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淋病奈瑟菌中锰对毒力因子和氧化应激抗性的调节作用。

Manganese regulation of virulence factors and oxidative stress resistance in Neisseria gonorrhoeae.

机构信息

Core Facilities for Proteomics Research, Institute of Biological Chemistry, Academia Sinica, Taipei, 115, Taiwan.

出版信息

J Proteomics. 2010 Mar 10;73(5):899-916. doi: 10.1016/j.jprot.2009.12.001. Epub 2009 Dec 11.

Abstract

Neisseria gonorrhoeae has evolved a complex and novel network of oxidative stress responses, including defence mechanisms that are dependent on manganese (Mn). We performed systematic analyses at the transcriptomic and proteomic (1D SDS-PAGE and Isotope-Coded Affinity Tag [ICAT]) levels to investigate the global expression changes that take place in a high Mn environment, which results in a Mn-dependent oxidative stress resistance phenotype. These studies revealed that there were proteins regulated at the post-transcriptional level under conditions of increased Mn concentration, including proteins involved in virulence (e.g., pilin, a key adhesin), oxidative stress defence (e.g., superoxide dismutase), cellular metabolism, protein synthesis, RNA processing and cell division. Mn regulation of inorganic pyrophosphatase (Ppa) indicated the potential involvement of phosphate metabolism in the Mn-dependent oxidative stress defence. A detailed analysis of the role of Ppa and polyphosphate kinase (Ppk) in the gonococcal oxidative stress response revealed that ppk and ppa mutant strains showed increased resistance to oxidative stress. Investigation of these mutants grown with high Mn suggests that phosphate and pyrophosphate are involved in Mn-dependent oxidative stress resistance.

摘要

淋病奈瑟菌已经进化出了一套复杂而新颖的氧化应激反应网络,包括依赖于锰 (Mn) 的防御机制。我们在转录组和蛋白质组(1D SDS-PAGE 和同位素编码亲和标签 [ICAT])水平上进行了系统分析,以研究在高 Mn 环境中发生的全局表达变化,这导致了一种 Mn 依赖性的抗氧化应激抗性表型。这些研究表明,在 Mn 浓度增加的条件下,有蛋白质在转录后水平受到调节,包括与毒力相关的蛋白质(例如,菌毛,一种关键的黏附素)、氧化应激防御(例如,超氧化物歧化酶)、细胞代谢、蛋白质合成、RNA 处理和细胞分裂。Mn 对无机焦磷酸酶(Ppa)的调节表明,磷酸盐代谢可能参与了 Mn 依赖性的氧化应激防御。对 Ppa 和多磷酸激酶(Ppk)在淋病奈瑟菌氧化应激反应中的作用的详细分析表明,ppk 和 ppa 突变株对氧化应激的抵抗力增强。对这些在高 Mn 条件下生长的突变株的研究表明,磷酸盐和焦磷酸盐参与了 Mn 依赖性的氧化应激抗性。

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