Live cell imaging of SOS and prophage dynamics in isogenic bacterial populations

被引:28
|
作者
Helfrich, Stefan [1 ]
Pfeifer, Eugen [1 ]
Kraemer, Christina [1 ]
Sachs, Christian Carsten [1 ]
Wiechert, Wolfgang [1 ]
Kohlheyer, Dietrich [1 ]
Noeh, Katharina [1 ]
Frunzke, Julia [1 ]
机构
[1] Forschungszentrum Julich, Inst Bio & Geowissensch, IBG Biotechnol 1, D-52425 Julich, Germany
关键词
ESCHERICHIA-COLI; CORYNEBACTERIUM-GLUTAMICUM; MOLECULAR ANALYSIS; INDUCTION; DNA; MUTATION; CLONING; REPLICATION; EXPRESSION; MECHANISM;
D O I
10.1111/mmi.13147
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Almost all bacterial genomes contain DNA of viral origin, including functional prophages or degenerated phage elements. A frequent but often unnoted phenomenon is the spontaneous induction of prophage elements (SPI) even in the absence of an external stimulus. In this study, we have analyzed SPI of the large, degenerated prophage CGP3 (187kbp), which is integrated into the genome of the Gram-positive Corynebacterium glutamicumATCC 13032. Time-lapse fluorescence microscopy of fluorescent reporter strains grown in microfluidic chips revealed the sporadic induction of the SOS response as a prominent trigger of CGP3 SPI but also displayed a considerable fraction (approximate to 30%) of RecA-independent SPI. Whereas approx. 20% of SOS-induced cells recovered from this stress and resumed growth, the spontaneous induction of CGP3 always led to a stop of growth and likely cell death. A carbon source starvation experiment clearly emphasized that SPI only occurs in actively proliferating cells, whereas sporadic SOS induction was still observed in resting cells. These data highlight the impact of sporadic DNA damage on the activity of prophage elements and provide a time-resolved, quantitative description of SPI as general phenomenon of bacterial populations.
引用
收藏
页码:636 / 650
页数:15
相关论文
共 50 条
  • [21] Live cell imaging of phosphoinositide dynamics with fluorescent protein domains
    Varnai, Peter
    Balla, Tamas
    BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2006, 1761 (08): : 957 - 967
  • [22] Emergence and maintenance of phenotypic heterogeneity in isogenic cell populations
    Paldi, A.
    DIFFERENTIATION, 2006, 74 (08) : 450 - 450
  • [23] Study of subcellular dynamics on cell-substrate interactions by live cell imaging
    Lin, Chuang-Yu
    Li, Li-Tzu
    Su, Wen-Ta
    JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2014, 102 (04) : 1149 - 1154
  • [24] Fluorescent probes for analyzing live cell populations through flow and imaging cytometry
    Li, Zaiguo
    Alvarez, Mark
    Pande, Praveen
    Shen, Dee
    Patton, Wayne F.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2011, 242
  • [25] Live imaging of endosome dynamics
    Kerr, Markus
    Teasdale, Rohan D.
    SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2014, 31 : 11 - 19
  • [26] Live cell imaging
    不详
    CHEMISTRY & INDUSTRY, 2006, (16) : 36 - 36
  • [27] Optical imaging fiber-based live bacterial cell array biosensor
    Biran, I
    Rissin, DM
    Ron, EZ
    Walt, DR
    ANALYTICAL BIOCHEMISTRY, 2003, 315 (01) : 106 - 113
  • [28] Live cell imaging
    Coulton, G
    HISTOCHEMICAL JOURNAL, 1998, 30 (03): : 121 - 122
  • [29] Live cell imaging of bacterial cells: Pyrenoylpyrrole-based fluorescence labeling
    Divakar, Mathiyazhagan Arun
    Shanmugam, Sivakumar
    CHEMICAL BIOLOGY & DRUG DESIGN, 2017, 90 (04) : 554 - 560
  • [30] A Live Cell Imaging Microfluidic Model for Studying Extravasation of Bloodborne Bacterial Pathogens
    Bergevin, Michele D.
    Boczula, Anna E.
    Caruso, Laura-lee
    Persson, Henrik
    Simmons, Craig A.
    Moriarty, Tara J.
    CELLULAR MICROBIOLOGY, 2022, 2022