Department of Pediatrics, The Pennsylvania State University College of Medicine, Hershey, PA, 17033, USA.
Department of Pediatrics, The Pennsylvania State University College of Medicine, Hershey, PA, 17033, USA; Biobehavioral Laboratory, The University of North Carolina at Chapel Hill, School of Nursing, Chapel Hill, NC, 27599, USA.
Respir Med. 2019 May;151:133-138. doi: 10.1016/j.rmed.2019.04.012. Epub 2019 Apr 13.
Cystic Fibrosis (CF) is the most common life limiting genetic disorder, characterized by chronic respiratory failure secondary to inflammation and chronic bacterial lung infection. Pseudomonas aeruginosa lung infection is associated with more severe lung disease and rapid progression of respiratory failure when compared to Staphylococcus aureus infection. We hypothesized that a specific signature of epigenetic factors targeting specific gene transcripts contributes to the increased morbidity seen in CF patients with chronic Pseudomonas infection.
We collected exhaled breath condensate (EBC) from 27 subjects and evaluated miRNA signatures in these samples using commercial PCR array. We identified predicted mRNA targets and associated signaling pathways using Ingenuity Pathway Analysis.
We found 11 differentially expressed miRNAs in EBC of patients infected with Pseudomonas aeruginosa compared to EBC from CF patients who were not chronically infected with Pseudomonas aeruginosa (p < 0.05). Six of these miRNAs (hsa-miRNA-1247, hsa-miRNA-1276, hsa-miRNA-449c, hsa-miRNA-3170, hsa-miRNA-432-5p and hsa-miR-548) were significantly different in the CF Pseudomonas positive group when compared to both the CF Pseudomonas negative group and healthy control group. Ingenuity pathway analysis (IPA) revealed organismal injury and abnormalities, reproductive system disease and cancer as the top diseases and bio functions associated with these miRNAs. IPA also detected RELA, JUN, TNF, IL-10, CTNNB1, IL-13, SERPINB8, CALM1, STARD3NL, SFI1, CD55, RPS6KA4, TTC36 and HIST1H3D as the top target genes for these miRNAs.
Our study identified 6 miRNAs as epigenetic factors specifically associated with chronic Pseudomonas infection in patients with CF.
囊性纤维化(CF)是最常见的致命性遗传疾病,其特征是慢性呼吸道衰竭,继发于炎症和慢性细菌性肺部感染。与金黄色葡萄球菌感染相比,铜绿假单胞菌肺部感染与更严重的肺部疾病和呼吸衰竭的快速进展有关。我们假设,针对特定基因转录本的特定表观遗传因子特征导致 CF 患者慢性铜绿假单胞菌感染时发病率增加。
我们收集了 27 名受试者的呼出气冷凝物(EBC),并使用商业 PCR 阵列评估了这些样本中的 miRNA 特征。我们使用 Ingenuity 通路分析确定了预测的 mRNA 靶标和相关信号通路。
我们发现,与未慢性感染铜绿假单胞菌的 CF 患者的 EBC 相比,慢性感染铜绿假单胞菌的 CF 患者的 EBC 中有 11 个 miRNA 表达差异(p < 0.05)。在 CF 铜绿假单胞菌阳性组中,有 6 个 miRNA(hsa-miRNA-1247、hsa-miRNA-1276、hsa-miRNA-449c、hsa-miRNA-3170、hsa-miRNA-432-5p 和 hsa-miR-548)与 CF 铜绿假单胞菌阴性组和健康对照组相比存在显著差异。IPA 揭示了机体损伤和异常、生殖系统疾病和癌症是与这些 miRNA 相关的前三大疾病和生物功能。IPA 还检测到 RELA、JUN、TNF、IL-10、CTNNB1、IL-13、SERPINB8、CALM1、STARD3NL、SFI1、CD55、RPS6KA4、TTC36 和 HIST1H3D 是这些 miRNA 的前三大靶基因。
我们的研究确定了 6 个 miRNA 作为与 CF 患者慢性铜绿假单胞菌感染特异性相关的表观遗传因子。