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Updated: May 22, 2026

Visualization of Bacterial Resistance using Fluorescent Antibiotic Probes
Published on: March 2, 2020
Artificial intelligence-assisted phenotyping of drug-resistant bacteria using a monosaccharide-based fluorescent
Zhuo-Fan Zhang1, Wen-Zhen Gui1, Yi-Fan Tang2
1Key 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.
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 Pseudomonas aeruginosa (P. aeruginosa) expressing bacterial lectins (LecA and LecB) selective for d-galactose, l-fucose and d-mannose. However, minimal fluorescence changes were seen when the glycoprobes were incubated with other bacterial strains lacking lectin expression. The use of ensemble learning to process the acquired sensing signals further enabled the accurate discrimination of clinically isolated, drug-resistant P. aeruginosa from drug-sensitive strains. Interestingly, using AI-assisted array sensing, we also achieved the phenotyping of P. aeruginosa after long-term exposure to mechanistically different antibiotics, thus highlighting the effectiveness of this approach for precision medicine.
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