Evidence map›Paper›PMID 41724709›Full record

ArticleMicrobiologyOpen2026

Genomic Epidemiology and Machine Learning-Based Drug Discovery for Antimicrobial Resistant Diarrheagenic Escherichia coli.

Ayesha Masood, Fatima Noor, Abdu Rehman, Mohsin Gulzar Barq, Shazia Iqbal, Muhammad Qasim Ali, Shahzad Ahmad, Syed Zeeshan Haider Naqvi

Abstract read
In one paragraph

Article in MicrobiologyOpen, 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.

Ayesha MasoodInstitute of Molecular Biology and Biotechnology (IMBB), The University of Lahore, Lahore, Pakistan.
Fatima NoorInstitute of Molecular Biology and Biotechnology (IMBB), The University of Lahore, Lahore, Pakistan.
Abdu RehmanCenter of Bioinformatics, College of Life Sciences, Northwest Agriculture and Forestry University, Yangling, Shaanxi, China.ORCID 0000-0003-0570-6224
Mohsin Gulzar BarqDepartment of Microbiology, University of Central Punjab (UCP), Lahore, Pakistan.
Shazia IqbalFaculty of Medicine and Health Sciences, The University of Buckingham, Buckingham, UK.
Muhammad Qasim AliMicrobiology Department of Gulab Devi Educational Complex, Lahore, Pakistan.
Shahzad AhmadFaculty of Medicine and Health Sciences, The University of Buckingham, Buckingham, UK.ORCID 0000-0002-3953-593X
Syed Zeeshan Haider NaqviInstitute of Molecular Biology and Biotechnology (IMBB), The University of Lahore, Lahore, Pakistan.

Funding

The University of Buckingham, Buckingham, United Kingdom
6 · The paper itself

Abstract

Diarrheagenic Escherichia coli (DEC) is a leading cause of pediatric diarrhea, with antimicrobial resistance (AMR) complicating treatment. This study analyzed 350 E. coli isolates (175 DEC and 175 non-DEC) to determine molecular pathotypes, resistance patterns, and therapeutic targets. Polymerase chain reaction and 16S ribosomal RNA sequencing identified enteropathogenic E. coli as the most prevalent DEC pathotype (35%), followed by enterotoxigenic E. coli (25%), enterohemorrhagic E. coli (15%), enteroinvasive E. coli (10%), and diffusely adherent E. coli (20%). Phylogenetic analysis confirmed distinct clustering between DEC and non-DEC strains, revealing their evolutionary relationships. Antimicrobial susceptibility testing showed high resistance to ampicillin (87.6%), trimethoprim-sulfamethoxazole (75.5%), and erythromycin (100%), while carbapenems and colistin retained effectiveness. Functional analysis using phylogenetic investigation of communities by reconstruction of unobserved states (PICRUSt) indicated enhanced metabolic and immune-related functions in DEC strains, differentiating them from non-DEC strains. Machine learning and bioinformatics-driven drug discovery identified Alatamide and Isosativan as potential therapeutic compounds, exhibiting strong binding affinities and structural stability against DEC virulence targets through molecular docking and molecular dynamics simulations. This study provides critical insights into the epidemiology, genetic diversity, and resistance patterns of DEC and non-DEC strains. The integration of bioinformatics and machine learning offers a promising strategy for discovering alternative treatments. Continuous AMR surveillance, responsible antibiotic use, and further experimental validation of identified drug candidates are essential to managing E. coli-associated diarrheal infections in pediatric populations and mitigating the global burden of multidrug-resistant pathogens.

Indexed as

Anti-Bacterial AgentsDiarrheaDrug DiscoveryEscherichia coliEscherichia coli InfectionsMachine LearningDrug Resistance, BacterialDrug Resistance, Multiple, BacterialEnteropathogenic Escherichia coliHumansMicrobial Sensitivity TestsMolecular Docking SimulationMolecular EpidemiologyPhylogenyRNA, Ribosomal, 16SAnti-Bacterial AgentsRNA, Ribosomal, 16Sdiarrheagenic Escherichia colimachine learningmolecular dockingmolecular dynamic simulationresistance

Identifiers

PMID41724709
PMCPMC12927950

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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.