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Prokaryotic expression and functional analysis of the Mb1514 gene in Mycobacterium bovis

机译:Mb1514基因在牛分枝杆菌中的原核表达及功能分析

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The ability of mycobacteria to grow and invade target tissues is the key component in the process of Mycobacterium bovis infection. Therefore, analysis of the proteins responsible for cell invasion will assist clinicians in combating bovine tuberculosis. The Mb1514 gene of M. bovis encodes a hypothetical invasion protein (designated here as MbINV protein), whose function has not yet been directly identified. In this study, the Mb1514 gene from M. bovis was cloned, and expressed in E. coli. The recombinant MbINV protein (a single band of approximately 28 kDa) was purified for biological analysis. Our data demonstrated that recombinant MbINV protein significantly inhibited the viability of RAW264.7 macrophages in a dose-dependent manner (P < 0.05), and induced cell necrosis, indicating that the protein is toxic. MbINV protein infection significantly enhanced the mRNA expression levels of TNF-α, IL-1β, and NOS2 (P < 0.01), suggesting that MbINV protein may be one of the virulence factors which directly interact with macrophages and modulate the host immune response to M. bovis. An invasion inhibition assay showed that MbINV-inhibited M. bovis invasion of RAW264.7 cells in a concentration-dependant manner, demonstrating it is an invasion protein.
机译:分枝杆菌生长和侵袭目标组织的能力是牛分枝杆菌感染过程中的关键组成部分。因此,对负责细胞入侵的蛋白质进行分析将有助于临床医生对抗牛结核病。牛分枝杆菌的Mb1514基因编码一种假设的入侵蛋白(在此称为MbINV蛋白),其功能尚未被直接鉴定。在这项研究中,克隆了来自牛分枝杆菌的Mb1514基因,并在大肠杆菌中表达。纯化重组MbINV蛋白(约28 kDa的单条带)以进行生物学分析。我们的数据表明重组MbINV蛋白以剂量依赖性方式显着抑制RAW264.7巨噬细胞的活力(P <0.05),并诱导细胞坏死,表明该蛋白具有毒性。 MbINV蛋白感染显着增强了TNF-α,IL-1β和NOS2的mRNA表达水平(P <0.01),表明MbINV蛋白可能是直接与巨噬细胞相互作用并调节宿主对M免疫反应的毒力因子之一。牛侵袭抑制试验表明,MbINV抑制的牛分枝杆菌以浓度依赖的方式侵袭RAW264.7细胞,表明它是一种侵袭蛋白。

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