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Nitric Oxide as a Biomarker of Intracellular Salmonella Viability and Identification of the Bacteriostatic Activity of Protein Kinase A Inhibitor H-89

机译:一氧化氮作为细胞内沙门氏菌活力和蛋白质的抑菌活性的鉴定的生物标记物激酶a抑制剂H-89

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摘要

Salmonella enterica serovar Enteritidis is one of the most prevalent Salmonella serovars in poultry and is often associated with human salmonellosis. S. Enteritidis is known to suppress nitric oxide (NO) production in infected chicken macrophage HD11 cells, while dead S. Enteritidis stimulates a high level of NO production, suggesting a bacterial inhibitory effect on NO production. Based on these observations, the present study was conducted to evaluate whether NO production in S. Enteritidis-infected HD11 cells can be used as a biomarker to identify molecules that kill intracellular Salmonella. Since Salmonella are known to manipulate the host cell kinase network to facilitate intracellular survival, we screened a group of pharmaceutical inhibitors of various kinases to test our hypothesis. A protein kinase A inhibitor, H-89, was found to reverse the suppression of NO production in S. Enteritidis-infected HD11 cells. Production of NO in S. Enteritidis-infected HD11 cells increased significantly following treatment with H-89 at or above 20 µM. Inversely, the number of viable intracellular Salmonella decreased significantly in cells treated with H-89 at or above 30 µM. Furthermore, the growth rate of S. Enteritidis in culture was significantly inhibited by H-89 at concentrations from 20 to 100 µM. Our results demonstrate that NO-based screening using S. Enteritidis-infected HD11 cells is a viable tool to identify chemicals with anti-intracellular Salmonella activity. Using this method, we have shown H-89 has bacteriostatic activity against Salmonella, independent of host cell protein kinase A or Akt1 activity.
机译:肠炎沙门氏菌肠炎沙门氏菌是家禽中最普遍的沙门氏菌血清型之一,通常与人沙门氏菌病有关。已知肠炎沙门氏菌可抑制感染的鸡巨噬细胞HD11细胞中一氧化氮(NO)的产生,而死亡的肠炎沙门氏菌可刺激高水平的NO产生,表明细菌对NO产生具有抑制作用。基于这些观察,进行了本研究以评估在肠炎沙门氏菌感染的HD11细胞中是否不产生NO,可以用作生物标志物来鉴定杀死细胞内沙门氏菌的分子。由于已知沙门氏菌会操纵宿主细胞激酶网络以促进细胞内存活,因此我们筛选了一组各种激酶的药物抑制剂来检验我们的假设。发现一种蛋白激酶A抑制剂H-89可逆转肠炎沙门氏菌感染的HD11细胞对NO产生的抑制作用。用20 µM或以上的H-89处理后,经肠炎沙门氏菌感染的HD11细胞中NO的生成显着增加。相反,在30 µM或以上的H-89处理细胞中,存活的细胞内沙门氏菌数量显着减少。此外,浓度为20至100 µM的H-89可显着抑制培养肠炎链球菌的生长速率。我们的结果表明,使用肠炎沙门氏菌感染的HD11细胞进行的基于NO的筛选是鉴定具有抗细胞内沙门氏菌活性的化学品的可行工具。使用这种方法,我们已显示H-89具有抗沙门氏菌的抑菌活性,而与宿主细胞蛋白激酶A或Akt1活性无关。

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