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

被引:0
|
作者
Villa, Nicolas [1 ]
Tartari, Enrico [1 ]
Glicenstein, Simon [2 ]
de la Noue, Hugues de Villiers [3 ]
Picard, Emmanuel [2 ]
Marcoux, Pierre R. [4 ]
Zelsmann, Marc [5 ]
Resch, Gregory [3 ]
Hadji, Emmanuel [2 ]
Houdre, Romuald [1 ]
机构
[1] Ecole Polytech Fed Lausanne, Inst Phys, CH-1015 Lausanne, Switzerland
[2] Univ Grenoble Alpes, CEA, Grenoble INP, IRIG,PHELIQS, F-38000 Grenoble, France
[3] Lausanne Univ Hosp CHUV, Lab Bacteriophages & Phage Therapy, Ctr Res & Innovat Clin Pharmaceut Sci CRISP, CH-1011 Lausanne, Switzerland
[4] Univ Grenoble Alpes, CEA, LETI, DTIS,L4IV, F-38000 Grenoble, France
[5] Univ Grenoble Alpes, CNRS, CEA LETI Minatec, LTM, F-38054 Grenoble, France
基金
瑞士国家科学基金会;
关键词
bacteria; bacteriophages; biosensing; microfluidics; optical resonators; optical trapping; photonic crystals; REFRACTIVE-INDEX; PHAGE THERAPY; MANIPULATION; BACTERIA; CULTURE; PATIENT;
D O I
10.1002/smll.202308814
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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. image
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页数:9
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