Gradients in gene essentiality reshape antibacterial research

被引:11
|
作者
Hogan, Andrew M. [1 ]
Cardona, Silvia T. [1 ,2 ]
机构
[1] Univ Manitoba, Dept Microbiol, 45 Chancellors Circle, Winnipeg, MB R3T 2N2, Canada
[2] Univ Manitoba, Dept Med Microbiol & Infect Dis, Max Rady Coll Med, Room 543-745,Bannatyne Ave, Winnipeg, MB, Canada
基金
加拿大健康研究院;
关键词
essential gene; antibiotic discovery; genetic interaction; conditional essentiality; transposon mutagenesis; CRISPRi; cystic fibrosis; CONDITIONALLY ESSENTIAL GENES; TRANSPOSON MUTANT LIBRARY; SEQUENCE-SPECIFIC CONTROL; GENOME-SCALE ANALYSIS; ESCHERICHIA-COLI; CYSTIC-FIBROSIS; MYCOBACTERIUM-TUBERCULOSIS; PSEUDOMONAS-AERUGINOSA; BACILLUS-SUBTILIS; PROTEIN-DEGRADATION;
D O I
10.1093/femsre/fuac005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Essential genes encode the processes that are necessary for life. Until recently, commonly applied binary classifications left no space between essential and non-essential genes. In this review, we frame bacterial gene essentiality in the context of genetic networks. We explore how the quantitative properties of gene essentiality are influenced by the nature of the encoded process, environmental conditions and genetic background, including a strain's distinct evolutionary history. The covered topics have important consequences for antibacterials, which inhibit essential processes. We argue that the quantitative properties of essentiality can thus be used to prioritize antibacterial cellular targets and desired spectrum of activity in specific infection settings. We summarize our points with a case study on the core essential genome of the cystic fibrosis pathobiome and highlight avenues for targeted antibacterial development. This review explores the spectrum of gene essentiality in the context of the environment, genetic networks and evolution, with the goal of highlighting its applicability to antimicrobial research targeting specific pathogens and infection settings.
引用
收藏
页数:27
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