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Table · dataset · 2026

Parallelised detection of bacterial viability using an electrode array and the Exeter Multiscope - dataset

Listed in figshare and Loughborough Research Repository and GRANTS Data and UP Research Data Repository — shown once because both records carry DOI 10.24378/exe.32251290.v1

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<p dir="ltr">This is the supplemental data for <b>Parallelised detection of bacteria viability using an electrode array and the Exeter Multiscope</b>, published in Scientific Reports, volume 16, article 29903. doi.org/10.1038/s41598-026-66381-9</p><p dir="ltr">The research is summarised below:</p><p dir="ltr">Antimicrobial resistance remains a global existential threat. Given that antimicrobial therapy commonly starts before pathogen identification, rapid and scalable methods capable of determining effective antimicrobial compounds are needed.

In this paper, we demonstrate a 2 × 2 array of parallelised microscopes that uses low numerical aperture (NA=0.25) detection optics and LED excitation to determine bacterial viability based on their fluorescence response to an electrical stimulus. Following a 2-hour incubation, the fluorescent viability readout requires less than one minute. We use K-means clustering to classify pixels in a time lapse sequence of widefield fluorescence images and extract changes seen within bacterial clusters.

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We demonstrate sufficient sensitivity to measure fluorescence changes after electrical stimulation in a bacterial monolayer. To capture these subtle fluorescence changes at high signal-to-background ratios, we place a limit on the minimum optical density of the bacterial sample. This novel approach is scalable to 96-well formats using a suitable consumable electrode array.</p>

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Agricultural biotechnology 71% · Image 65%
Provenance · 4 source records, 35 field assertions
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