Department of Diagnostic and Biomedical Sciences, School of Dentistry, University of Texas Health Science Center, Houston, Texas, United States of America.
PLoS One. 2018 Aug 16;13(8):e0202233. doi: 10.1371/journal.pone.0202233. eCollection 2018.
The mitis group, a member of the genetically diverse viridans group streptococci, predominately colonizes the human oropharynx. This group has been shown to cause a wide range of infectious complications in humans, including bacteremia in patients with neutropenia, orbital cellulitis and infective endocarditis. Hydrogen peroxide (H2O2) has been identified as a virulence factor produced by this group of streptococci. More importantly, it has been shown that Streptococcus oralis and S. mitis induce epithelial cell and macrophage death via the production of H2O2. Previously, H2O2 mediated killing was observed in the nematode Caenorhabditis elegans in response to S. oralis and S. mitis. The genetically tractable model organism C. elegans is an excellent system to study mechanisms of pathogenicity and stress responses. Using this model, we observed rapid H2O2 mediated killing of the worms by S. gordonii in addition to S. mitis and S. oralis. Furthermore, we observed colonization of the intestine of the worms when exposed to S. gordonii suggesting the involvement of an infection-like process. In response to the H2O2 produced by the mitis group, we demonstrate the oxidative stress response is activated in the worms. The oxidative stress response transcription factor SKN-1 is required for the survival of the worms and provides protection against H2O2 produced by S. gordonii. We show during infection, H2O2 is required for the activation of SKN-1 and is mediated via the p38-MAPK pathway. The activation of the p38 signaling pathway in the presence of S. gordonii is not mediated by the endoplasmic reticulum (ER) transmembrane protein kinase IRE-1. However, IRE-1 is required for the survival of worms in response to S. gordonii. These finding suggests a parallel pathway senses H2O2 produced by the mitis group and activates the phosphorylation of p38. Additionally, the unfolded protein response plays an important role during infection.
缓症链球菌是多样性遗传的草绿色链球菌群的一个成员,主要定植于人类口咽部。该菌群已被证实可引起广泛的人类感染性并发症,包括中性粒细胞减少症患者的菌血症、眶蜂窝织炎和感染性心内膜炎。过氧化氢(H2O2)已被鉴定为该链球菌群产生的一种毒力因子。更重要的是,已经表明口腔链球菌和缓症链球菌通过产生 H2O2 诱导上皮细胞和巨噬细胞死亡。此前,在秀丽隐杆线虫中观察到 H2O2 介导的杀伤作用,以响应口腔链球菌和缓症链球菌。遗传上可操作的秀丽隐杆线虫模型生物是研究致病性和应激反应机制的极好系统。使用该模型,我们观察到除了缓症链球菌和口腔链球菌之外,S. gordonii 还能迅速介导 H2O2 杀伤线虫。此外,当暴露于 S. gordonii 时,我们观察到线虫的肠道定植,表明涉及类似感染的过程。针对缓症链球菌群产生的 H2O2,我们证明了氧化应激反应在蠕虫中被激活。氧化应激反应转录因子 SKN-1 是蠕虫存活所必需的,并为 S. gordonii 产生的 H2O2 提供保护。我们在感染期间表明,H2O2 是激活 SKN-1 所必需的,并且通过 p38-MAPK 途径介导。在存在 S. gordonii 的情况下,p38 信号通路的激活不是由内质网(ER)跨膜蛋白激酶 IRE-1 介导的。然而,IRE-1 是蠕虫对 S. gordonii 反应存活所必需的。这些发现表明,平行途径感知缓症链球菌群产生的 H2O2 并激活 p38 的磷酸化。此外,未折叠蛋白反应在感染过程中起着重要作用。