Evidence map›Paper›PMID 40173243›Full record

ArticleScience advances2025

A predatory gene drive for targeted control of self-transmissible plasmids.

Ryan Tsoi, Hye-In Son, Grayson S Hamrick, Katherine Tang, Jonathan H Bethke, Jia Lu, Rohan Maddamsetti, Lingchong You

Abstract read
In one paragraph

Article in Science advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

8 authors.

Ryan TsoiDepartment of Biomedical Engineering, Duke University, Durham, NC 27708, USA.ORCID 0009-0009-4880-7827
Hye-In SonDepartment of Biomedical Engineering, Duke University, Durham, NC 27708, USA.
Grayson S HamrickDepartment of Biomedical Engineering, Duke University, Durham, NC 27708, USA.ORCID 0000-0002-3149-538X
Katherine TangDepartment of Biomedical Engineering, Duke University, Durham, NC 27708, USA.ORCID 0009-0000-0946-6622
Jonathan H BethkeDepartment of Molecular Genetics and Microbiology, Duke University School of Medicine, Durham, NC 27708, USA.ORCID 0000-0002-9900-2369
Jia LuDepartment of Biomedical Engineering, Duke University, Durham, NC 27708, USA.ORCID 0000-0001-7363-5398
Rohan MaddamsettiDepartment of Biomedical Engineering, Duke University, Durham, NC 27708, USA.ORCID 0000-0003-3370-092X
Lingchong YouDepartment of Biomedical Engineering, Duke University, Durham, NC 27708, USA.ORCID 0000-0003-3725-4007

Funding

Tradeoffs between fitness costs and transfer rates in horizontal gene transferR01AI125604 · NIAID · DUKE UNIVERSITY · PI LINGCHONG YOU · 2017 to 2026
$3.3M
Targeted control of self-transmissible plasmids by using engineered interfering plasmidsR01EB031869 · NIBIB · DUKE UNIVERSITY · PI YOU, LINGCHONG · 2021 to 2024
$1.5M
NIAID NIH HHS R01 AI125604NIBIB NIH HHS R01 EB031869
6 · The paper itself

Abstract

Suppressing plasmid transfer in microbial communities has profound implications due to the role of horizontal gene transfer (HGT) in spreading and maintaining diverse functional traits such as metabolic functions, virulence factors, and antibiotic resistance. However, existing tools for inhibiting HGT are limited in their modes of delivery, efficacy, and scalability. Here, we present a versatile denial-of-spread (DoS) strategy to target and eliminate specific conjugative plasmids. Our strategy exploits retrotransfer, whereby an engineered DoS plasmid is introduced into host cells containing a target plasmid. Acting as a predatory gene drive, DoS propagates itself at the expense of the target plasmid, through competition or active elimination. Once the target plasmid is eradicated, DoS is removed via induced plasmid suicide, resulting in a community containing neither plasmid. The strategy is tunable and scalable for various conjugative plasmids, different mechanisms of plasmid inheritance interruption, and diverse environmental contexts. DoS represents a new tool for precise control of gene persistence in microbial communities.

Indexed as

Gene Drive TechnologyGene Transfer, HorizontalPlasmidsConjugation, Genetic

Identifiers

PMID40173243
PMCPMC11963995

What OpenQuestion holds

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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.