Fisher Carolyn R, Wyckoff Elizabeth E, Peng Eric D, Payne Shelley M
Department of Molecular Biosciences, The University of Texas at Austin, Austin, Texas, USA.
Department of Molecular Biosciences, The University of Texas at Austin, Austin, Texas, USA
J Bacteriol. 2016 Sep 22;198(20):2810-7. doi: 10.1128/JB.00215-16. Print 2016 Oct 15.
Manganese plays an important role in the cellular physiology and metabolism of bacterial species, including the human pathogen Vibrio cholerae The intracellular level of manganese ions is controlled through coordinated regulation of the import and export of this element. We have identified a putative manganese exporter (VC0022), named mneA (manganese exporter A), which is highly conserved among Vibrio spp. An mneA mutant exhibited sensitivity to manganese but not to other cations. Under high-manganese conditions, the mneA mutant showed an almost 50-fold increase in intracellular manganese levels and reduced intracellular iron relative to those of its wild-type parent, suggesting that the mutant's manganese sensitivity is due to the accumulation of toxic levels of manganese and reduced iron. Expression of mneA suppressed the manganese-sensitive phenotype of an Escherichia coli strain carrying a mutation in the nonhomologous manganese export gene, mntP, further supporting a manganese export function for V. cholerae MneA. The level of mneA mRNA was induced approximately 2.5-fold after addition of manganese to the medium, indicating regulation of this gene by manganese. This study offers the first insights into understanding manganese homeostasis in this important pathogen.
Bacterial cells control intracellular metal concentrations by coordinating acquisition in metal-limited environments with export in metal-excess environments. We identified a putative manganese export protein, MneA, in Vibrio cholerae An mneA mutant was sensitive to manganese, and this effect was specific to manganese. The mneA mutant accumulated high levels of intracellular manganese with a concomitant decrease in intracellular iron levels when grown in manganese-supplemented medium. Expression of mneA in trans suppressed the manganese sensitivity of an E. coli mntP mutant. This study is the first to investigate manganese export in V. cholerae.
锰在细菌物种(包括人类病原体霍乱弧菌)的细胞生理和代谢中起着重要作用。锰离子的细胞内水平通过对该元素进出口的协同调节来控制。我们鉴定出一种假定的锰输出蛋白(VC0022),命名为mneA(锰输出蛋白A),它在弧菌属中高度保守。mneA突变体对锰敏感,但对其他阳离子不敏感。在高锰条件下,相对于其野生型亲本,mneA突变体的细胞内锰水平增加了近50倍,细胞内铁减少,这表明突变体对锰的敏感性是由于有毒水平的锰积累和铁减少所致。mneA的表达抑制了携带非同源锰输出基因mntP突变的大肠杆菌菌株的锰敏感表型,进一步支持了霍乱弧菌MneA的锰输出功能。向培养基中添加锰后,mneA mRNA水平诱导增加约2.5倍,表明该基因受锰调节。这项研究为理解这种重要病原体中的锰稳态提供了初步见解。
细菌细胞通过在金属限制环境中的获取与金属过量环境中的输出相协调来控制细胞内金属浓度。我们在霍乱弧菌中鉴定出一种假定的锰输出蛋白MneA。mneA突变体对锰敏感,且这种效应是锰特异性的。当在补充锰的培养基中生长时,mneA突变体积聚了高水平的细胞内锰,同时细胞内铁水平下降。mneA的反式表达抑制了大肠杆菌mntP突变体的锰敏感性。这项研究首次对霍乱弧菌中的锰输出进行了研究。