Evidence map›Paper›PMID 42754710›Full record

ArticleNature microbiology2026

In vivo CRISPRi screens reveal Escherichia coli functional adaptations in the mouse gut.

Amandine Maire, Monica Ortelli, Emma Tkacz, Christoph Dehio, Benoit Chassaing, Harry Sokol, Nathalie Rolhion, David Bikard

Abstract read
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In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Amandine MaireInstitut Pasteur, Université Paris-Cité, UMR CNRS 3525, Synthetic Biology, Paris, France.
Monica OrtelliBiozentrum, University of Basel, Basel, Switzerland.ORCID http://orcid.org/0009-0009-3256-3987
Emma TkaczCentre de Recherche Saint-Antoine, Assistance Publique-Hôpitaux de Paris, Sorbonne Université, INSERM UMRS-938, Paris, France.
Christoph DehioBiozentrum, University of Basel, Basel, Switzerland.ORCID http://orcid.org/0000-0001-7288-1052
Benoit ChassaingInstitut Pasteur, Université Paris Cité, INSERM U1306, CNRS UMR6047, Microbiome-Host Interactions, Paris, France.ORCID http://orcid.org/0000-0002-4285-769X
Harry SokolCentre de Recherche Saint-Antoine, Assistance Publique-Hôpitaux de Paris, Sorbonne Université, INSERM UMRS-938, Paris, France.
Nathalie RolhionCentre de Recherche Saint-Antoine, Assistance Publique-Hôpitaux de Paris, Sorbonne Université, INSERM UMRS-938, Paris, France. nathalie.rolhion@inserm.fr.ORCID http://orcid.org/0000-0002-2946-4808
David BikardInstitut Pasteur, Université Paris-Cité, UMR CNRS 3525, Synthetic Biology, Paris, France. david.bikard@pasteur.fr.ORCID http://orcid.org/0000-0002-5729-1211

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-10-LABX-62-IBEIDEC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) 101044479Fondation pour la Recherche Médicale (Foundation for Medical Research in France) 51NF40_180541Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (Swiss National Science Foundation) 51NF40_180541
6 · The paper itself

Abstract

Escherichia coli exhibits remarkable genetic diversity that enables it to adapt to the intestinal environment. Here we establish an in vivo CRISPR interference platform that leverages bacterial gene fitness as a high-resolution functional reporter of E. coli adaptations within mice harbouring a defined minimal microbial community (OligoMM12). The screen revealed that diet profoundly shapes the metabolic landscape of E. coli and the essential gene profile identified cross-feeding interactions. Comparison between a laboratory strain (MG1655), a uropathogenic strain (CFT073) and an adherent-invasive E. coli (AIEC LF82) identified distinct genetic requirements for intestinal colonization, highlighting divergent motility, stress response and respiration strategies. In a host inflammatory environment, we found that AIEC LF82 preferably colonized the small intestine with a mobile genetic element, Gally prophage, playing an important role in modulating fitness. These findings provide a high-resolution genetic atlas of E. coli's functional adaptation and demonstrate the utility of functional genomics to probe the gut environment itself.

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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.