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In vitro activity of caspofungin against planktonic and sessile Candida sp. cells
Anna Serefko1, Beata Chudzik, Anna Malm
1Department of Pharmaceutical Microbiology, Medical University of Lublin, Chodiki 1, 20-093 Lublin, Poland.
Abstract:
Candida sp. may be regarded as one of the leading etiologic agents of hospital-acquired infections, including those related with the indwelling medical devices, which become colonized by the yeasts, accompanied by biofilm formation. In this paper we assayed in vitro susceptibility to caspofungin of planktonic and sessile cells of nasopharyngeal isolates of Candida sp. Two types of biomaterials were used - silicone elastomer-coated latex urinary Foley catheter and PCV Thorax catheter. The minimal inhibitory concentrations (MIC) of caspofungin for planktonic Candida sp. cells ranged from 0.008 to 0.031 mg/l, while the minimal fungicidal concentrations (MFC) from 0.008 to 0.062 mg/l, with MFC/MIC ratios < or = 2. The minimal concentration of caspofungin preventing adhesion process of Candida sp. on both biomaterials ranged from 0.004 to 0.031 mg/l, while preventing biofilm formation from 0.004 to 0.062 mg/l. In contrast, much higher minimal concentrations of caspofungin were needed to eradicate the mature biofilm (0.25 to >8 mg/l). In all cases, drug concentrations depended on the strain and the biomaterial used. Our preliminary data suggest that caspofungin, showing good anti-adherent activity in vitro against Candida sp., appears to be a potential agent rather for prophylaxis of the yeast infections associated with biomaterials but not for their treatment.
Insights
Caspofungin effectively prevents Candida sp. yeast adhesion and biofilm formation on medical devices in vitro. However, it is less effective at eradicating established biofilms, suggesting a prophylactic rather than therapeutic role.
Area of Science:
- Mycology
- Infectious Diseases
- Biomaterials Science
Background:
- Candida species are a major cause of hospital-acquired infections, particularly those linked to indwelling medical devices.
- Medical device colonization by Candida leads to biofilm formation, complicating treatment and increasing infection risk.
Purpose of the Study:
- To evaluate the in vitro susceptibility of planktonic and sessile Candida sp. cells to caspofungin.
- To assess caspofungin's efficacy in preventing adhesion and biofilm formation on two types of medical biomaterials.
Main Methods:
- In vitro susceptibility testing of Candida sp. (nasopharyngeal isolates) to caspofungin.
- Evaluation of caspofungin's effect on planktonic and sessile cells adhered to silicone elastomer-coated latex urinary Foley catheters and PCV Thorax catheters.
- Determination of minimal inhibitory concentrations (MIC), minimal fungicidal concentrations (MFC), and concentrations preventing adhesion and biofilm formation.
Main Results:
- Low MIC and MFC values for caspofungin against planktonic Candida sp. cells (MIC: 0.008–0.031 mg/l, MFC: 0.008–0.062 mg/l).
- Caspofungin demonstrated significant anti-adherent and anti-biofilm formation activity at low concentrations (0.004–0.062 mg/l).
- Eradication of mature biofilms required substantially higher caspofungin concentrations (0.25 to >8 mg/l), varying by strain and biomaterial.
Conclusions:
- Caspofungin exhibits potent in vitro anti-adherent activity against Candida sp. on medical biomaterials.
- The drug shows promise for the prophylaxis of yeast infections associated with medical devices.
- Caspofungin is less effective for treating established Candida biofilms on these materials.
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