肺实质中血红蛋白的氧化有助于肺炎球菌分化为被包裹的细菌。

Babek Alibayov, Ana G Jop Vidal, Landon Murin, Anna Scasny, Kenichi Takeshita, Komal Beeton, Kristin S Edwards, Tracy Punshon, Brian P Jackson, Larry S McDaniel, Jorge E Vidal
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引用次数: 0

摘要

肺炎球菌肺炎引起肺实质细胞毒性,但其潜在机制涉及多种因素导致细胞死亡。在这里,我们发现由肺炎链球菌产生的过氧化氢(spn - h2o2)通过氧化血红蛋白起关键作用,导致其聚合并随后释放不稳定的血红素。在生理相关水平上,血红素选择了包膜肺炎球菌群体。在缺乏荚膜和spn - h2o2的情况下,宿主细胞内血红素对肺炎球菌表现出毒性,从而发挥抗菌机制。进一步的研究表明血红素介导的毒性需要ABC转运蛋白GlnPQ。体内实验表明,肺炎球菌通过非蛋白水解降解肌动蛋白、微管蛋白和GAPDH等细胞内蛋白,释放h2o2,引起支气管和肺泡细胞毒性。总的来说,我们的研究结果揭示了氧化应激介导的肺毒性机制,该机制有利于包裹性肺炎球菌的生长,这表明通过靶向氧化反应具有治疗潜力。图片摘要:重点:肺炎链球菌在体内氧化血红蛋白,促进分化成囊化肺炎球菌。分化后的肺炎链球菌产生荚膜和过氧化氢(spn - h2o2)作为防御宿主血红素介导毒性的机制。spn - h2o2诱导的肺毒性导致细胞内蛋白微管蛋白、肌动蛋白和GAPDH的氧化和非蛋白水解降解。ABC转运蛋白GlnPQ是一种血红素结合复合体,使Spn易受血红素毒性影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Heme-Mediated Selection of Encapsulated Streptococcus pneumoniae in the Lungs by Oxidative Stress.

Streptococcus pneumoniae (the pneumococcus) causes cytotoxicity and encapsulates within the lung parenchyma, leading to pneumococcal pneumonia. However, the underlying mechanisms remain unclear and likely involve multiple bacterial and host factors. We investigated the selection process of encapsulated pneumococci, a critical factor in lung damage during pneumococcal pneumonia. Our study revealed that pneumococci initially lack capsules but re-encapsulate upon reaching the alveoli. This process is driven by S. pneumoniae-derived hydrogen peroxide (Spn-H2O2), which oxidizes lung hemoglobin, leading to heme release and polymerized hemoglobin formation. Physiologically relevant levels of heme were found to promote the selection of encapsulated bacteria. Furthermore, encapsulation protects bacteria from intracellular heme toxicity, a defense absent in non-encapsulated strains. Ultrastructural analysis demonstrated interactions between hemoglobin and both encapsulated and non-encapsulated pneumococci in human sputum. These findings reveal a critical connection between oxidative stress-mediated lung damage and the selection of encapsulated pneumococci, suggesting potential therapeutic avenues by targeting these oxidative processes.

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