生物
毒力
结核分枝杆菌
抗药性
传输(电信)
肺结核
抄写(语言学)
表型
病毒学
转录因子
遗传学
基因表达
疾病
微生物学
遗传变异
基因表达调控
细菌遗传学
基因表达谱
基因组
转录组
核糖核酸
毒力因子
深度测序
抗生素耐药性
转录调控
分枝杆菌
基因型
DNA测序
基因
作者
Peter H. Culviner,Abigail M Frey,Qingyun Liu,Đặng Thị Minh Hà,Phan Vuong Khac Thai,Do Dang Anh Thu,Nguyen Le Quang,Róger Calderón,Leonid Lecca,Maxine Caws,Sarah J. Dunstan,Megan Murray,Nguyễn Thụy Thương Thương,Sarah M. Fortune
出处
期刊:Cell
[Cell Press]
日期:2025-09-30
卷期号:188 (23): 6620-6635.e14
被引量:7
标识
DOI:10.1016/j.cell.2025.09.005
摘要
Mycobacterium tuberculosis (Mtb) has co-evolved with humans for thousands of years and is characterized by variation in virulence, transmissibility, and disease phenotypes. To identify bacterial contributors to phenotypic diversity, we developed new RNA sequencing (RNA-seq) and phylogenomic tools to capture hundreds of Mtb isolate transcriptomes, link transcriptional and genetic variation, and find associations between variants and epidemiologic traits. Across 274 Mtb clinical isolates, we uncovered unexpected diversity in virulence gene expression, which we linked to known and unknown regulators. Surprisingly, we found that many isolates harbor variants associated with decreased expression of EsxA (Esat6) and EsxB (Cfp10), which are virulence effectors, dominant T cell antigens, and immunodiagnostic targets. Across >55,000 isolates, these variants associate with increased transmissibility, especially in drug-resistant Mtb strains. Our data suggest expression of Mtb virulence genes is evolving in response to drug-linked pressure, raising concerns about use of these targets in immunodiagnostics and next-generation vaccines.
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