopes of a serovar A strain of A. paragallinarum by using a random 12-peptide library, and evaluated the immunogenicity in chickens of the selected mimotope. Polyclonal antibody directed against A. paragallinarum strain 0083 (serovar A) was used as the target antibody and phage clones binding to this target were screened from the 12-mer random peptide library. More than 50% of the phage clones selected in the third round carried the consensus peptide motif sequence A-DP(M)L. The phage clones containing the peptide motif reacted with the target antibody and this interaction could be blocked, in a dose-dependent manner, by A. paragallinarum. One of the peptide sequences, YGLLAVDPLFKP, was selected and the corresponding oligonucleotide sequence was synthesized and then inserted into the expression vector pFliTrx. The recombinant plasmid was transferred into an expression host Escherichia coli GI826 by electroporation, resulting in a recombinant E. coli expressing the peptide on the bacterial surface. Intramuscular injection of the epitope-expressing recombinant bacteria into chickens induced a specific serological response to serovar A. A. paragallinarum. The chickens given the recombinant E. coli showed significant protection against challenge with A. paragallinarum 0083. These results indicated a potential for the use of the mimotope in the development of molecular vaccines for infectious coryza.
副鸡禽杆菌是传染性鼻炎的病原体。这种重要病原菌的保护性抗原尚未明确鉴定。在本文中,我们应用噬菌体展示技术,利用随机12肽库筛选副鸡禽杆菌A血清型菌株的免疫显性模拟表位,并评估所选模拟表位在鸡体内的免疫原性。以抗副鸡禽杆菌0083菌株(A血清型)的多克隆抗体作为靶抗体,从12聚体随机肽库中筛选与该靶标结合的噬菌体克隆。第三轮筛选出的噬菌体克隆中,超过50%携带共有肽基序序列A-DP(M)L。含有该肽基序的噬菌体克隆与靶抗体发生反应,且这种相互作用可被副鸡禽杆菌以剂量依赖的方式阻断。选择其中一个肽序列YGLLAVDPLFKP,合成相应的寡核苷酸序列,然后插入表达载体pFliTrx。通过电穿孔将重组质粒转入表达宿主大肠杆菌GI826,得到在细菌表面表达该肽的重组大肠杆菌。将表达表位的重组细菌肌肉注射到鸡体内,可诱导鸡对A血清型副鸡禽杆菌产生特异性血清学反应。接种重组大肠杆菌的鸡对副鸡禽杆菌0083的攻击表现出显著的保护作用。这些结果表明,该模拟表位在传染性鼻炎分子疫苗的开发中具有应用潜力。