Evidence map›Paper›PMID 42164444›Full record

ArticleChemical science2026

Artificial intelligence-assisted phenotyping of drug-resistant bacteria using a monosaccharide-based fluorescent sensor array.

Zhuo-Fan Zhang, Wen-Zhen Gui, Yi-Fan Tang, Hui-Qi Gan, Xi-Le Hu, Tony D James, Shengbing Yang, Qian Liu, Xiao-Peng He

Abstract read
In one paragraph

Article in Chemical science, 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

9 authors.

Zhuo-Fan ZhangKey Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Centre, School of Chemistry and Molecular Engineering. East China University of Science & Technology Shanghai 200237 China xlhu@ecust.edu.cn xphe@ecust.edu.cn.
Wen-Zhen GuiKey Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Centre, School of Chemistry and Molecular Engineering. East China University of Science & Technology Shanghai 200237 China xlhu@ecust.edu.cn xphe@ecust.edu.cn.
Yi-Fan TangAcademy of Pharmacy Xi'an-Jiaotong Liverpool University Suzhou 215123 China.
Hui-Qi GanKey Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Centre, School of Chemistry and Molecular Engineering. East China University of Science & Technology Shanghai 200237 China xlhu@ecust.edu.cn xphe@ecust.edu.cn.
Xi-Le HuKey Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Centre, School of Chemistry and Molecular Engineering. East China University of Science & Technology Shanghai 200237 China xlhu@ecust.edu.cn xphe@ecust.edu.cn.
Tony D JamesDepartment of Chemistry, University of Bath Bath BA2 7AY UK t.d.james@bath.ac.uk.ORCID https://orcid.org/0000-0002-4095-2191
Shengbing YangShanghai Key Laboratory of Orthopedic Implants, Department of Orthopedic Surgery, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine Shanghai 200011 China shengbingyang@shusmu.edu.cn.
Qian LiuDepartment of Laboratory Medicine, Ren Ji Hospital 160 Pujian Road Shanghai 200127 China liuqian_rj@shsmu.edu.cn.
Xiao-Peng HeKey Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Centre, School of Chemistry and Molecular Engineering. East China University of Science & Technology Shanghai 200237 China xlhu@ecust.edu.cn xphe@ecust.edu.cn.ORCID https://orcid.org/0000-0002-8736-3511

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemical tools capable of effectively phenotyping drug-resistant bacteria can help improve therapeutic efficacy toward bacterial infections. While conventional techniques rely on labor-intensive procedures for the determination of bacterial susceptibility to antibiotics, here we developed a sensor array based on fluorogen-labelled monosaccharides to accurately phenotype drug-resistant bacteria with the assistance of artificial intelligence (AI). d-Glucose, d-galactose, l-fucose and d-mannose, which are common monomeric building blocks of natural glycans, were labelled with a "conformationally-adaptive" fluorophore (DPAC) with two different linkers, giving rise to a sensor array that consists of eight fluorescent glycoprobes. Using homogeneous high-throughput screening, we found that all the glycoprobes exhibited sensitive ratiometric fluorescence changes in the presence of

Identifiers

PMID42164444
PMCPMC13186398

What Socratic holds

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LicenceCC BY
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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.