首页> 外文期刊>Journal of animal and veterinary advances >Interaction Between VirB5 of Brucella Type IV Secretion System (TFSS) and Ferritin Heavy Polypeptide 1 (FTH1) in Murine Macrophage
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Interaction Between VirB5 of Brucella Type IV Secretion System (TFSS) and Ferritin Heavy Polypeptide 1 (FTH1) in Murine Macrophage

机译:布鲁氏杆菌IV型分泌系统(TFSS)的VirB5与小鼠巨噬细胞中铁蛋白重肽1(FTH1)的相互作用。

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摘要

TFSS is an important virulence factor of Brucella, organized as one operon containing 12 different across the cell wall bacterial proteins among which VirB5 regulates the host phagocytosis of Brucella and the transportation of Brucella in the host cells. This study has constructed cDNA library from Brucella melitensis 16M-infected murine macrophage Raw264.7, identified and confirmed the interaction between Brucella VirB5 and FTH1 of RAW264.7 using yeast two-hybrid and Co-Immunoprecipitation (Co-IP) technologies. Subsequently, the morphological changes and the expression of apoptosis-related genes in Brucella-infected RAW264.7 cells have been investigated with Electron Microscope (EM) and real-time quantitative RT-PCR, respectively. The present study has demonstrated that VirB5 and FTH1 play important roles in intracellular parasitism of Brucella and inhibition of FHT1 expression accelerates the apoptosis of macrophage.
机译:TFSS是布鲁氏菌的重要毒力因子,组织为一个操纵子,含有12种跨细胞壁的细菌蛋白,其中VirB5调节布鲁氏菌的宿主吞噬作用和布鲁氏菌在宿主细胞中的运输。本研究利用酵母双杂交和共免疫沉淀(Co-IP)技术从布鲁氏菌16M感染的鼠巨噬细胞Raw264.7构建了cDNA文库,鉴定并证实了布鲁氏菌VirB5与RAW264.7的FTH1之间的相互作用。随后,分别用电子显微镜(EM)和实时定量RT-PCR研究了布鲁氏菌感染的RAW264.7细胞的形态变化和凋亡相关基因的表达。本研究表明,VirB5和FTH1在布鲁氏菌的细胞内寄生中起重要作用,抑制FHT1表达可加速巨噬细胞的凋亡。

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