Published August 2026 | Version v1
Dissertation Open

Transcriptomic Insights on the Fungal Response to Antimicrobial Nanopatterned Surfaces

  • 1. ROR icon University of Chicago

Contributors

  • 1. ROR icon University of Chicago

Description

Nanopatterned surfaces have many unique properties conferred to them by virtue of their nano scale. As methods of nanofabrication have advanced, nanopatterned surfaces are of increasing interest for these properties. Nanopatterned surfaces with antimicrobial effects are one such example. By reducing microbial adhesion or acting with microbicidal efficiency on microbes that adhere on the surface, antimicrobial nanomaterials (AMNs) can confer resistance to biofouling without the use of antimicrobial drugs—which are rapidly losing their effectiveness due to the growing population of drug-resistant microbes. It is unclear what responses, if any, microbes may mount to resist antimicrobial nanofeatures and overcome these multifaceted effects. Understanding how microbes may resist the antimicrobial effects of AMNs to colonize their surfaces is imperative to gaining a complete understanding of how antimicrobial surfaces can be effectively deployed. In this thesis, I have used transcriptomics, fluorescent microscopy, and scanning electron microscopy to examine the AMN-induced stress response of three fungal microbe species (S. cerevisiae, C. albicans, and C. auris) exposed to four types of black silicon (bSi) AMNs. I have found that the induced stress response correlates with the antimicrobial effect. Furthermore, I show that C. albicans exhibit the strongest stress response, followed by C. auris then S. cerevisiae. Overall, I have established a new modality of examining the microbe-AMN interaction dynamic by incorporating the use of transcriptomics.

Other

Additionally contained within this thesis are two other works which I co-first authored throughout my PhD, entitled “Integration of silicon chip microstructures for in-line microbial cell lysis in soft microfluidics” (DOI: 10.1039/D2LC00896C) and “Capture, Confine, Characterize: High-Throughput Dielectrophoresis-Based Single-Cell Microfluidics Platform to Analyze Mammalian and Yeast Cells Using Raman Spectroscopy” (DOI: 10.1002/smll.202508692).

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Additional details

Funding

National Institutes of Health
NIH Director's New Innovator Awards (DP2)
National Institutes of Health
Collaborative Program Grant for Multidisciplinary Teams (RM1)

UChicago Information

Division(s)
Physical Sciences Division
Department(s)
Chemistry