Key Laboratory of Medical Molecular Virology and Institute of Biomedical Sciences, Fudan University, Shanghai, China.
PLoS One. 2011;6(10):e25832. doi: 10.1371/journal.pone.0025832. Epub 2011 Oct 7.
The mechanism of latent tuberculosis (TB) infection remains elusive. Several host factors that are involved in this complex process were previously identified. Micro RNAs (miRNAs) are endogenous ∼22 nt RNAs that play important regulatory roles in a wide range of biological processes. Several studies demonstrated the clinical usefulness of miRNAs as diagnostic or prognostic biomarkers in various malignancies and in a few nonmalignant diseases. To study the role of miRNAs in the transition from latent to active TB and to discover candidate biomarkers of this transition, we used human miRNA microarrays to probe the transcriptome of peripheral blood mononuclear cells (PBMCs) in patients with active TB, latent TB infection (LTBI), and healthy controls. Using the software package BRB Array Tools for data analyses, 17 miRNAs were differentially expressed between the three groups (P<0.01). Hierarchical clustering of the 17 miRNAs expression profiles showed that individuals with active TB clustered independently of individuals with LTBI or from healthy controls. Using the predicted target genes and previously published genome-wide transcriptional profiles, we constructed the regulatory networks of miRNAs that were differentially expressed between active TB and LTBI. The regulatory network revealed that several miRNAs, with previously established functions in hematopoietic cell differentiation and their target genes may be involved in the transition from latent to active TB. These results increase the understanding of the molecular basis of LTBI and confirm that some miRNAs may control gene expression of pathways that are important for the pathogenesis of this infectious disease.
潜伏性结核病 (TB) 感染的机制仍然难以捉摸。以前已经确定了几个参与这一复杂过程的宿主因素。微 RNA(miRNA)是内源性的约 22 个核苷酸 RNA,在广泛的生物学过程中发挥着重要的调节作用。几项研究表明,miRNA 作为各种恶性肿瘤和少数非恶性疾病的诊断或预后生物标志物具有临床实用性。为了研究 miRNA 在潜伏性 TB 向活动性 TB 转变中的作用,并发现这一转变的候选生物标志物,我们使用人类 miRNA 微阵列探测活动性 TB、潜伏性 TB 感染 (LTBI) 和健康对照者外周血单核细胞 (PBMC) 的转录组。使用 BRB Array Tools 软件包进行数据分析,在三组之间有 17 个 miRNA 差异表达(P<0.01)。17 个 miRNA 表达谱的层次聚类显示,活动性 TB 个体与 LTBI 个体或健康对照者聚类独立。使用预测的靶基因和先前发表的全基因组转录谱,我们构建了 miRNA 在活动性 TB 和 LTBI 之间差异表达的调控网络。该调控网络表明,一些 miRNA 可能与造血细胞分化的已有功能有关,并且它们的靶基因可能参与从潜伏性到活动性 TB 的转变。这些结果增加了对 LTBI 分子基础的理解,并证实了一些 miRNA 可能控制对这种传染病发病机制很重要的途径的基因表达。