THEME: "The Role of New Technologies in the Fields of Catalysis and Chemical Science"
University of Colorado, USA
Title: Light-Activated Quantum Dot Potentiation of Antibiotics to Treat Drug-Resistant Biofilms
Dana F. Stamo is a second-year
Biological Engineering PhD student at the University of Colorado Boulder where
she does research on novel therapeutics for hard-to-treat infectious diseases. In
2019, Dana graduated from the University of Colorado Boulder with her
Bachelor’s degree in Chemical & Biological Engineering. An artist in her
free time, Dana often blurs the line between art and science, using creativity
and design principles in her approach to engineering. When she isn’t doing art
or science, you’ll find Dana hiking the Colorado Rockies, skating, or reading.
Antimicrobial
resistance is one of the biggest threats to global health and demands
alternative therapies for multi-drug resistant (MDR) infections.
Light-activated quantum dots (QDs) are a versatile candidate for treating MDR
bacteria without harming mammalian cells. Furthermore, their ease of diffusion
and ability to photo-potentiate allows for precise, localized treatment and
their dynamic tunability keeps them in pace with bacterial evolution. While QDs
are shown to be a viable alternative therapy for planktonic cultures, they have
not been applied in treating bacterial biofilms (a common growth form that affords
bacterial strains more resistance and persistence to immune and traditional
drug attack). Additionally, the mechanism of QD attack—production of reactive
oxygen species—and sub-breakpoint antibiotic treatments have been shown to
stimulate biofilm formation, especially in clinical isolates. Herein, we
demonstrate the previously observed mono-therapeutic stimulation of biofilm
formation and apply QD-antibiotic combination therapies to overcome and nearly
eradicate 48-hour, early-stage, static biofilms of Escherichia coli K12,
methicillin-resistant Staphylococcus aureus, and Pseudomonas
aeruginosa. These results lay the groundwork for QD-antibiotic combination
treatments for late-stage clinical and industrial biofilms, contributing to the
development of QD nanotherapeutics for combating MDR superbugs.