Genome-wide transcription response of Staphylococcus epidermidis to heat shock and medically relevant glucose levels

Skin serves as both barrier and interface between body and environment. Skin microbes are intermediaries evolved to respond, transduce, or act in response to changing environmental or physiological conditions. We quantified genome-wide changes in gene expression levels for one abundant skin commensa...

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Published in:Frontiers in microbiology Vol. 15; p. 1408796
Main Authors: Benjamin, Kaisha N, Goyal, Aditi, Nair, Ramesh V, Endy, Drew
Format: Journal Article
Language:English
Published: Switzerland Frontiers Media S.A 22-07-2024
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Summary:Skin serves as both barrier and interface between body and environment. Skin microbes are intermediaries evolved to respond, transduce, or act in response to changing environmental or physiological conditions. We quantified genome-wide changes in gene expression levels for one abundant skin commensal, , in response to an internal physiological signal, glucose levels, and an external environmental signal, temperature. We found 85 of 2,354 genes change up to 34-fold in response to medically relevant changes in glucose concentration (0-17 mM; adj ≤0.05). We observed carbon catabolite repression in response to a range of glucose spikes, as well as upregulation of genes involved in glucose utilization in response to persistent glucose. We observed 366 differentially expressed genes in response to a physiologically relevant change in temperature (37-45°C; adj ≤ 0.05) and an heat-shock response that mostly resembles the heat-shock response of related staphylococcal species. DNA motif analysis revealed CtsR and CIRCE operator sequences arranged in tandem upstream of and operons. We identified and curated 38 glucose-responsive genes as candidate ON or OFF switches for use in controlling synthetic genetic systems. Such systems might be used to instrument the skin microbiome or help control microbes bioengineered to serve as embedded diagnostics, monitoring, or treatment platforms.
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Vineet Kumar, The University of Texas at Austin, United States
Reviewed by: Becky Hess, Pacific Northwest National Laboratory (DOE), United States
These authors have contributed equally to this work and share first authorship
Edited by: Christoph Engl, Queen Mary University of London, United Kingdom
ISSN:1664-302X
1664-302X
DOI:10.3389/fmicb.2024.1408796