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Droplet-based methodology for investigating bacterial population dynamics in response to phage exposure

Abstract:
An alarming rise in antimicrobial resistance worldwide has spurred efforts into the search for alternatives to antibiotic treatments. The use of bacteriophages, bacterial viruses harmless to humans, represents a promising approach with potential to treat bacterial infections (phage therapy). Recent advances in microscopy-based single-cell techniques have allowed researchers to develop new quantitative methodologies for assessing the interactions between bacteria and phages, especially the ability of phages to eradicate bacterial pathogen populations and to modulate growth of both commensal and pathogen populations. Here we combine droplet microfluidics with fluorescence time-lapse microscopy to characterize the growth and lysis dynamics of the bacterium Escherichia coli confined in droplets when challenged with phage. We investigated phages that promote lysis of infected E. coli cells, specifically, a phage species with DNA genome, T7 (Escherichia virus T7) and two phage species with RNA genomes, MS2 (Emesvirus zinderi) and Qβ (Qubevirus durum). Our microfluidic trapping device generated and immobilized picoliter-sized droplets, enabling stable imaging of bacterial growth and lysis in a temperature-controlled setup. Temporal information on bacterial population size was recorded for up to 25 h, allowing us to determine growth rates of bacterial populations and helping us uncover the extent and speed of phage infection. In the long-term, the development of novel microfluidic single-cell and population-level approaches will expedite research towards fundamental understanding of the genetic and molecular basis of rapid phage-induced lysis and eco-evolutionary aspects of bacteria-phage dynamics, and ultimately help identify key factors influencing the success of phage therapy
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.3389/fmicb.2023.1260196

Authors

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Role:
Author
ORCID:
0000-0001-9068-6090
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Role:
Author
ORCID:
0009-0002-3756-4865
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-0866-7470
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Role:
Author
ORCID:
0000-0003-0876-3187
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Role:
Author
ORCID:
0000-0003-0604-7224


Publisher:
Frontiers Media
Journal:
Frontiers in Microbiology More from this journal
Volume:
14
Pages:
1260196-1260196
Publication date:
2023-11-21
DOI:
EISSN:
1664-302X
ISSN:
1664-302X


Language:
English
Keywords:
Pubs id:
2432813
Local pid:
pubs:2432813
Source identifiers:
W4388940279
Deposit date:
2026-06-12
ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

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