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首页> 外文期刊>Pesquisa Veterinaria Brasileira >Selection, characterization and cloning of the fljB and groEL genes agonists of the innate immune system pattern recognition receptors of birds
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Selection, characterization and cloning of the fljB and groEL genes agonists of the innate immune system pattern recognition receptors of birds

机译:鸟类先天免疫系统模式识别受体的fljB和groEL基因激动剂的选择,表征和克隆

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> face="verdana" size="2">The recombinant production of innate immune system pattern recognition receptor agonists has provided a new tool for the production of immunostimulants for animals. The molecular pattern associated with the pathogen (PAMP), flagellin, coded by the fljB gene from Salmonella Typhimirium, and the molecular pattern associated to the damage (DAMP), HSP60, coded by the groEL gene from S. Typhimurium and S. Enteritidis, are recognized by pattern recognition receptors (PRRs) of the innate immune system of birds. In the present study, we performed the cloning of genetic fragments of the genes fljB, from S. Typhimurium, and groEL from S. Typhimurium and S. Enteritidis inserted in expression vector pET100/D-TOPO and transformed in E. coli TO10 cells. The clones were evaluated by colony PCR, plasmidial DNA PCR and genome sequencing in order to confirm the presence of these genes. In the colony PCR, we identified the presence of genes groEL (S. Enteritidis), groEL (S. Typhimurium) and fljB (S. Typhimurium) in 80%, 60% and 80% of the transformed colonies, respectively. The cloning system adopted allowed the production of HSP60 genetic fragment clones and flagellin of Salmonella strains, allowing the posterior use of these clones in gene expression trials, with the future potential of being used as non-specific immunostimulants for birds.
机译:> face =“ verdana” size =“ 2”>先天免疫系统模式识别受体激动剂的重组生产为动物免疫刺激剂的生产提供了新的工具。 沙门氏菌鼠伤寒的fljB基因编码的与病原体(PAMP)鞭毛蛋白有关的分子模式,与

groEL基因编码的与损伤(DAMP)HSP60相关的分子模式。 i> S。 鼠伤寒 和 S。肠炎,是由鸟类先天免疫系统的模式识别受体(PRR)识别的。在本研究中,我们从iS克隆了fljB基因的遗传片段。 鼠伤寒和 S中的groEL。 鼠伤寒 和 S。 肠炎沙门氏菌插入表达载体pET100 / D-TOPO中并在 E中转化。大肠杆菌TO10细胞。通过菌落PCR,质粒DNA PCR和基因组测序评估克隆,以证实这些基因的存在。在菌落PCR中,我们鉴定出存在基因groEL( S。Enteritidis ),groEL( S。 Typhimurium)和fljB( S。鼠伤寒杆菌)分别占转化菌落的80%,60%和80%。所采用的克隆系统允许生产HSP60基因片段克隆和沙门氏菌的鞭毛蛋白,从而允许这些克隆在基因表达试验中后继使用,并有可能被用作非特异性免疫刺激剂。鸟。

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