Kenya Medical Research Institute, Nairobi, Kenya.
PLoS One. 2012;7(1):e30048. doi: 10.1371/journal.pone.0030048. Epub 2012 Jan 26.
To identify novel biomarkers for HIV-1 resistance, including pathways that may be critical in anti-HIV-1 vaccine design, we carried out a gene expression analysis on blood samples obtained from HIV-1 highly exposed seronegatives (HESN) from a commercial sex worker cohort in Nairobi and compared their profiles to HIV-1 negative controls. Whole blood samples were collected from 43 HIV-1 resistant sex workers and a similar number of controls. Total RNA was extracted and hybridized to the Affymetrix HUG 133 Plus 2.0 micro arrays (Affymetrix, Santa Clara CA). Output data was analysed through ArrayAssist software (Agilent, San Jose CA). More than 2,274 probe sets were differentially expressed in the HESN as compared to the control group (fold change ≥1.3; p value ≤0.0001, FDR <0.05). Unsupervised hierarchical clustering of the differentially expressed genes readily distinguished HESNs from controls. Pathway analysis through the KEGG signaling database revealed a majority of the impacted pathways (13 of 15, 87%) had genes that were significantly down regulated. The most down expressed pathways were glycolysis/gluconeogenesis, pentose phosphate, phosphatidyl inositol, natural killer cell cytotoxicity and T-cell receptor signaling. Ribosomal protein synthesis and tight junction genes were up regulated. We infer that the hallmark of HIV-1 resistance is down regulation of genes in key signaling pathways that HIV-1 depends on for infection.
为了鉴定 HIV-1 耐药的新生物标志物,包括在抗 HIV-1 疫苗设计中可能至关重要的途径,我们对从内罗毕商业性工作者队列中获得的 HIV-1 高度暴露血清阴性者(HESN)的血液样本进行了基因表达分析,并将其与 HIV-1 阴性对照进行了比较。从 43 名 HIV-1 耐药性性工作者和数量相似的对照者中采集了全血样本。提取总 RNA 并与 Affymetrix HUG 133 Plus 2.0 微阵列(Affymetrix,Santa Clara CA)杂交。通过 ArrayAssist 软件(Agilent,San Jose CA)分析输出数据。与对照组相比,HESN 中超过 2274 个探针集表达差异(倍数变化≥1.3;p 值≤0.0001, FDR <0.05)。差异表达基因的无监督层次聚类很容易将 HESN 与对照组区分开来。通过 KEGG 信号数据库进行的途径分析表明,受影响的途径中的大多数(15 个途径中的 13 个,87%)的基因表达显著下调。表达下调最明显的途径是糖酵解/糖异生、戊糖磷酸、磷酸肌醇、自然杀伤细胞细胞毒性和 T 细胞受体信号。核糖体蛋白合成和紧密连接基因上调。我们推断,HIV-1 耐药的标志是 HIV-1 感染所依赖的关键信号通路中的基因下调。