Evidence map›Paper›PMID 42627671›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

Artificial Intelligence-Empowered Single-Cell Phenotyping for Rapid, Automated Pathogen Diagnostics.

Sabita Khadka, Bushra Raahat, Spyros Tragoudas, Hui Li

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 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

4 authors.

Sabita KhadkaSchool of Electrical, Computer, and Biomedical Engineering, Southern Illinois University, Carbondale, Illinois, USA.
Bushra RaahatSchool of Electrical, Computer, and Biomedical Engineering, Southern Illinois University, Carbondale, Illinois, USA.
Spyros TragoudasSchool of Electrical, Computer, and Biomedical Engineering, Southern Illinois University, Carbondale, Illinois, USA.
Hui LiSchool of Electrical, Computer, and Biomedical Engineering, Southern Illinois University, Carbondale, Illinois, USA.ORCID https://orcid.org/0000-0001-6725-4468

Funding

SIU System Collaborative Grant AwardSouthern Illinois University
6 · The paper itself

Abstract

Accurate bacterial identification and antimicrobial susceptibility testing (AST) are essential for timely clinical decision-making. Conventional diagnostic methods typically require 24-48 h, leading to inappropriate empirical therapy, accelerating antimicrobial resistance, and worsening patient outcomes. Here, we present an integrated diagnostic platform that combines microfluidic single-cell bacterial detection with artificial intelligence (AI)-driven analysis for rapid phenotypic AST. The microfluidic device enables stable time-lapse detection of individual bacterial cells under designated, controlled antibiotic exposure, with a U-Net-based AI model that automatically segments and quantifies the drug response of individual bacterial cells using phase-contrast microscopy images. The trained model identified 96% of individual Escherichia coli (E. coli) cells and showed no false-positive predictions on bacteria-free images. Applied to AST, the integrated system quantified dose-dependent growth inhibition of E. coli exposed to ciprofloxacin and trimethoprim/sulfamethoxazole, yielding resistance profiles, along with minimum inhibitory concentrations (MICs), within 2 h. These results are consistent with standard broth microdilution, demonstrating the potential of integrating microfluidics and AI for rapid, automated, and single-cell-resolved pathogen diagnosis. Beyond rapid AST, the integrated microfluidic-AI platform was further evaluated for automated identification of targeted infections, including E. coli and Staphylococcus aureus (S. aureus) in the presence of blood matrices.

Indexed as

deep learning analysisinfection diagnosisrapid antimicrobial susceptibility testsingle‐cell detection

Identifiers

PMID42627671
PMCPMC13496276

What OpenQuestion 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 OpenQuestion graph.