结核分枝杆菌
基岩
生物信息学
利福平
肺结核
转录组
抗药性
抗生素
乙胺丁醇
生物
吡嗪酰胺
利奈唑啉
异烟肼
微生物学
抗生素耐药性
基因
遗传学
医学
基因表达
细菌
万古霉素
病理
金黄色葡萄球菌
标识
DOI:10.1016/j.ijtb.2023.06.010
摘要
The emergence of drug resistant Mycobacterium tuberculosis strains increases the burden on the treatment of tuberculosis. In this study, through in-silico transcriptome analysis of drug-treated M. tuberculosis samples, novel drug targets for the treatment of drug resistance in tuberculosis were identified. Gene expression datasets of tuberculosis patients samples treated with different antibiotics (Isoniazid, Rifampicin, Pyrazinamide, Bedaquiline and Linezolid) were considered in this study. DESeq2 was used to identify the differentially regulated genes. Novel genes which were up-regulated during antibiotic treatment were identified which could be antibiotic resistance factors. Further, to understand the resistance mechanism of the novel genes, we performed gene ontology and gene network analysis for the differentially up-regulated genes. Thus, the in-silico transcriptome analysis paves way for a deeper understanding of the antibiotic resistance in M. tuberculosis.
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