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Label-free 1D microfluidic dipstick counting of microbial colonies and bacteriophage plaques

Label-free 1D microfluidic dipstick counting of microbial colonies and bacteriophage plaques
Label-free 1D microfluidic dipstick counting of microbial colonies and bacteriophage plaques
Counting viable bacterial cells and functional bacteriophage is fundamental to microbiology underpinning research, surveillance, biopharmaceuticals and diagnostics. Colony forming unit (CFU) and plaque forming unit (PFU) counting still requires slow and laborious solid culture on agar in Petri dishes or plates. Here, we show that dip-stick microfluidic strips can be used without growth indicator dye for rapid and simple CFU ml−1 and PFU ml−1 measurement. We demonstrate for the first time that fluoropolymer microcapillaries combined with digital imaging allow bacteriophage plaques to be counted rapidly in a dip-and-test format. The microfluidic length scales offer a linear 1-dimensional alternative to a 2D solid agar medium surface, with colonies or plaques clearly visible as “dashes” or “gaps”. An inexpensive open source darkfield biosensor system using Raspberry Pi imaging permits label-free detection and counting of colonies or plaques within 4–8 hours in a linear, liquid matrix within ∼200 μm inner diameter microcapillaries. We obtained full quantitative agreement between 1D microfluidic colony counting in dipsticks versus conventional 2D solid agar Petri dish plates for S. aureus and E. coli, and for T2 phage and phage K, but up to 6 times faster. Time-lapse darkfield imaging permitted detailed kinetic analysis of colony growth in the microcapillaries, providing new insight into microfluidic microbiology and colony growth, not possible with Petri dishes. Surprisingly, whilst E. coli colonies appeared earlier, subsequent colony expansion was faster along the microcapillaries for S. aureus. This may be explained by the microenvironment offered for 1D colony growth within microcapillaries, linked to a mass balance between nutrient (glucose) diffusion and bacterial growth kinetics. Counting individual colonies in liquid medium was not possible for motile strains that spread rapidly along the capillary, however inclusion of soft agar inhibited spreading, making this new simple dip-and-test counting method applicable to both motile and non-motile bacteria. Label-free dipstick colony and plaque counting has potential for many analytical microbial tasks, and the innovation of 1D colony counting has relevance to other microfluidic microbiology.
1473-0197
2820-2831
Dönmez, Sultan İlayda
640c098c-267c-4af0-8925-70ba1cab5321
Needs, Sarah H.
24425556-99e3-4c46-995b-2381776a0a38
Osborn, Helen M.I.
06b84ced-f441-44b3-a72d-ea0e01a43da6
Reis, Nuno M.
898670e7-a794-4302-81ce-03a4d86cc17a
Edwards, Alexander D.
bc3d9b93-a533-4144-937b-c673d0a28879
Dönmez, Sultan İlayda
640c098c-267c-4af0-8925-70ba1cab5321
Needs, Sarah H.
24425556-99e3-4c46-995b-2381776a0a38
Osborn, Helen M.I.
06b84ced-f441-44b3-a72d-ea0e01a43da6
Reis, Nuno M.
898670e7-a794-4302-81ce-03a4d86cc17a
Edwards, Alexander D.
bc3d9b93-a533-4144-937b-c673d0a28879

Dönmez, Sultan İlayda, Needs, Sarah H., Osborn, Helen M.I., Reis, Nuno M. and Edwards, Alexander D. (2022) Label-free 1D microfluidic dipstick counting of microbial colonies and bacteriophage plaques. Lab on a Chip, 22, 2820-2831. (doi:10.1039/D2LC00280A).

Record type: Article

Abstract

Counting viable bacterial cells and functional bacteriophage is fundamental to microbiology underpinning research, surveillance, biopharmaceuticals and diagnostics. Colony forming unit (CFU) and plaque forming unit (PFU) counting still requires slow and laborious solid culture on agar in Petri dishes or plates. Here, we show that dip-stick microfluidic strips can be used without growth indicator dye for rapid and simple CFU ml−1 and PFU ml−1 measurement. We demonstrate for the first time that fluoropolymer microcapillaries combined with digital imaging allow bacteriophage plaques to be counted rapidly in a dip-and-test format. The microfluidic length scales offer a linear 1-dimensional alternative to a 2D solid agar medium surface, with colonies or plaques clearly visible as “dashes” or “gaps”. An inexpensive open source darkfield biosensor system using Raspberry Pi imaging permits label-free detection and counting of colonies or plaques within 4–8 hours in a linear, liquid matrix within ∼200 μm inner diameter microcapillaries. We obtained full quantitative agreement between 1D microfluidic colony counting in dipsticks versus conventional 2D solid agar Petri dish plates for S. aureus and E. coli, and for T2 phage and phage K, but up to 6 times faster. Time-lapse darkfield imaging permitted detailed kinetic analysis of colony growth in the microcapillaries, providing new insight into microfluidic microbiology and colony growth, not possible with Petri dishes. Surprisingly, whilst E. coli colonies appeared earlier, subsequent colony expansion was faster along the microcapillaries for S. aureus. This may be explained by the microenvironment offered for 1D colony growth within microcapillaries, linked to a mass balance between nutrient (glucose) diffusion and bacterial growth kinetics. Counting individual colonies in liquid medium was not possible for motile strains that spread rapidly along the capillary, however inclusion of soft agar inhibited spreading, making this new simple dip-and-test counting method applicable to both motile and non-motile bacteria. Label-free dipstick colony and plaque counting has potential for many analytical microbial tasks, and the innovation of 1D colony counting has relevance to other microfluidic microbiology.

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Accepted/In Press date: 1 July 2022
e-pub ahead of print date: 6 July 2022
Published date: 15 November 2022

Identifiers

Local EPrints ID: 495099
URI: http://eprints.soton.ac.uk/id/eprint/495099
ISSN: 1473-0197
PURE UUID: d615f607-c461-4ed4-aaaf-80955508c067
ORCID for Alexander D. Edwards: ORCID iD orcid.org/0000-0003-2369-989X

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Date deposited: 29 Oct 2024 17:41
Last modified: 30 Oct 2024 03:06

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Contributors

Author: Sultan İlayda Dönmez
Author: Sarah H. Needs
Author: Helen M.I. Osborn
Author: Nuno M. Reis
Author: Alexander D. Edwards ORCID iD

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