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Burkholderia mallei and Burkholderia pseudomallei Cluster 1 Type VI Secretion System Gene Expression Is Negatively Regulated by Iron and Zinc

机译:铁和锌对伯克霍尔德氏菌和假伯克霍尔德氏菌丛1型VI分泌系统基因表达负调控。

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摘要

Burkholderia mallei is a facultative intracellular pathogen that causes glanders in humans and animals. Previous studies have demonstrated that the cluster 1 type VI secretion system (T6SS-1) expressed by this organism is essential for virulence in hamsters and is positively regulated by the VirAG two-component system. Recently, we have shown that T6SS-1 gene expression is up-regulated following internalization of this pathogen into phagocytic cells and that this system promotes multinucleated giant cell formation in infected tissue culture monolayers. In the present study, we further investigated the complex regulation of this important virulence factor. To assess T6SS-1 expression, B. mallei strains were cultured in various media conditions and Hcp1 production was analyzed by Western immunoblotting. Transcript levels of several VirAG-regulated genes (bimA, tssA, hcp1 and tssM) were also determined using quantitative real time PCR. Consistent with previous observations, T6SS-1 was not expressed during growth of B. mallei in rich media. Curiously, growth of the organism in minimal media (M9G) or minimal media plus casamino acids (M9CG) facilitated robust expression of T6SS-1 genes whereas growth in minimal media plus tryptone (M9TG) did not. Investigation of this phenomenon confirmed a regulatory role for VirAG in this process. Additionally, T6SS-1 gene expression was significantly down-regulated by the addition of iron and zinc to M9CG. Other genes under the control of VirAG did not appear to be as tightly regulated by these divalent metals. Similar results were observed for B. pseudomallei, but not for B. thailandensis. Collectively, our findings indicate that in addition to being positively regulated by VirAG, B. mallei and B. pseudomallei T6SS-1 gene expression is negatively regulated by iron and zinc.
机译:伯克霍尔德氏菌是一种兼性的细胞内病原体,可在人和动物中引起腺体。先前的研究表明,这种生物体表达的簇1型VI分泌系统(T6SS-1)对于仓鼠的毒力至关重要,并且受VirAG两组分系统的正调控。最近,我们已经表明该病原体内化进入吞噬细胞后,T6SS-1基因表达被上调,并且该系统促进了被感染组织培养单层中多核巨细胞的形成。在本研究中,我们进一步研究了该重要毒力因子的复杂调控。为了评估T6SS-1的表达,在各种培养基条件下培养了B. mallei菌株,并通过Western免疫印迹分析了Hcp1的产生。还使用定量实时PCR测定了几个VirAG调控基因(bimA,tssA,hcp1和tssM)的转录水平。与以前的观察结果一致,在富媒体中马来芽孢杆菌的生长过程中未表达T6SS-1。奇怪的是,有机体在基本培养基(M9G)或基本培养基加酪蛋白氨基酸(M9CG)中的生长促进了T6SS-1基因的稳健表达,而在基本培养基和胰蛋白((M9TG)中的生长却没有。对这一现象的研究证实了VirAG在此过程中的调节作用。此外,通过向M9CG中添加铁和锌,T6SS-1基因表达显着下调。在VirAG的控制下,其他基因似乎不受这些二价金属的严格调控。对于假芽孢杆菌(B. pseudomallei)观察到了相似的结果,但对于泰国芽孢杆菌(B. thailandensis)没有观察到。总体而言,我们的发现表明,除了受VirAG的正调控外,B。Mallei和B. pseudomallei T6SS-1基因表达还受到铁和锌的负调控。

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