Drinking water contamination, often caused by bacteria, leads to substantial numbers of diarrhea deaths each year, especially in developing regions. Human urine as a source of fertilizer, when handled improperly, can contaminate drinking water. One dominant bacterial pathogen in urine is Escherichia coli , which can trigger serious waterborne/foodborne diseases. Considering the prevalence of the multi-drug resistant extended-spectrum beta-lactamase (ESBL) producing E. coli , a rapid detection method for resistance is highly desired. In this work, we developed a method for quick identification of E. coli and, at the same time, capable of removal of general bacterial pathogens from human urine. A specific peptide GRHIFWRRGGGHKVAPR, reported to have a strong affinity to E. coli , was utilized to modify the PEGylated magnetic nanoclusters, resulting in a specific capture and enrichment of E. coli from the bacteria-spiked artificial urine. Subsequently, a novel luminescent probe was applied to rapidly identify the antimicrobial resistance of the collected E. coli within 30 min. These functionalized magnetic nanoclusters demonstrate a promising prospect to rapidly detect ESBL E. coli in urine and contribute to reducing drinking water contamination.
Keyphrases
- drinking water
- escherichia coli
- antimicrobial resistance
- drug resistant
- health risk
- loop mediated isothermal amplification
- sensitive detection
- health risk assessment
- klebsiella pneumoniae
- label free
- endothelial cells
- molecularly imprinted
- biofilm formation
- quantum dots
- multidrug resistant
- acinetobacter baumannii
- fluorescent probe
- energy transfer
- mass spectrometry
- gram negative
- high resolution
- clostridium difficile
- recombinant human
- bioinformatics analysis