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鉴定 H7 禽流感病毒血凝素蛋白中的抗原表位。

Identification of antigenic epitopes in the haemagglutinin protein of H7 avian influenza virus.

机构信息

MOE Joint International Research Laboratory of Animal Health and Food Safety, Institute of Immunology, Nanjing Agricultural University, Nanjing, People's Republic of China.

Jiangsu Engineering Laboratory of Animal Immunology, Institute of Immunology, Nanjing Agricultural University, Nanjing, People's Republic of China.

出版信息

Avian Pathol. 2020 Feb;49(1):62-73. doi: 10.1080/03079457.2019.1666971. Epub 2019 Oct 8.

Abstract

The H7 subtype avian influenza virus (AIV) has been reported to infect not only poultry but also humans. The haemagglutinin (HA) protein is the major surface antigen of AIV and plays an important role in viral infection. In this study, five monoclonal antibodies (mAbs, 2F8, 3F6, 5C11, 5E2 and 5C12) against the HA protein of H7 virus were produced and characterized. Epitope mapping indicated that RESGSS was the minimal linear epitope recognized by the mAbs 2F8/3F6/5C11, and mAbs 5E2/5C12 recognized the epitope 103-145aa. The protein sequence alignment of HA indicated that the two epitopes were not found in other subtypes of AIV, and none of the five mAbs cross-reacted with other subtypes, suggesting these mAbs are specific to H7 virus. The epitope RESGSS was highly conserved among Eurasian lineage strains of H7 AIV, whereas three amino acid substitutions (E104R, E104K and E104G) in the epitope occurred in 98.44% of North-American lineage strains. Any of these single mutations prevented the mutated epitope from being recognized by mAbs 2F8/3F6/5C11; thus, these mAbs can distinguish between Eurasian and North-American lineages of H7 strains. Furthermore, the mAbs 2F8, 3F6 and 5C11 could be highly blocked with H7-positive serum in blocking assays, revealing that RESGSS may be a dominant epitope stimulating the production of antibodies during viral infection. These results may facilitate future investigations into the structure and function of HA protein, as well as surveillance and detection of H7 virus.Five mAbs against HA protein of H7 AIV were generated and characterized.Two novel epitopes RESGSS and 103-145aa were identified.The epitope RESGSS differs between Eurasian and North-American lineages.The mAbs 2F8, 3F6 and 5C11 could distinguish two lineages of H7 strains.

摘要

本研究制备并鉴定了针对 H7 亚型禽流感病毒(AIV)血凝素(HA)蛋白的 5 株单克隆抗体(mAb),2F8、3F6、5C11、5E2 和 5C12。表位作图表明,RESGSS 是 mAb 2F8/3F6/5C11 识别的最小线性表位,而 mAb 5E2/5C12 识别 103-145aa 表位。HA 蛋白序列比对表明,这两个表位未在其他 AIV 亚型中发现,且这 5 株 mAb 均与其他亚型无交叉反应,提示这些 mAb 特异性识别 H7 病毒。表位 RESGSS 在欧亚谱系 H7 AIV 株中高度保守,而表位中 3 个氨基酸(E104R、E104K 和 E104G)的取代则发生在 98.44%的北美谱系株中。这 3 种突变中的任何一种都阻止了突变表位被 mAb 2F8/3F6/5C11 识别,因此,这些 mAb 可区分 H7 病毒的欧亚和北美谱系。此外,在阻断试验中,mAb 2F8、3F6 和 5C11 可被 H7 阳性血清高度阻断,表明 RESGSS 可能是病毒感染期间刺激抗体产生的优势表位。这些结果可能有助于进一步研究 HA 蛋白的结构和功能,以及 H7 病毒的监测和检测。

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