Bou Ghanem Elsa N, Clark Stacie, Roggensack Sara E, McIver Sally R, Alcaide Pilar, Haydon Philip G, Leong John M
Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, Massachusetts, United States of America.
Program in Molecular Microbiology, Sackler School of Graduate Biomedical Sciences, Tufts University, Boston, Massachusetts, United States of America.
PLoS Pathog. 2015 Aug 27;11(8):e1005126. doi: 10.1371/journal.ppat.1005126. eCollection 2015 Aug.
An important determinant of disease following Streptococcus pneumoniae (pneumococcus) lung infection is pulmonary inflammation mediated by polymorphonuclear leukocytes (PMNs). We found that upon intratracheal challenge of mice, recruitment of PMNs into the lungs within the first 3 hours coincided with decreased pulmonary pneumococci, whereas large numbers of pulmonary PMNs beyond 12 hours correlated with a greater bacterial burden. Indeed, mice that survived infection largely resolved inflammation by 72 hours, and PMN depletion at peak infiltration, i.e. 18 hours post-infection, lowered bacterial numbers and enhanced survival. We investigated host signaling pathways that influence both pneumococcus clearance and pulmonary inflammation. Pharmacologic inhibition and/or genetic ablation of enzymes that generate extracellular adenosine (EAD) (e.g. the ectoenzyme CD73) or degrade EAD (e.g. adenosine deaminase) revealed that EAD dramatically increases murine resistance to S. pneumoniae lung infection. Moreover, adenosine diminished PMN movement across endothelial monolayers in vitro, and although inhibition or deficiency of CD73 had no discernible impact on PMN recruitment within the first 6 hours after intratracheal inoculation of mice, these measures enhanced PMN numbers in the pulmonary interstitium after 18 hours of infection, culminating in dramatically elevated numbers of pulmonary PMNs at three days post-infection. When assessed at this time point, CD73-/- mice displayed increased levels of cellular factors that promote leukocyte migration, such as CXCL2 chemokine in the murine lung, as well as CXCR2 and β-2 integrin on the surface of pulmonary PMNs. The enhanced pneumococcal susceptibility of CD73-/- mice was significantly reversed by PMN depletion following infection, suggesting that EAD-mediated resistance is largely mediated by its effects on PMNs. Finally, CD73-inhibition diminished the ability of PMNs to kill pneumococci in vitro, suggesting that EAD alters both the recruitment and bacteriocidal function of PMNs. The EAD-pathway may provide a therapeutic target for regulating potentially harmful inflammatory host responses during Gram-positive bacterial pneumonia.
肺炎链球菌肺部感染后疾病的一个重要决定因素是由多形核白细胞(PMN)介导的肺部炎症。我们发现,对小鼠进行气管内攻击后,最初3小时内PMN向肺部的募集与肺部肺炎球菌数量减少同时发生,而12小时后大量的肺部PMN与更高的细菌负荷相关。事实上,在感染后存活下来的小鼠在72小时内炎症基本消退,在浸润高峰期(即感染后18小时)耗尽PMN可降低细菌数量并提高存活率。我们研究了影响肺炎球菌清除和肺部炎症的宿主信号通路。对产生细胞外腺苷(EAD)的酶(如胞外酶CD73)或降解EAD的酶(如腺苷脱氨酶)进行药理抑制和/或基因敲除后发现,EAD可显著增强小鼠对肺炎链球菌肺部感染的抵抗力。此外,腺苷在体外减少了PMN穿过内皮单层的移动,虽然抑制或缺乏CD73对小鼠气管内接种后最初6小时内的PMN募集没有明显影响,但这些措施在感染18小时后增加了肺间质中的PMN数量,最终导致感染后三天肺部PMN数量急剧增加。在这个时间点进行评估时,CD73基因敲除小鼠体内促进白细胞迁移的细胞因子水平升高,如小鼠肺中的CXCL2趋化因子,以及肺部PMN表面的CXCR2和β-2整合素。感染后耗尽PMN可显著逆转CD73基因敲除小鼠增强的肺炎球菌易感性,这表明EAD介导的抵抗力很大程度上是通过其对PMN的作用来介导的。最后,抑制CD73可降低PMN在体外杀死肺炎球菌的能力,这表明EAD改变了PMN的募集和杀菌功能。EAD途径可能为调节革兰氏阳性菌肺炎期间潜在有害的炎症宿主反应提供一个治疗靶点。