Increased Expression of Periplasmic Cu,Zn Superoxide Dismutase Enhances Survival of Escherichia coli Invasive Strains within Nonphagocytic Cells
DNA, Bacterial
0301 basic medicine
enzyme induction
gene overexpression
Gene Expression
Endosomes
Electron
Plasmid
copper zinc superoxide dismutase
03 medical and health sciences
Escherichia coli Protein
Escherichia coli Invasive Strains; Periplasmic Cu,Zn Superoxide Dismutase; Nonphagocytic Cells
Escherichia coli
Humans
human
strain difference
endosome
Settore BIO/10 - BIOCHIMICA
bacterium competence
oxidative stre
Microscopy
Base Sequence
Virulence
Superoxide Dismutase
human cell
Escherichia coli Proteins
article
Bacterial
Yersinia pseudotuberculosi
DNA
phagocytosi
Hydrogen-Ion Concentration
3. Good health
Microscopy, Electron
Oxidative Stress
intracellular killing
priority journal
Genes
Genes, Bacterial
copper zinc superoxide dismutase; article; bacterium competence; endosome; enzyme induction; epithelium cell; Escherichia coli; gene overexpression; HeLa cell; human; human cell; intracellular killing; oxidative stress; phagocytosis; priority journal; strain difference; Yersinia pseudotuberculosis; Base Sequence; DNA, Bacterial; Endosomes; Escherichia coli; Escherichia coli Proteins; Gene Expression; Genes, Bacterial; Hela Cells; Humans; Hydrogen-Ion Concentration; Microscopy, Electron; Oxidative Stress; Plasmids; Superoxide Dismutase; Virulence
epithelium cell
HeLa cell
HeLa Cells
Plasmids
DOI:
10.1128/iai.68.1.30-37.2000
Publication Date:
2009-05-01T17:57:25Z
AUTHORS (10)
ABSTRACT
ABSTRACT We have studied the influence of periplasmic Cu,Zn superoxide dismutase on intracellular survival Escherichia coli strains able to invade epithelial cells by expression inv gene from Yersinia pseudotuberculosis but unable multiply intracellularly. Intracellular viability assays, confirmed electron microscopy observations, showed that invasive E. engineered increase production are much more resistant killing than containing only chromosomal sodC copy. However, we found a slight difference in within HeLa between -null mutant and its isogenic wild-type strain. Such small correlates with very low this enzyme also observed acid- oxidative stress-sensitive HB101(pRI203) is rapidly killed GC4468(pRI203). The high mortality HB101(pRI203), independent acidification endosome, abolished overexpression . Our data suggest oxyradicals involved mechanisms bacterial high-level provides bacteria an effective protection against damage. propose could offer important selective advantage host expressing levels enzyme.
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