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Optical Trapping and Fast Discrimination of Label‐Free Bacteriophages at the Single Virion Level

There is a recent resurgence of interest in phage therapy (the therapeutic use of bacterial viruses) as an approach to eliminating difficult‐to‐treat infections. However, existing approaches for therapeutic phage selection and virulence testing are time‐consuming, host‐dependent, and facing reproduc...

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Bibliographic Details
Published in:Small (Weinheim an der Bergstrasse, Germany) Germany), 2024-07, Vol.20 (27), p.e2308814-n/a
Main Authors: Villa, Nicolas, Tartari, Enrico, Glicenstein, Simon, de Villiers de la Noue, Hugues, Picard, Emmanuel, Marcoux, Pierre R., Zelsmann, Marc, Resch, Grégory, Hadji, Emmanuel, Houdré, Romuald
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Language:English
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Summary:There is a recent resurgence of interest in phage therapy (the therapeutic use of bacterial viruses) as an approach to eliminating difficult‐to‐treat infections. However, existing approaches for therapeutic phage selection and virulence testing are time‐consuming, host‐dependent, and facing reproducibility issues. Here, this study presents an innovative approach wherein integrated resonant photonic crystal (PhC) cavities in silicon are used as optical nanotweezers for probing and manipulating single bacteria and single virions with low optical power. This study demonstrates that these nanocavities differentiate between a bacterium and a phage without labeling or specific surface bioreceptors. Furthermore, by tailoring the spatial extent of the resonant optical mode in the low‐index medium, phage distinction across phenotypically distinct phage families is demonstrated. The work paves the road to the implementation of optical nanotweezers in phage therapy protocols. An optical tweezer is developed which is able to operate at the single virion level without any need for virion pre‐labeling nor surface bioreceptors and sensitive enough to detect the presence of one, two, three, or more virions, here bacteriophages, as well as to distinguish different phages from phenotypically distinct families.
ISSN:1613-6810
1613-6829
1613-6829
DOI:10.1002/smll.202308814