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锰外流系统mntE在肺炎链球菌信号传导和致病机制中的作用。

Role of the manganese efflux system mntE for signalling and pathogenesis in Streptococcus pneumoniae.

作者信息

Rosch Jason W, Gao Geli, Ridout Granger, Wang Yong-Dong, Tuomanen Elaine I

机构信息

Department of Infectious Diseases, St Jude's Children's Research Hospital, Memphis, TN 38105, USA.

出版信息

Mol Microbiol. 2009 Apr;72(1):12-25. doi: 10.1111/j.1365-2958.2009.06638.x. Epub 2009 Feb 17.

Abstract

The ability of bacteria to sense and respond to both environmental and intracellular metal concentrations plays an important role in pathogenesis. The acquisition of manganese is vital for the virulence of several bacterial species. Although manganese uptake systems have been well studied in bacteria, no manganese efflux system has yet been identified. In this study we have identified a cation diffusion facilitator (CDF) protein (Sp1552) of unknown substrate specificity that functions as a manganese export system in Streptococcus pneumoniae. We designated the gene for this manganese efflux system mntE and found that the mutant strain was highly sensitive to manganese stress. Although the mutant was more resistant to oxidative stress and produced more H(2)O(2) and pili, it had reduced virulence in a murine model of infection, indicating that manganese export plays a role in host pathogenesis. There was a distinct differential transcriptional response to extracellular and intracellular manganese accumulation. Our study indicates that manganese efflux is required for invasive disease and may provide a useful antimicrobial target to devise future therapeutics.

摘要

细菌感知并响应环境和细胞内金属浓度的能力在发病机制中起着重要作用。锰的获取对多种细菌的毒力至关重要。尽管细菌中的锰摄取系统已得到充分研究,但尚未鉴定出锰外排系统。在本研究中,我们鉴定了一种底物特异性未知的阳离子扩散促进剂(CDF)蛋白(Sp1552),其在肺炎链球菌中作为锰输出系统发挥作用。我们将这个锰外排系统的基因命名为mntE,并发现突变株对锰胁迫高度敏感。尽管该突变体对氧化应激更具抗性且产生更多的H₂O₂和菌毛,但其在小鼠感染模型中的毒力降低,这表明锰输出在宿主发病机制中起作用。对细胞外和细胞内锰积累存在明显的差异转录反应。我们的研究表明,锰外排是侵袭性疾病所必需的,并且可能为设计未来的治疗方法提供一个有用的抗菌靶点。

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