Evidence map›Paper›PMID 40681864›Full record

ArticleNature biomedical engineering2025

Precise virulence inactivation using a CRISPR-associated transposase for combating Enterobacteriaceae gut pathogens.

Carlotta Ronda, Tyler Perdue, Logan Schwanz, Diego Rivera Gelsinger, Leonie Brockmann, Andrew Kaufman, Yiming Huang, Samuel H Sternberg, Harris H Wang

Abstract read
In one paragraph

Article in Nature biomedical engineering, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Research square · 2026
    Article
  5. bioRxiv : the preprint server for biology · 2026
    Article
  6. Article
  7. 2025 in review.Nature biomedical engineering · 2025
    Article
  8. Article
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

9 authors.

Carlotta Ronda *Department of System Biology, Columbia University, New York, NY, USA.
Tyler Perdue *Department of System Biology, Columbia University, New York, NY, USA.
Logan SchwanzDepartment of System Biology, Columbia University, New York, NY, USA.
Diego Rivera GelsingerDepartment of System Biology, Columbia University, New York, NY, USA.
Leonie BrockmannDepartment of System Biology, Columbia University, New York, NY, USA.
Andrew KaufmanDepartment of System Biology, Columbia University, New York, NY, USA.
Yiming HuangDepartment of System Biology, Columbia University, New York, NY, USA.ORCID http://orcid.org/0000-0003-1932-2803
Samuel H SternbergDepartment of Biochemistry and Molecular Biophysics, Columbia University, New York, NY, USA.ORCID http://orcid.org/0000-0001-8240-9114
Harris H WangDepartment of System Biology, Columbia University, New York, NY, USA. harris.wang@columbia.edu.ORCID http://orcid.org/0000-0003-2164-4318

Funding

The Organoid and Cell Culture CoreP30DK132710 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Utpal Pajvani · 2022 to 2026
$7.2M
Micron-scale Spatial Metagenomic Mapping of Microbial Biogeography in the Gastrointestinal TractR01AI132403 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Harris H Wang · 2017 to 2026
$6.0M
Ecological dynamics and metabolic interactions in thegut microbiome across space and timeR01DK118044 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI VITKUP, DENNIS, WANG, HARRIS H · 2018 to 2022
$3.4M
A high-performance and versatile technology for precision microbiome engineeringR01EB031935 · NIBIB · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Samuel Henry Sternberg, Harris H Wang · 2021 to 2026
$3.3M
Leveraging Programmable Integrases for Human Genome EngineeringDP2HG011650 · NHGRI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI STERNBERG, SAMUEL HENRY · 2020 to 2020
$2.4M
Impact of CRISPR-associated transposons on anti-phage immunity in Vibrio choleraeR21AI168976 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI STERNBERG, SAMUEL HENRY · 2022 to 2023
$446k
Discovery of immunomodulatory gut microbes with MAGICR21AI146817 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI IVANOV, IVAYLO IVANOV · 2019 to 2020
$437k
Burroughs Wellcome Fund (BWF) 1016691NHGRI NIH HHS DP2 HG011650NIAID NIH HHS R01 AI132403NIAID NIH HHS R21 AI146817NIAID NIH HHS R21 AI168976NIBIB NIH HHS R01 EB031935NIDDK NIH HHS P30 DK132710NIDDK NIH HHS R01 DK118044Simons Foundation 527896U.S. Department of Defense (United States Department of Defense) S-168-4X5-001U.S. Department of Health & Human Services | National Institutes of Health (NIH) 1R01DK118044U.S. Department of Health & Human Services | National Institutes of Health (NIH) 1R01EB031935U.S. Department of Health & Human Services | National Institutes of Health (NIH) 1R21AI146817U.S. Department of Health & Human Services | National Institutes of Health (NIH) 2R01AI132403U.S. Department of Health & Human Services | National Institutes of Health (NIH) DP2HG011650U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01EB031935U.S. Department of Health & Human Services | National Institutes of Health (NIH) R21AI68976
6 · The paper itself

Abstract

Targeted gene manipulation in a complex microbial community is an enabling technology for precise microbiome editing. Here we introduce BACTRINS, an in situ microbiome engineering platform designed for efficient and precise genomic insertion of a desired payload and simultaneous knockout of target genes. This system leverages conjugation-mediated delivery of CRISPR-associated transposases to achieve RNA-guided genomic integration, allowing precise insertion of a therapeutic payload while neutralizing pathogen virulence without causing cell death. When applied against an Enterobacteriaceae Shiga toxin-producing pathogen in the gut, this system delivers a CRISPR-associated transposase by bacterial conjugation for site-specific inactivation of the Shiga toxin gene and integration of a nanobody therapeutic payload to disrupt pathogen attachment. A single dose of this therapy results in high-efficiency Shiga gene inactivation and improved survival in a murine infection model of Shiga-producing pathogen. This work establishes a new type of live bacterial therapeutic capable of reducing gut infections by transforming toxigenic pathogens into commensal protectors.

Indexed as

Clustered Regularly Interspaced Short Palindromic RepeatsCRISPR-Cas SystemsEnterobacteriaceaeEnterobacteriaceae InfectionsGastrointestinal MicrobiomeTransposasesAnimalsGene EditingHumansMiceShiga ToxinVirulenceShiga ToxinTransposases

Identifiers

PMID40681864
PMCPMC12915489

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.