Song Shulin, Gan Donghui, Wu Di, Li Ting, Zhang Shiqian, Lu Yibo, Jin Guanqiao
Department of Radiology, Guangxi Medical University Cancer Hospital, Nanning, 530023, Guangxi, China.
Department of Radiology, The Fourth People's Hospital of Nanning, Nanning, 530023, Guangxi, China.
Mol Biotechnol. 2024 Oct 24. doi: 10.1007/s12033-024-01299-z.
The issue of multi-drug-resistant tuberculosis (MDR-TB) presents a substantial challenge to global public health. Regrettably, the diagnosis of drug-resistant tuberculosis (DR-TB) frequently necessitates an extended period or more extensive laboratory resources. The swift identification of MDR-TB poses a particularly challenging endeavor. To identify the biomarkers indicative of multi-drug resistance, we conducted a screening of the GSE147689 dataset for differentially expressed genes (DEGs) and subsequently conducted a gene enrichment analysis. Our analysis identified a total of 117 DEGs, concentrated in pathways related to the immune response. Three machine learning methods, namely random forest, decision tree, and support vector machine recursive feature elimination (SVM-RFE), were implemented to identify the top 10 genes according to their feature importance scores. A4GALT and S1PR1, which were identified as common genes among the three methods, were selected as potential molecular markers for distinguishing between MDR-TB and drug-susceptible tuberculosis (DS-TB). These markers were subsequently validated using the GSE147690 dataset. The findings suggested that A4GALT exhibited area under the curve (AUC) values of 0.8571 and 0.7121 in the training and test datasets, respectively, for distinguishing between MDR-TB and DS-TB. S1PR1 demonstrated AUC values of 0.8163 and 0.5404 in the training and test datasets, respectively. When A4GALT and S1PR1 were combined, the AUC values in the training and test datasets were 0.881 and 0.7551, respectively. The relationship between hub genes and 28 immune cells infiltrating MDR-TB was investigated using single sample gene enrichment analysis (ssGSEA). The findings indicated that MDR-TB samples exhibited a higher proportion of type 1 T helper cells and a lower proportion of activated dendritic cells in contrast to DS-TB samples. A negative correlation was observed between A4GALT and type 1 T helper cells, whereas a positive correlation was found with activated dendritic cells. S1PR1 exhibited a positive correlation with type 1 T helper cells and a negative correlation with activated dendritic cells. Furthermore, our study utilized connectivity map analysis to identify nine potential medications, including verapamil, for treating MDR-TB. In conclusion, our research identified two molecular indicators for the differentiation between MDR-TB and DS-TB and identified a total of nine potential medications for MDR-TB.
耐多药结核病(MDR-TB)问题给全球公共卫生带来了重大挑战。遗憾的是,耐药结核病(DR-TB)的诊断通常需要较长时间或更广泛的实验室资源。快速识别MDR-TB是一项特别具有挑战性的工作。为了识别指示耐多药的生物标志物,我们对GSE147689数据集进行了差异表达基因(DEG)筛选,随后进行了基因富集分析。我们的分析共鉴定出117个DEG,集中在与免疫反应相关的途径中。实施了三种机器学习方法,即随机森林、决策树和支持向量机递归特征消除(SVM-RFE),以根据其特征重要性得分识别前10个基因。在这三种方法中被鉴定为共同基因的A4GALT和S1PR1被选为区分MDR-TB和药物敏感结核病(DS-TB)的潜在分子标志物。随后使用GSE147690数据集对这些标志物进行了验证。结果表明,A4GALT在训练和测试数据集中区分MDR-TB和DS-TB的曲线下面积(AUC)值分别为0.8571和0.7121。S1PR1在训练和测试数据集中的AUC值分别为0.8163和0.5404。当A4GALT和S1PR1联合使用时,训练和测试数据集中的AUC值分别为0.881和0.7551。使用单样本基因富集分析(ssGSEA)研究了中心基因与浸润MDR-TB的28种免疫细胞之间的关系。结果表明,与DS-TB样本相比,MDR-TB样本中1型辅助性T细胞的比例更高,活化树突状细胞的比例更低。观察到A4GALT与1型辅助性T细胞呈负相关,而与活化树突状细胞呈正相关。S1PR1与1型辅助性T细胞呈正相关,与活化树突状细胞呈负相关。此外,我们的研究利用连接图谱分析确定了九种潜在药物,包括维拉帕米,用于治疗MDR-TB。总之,我们的研究确定了两种区分MDR-TB和DS-TB的分子指标,并确定了总共九种治疗MDR-TB的潜在药物。