Premium
Enhanced pathogenicity of biofilm‐negative S taphylococcus epidermidis isolated from platelet preparations
Author(s) -
Hodgson Scott D.,
GrecoStewart Valerie,
Jimenez Celine S.,
Sifri Costi D.,
Brassinga Ann Karen C.,
RamirezArcos Sandra
Publication year - 2014
Publication title -
transfusion
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.045
H-Index - 132
eISSN - 1537-2995
pISSN - 0041-1132
DOI - 10.1111/trf.12308
Subject(s) - biofilm , virulence , microbiology and biotechnology , staphylococcus epidermidis , biology , operon , bacteria , crystal violet , gene , genetics , escherichia coli , staphylococcus aureus
Background The platelet (PLT) storage environment triggers the formation of surface‐attached aggregates known as biofilms by the common PLT contaminant S taphylococcus epidermidis. The biofilm matrix is largely composed of polysaccharide intercellular adhesin ( PIA ) mediated by the icaADBC operon. However, PIA ‐negative S . epidermidis has been reported to form biofilms in PLT concentrates ( PCs ). Since biofilm formation is associated with increased virulence, this study was aimed at determining if PIA ‐negative S . epidermidis grown in PCs presents enhanced virulence using the nematode C aenorhabditis elegans as a host model for bacterial pathogenesis. Study Design and Methods Biofilm‐positive S . epidermidis ATCC 35984 and 9142, which carry the icaADBC operon, and biofilm‐negative S . epidermidis ATCC 12228 and 9142 Δ icaA were grown in regular media and in PCs and biofilm formation was quantified using a crystal violet assay. The virulence of these strains after passage through PCs was tested using nematode killing assays. Nematode survival was calculated using the K aplan‐ M eier method and statistical differences were determined by log‐rank analysis. Results All S . epidermidis strains were able to form biofilms in PCs . Although persistence of a biofilm‐positive phenotype in the biofilm‐negative strains grown in PCs was not observed after passage in regular medium, the virulence of all strains was significantly increased as demonstrated by shortened life spans of the nematodes in C . elegans killing assays. Conclusion Our findings highlight the potential of an increased risk of nosocomial infections caused by S . epidermidis in transfusion recipients since PC storage conditions promote biofilm formation, and possibly pathogenicity, of strains traditionally known to be attenuated for virulence.