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牙龈卟啉单胞菌FeoB2在金属摄取和氧化应激保护中的作用。

Role of Porphyromonas gingivalis FeoB2 in metal uptake and oxidative stress protection.

作者信息

He Jia, Miyazaki Hiroshi, Anaya Cecilia, Yu Fan, Yeudall W Andrew, Lewis Janina P

机构信息

Philips Institute of Oral and Craniofacial Molecular Biology, School of Dentistry, Virginia Commonwealth University, P.O. Box 980566, Richmond, VA 23298, USA.

出版信息

Infect Immun. 2006 Jul;74(7):4214-23. doi: 10.1128/IAI.00014-06.

Abstract

Porphyromonas gingivalis, a gram-negative anaerobic bacterium, is a recognized periodontopathogen. It exhibits a high degree of aerotolerance and is able to survive in host cells, indicating that efficient oxidative stress protection mechanisms must be present in this organism. Manganese homeostasis plays a major role in oxidative stress protection in a variety of organisms; however, the transport and role of this metal in P. gingivalis is not well understood. Analysis of the genome of P. gingivalis W83 revealed the presence of two genes encoding homologs of a ferrous iron transport protein, FeoB1 and FeoB2. FeoB2 has been implicated in manganese accumulation in P. gingivalis. We sought to determine the role of the FeoB2 protein in metal transport as well as its contribution to resistance to oxygen radicals. Quantitative reverse transcriptase PCR analyses demonstrated that expression of feoB2 is induced in the presence of oxygen. The role of FeoB2 was investigated using an isogenic mutant strain deficient in the putative transporter. We characterized the FeoB2-mediated metal transport using (55)Fe(2+) and (54)Mn(2+). The FeoB2-deficient mutant had dramatically reduced rates of manganese uptake (0.028 pmol/min/10(7) bacteria) compared with the parental strain (0.33 pmol/min/10(7) bacteria) (after 20 min of uptake using 50 nM of (54)Mn(2+)). The iron uptake rates, however, were higher in the mutant strain (0.75 pmol/min/10(7) bacteria) than in the wild type (0.39 pmol/min/10(7) bacteria). Interestingly, reduced survival rates were also noted for the mutant strain after exposure to H(2)O(2) and to atmospheric oxygen compared to the parental strain cultured under the same conditions. In addition, in vitro infection of host cells with the wild type, the FeoB2-deficient mutant, and the same-site revertant revealed that the mutant had a significantly decreased capability for intracellular survival in the host cells compared to the wild-type strain. Our results demonstrate that feoB2 encodes a major manganese transporter required for protection of the bacterium from oxidative stress generated by atmospheric oxygen and H(2)O(2). Furthermore, we show that FeoB2 and acquisition of manganese are required for intracellular survival of P. gingivalis in host cells.

摘要

牙龈卟啉单胞菌是一种革兰氏阴性厌氧菌,是公认的牙周病原体。它表现出高度的耐氧性,能够在宿主细胞中存活,这表明该生物体中必定存在有效的氧化应激保护机制。锰稳态在多种生物体的氧化应激保护中起主要作用;然而,这种金属在牙龈卟啉单胞菌中的转运和作用尚未得到充分了解。对牙龈卟啉单胞菌W83基因组的分析揭示了两个编码亚铁转运蛋白同源物的基因,即FeoB1和FeoB2。FeoB2与牙龈卟啉单胞菌中的锰积累有关。我们试图确定FeoB2蛋白在金属转运中的作用及其对抵抗氧自由基的贡献。定量逆转录酶PCR分析表明,在有氧条件下feoB2的表达被诱导。使用推定转运蛋白缺陷的同基因突变株研究了FeoB2的作用。我们使用(55)Fe(2+)和(54)Mn(2+)对FeoB2介导的金属转运进行了表征。与亲本菌株(0.33 pmol/分钟/10(7)个细菌)相比,FeoB2缺陷型突变株的锰摄取率显著降低(0.028 pmol/分钟/10(7)个细菌)(使用50 nM的(54)Mn(2+)摄取20分钟后)。然而,突变株的铁摄取率(0.75 pmol/分钟/10(7)个细菌)高于野生型(0.39 pmol/分钟/10(7)个细菌)。有趣的是,与在相同条件下培养的亲本菌株相比,突变株在暴露于H(2)O(2)和大气氧后存活率也降低。此外,用野生型、FeoB2缺陷型突变株和同一位点回复株对宿主细胞进行体外感染,结果显示与野生型菌株相比,突变株在宿主细胞内的存活能力显著降低。我们的结果表明,feoB2编码一种主要的锰转运蛋白,该蛋白是保护细菌免受大气氧和H(2)O(2)产生的氧化应激所必需的。此外,我们表明FeoB2和锰的获取是牙龈卟啉单胞菌在宿主细胞内生存所必需的。

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