Abstract
Macrophages are armed with multiple oxygen-dependent and -independent bactericidal properties. However, the respiratory burst, generating reactive oxygen species, is believed to be a major cause of bacterial killing. We exploited the susceptibility of Escherichia coli in macrophages to characterize the effects of the respiratory burst on intracellular bacteria. We show that E. coli strains recovered from J774 macrophages exhibit high rates of mutations. We report that the DNA damage generated inside macrophages includes DNA strand breaks and the modification 8-oxo-2'-deoxyguanosine, which are typical oxidative lesions. Interestingly, we found that under these conditions, early in the infection the majority of E. coli cells are viable but gene expression is inhibited. Our findings demonstrate that macrophages can cause severe DNA damage to intracellular bacteria. Our results also suggest that protection against the macrophage-induced DNA damage is an important component of the bacterial defense mechanism within macrophages.
MeSH Terms
Animals
Cell Line
DNA Damage
DNA, Bacterial/chemistry,drug effects
Escherichia coli/genetics,physiology
Green Fluorescent Proteins
Hydrogen Peroxide/pharmacology
Lac Operon
Luminescent Proteins/biosynthesis
Macrophage Activation
Macrophages/drug effects,microbiology,physiology
Oxidative Stress
Recombinant Proteins/biosynthesis
Respiratory Burst
Salmonella/genetics,physiology
Tetradecanoylphorbol Acetate/pharmacology
Transfection
Chemicals
DNA, Bacterial
Luminescent Proteins
Recombinant Proteins
Green Fluorescent Proteins
Hydrogen Peroxide
Tetradecanoylphorbol Acetate
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Schlosser-Silverman E
Department of Molecular Genetics and Biotechnology, The Hebrew University-Hadassah Medical School, The Hebrew University, Jerusalem, Israel.
Elgrably-Weiss M
Rosenshine I
Kohen R
Altuvia S
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