4.5 Article

Spiked Nanostructures Disrupt Fungal Biofilm and Impart Increased Sensitivity to Antifungal Treatment

期刊

ADVANCED MATERIALS INTERFACES
卷 9, 期 12, 页码 -

出版社

WILEY
DOI: 10.1002/admi.202102353

关键词

antifungal drugs; hydrothermal etching; implants; mechano-bactericidal effect; morphogenesis

资金

  1. Department of Industry, Science, Energy and Resources (Innovative Manufacturing CRC Ltd) Global Orthopaedic Technology Pty Ltd [IMCRC/GOT/130318]
  2. Corin Australia
  3. University of South Australia
  4. NHMRC [GNT1194466]

向作者/读者索取更多资源

There is a growing global demand for medically implanted devices, while the incidence of implant associated infection is also increasing. This study explores the interaction between the fungal pathogen Candida albicans and an antimicrobial surface with nanoscale protrusions. The findings suggest that the nanostructured surface can inhibit the growth and hyphal transition of C. albicans, as well as affect the expression of virulence-associated genes. Additionally, the study demonstrates that the antifungal drug amphotericin B is more effective against C. albicans cultured on the nanostructured surface compared to a smooth control surface.
There is a globally increasing demand for medically implanted devices, partly spurred by an aging population. In parallel, there is a proportionate increase in implant associated infection. Much focus has been directed toward the development of techniques to fabricate nanostructured antimicrobial biomaterials to mitigate infection. The present study investigates the interaction of the fungal pathogen Candida albicans with an antimicrobial surface bearing nanoscale protrusions. C. albicans cells were observed to be affected by cell wall stress, which impeded its ability to switch to a hyphal phenotype. There are significant differences in the expression of C. albicans virulence-associated genes between the untreated and nanostructured surfaces. To determine whether the observed inhibition of C. albicans would also sensitize it to antifungal drugs, a culture is established for 3 days on the nanostructured surface before being treated with the antifungal drug amphotericin B. The drug was able to kill all cells on the nanostructured surface at sub-clinical concentrations, while remaining ineffective against cultures grown on a smooth control surface. These findings may eventually prove to be impactful in the clinic, as clinicians may be able to reduce antifungal drug dosages and minimize the effects of drug associated toxicity.

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