Investigation of the effect of β-lactam antibiotics and serum on growth and gene expression in Escherichia coli strain JJ1886
β-Lactamase-producing Escherichia coli strain JJ1886 is an epidemic clone with high virulence properties. Because this strain can survive in the bloodstream, we aimed here to understand how β-lactam antibiotics and human serum affect the growth and gene expression of this bacterium. We report the ti...
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Veröffentlicht in: | Turkish journal of medical sciences 2018-12, Vol.48 (6), p.1340-1350 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | β-Lactamase-producing
Escherichia coli
strain JJ1886 is an epidemic clone with high virulence properties. Because
this
strain can survive in the bloodstream, we aimed here to understand how β-lactam antibiotics and human serum affect the growth
and gene expression of this bacterium.
We report the time-dependent growth effect of normal human serum and heat-inactivated serum, together
with β-lactam antibiotics (including cefotaxime, ceftazidime, and carbenicillin), for
E. coli
strain JJ1886. Relative gene expression of
β-lactamase-related genes (encoding the β-lactamase regulator, CTX-M-15, and peptidoglycan glycosyltransferase) and serum survival-
associated genes (encoding lipoprotein NlpI, murein lipoprotein, lipopolysaccharide core heptose (I) kinase, lipopolysaccharide
biosynthesis protein, capsule synthesis protein, and phosphate transport system) were investigated by RT-qPCR.
Cells proliferated during the exponential growth phase when the bacterium was treated with human serum. However,
cefotaxime and ceftazidime together with serum had a bactericidal effect at each of the tested time points. Downregulation was observed
in gene-encoding lipoprotein NlpI as a result of treatment with carbenicillin.
Serum plus cefotaxime or ceftazidime had bactericidal activities. When the bacterium was treated with human serum and
β-lactam antibiotics, there were no significant changes in relative gene expression, except for the
nlpI
gene. |
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ISSN: | 1300-0144 1303-6165 |
DOI: | 10.3906/sag-1803-121 |