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
相关论文
共 50 条
  • [11] Assessing persister awakening dynamics following antibiotic treatment in E. coli
    Wilmaerts, Dorien
    Govers, Sander K.
    Michiels, Jan
    STAR PROTOCOLS, 2022, 3 (03):
  • [12] On the record with E. coli DNA
    Borkowski, Olivier
    Gilbert, Charlie
    Ellis, Tom
    SCIENCE, 2016, 353 (6298) : 444 - 445
  • [13] Cataloging E. coli DNA
    Water Environment and Technology, 1997, 9 (08):
  • [14] A General Model for Toxin-Antitoxin Module Dynamics Can Explain Persister Cell Formation in E. coli
    Gelens, Lendert
    Hill, Lydia
    Vandervelde, Alexandra
    Danckaert, Jan
    Loris, Remy
    PLOS COMPUTATIONAL BIOLOGY, 2013, 9 (08)
  • [15] DNA sliding and loop formation by E. coli SMC complex: MukBEF
    Zhou, Man
    BIOCHEMISTRY AND BIOPHYSICS REPORTS, 2022, 31
  • [16] DNA sliding and loop formation by E. coli SMC complex: MukBEF
    Zhou, Man
    BIOCHEMISTRY AND BIOPHYSICS REPORTS, 2022, 31
  • [17] Engineering DNA Looping in E. Coli
    Becker, Nicole A.
    Schwab, Tanya L.
    Clark, Karl J.
    Maher, L. James, III
    BIOPHYSICAL JOURNAL, 2017, 112 (03) : 68A - 68A
  • [18] dinB gene encodes a novel E. coli DNA polymerase, DNA pol IV, involved in mutagenesis
    Wagner, Jerome
    Gruz, Petr
    Kim, Su-Ryang
    Yamada, Masami
    Matsui, Keiko
    Fuchs, Robert P.P.
    Nohmi, Takehiko
    Molecular Cell, 4 (02): : 281 - 286
  • [19] A genome-wide approach to identify the genes involved in biofilm formation in E. coli
    Niba, Emma Tabe Eko
    Naka, Yoshiaki
    Nagase, Megumi
    Mori, Hirotada
    Kitakawa, Madoka
    DNA RESEARCH, 2007, 14 (06) : 237 - 246
  • [20] Lowering DNA binding affinity of SssI DNA methyltransferase does not enhance the specificity of targeted DNA methylation in E. coli
    Krystyna Ślaska-Kiss
    Nikolett Zsibrita
    Mihály Koncz
    Pál Albert
    Ákos Csábrádi
    Sarolta Szentes
    Antal Kiss
    Scientific Reports, 11