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Apoptosis Toll-like RIG-I-like and NOD-like Receptors Are Pathways Jointly Induced by Diverse Respiratory Bacterial and Viral Pathogens

机译:细胞凋亡Toll样RIG-I样和NOD样受体是多种呼吸细菌和病毒病原体共同诱导的途径。

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摘要

Lower respiratory tract infections are among the top five leading causes of human death. Fighting these infections is therefore a world health priority. Searching for induced alterations in host gene expression shared by several relevant respiratory pathogens represents an alternative to identify new targets for wide-range host-oriented therapeutics. With this aim, alveolar macrophages were independently infected with three unrelated bacterial (Streptococcus pneumoniae, Klebsiella pneumoniae, and Staphylococcus aureus) and two dissimilar viral (respiratory syncytial virus and influenza A virus) respiratory pathogens, all of them highly relevant for human health. Cells were also activated with bacterial lipopolysaccharide (LPS) as a prototypical pathogen-associated molecular pattern. Patterns of differentially expressed cellular genes shared by the indicated pathogens were searched by microarray analysis. Most of the commonly up-regulated host genes were related to the innate immune response and/or apoptosis, with Toll-like, RIG-I-like and NOD-like receptors among the top 10 signaling pathways with over-expressed genes. These results identify new potential broad-spectrum targets to fight the important human infections caused by the bacteria and viruses studied here.
机译:下呼吸道感染是人类死亡的五大主要原因。因此,与这些感染作斗争是世界卫生的重中之重。寻找由几种相关的呼吸道病原体共有的宿主基因表达的诱导改变代表了一种为大范围以宿主为导向的治疗方法确定新靶标的选择。为了这个目的,肺泡巨噬细胞被三种无关的细菌(肺炎链球菌,肺炎克雷伯菌和金黄色葡萄球菌)和两种不同的病毒(呼吸道合胞病毒和甲型流感病毒)呼吸道病原体独立感染,它们均与人类健康高度相关。细胞也被细菌脂多糖(LPS)激活,作为典型的病原体相关分子模式。通过微阵列分析搜索由指定病原体共有的差异表达的细胞基因的模式。大多数通常上调的宿主基因与先天免疫应答和/或细胞凋亡有关,在表达过量的前十个信号通路中,有Toll样,RIG-I样和NOD样受体。这些结果确定了新的潜在广谱靶标,以对抗由此处研究的细菌和病毒引起的重要的人类感染。

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