DNA adenine methylation is involved in persister formation in E. coli

被引:20
|
作者
Xu, Yuanyuan [1 ]
Liu, Shuang [1 ]
Zhang, Ying [2 ]
Zhang, Wenhong [1 ]
机构
[1] Fudan Univ, Dept Infect Dis, Huashan Hosp, Shanghai 200040, Peoples R China
[2] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Mol Microbiol & Immunol, Baltimore, MD 21205 USA
基金
美国国家科学基金会;
关键词
Persister; DNA adenine methylation; Methylome; Transcriptome; Urinary tract infection; URINARY-TRACT-INFECTIONS; UROPATHOGENIC ESCHERICHIA-COLI; MULTIPLE ANTIBIOTICS; CYTOSINE METHYLATION; SINGLE-MOLECULE; GENE-EXPRESSION; TOLERANCE; MECHANISMS; STRESSES; EPIDEMIOLOGY;
D O I
10.1016/j.micres.2021.126709
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Uropathogenic Escherichia coli (UPEC) is a major cause of urinary tract infections (UTI). UPEC persister bacteria play crucial roles in clinical treatment failure and relapse. Although DNA methylation is known to regulate gene expression, its role in persister formation has not been investigated. Here, we show that Delta dam (adenine methylase) mutant from UPEC strain UTI89 had significant defect in persister formation and complementation of the Delta dam mutant restored this defect. Using PacBio sequencing of methylome and RNA sequencing of Delta dam, we defined, for the first time, the role of Dam in persister formation. We found that Delta dam mutation had an overwhelming effect on demethylation of the genome and the demethylation sites affected expression of genes involved in broad transcriptional and metabolic processes. Using comparative COG analysis of methylome and transcriptome, we demonstrate that Dam mediates persister formation through transcriptional control, cell motility, DNA repair and metabolite transport processes. These findings provide the first evidence and molecular basis for DNA methylation mediated persister formation and implicate Dam DNA methylation as a potential drug target for persister bacteria.
引用
收藏
页数:12
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