Evidence map›Paper›PMID 39160293›Full record

ArticleNature microbiology2024

Non-canonical start codons confer context-dependent advantages in carbohydrate utilization for commensal E. coli in the murine gut.

Yassine Cherrak, Miguel Angel Salazar, Nicolas Näpflin, Lukas Malfertheiner, Mathias K-M Herzog, Christopher Schubert, Christian von Mering, Wolf-Dietrich Hardt

Abstract read
In one paragraph

Article in Nature microbiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Yassine Cherrak *Institute of Microbiology, Department of Biology, ETH Zurich, Zurich, Switzerland. ycherrak@biol.ethz.ch.ORCID http://orcid.org/0000-0002-6643-2397
Miguel Angel Salazar *Institute of Microbiology, Department of Biology, ETH Zurich, Zurich, Switzerland.ORCID http://orcid.org/0009-0005-5090-3448
Nicolas NäpflinDepartment of Molecular Life Sciences and Swiss Institute of Bioinformatics, University of Zurich, Zurich, Switzerland.ORCID http://orcid.org/0000-0001-6845-7400
Lukas MalfertheinerDepartment of Molecular Life Sciences and Swiss Institute of Bioinformatics, University of Zurich, Zurich, Switzerland.ORCID http://orcid.org/0000-0002-5697-2007
Mathias K-M HerzogInstitute of Microbiology, Department of Biology, ETH Zurich, Zurich, Switzerland.
Christopher SchubertInstitute of Microbiology, Department of Biology, ETH Zurich, Zurich, Switzerland.ORCID http://orcid.org/0000-0002-7921-1470
Christian von MeringDepartment of Molecular Life Sciences and Swiss Institute of Bioinformatics, University of Zurich, Zurich, Switzerland.
Wolf-Dietrich HardtInstitute of Microbiology, Department of Biology, ETH Zurich, Zurich, Switzerland. hardt@micro.biol.ethz.ch.ORCID http://orcid.org/0000-0002-9892-6420

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Resource competition is a driver of gut microbiota composition. Bacteria can outcompete metabolically similar rivals through the limitation of shared growth-fuelling nutrients. The mechanisms underlying this remain unclear for bacteria with identical sets of metabolic genes. Here we analysed the lactose utilization operon in the murine commensal Escherichia coli 8178. Using in vitro and in vivo approaches, we showed that translation of the lactose utilization repressor gene lacI from its native non-canonical GTG start codon increases the basal expression of the lactose utilization cluster, enhancing adaptation to lactose consumption. Consequently, a strain carrying the wild type lacI GTG start codon outperformed the lacI ATG start codon mutant in the mouse intestine. This advantage was attenuated upon limiting host lactose intake through diet shift or altering the mutant frequency, emphasizing the context-dependent effect of a single nucleotide change on the bacterial fitness of a common member of the gut microbiota. Coupled with a genomic analysis highlighting the selection of non-ATG start codons in sugar utilization regulator genes across the Enterobacteriaceae family, our data exposed an unsuspected function of non-canonical start codons in metabolic competition.

Indexed as

Codon, InitiatorEscherichia coliGastrointestinal MicrobiomeLactoseAnimalsCarbohydrate MetabolismEscherichia coli ProteinsGene Expression Regulation, BacterialLac OperonLac RepressorsMiceMice, Inbred C57BLOperonSymbiosisCodon, InitiatorEscherichia coli ProteinsLac RepressorsLactose

Identifiers

PMID39160293
PMCPMC11445065

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Registered trials

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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.