Abstract
Foreign-body infection (FBI) is notoriously resistant to eradication by antibiotic treatment. It is hypothesized that reduced bacterial metabolic activity contributes to this resistance. We examined the metabolic activity of Staphylococcus epidermidis in 204 samples recovered during in vitro foreign-body colonization and in 424 samples recovered during in vivo FBI in a rat model. Metabolic activity was measured by determining the amount of 16S rRNA per genome by quantitative PCR. The initial foreign-body-associated growth proved to be a metabolically active process, both in vitro and in vivo. The initial 16S rRNA content was similar to that observed during in vitro exponential-growth phase. However, during late in vivo FBI, a 114-fold (P << 0.0001) decrease in the 16S rRNA content was observed, indicating that there was markedly decreased metabolic activity. This decreased metabolic activity during late FBI can explain at least in part why such infections are so difficult to eradicate with conventional antibiotic treatment.
MeSH Terms
Animals
Catheters, Indwelling/microbiology
Disease Models, Animal
Foreign-Body Reaction/microbiology
Germ-Free Life
Polymerase Chain Reaction
Polyurethanes
RNA, Bacterial/analysis
RNA, Ribosomal, 16S/analysis
Rats
Rats, Inbred F344
Staphylococcal Infections/microbiology
Staphylococcus epidermidis/genetics,metabolism
Time Factors
Chemicals
Polyurethanes
RNA, Bacterial
RNA, Ribosomal, 16S
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Vandecasteele Stefaan Johan
Infectious Diseases Research Group, Department of Microbiology and Immunology, Rega Institute for Medical Research and Internal Medicine and Infectious Diseases, University Hospital Leuven, Leuven, Belgium.
[email protected]
Peetermans Willy Eduard
Carbonez An
Van Eldere Johan
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