Using bacterial population dynamics to count phages and their lysogens.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
06 Sep 2024
Historique:
received: 17 10 2023
accepted: 20 08 2024
medline: 7 9 2024
pubmed: 7 9 2024
entrez: 6 9 2024
Statut: epublish

Résumé

Traditional assays for counting bacteriophages and their lysogens are labor-intensive and perturbative to the host cells. Here, we present a high-throughput infection method in a microplate reader, where the growth dynamics of the infected culture is measured using the optical density (OD). We find that the OD at which the culture lyses scales linearly with the logarithm of the initial phage concentration, providing a way of measuring phage numbers over nine orders of magnitude and down to single-phage sensitivity. Interpreting the measured dynamics using a mathematical model allows us to infer the phage growth rate, which is a function of the phage-cell encounter rate, latent period, and burst size. Adding antibiotic selection provides the ability to measure the rate of host lysogenization. Using this method, we found that when E. coli growth slows down, the lytic growth rate of lambda phages decreases, and the propensity for lysogeny increases, demonstrating how host physiology influences the viral developmental program.

Identifiants

pubmed: 39242585
doi: 10.1038/s41467-024-51913-6
pii: 10.1038/s41467-024-51913-6
doi:

Substances chimiques

Anti-Bacterial Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

7814

Subventions

Organisme : NIGMS NIH HHS
ID : R35 GM140709
Pays : United States
Organisme : Alfred P. Sloan Foundation
ID : G-2023-19649
Organisme : National Science Foundation (NSF)
ID : 2243257

Informations de copyright

© 2024. The Author(s).

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Auteurs

Yuncong Geng (Y)

Department of Physics, University of Illinois Urbana-Champaign, Urbana, IL, 61801, USA.
Center for Biophysics and Quantitative Biology, University of Illinois Urbana-Champaign, Urbana, IL, 61801, USA.

Thu Vu Phuc Nguyen (TVP)

Department of Physics, University of Illinois Urbana-Champaign, Urbana, IL, 61801, USA.
Verna and Marrs McLean Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, TX, 77030, USA.
Department of Molecular Biology, Princeton University, Princeton, NJ, 08544, USA.

Ehsan Homaee (E)

Department of Physics, University of Illinois Urbana-Champaign, Urbana, IL, 61801, USA.
Center for Biophysics and Quantitative Biology, University of Illinois Urbana-Champaign, Urbana, IL, 61801, USA.

Ido Golding (I)

Department of Physics, University of Illinois Urbana-Champaign, Urbana, IL, 61801, USA. igolding@illinois.edu.
Center for Biophysics and Quantitative Biology, University of Illinois Urbana-Champaign, Urbana, IL, 61801, USA. igolding@illinois.edu.
Verna and Marrs McLean Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, TX, 77030, USA. igolding@illinois.edu.
Department of Microbiology, University of Illinois Urbana-Champaign, Urbana, IL, 61801, USA. igolding@illinois.edu.

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