Dispersing and Sonoporating Biofilm-Associated Bacteria with Sonobactericide
Kirby R. Lattwein (Erasmus MC)
Inés Beekers (Erasmus MC)
Joop J.P. Kouijzer (Erasmus MC)
Mariël Leon-Grooters (Erasmus MC)
Simone A.G. Langeveld (Erasmus MC)
Tom van Rooij (Erasmus MC)
Antonius F.W. van der Steen (TU Delft - ImPhys/Medical Imaging, Erasmus MC)
Nico de Jong (Erasmus MC, TU Delft - ImPhys/Medical Imaging)
Willem J.B. van Wamel (Erasmus MC)
Klazina Kooiman (Erasmus MC)
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Abstract
Bacteria encased in a biofilm poses significant challenges to successful treatment, since both the immune system and antibiotics are ineffective. Sonobactericide, which uses ultrasound and microbubbles, is a potential new strategy for increasing antimicrobial effectiveness or directly killing bacteria. Several studies suggest that sonobactericide can lead to bacterial dispersion or sonoporation (i.e., cell membrane permeabilization); however, real-time observations distinguishing individual bacteria during and directly after insonification are missing. Therefore, in this study, we investigated, in real-time and at high-resolution, the effects of ultrasound-induced microbubble oscillation on Staphylococcus aureus biofilms, without or with an antibiotic (oxacillin, 1 µg/mL). Biofilms were exposed to ultrasound (2 MHz, 100–400 kPa, 100–1000 cycles, every second for 30 s) during time-lapse confocal microscopy recordings of 10 min. Bacterial responses were quantified using post hoc image analysis with particle counting. Bacterial dispersion was observed as the dominant effect over sonoporation, resulting from oscillating microbubbles. Increasing pressure and cycles both led to significantly more dispersion, with the highest pressure leading to the most biofilm removal (up to 83.7%). Antibiotic presence led to more variable treatment responses, yet did not significantly impact the therapeutic efficacy of sonobactericide, suggesting synergism is not an immediate effect. These findings elucidate the direct effects induced by sonobactericide to best utilize its potential as a biofilm treatment strategy.