On-Chip Optical Nano-Tweezers for Culture-Less Fast Bacterial Viability Assessment.

nanophotonic tweezers nanoscale optical sensing optical trapping single-cell characterization viability assessment

Journal

Small (Weinheim an der Bergstrasse, Germany)
ISSN: 1613-6829
Titre abrégé: Small
Pays: Germany
ID NLM: 101235338

Informations de publication

Date de publication:
01 2022
Historique:
revised: 30 09 2021
received: 28 06 2021
pubmed: 17 11 2021
medline: 19 3 2022
entrez: 16 11 2021
Statut: ppublish

Résumé

Because of antibiotics misuse, the dramatic growth of antibioresistance threatens public health. Tests are indeed culture-based, and require therefore one to two days. This long time-to-result implies the use of large-spectrum antibiotherapies as a first step, in absence of pathogen characterization. Here, a breakthrough approach for a culture-less fast assessment of bacterial response to stress is proposed. It is based on non-destructive on-chip optical tweezing. A laser loads an optical nanobeam cavity whose evanescent part of the resonant field acts as a nano-tweezer for bacteria surrounding the cavity. Once optically trapped, the bacterium-nanobeam cavity interaction induces a shift of the resonance driven by the bacterial cell wall optical index. The analysis of the wavelength shift yields an assessment of viability upon stress at the single-cell scale. As a proof of concept, bacteria are stressed by incursion, before optical trapping, at different temperatures (45, 51, and 70 °C). Optical index changes correlate with the degree of thermal stress allowing to sort viable and dead bacteria. With this disruptive diagnosis method, bacterial viability upon stress is probed much faster (typically less than 4 h) than with conventional culture-based enumeration methods (24 h).

Identifiants

pubmed: 34784093
doi: 10.1002/smll.202103765
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2103765

Informations de copyright

© 2021 Wiley-VCH GmbH.

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Auteurs

Manon Tardif (M)

Univ. Grenoble Alpes, Grenoble INP, CEA, IRIG, Pheliqs, SiNaPS Lab, Grenoble, F-38000, France.
Univ. Grenoble Alpes, CNRS, LTM, Grenoble, F-38000, France.

Emmanuel Picard (E)

Univ. Grenoble Alpes, Grenoble INP, CEA, IRIG, Pheliqs, SiNaPS Lab, Grenoble, F-38000, France.

Victor Gaude (V)

Univ. Grenoble Alpes, CNRS, LTM, Grenoble, F-38000, France.

Jean-Baptiste Jager (JB)

Univ. Grenoble Alpes, Grenoble INP, CEA, IRIG, Pheliqs, SiNaPS Lab, Grenoble, F-38000, France.

David Peyrade (D)

Univ. Grenoble Alpes, CNRS, LTM, Grenoble, F-38000, France.

Emmanuel Hadji (E)

Univ. Grenoble Alpes, Grenoble INP, CEA, IRIG, Pheliqs, SiNaPS Lab, Grenoble, F-38000, France.

Pierre R Marcoux (PR)

Univ. Grenoble Alpes, CEA, LETI, DTBS, LSIV, Grenoble, F-38000, France.

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