4.6 Article

Lack of Direct Correlation between Biofilm Formation and Antimicrobial Resistance in Clinical Staphylococcus epidermidis Isolates from an Italian Hospital

Journal

MICROORGANISMS
Volume 10, Issue 6, Pages -

Publisher

MDPI
DOI: 10.3390/microorganisms10061163

Keywords

Staphylococcus epidermidis; biofilm; crystal violet; antibiotic resistance polysaccharide intercellular adhesin (PIA); Congo red agar

Categories

Funding

  1. PFIZER
  2. Department of Bioscience

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Staphylococcus epidermidis is an opportunistic pathogen that can cause nosocomial infections. A study conducted in an Italian hospital found that only a minority of S. epidermidis isolates displayed biofilm formation, regardless of their source. However, among the biofilm-producing isolates, those from catheters were the most efficient in biofilm formation. Interestingly, the production levels of PIA, the main extracellular polysaccharide of S. epidermidis, were similar in most isolates, including strong biofilm producers, compared to reference strains classified as non-biofilm formers. This suggests that high levels of PIA production may not confer a particular advantage for clinical isolates. The study also found that the correlation between biofilm production and decreased antibiotic sensitivity differed among the clinical isolates.
Staphylococcus epidermidis is an opportunistic pathogen and a frequent cause of nosocomial infections. In this work, we show that, among 51 S. epidermidis isolates from an Italian hospital, only a minority displayed biofilm formation, regardless of their isolation source (peripheral blood, catheter, or skin wounds); however, among the biofilm-producing isolates, those from catheters were the most efficient in biofilm formation. Interestingly, most isolates including strong biofilm producers displayed production levels of PIA (polysaccharide intercellular adhesin), the main S. epidermidis extracellular polysaccharide, similar to reference S. epidermidis strains classified as non-biofilm formers, and much lower than those classified as intermediate or high biofilm formers, possibly suggesting that high levels of PIA production do not confer a particular advantage for clinical isolates. Finally, while for the reference S. epidermidis strains the biofilm production clearly correlated with the decreased sensitivity to antibiotics, in particular, protein synthesis inhibitors, in our clinical isolates, such positive correlation was limited to tetracycline. In contrast, we observed an inverse correlation between biofilm formation and the minimal inhibitory concentrations for levofloxacin and teicoplanin. In addition, in growth conditions favoring PIA production, the biofilm-forming isolates showed increased sensitivity to daptomycin, clindamycin, and erythromycin, with increased tolerance to the trimethoprim/sulfamethoxazole association. The lack of direct correlation between the biofilm production and increased tolerance to antibiotics in S. epidermidis isolates from a clinical setting would suggest, at least for some antimicrobials, the possible existence of a trade-off between the production of biofilm determinants and antibiotic resistance.

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