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Updated: Aug 13, 2026

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'Bioluminescent' Reporter Phage for the Detection of Category A Bacterial Pathogens
Published on: July 8, 2011
An In Situ Dual-Mode Bacterial Detection Technique Allowing Both Direct Visual Colorimetric Screening and ATP
Cong Cao1, Rong Feng1, Zhenzhong Yu1
1School of Material Science and Chemical Engineering, Ningbo University, Ningbo315211, China.
Analytical Chemistry
|August 11, 2026
Summary
A novel dual-mode platform rapidly detects foodborne bacteria using phage-immobilized hydrogels. Visual color changes and bioluminescence confirm pathogen presence, ensuring food safety with on-site analysis.
Area of Science:
- Microbiology
- Materials Science
- Analytical Chemistry
Background:
- Foodborne pathogenic bacteria pose significant risks to public health and food safety due to their rapid reproduction.
- Accurate and rapid detection methods for these pathogens are essential for effective control and prevention.
Purpose of the Study:
- To develop a dual-mode in situ detection platform for rapid and accurate bacterial analysis.
- To enable on-site detection without large-scale instrumentation.
Main Methods:
- A phage-immobilized hydrogel stir bar captures target bacteria, causing a pH-induced color change (colorimetric detection).
- Embedded ZnO/ZIF generates reactive oxygen species (ROS) under light, killing bacteria and releasing ATP.
- ATP triggers a bioluminescence reaction quantified by a hand-held sensor, providing a second detection mode.
Main Results:
- The dual-mode platform achieved rapid on-site detection of live bacteria within 35 minutes.
- Detection range: 10³ to 10⁹ CFU·mL⁻¹, with a colorimetric LOD of 10³ CFU·mL⁻¹.
- Bioluminescence mode achieved a limit of quantification (LOQ) of 30 CFU·mL⁻¹, with mutual verification enhancing accuracy and sensitivity.
Conclusions:
- The developed platform offers a sensitive, accurate, and rapid dual-mode detection method for foodborne pathogens.
- Its portable nature facilitates on-site screening and analysis, improving food safety measures.

