Evidence map›Paper›PMID 42325637›Full record

ReviewACS bio & med chem Au2026

Advancements in Technologies Targeting Horizontal Gene TransferRoutes to Control Drug Resistance Evolution.

Samuel Chetachukwu Adegoke, Md Adnan Karim, Maurelio Cabo Jr, Ignatius Senyo Yao Yawlui, Dennis LaJeunesse

Abstract readReview
In one paragraph

Review in ACS bio & med chem Au, 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

5 authors.

Samuel Chetachukwu AdegokeDepartment of Nanoscience, Joint School of Nanoscience and Nanoengineering, E Gate City Blvd, Greensboro, North Carolina 27401, United States.ORCID https://orcid.org/0000-0003-2261-2430
Md Adnan KarimDepartment of Nanoscience, Joint School of Nanoscience and Nanoengineering, E Gate City Blvd, Greensboro, North Carolina 27401, United States.
Maurelio Cabo JrDepartment of Nanoscience, Joint School of Nanoscience and Nanoengineering, E Gate City Blvd, Greensboro, North Carolina 27401, United States.ORCID https://orcid.org/0000-0003-2339-7998
Ignatius Senyo Yao YawluiDepartment of Nanoscience, Joint School of Nanoscience and Nanoengineering, E Gate City Blvd, Greensboro, North Carolina 27401, United States.
Dennis LaJeunesseDepartment of Nanoscience, Joint School of Nanoscience and Nanoengineering, E Gate City Blvd, Greensboro, North Carolina 27401, United States.ORCID https://orcid.org/0000-0001-5049-8968

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The global rise of multidrug-resistant (MDR) bacteria poses a major public health crisis, threatening the effectiveness of modern medicine. Traditional antibiotic development struggles to keep pace with bacterial evolution, largely due to the rapid dissemination of antibiotic resistance genes via horizontal gene transfer (HGT). HGT mechanisms both canonical and noncanonical enable bacteria to acquire resistance traits defining species and even special challenges. In this review, we cover the current understanding of HGT in spreading antibiotic resistance and explore possible strategies to control HGT and slow the spread of antimicrobial resistance. Recent advances highlight the potential of synthetic competence inhibitors, advanced oxidation processes (AOPs), CRISPR-Cas technologies, gene drives, and antiplasmids to disrupt horizontal gene flow and mitigate resistance evolution. Despite promising laboratory results, challenges remain in translating these approaches into clinical and environmental applications. Blocking HGT could complement antimicrobial stewardship programs and traditional antibiotic therapies by curbing the emergence of new resistant strains at their genetic roots. By targeting the foundational mechanisms of resistance acquisition, these strategies offer a proactive pathway to extend the efficacy of existing antibiotics and prevent a "postantibiotic" era. Ongoing research into bacterial pathogenesis, genome defense systems, and innovative gene-editing technologies will be critical to developing effective, scalable solutions for managing MDR infections worldwide.

Indexed as

advance oxidation process (AOP)antiplasmids systemscompetence blockersextended-spectrum β-lactamases (ESBLs)gene driveshorizontal gene transfermultidrug resistancenatural transformationresistance evolution

Identifiers

PMID42325637
PMCPMC13281022

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.