RAPID'E. coli 2 agar (Bio-Rad Laboratories, Hercules, CA) is a chromogenic medium for differentiation and enumeration of E. coli and non-E. coli coliform bacteria in food. The principle of RAPID'E. coli 2 medium relies on simultaneous detection of 2 enzymatic activities, P-D-glucuronidase (GLUC) and beta-D-galactosidase (GAL). Coliforms, other than E. coli (GAL+/GLUC-), form blue to green colonies, whereas, specifically, E. coli (GAL+/GLUC+) form violet colonies. Eleven foods (raw ground beef, raw boneless pork, fermented sausage, processed ham, processed turkey, frozen turkey breast, raw ground chicken, cottage cheese, ricotta cheese, raw milk, and dry infant formula) were validated, comparing the performance of RAPID'E. coli 2 agar to the reference method AOAC 966.24. Two sample incubation temperatures were evaluated, 37 and 44 degrees C, testing a mixture of naturally and artificially contaminated foods. If naturally contaminated food was not available, the matrix was artificially inoculated with one E. coli strain and one non-E. coli coliform strain. Method comparison studies demonstrated some statistical differences between the 2 methods, which are expected when a plating method is compared to a most probable number method. Inclusivity and exclusivity rates of the medium were 99 and 94%, respectively. The RAPID'E. coli 2 method was shown to be stable when minor variations were introduced.
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Biosens Bioelectron
January 2025
Sensor Engineering Department, Faculty of Science and Engineering, Maastricht University, P.O. Box 616, 6200 MD, Maastricht, the Netherlands.
Effective bacterial detection is crucial for health diagnostics, particularly for the detection of pathogenic species like Escherichia coli (E. coli), which is responsible for up to 90% of urinary tract infections (UTIs), is especially crucial. Current detection methods are time-consuming, often delaying diagnosis and treatment.
View Article and Find Full Text PDFBiosensors (Basel)
June 2024
Department of Bioengineering, University of Texas at Dallas, Richardson, TX 75080, USA.
Mikrochim Acta
April 2024
State Key Laboratory of Hydrology-Water Resources and Hydraulic Engineering, Hohai University, Nanjing, 210098, China.
The culture-based methods for viable Escherichia coli (E. coli) detection suffer from long detection time and laborious procedures, whereas the molecule tests and immune recognition technologies lack live/dead E. coli differentiation.
View Article and Find Full Text PDFAnal Chim Acta
January 2024
School of Electrical and Electronic Engineering, Nanyang Technological University, Singapore, 639798, Singapore. Electronic address:
Background: The identification and quantification of viable Escherichia coli (E. coli) are important in multiple fields including the development of antimicrobial materials, water quality, food safety and infections diagnosis. However, the standard culture-based methods of viable E.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2023
Anhui Institute of Ecological Civilization, Anhui Jianzhu University, Hefei 230601, Anhui, P. R. China.
Because of the limitations of traditional chlorine-based bactericidal water treatment, such as the formation of disinfection byproducts (DBPs) and resistance to chlorine, novel approaches and materials are required for effective disinfection of water. This study focuses on the development of a new sterilization material, Ag/NH-MIL-125(Ti), which was designed to effectively inactivate in water. The effectiveness of the as-designed material stems from the synergistic interactions between Ag nanoparticles (NPs) and photoactive metal-organic frameworks (MOFs).
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