Institute of Virology, Leipzig University, Leipzig, Germany.
Institute of Virology, Leipzig University, Leipzig, Germany; Avian and Rabbit Diseases Department, Faculty of Veterinary Medicine, Sadat City University, Egypt.
Virus Res. 2015 Mar 2;199:46-55. doi: 10.1016/j.virusres.2015.01.006. Epub 2015 Jan 17.
H5-specific monoclonal antibodies may serve as valuable tools for rapid diagnosis of H5N1 avian influenza virus. Therefore, conserved H5-specific sequences of the haemagglutinin (HA) protein were expressed in Pichia pastoris and used for generation of monoclonal antibodies (mAbs). The two mAbs, FD6 and HE4, were strongly reactive against native HA protein and exhibited specificity for subtype H5. By epitope mapping linear epitopes of mAbs were identified that are highly conserved among influenza A virus of subtype H5. Additionally no sequence similarities to homologous regions on HA proteins of other influenza A virus subtypes (i.e. H1, H3, H7, H9) were detected by sequence alignment analysis. Both mAbs did not cross react with native or denatured HA proteins of other influenza A virus subtypes. Furthermore, using ELISA and immunofluorescence test mAb FD6 reacted only to the native H5 protein of recently circulating highly pathogenic H5N1 influenza viruses but not to low pathogenic H5N1 isolates. In conclusion, the use of the two mAbs in non-molecular tests like antigen-capture-ELISA appears promising for detecting influenza A H5N1 virus.
H5 特异性单克隆抗体可作为快速诊断 H5N1 禽流感病毒的有价值工具。因此,在巴斯德毕赤酵母中表达了血凝素(HA)蛋白的保守 H5 特异性序列,并用于生成单克隆抗体(mAb)。两种 mAb,FD6 和 HE4,与天然 HA 蛋白强烈反应,并且对亚型 H5 具有特异性。通过表位作图,鉴定出 mAb 的线性表位,这些表位在 H5 亚型的流感病毒中高度保守。此外,通过序列比对分析,未检测到与其他流感 A 病毒亚型(即 H1、H3、H7、H9)HA 蛋白同源区域的序列相似性。两种 mAb 均与其他流感 A 病毒亚型的天然或变性 HA 蛋白无交叉反应。此外,使用 ELISA 和免疫荧光试验,mAb FD6 仅与最近流行的高致病性 H5N1 流感病毒的天然 H5 蛋白反应,而与低致病性 H5N1 分离株不反应。总之,在非分子检测中使用这两种 mAb(如抗原捕获 ELISA)似乎有望检测到甲型 H5N1 流感病毒。