Staphylococcus epidermidis: metabolic adaptation and biofilm formation in response to different oxygen concentrations
Author(s) -
Cristina UribeAlvarez,
Natalia ChiqueteFélix,
Martha Lucinda Contreras-Zentella,
Sergio GuerreroCastillo,
Antonio Peña,
Salvador UribeCarvajal
Publication year - 2015
Publication title -
pathogens and disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.983
H-Index - 105
ISSN - 2049-632X
DOI - 10.1093/femspd/ftv111
Subject(s) - dehydrogenase , biochemistry , respiratory chain , biofilm , lactate dehydrogenase , succinate dehydrogenase , alcohol dehydrogenase , oxidoreductase , nitrate reductase , staphylococcus epidermidis , pyruvate dehydrogenase complex , microbiology and biotechnology , chemistry , biology , reductase , enzyme , bacteria , staphylococcus aureus , genetics
Staphylococcus epidermidis has become a major health hazard. It is necessary to study its metabolism and hopefully uncover therapeutic targets. Cultivating S. epidermidis at increasing oxygen concentration [O2] enhanced growth, while inhibiting biofilm formation. Respiratory oxido-reductases were differentially expressed, probably to prevent reactive oxygen species (ROS) formation. Under aerobiosis, S. epidermidis expressed high oxido-reductase activities, including glycerol-3-phosphate dehydrogenase, pyruvate dehydrogenase, ethanol dehydrogenase and succinate dehydrogenase, as well as cytochromes bo and aa3; little tendency to form biofilms was observed. Under micro-aerobiosis, pyruvate dehydrogenase and ethanol dehydrogenase decreased while glycerol-3-phosphate dehydrogenase and succinate dehydrogenase nearly disappeared; cytochrome bo was present; anaerobic nitrate reductase activity was observed; biofilm formation increased slightly. Under anaerobiosis, biofilms grew; low ethanol dehydrogenase, pyruvate dehydrogenase and cytochrome bo were still present; nitrate dehydrogenase was the main terminal electron acceptor. KCN inhibited the aerobic respiratory chain and increased biofilm formation. In contrast, methylamine inhibited both nitrate reductase and biofilm formation. The correlation between the expression and/or activity or redox enzymes and biofilm-formation activities suggests that these are possible therapeutic targets to erradicate S. epidermidis.
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