Label-free smartphone quantitation of bacteria by darkfield imaging of light scattering in fluoropolymer micro capillary film allows portable detection of bacteriophage lysis
Label-free smartphone quantitation of bacteria by darkfield imaging of light scattering in fluoropolymer micro capillary film allows portable detection of bacteriophage lysis
Conventional methods for the detection and quantitation of bacteria are slow, laborious and require a laboratory. Microfluidic systems offer faster and portable testing, and smartphone cameras can record colorimetric or fluorometric bioassays, but this requires dye addition. Here, we demonstrate for the first time label-free smartphone detection of bacterial light scattering by darkfield microfluidic imaging to measure bacteria and bacteriophage lysis. A single LED and portable 3D printed imaging box allowed bacterial concentration and growth to be measured by direct imaging of bacterial light scattering. Bacteriophage lysis was detected within a 10-channel microfluidic device made from melt-extruded fluoropolymer micro capillary film, allowing rapid detection of host specificity. Elimination of unwanted reflections and optimising illumination angle are critical for successful darkfield bacterial imaging, with 15° giving maximal intensity. Bacterial sedimentation was directly observed within microfluidic devices, and detection sensitivity significantly increased by allowing bacteria to sediment for 30 min. With this simple, low-cost, 3D printed system bacterial concentrations down to an optical density of 0.1 could be measured corresponding to 8 × 104 colony forming units (CFU) per microdevice, approaching the sensitivity of conventional spectrophotometers. Bacteriophage lysis could be detected at a range of starting cell concentrations. With a low starting cell concentration, the increase in light scatter signal with incubation was prevented in the presence of bacteriophage. Conversely, with high starting cell concentration, the light scatter signal detected at the start was clearly eliminated when phage were added, indicating this simple system allows direct visualisation of bacteriophage eliminating light scattering by lysis.
Donmez, Sultan Itayda
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Needs, Sarah H.
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Osborn, Helen M.I.
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Edwards, Alexander D.
bc3d9b93-a533-4144-937b-c673d0a28879
6 August 2020
Donmez, Sultan Itayda
d603a603-da60-4e73-b3ac-966f4684f4a0
Needs, Sarah H.
6dd8aa24-d1de-4429-9b0a-65e82204db58
Osborn, Helen M.I.
dfe7b84a-38d7-49d3-a57a-b445b33d884e
Edwards, Alexander D.
bc3d9b93-a533-4144-937b-c673d0a28879
Donmez, Sultan Itayda, Needs, Sarah H., Osborn, Helen M.I. and Edwards, Alexander D.
(2020)
Label-free smartphone quantitation of bacteria by darkfield imaging of light scattering in fluoropolymer micro capillary film allows portable detection of bacteriophage lysis.
Sensors and Actuators B: Chemical, 323, [128645].
(doi:10.1016/j.snb.2020.128645).
Abstract
Conventional methods for the detection and quantitation of bacteria are slow, laborious and require a laboratory. Microfluidic systems offer faster and portable testing, and smartphone cameras can record colorimetric or fluorometric bioassays, but this requires dye addition. Here, we demonstrate for the first time label-free smartphone detection of bacterial light scattering by darkfield microfluidic imaging to measure bacteria and bacteriophage lysis. A single LED and portable 3D printed imaging box allowed bacterial concentration and growth to be measured by direct imaging of bacterial light scattering. Bacteriophage lysis was detected within a 10-channel microfluidic device made from melt-extruded fluoropolymer micro capillary film, allowing rapid detection of host specificity. Elimination of unwanted reflections and optimising illumination angle are critical for successful darkfield bacterial imaging, with 15° giving maximal intensity. Bacterial sedimentation was directly observed within microfluidic devices, and detection sensitivity significantly increased by allowing bacteria to sediment for 30 min. With this simple, low-cost, 3D printed system bacterial concentrations down to an optical density of 0.1 could be measured corresponding to 8 × 104 colony forming units (CFU) per microdevice, approaching the sensitivity of conventional spectrophotometers. Bacteriophage lysis could be detected at a range of starting cell concentrations. With a low starting cell concentration, the increase in light scatter signal with incubation was prevented in the presence of bacteriophage. Conversely, with high starting cell concentration, the light scatter signal detected at the start was clearly eliminated when phage were added, indicating this simple system allows direct visualisation of bacteriophage eliminating light scattering by lysis.
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Donmez_manuscript_Accepted manuscript
- Accepted Manuscript
More information
Accepted/In Press date: 23 July 2020
e-pub ahead of print date: 1 August 2020
Published date: 6 August 2020
Identifiers
Local EPrints ID: 494658
URI: http://eprints.soton.ac.uk/id/eprint/494658
ISSN: 0925-4005
PURE UUID: 3eeb4ae4-29c1-484a-9763-da6c7e03f9b7
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Date deposited: 11 Oct 2024 17:00
Last modified: 12 Oct 2024 04:01
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Contributors
Author:
Sultan Itayda Donmez
Author:
Sarah H. Needs
Author:
Helen M.I. Osborn
Author:
Alexander D. Edwards
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