Commonalities of Mycobacterium tuberculosis Transcriptomes in Response to Defined Persisting Macrophage Stresses

被引:11
|
作者
Vilcheze, Catherine [1 ]
Yan, Bo [2 ]
Casey, Rosalyn [3 ]
Hingley-Wilson, Suzie [3 ]
Ettwiller, Laurence [2 ]
Jacobs, William R., Jr. [1 ]
机构
[1] Albert Einstein Coll Med, Dept Microbiol & Immunol, Bronx, NY 10461 USA
[2] New England Biolabs Inc, Genome Biol Div, Res Dept, Ipswich, MA USA
[3] Univ Surrey, Fac Hlth & Med Sci, Sch Biosci & Med, Dept Microbial Sci, Guildford, England
来源
FRONTIERS IN IMMUNOLOGY | 2022年 / 13卷
基金
美国国家卫生研究院; 英国医学研究理事会;
关键词
RNA-seq; tuberculosis; starvation; pH; hypoxia; dormancy; GENE-EXPRESSION; RNA-SEQ; METHYLCITRATE CYCLE; ESSENTIAL REGULATOR; CALMETTE-GUERIN; BOVIS BCG; BIOSYNTHESIS; METABOLISM; VIRULENCE; ADAPTATION;
D O I
10.3389/fimmu.2022.909904
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
As the goal of a bacterium is to become bacteria, evolution has imposed continued selections for gene expression. The intracellular pathogen Mycobacterium tuberculosis, the causative agent of tuberculosis, has adopted a fine-tuned response to survive its host's methods to aggressively eradicate invaders. The development of microarrays and later RNA sequencing has led to a better understanding of biological processes controlling the relationship between host and pathogens. In this study, RNA-seq was performed to detail the transcriptomes of M. tuberculosis grown in various conditions related to stresses endured by M. tuberculosis during host infection and to delineate a general stress response incurring during persisting macrophage stresses. M. tuberculosis was subjected to long-term growth, nutrient starvation, hypoxic and acidic environments. The commonalities between these stresses point to M. tuberculosis maneuvering to exploit propionate metabolism for lipid synthesis or to withstand propionate toxicity whilst in the intracellular environment. While nearly all stresses led to a general shutdown of most biological processes, up-regulation of pathways involved in the synthesis of amino acids, cofactors, and lipids were observed only in hypoxic M. tuberculosis. This data reveals genes and gene cohorts that are specifically or exclusively induced during all of these persisting stresses. Such knowledge could be used to design novel drug targets or to define possible M. tuberculosis vulnerabilities for vaccine development. Furthermore, the disruption of specific functions from this gene set will enhance our understanding of the evolutionary forces that have caused the tubercle bacillus to be a highly successful pathogen.
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页数:18
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