Metabolic Labeling and Digital Microfluidic Single‐Cell Sequencing for Single Bacterial Genotypic‐Phenotypic Analysis

Author:

Guo Junnan1,Sun Di2,Li Kunjie1,Dai Qi1,Geng Shichen1,Yang Yuanyuan1,Mo Mengwu1,Zhu Zhi1,Shao Chen1,Wang Wei2,Song Jia3,Yang Chaoyong12ORCID,Zhang Huimin1ORCID

Affiliation:

1. Department of Chemical Biology College of Chemistry and Chemical Engineering School of Life Sciences Innovation Laboratory for Sciences and Technologies of Energy Materials of Fujian Province (IKKEM) Xiamen University Xiamen 361005 China

2. Institute of Molecular Medicine Renji Hospital School of Medicine Shanghai Jiao Tong University Shanghai 200127 China

3. Institute for Developmental and Regenerative Cardiovascular Medicine Xinhua Hospital Shanghai Jiao Tong University School of Medicine Shanghai 200092 China

Abstract

AbstractAccurate assessment of phenotypic and genotypic characteristics of bacteria can facilitate comprehensive cataloguing of all the resistance factors for better understanding of antibiotic resistance. However, current methods primarily focus on individual phenotypic or genotypic profiles across different colonies. Here, a Digital microfluidic‐based automated assay for whole‐genome sequencing of single‐antibiotic‐resistant bacteria is reported, enabling Genotypic and Phenotypic Analysis of antibiotic‐resistant strains (Digital‐GPA). Digital‐GPA can efficiently isolate and sequence antibiotic‐resistant bacteria illuminated by fluorescent D‐amino acid (FDAA)‐labeling, producing high‐quality single‐cell amplified genomes (SAGs). This enables identifications of both minor and major mutations, pinpointing substrains with distinctive resistance mechanisms. Digital‐GPA can directly process clinical samples to detect and sequence resistant pathogens without bacterial culture, subsequently provide genetic profiles of antibiotic susceptibility, promising to expedite the analysis of hard‐to‐culture or slow‐growing bacteria. Overall, Digital‐GPA opens a new avenue for antibiotic resistance analysis by providing accurate and comprehensive molecular profiles of antibiotic resistance at single‐cell resolution.

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Natural Science Foundation of Fujian Province

National Key Research and Development Program of China

Publisher

Wiley

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