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首页> 外文期刊>Virus Research: An International Journal of Molecular and Cellular Virology >Identification of immunodominant T-cell epitopes in membrane protein of highly pathogenic porcine reproductive and respiratory syndrome virus.
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Identification of immunodominant T-cell epitopes in membrane protein of highly pathogenic porcine reproductive and respiratory syndrome virus.

机译:immunodominant t细胞抗原表位的识别高致病性猪的膜蛋白繁殖与呼吸综合征病毒。

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摘要

The development of cell-mediated immunity has been known extremely important in clearing porcine reproductive and respiratory syndrome virus (PRRSV) in infected pigs. However, the PRRS immunology regarding the interaction of T-cells and PRRSV proteins is poorly understood. To identify the T-cell immunodominant epitopes on the membrane (M) protein of PRRSV, a series of 31 overlapping pentadecapeptides covering the entire M protein were designed and synthesized. These peptides were screened by ELIspot analysis for their capabilities to elicit interferon-gamma (IFN-gamma) responses in the peripheral blood mononuclear cells (PBMCs), which were collected from pigs immunized with attenuated PRRSV HuN4-F112 strain and challenged with highly pathogenic HuN4 strain. After three rounds of screening, 4 peptides (M3, M6, M8 and M12) were shown to elicit high expression of IFN-gamma. The stimulation of high IFN-gamma transcription in PBMCs by these 4 peptides was further confirmed in real-time PCR. The sequence alignment revealed that the epitope represented by peptide M6 was fully conserved in all of examined 42 North American genotype II PRRSV isolates and the epitopes represented by peptides M3, M8 and M12 showed 2-4 amino acid replacements. The finding of 4 T-cell immunodominant epitopes in the M protein of PRRSV will be beneficial to the understanding of the development of cell-mediated immunity.
机译:细胞介导免疫的发展已知在清算猪非常重要繁殖与呼吸综合征病毒(PRRSV)感染猪。免疫学有关t细胞之间的交互和PRRSV蛋白知之甚少。确定t细胞immunodominant抗原表位PRRSV的膜蛋白(M),一系列的31重叠pentadecapeptides覆盖整个设计并合成M蛋白。有关酶联免疫斑点分析多肽筛选了他们的能力引起移行(IFN-gamma)外周血中反应单核细胞(PBMCs),收集从猪接种减毒PRRSV与高度HuN4-F112应变和挑战致病性HuN4毒株。筛选4肽(M3, M6 M8和M12)引出IFN-gamma的高表达。刺激高IFN-gamma转录的PBMCs由这四肽被进一步证实实时PCR。为代表的表位肽M6完全守恒的检查42北美国II基因型PRRSV隔离和抗原表位肽所代表的M3, M8和M12显示2 - 4氨基酸替换。4 t细胞immunodominant抗原表位的M蛋白质PRRSV将是有益的理解细胞的发展免疫力。

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