Evidence map›Paper›PMID 42873737›Full record

ArticlePloS one2026

WISH-barcoding of Salmonella Typhimurium ATCC14028s strains for population dynamics studies in vivo.

Christopher Schubert, Jeongmin Kim, Nicolas Näpflin, Melanie Hoos, Jemina Huuskonen, Christian von Mering, Wolf-Dietrich Hardt

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Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Christopher SchubertInstitute of Microbiology, Department of Biology, ETH Zurich, Zurich, Switzerland.
Jeongmin KimInstitute of Microbiology, Department of Biology, ETH Zurich, Zurich, Switzerland.ORCID https://orcid.org/0009-0004-0680-0540
Nicolas NäpflinDepartment of Molecular Life Science and Swiss Institute of Bioinformatics, University of Zurich, Zurich, Switzerland.ORCID https://orcid.org/0000-0001-6845-7400
Melanie HoosInstitute of Microbiology, Department of Biology, ETH Zurich, Zurich, Switzerland.ORCID https://orcid.org/0009-0008-1268-1305
Jemina HuuskonenInstitute of Microbiology, Department of Biology, ETH Zurich, Zurich, Switzerland.
Christian von MeringDepartment of Molecular Life Science and Swiss Institute of Bioinformatics, University of Zurich, Zurich, Switzerland.ORCID https://orcid.org/0000-0001-7734-9102
Wolf-Dietrich HardtInstitute of Microbiology, Department of Biology, ETH Zurich, Zurich, Switzerland.ORCID https://orcid.org/0000-0002-9892-6420

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBarcoding of isogenic strains is a powerful approach to assess pathogen population dynamics during infection. Here, we adapted WISH-barcoding to Salmonella Typhimurium ATCC14028s to evaluate its suitability for pooled infection experiments in streptomycin-pretreated mouse models.

resultsWISH-barcoded wild-type pools showed pronounced population instability, characterized by reproducible strain loss and segregation into high- and low-fitness subpopulations. Whole-genome sequencing identified recurrent mutations in the methyltransferase gene rsmG and loss of the P3 plasmid carrying streptomycin resistance in low-fitness strains; neither was observed in ΔinvG or ΔssaV pools. We propose that rsmG mutations were enriched during strain construction carried out under streptomycin selection, following loss of the P3 plasmid. Control experiments demonstrated that rsmG mutations and P3 loss are counter-selected in vivo and attenuate gut-luminal colonization in streptomycin-pretreated mice.

conclusionWhile population dynamics experiments with ATCC14028s are feasible in principle, wild-type strains are prone to acquiring fitness-altering mutations during in vitro construction when using the P3 plasmid and streptomycin, highlighting the need for careful pool validation prior to use and for minimizing antibiotic exposure during strain construction when the strain of interest has no natural resistance, to reduce the risk of selecting mutations.

Indexed as

Salmonella typhimuriumAnimalsAnti-Bacterial AgentsBacterial ProteinsDrug Resistance, BacterialMiceMutationPlasmidsPopulation DynamicsStreptomycinAnti-Bacterial AgentsBacterial ProteinsStreptomycin

Identifiers

PMID42873737
PMCPMC13667820

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.