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Customizable PCR-microplate array for differential identification of multiple pathogens
Abdela Woubit1, Teshome Yehualaeshet, Sherrelle Roberts
1Department of Pathobiology, College of Veterinary Medicine, Nursing and Allied Health, Tuskegee University, Tuskegee, Alabama 36088, USA. wabdela@mytu.tuskegee.edu.
Abstract:
Customizable PCR-microplate arrays were developed for the rapid identification of Salmonella Typhimurium, Salmonella Saintpaul, Salmonella Typhi, Shigella dysenteriae, Escherichia coli O157:H7, Francisella tularensis subsp. tularensis, Francisella tularensis subsp. novicida, Vibrio cholerae, Vibrio parahaemolyticus, Yersinia pestis, and Yersinia pseudotuberculosis. Previously, we identified highly specific primers targeting each of these pathogens. Here, we report the development of customizable PCR-microplate arrays for simultaneous identification of the pathogens using the primers identified. A mixed aliquot of genomic DNA from 38 strains was used to validate three PCR-microplate array formats. Identical PCR conditions were used to run all the samples on the three formats. Specific amplifications were obtained on all three custom plates. In preliminary tests performed to evaluate the sensitivity of these assays in samples inoculated in the laboratory with Salmonella Typhimurium, amplifications were obtained from 1 g of beef hot dog inoculated at as low as 9 CFU/ml or from milk inoculated at as low as 78 CFU/ml. Such microplate arrays could be valuable tools for initial identification or secondary confirmation of contamination by these pathogens.
Insights
New customizable PCR-microplate arrays enable rapid, simultaneous identification of dangerous foodborne pathogens like Salmonella and E. coli. These validated assays offer high sensitivity for contamination detection in food products.
Area of Science:
- Microbiology
- Molecular Biology
- Food Safety
Background:
- Accurate and rapid identification of foodborne pathogens is crucial for public health.
- Existing methods can be time-consuming or lack multiplexing capabilities.
Purpose of the Study:
- To develop and validate customizable PCR-microplate arrays for simultaneous detection of multiple bacterial pathogens.
- To assess the sensitivity of these arrays in food matrices.
Main Methods:
- Design of specific primers for target pathogens.
- Development of customizable PCR-microplate arrays.
- Validation using genomic DNA from 38 strains and spiked food samples (beef hot dogs, milk).
Main Results:
- Successful development of three PCR-microplate array formats.
- Specific amplifications achieved for all target pathogens across all formats.
- High sensitivity demonstrated, detecting Salmonella Typhimurium at 9 CFU/ml in beef hot dogs and 78 CFU/ml in milk.
Conclusions:
- Customizable PCR-microplate arrays are effective tools for simultaneous pathogen identification.
- These arrays can serve as valuable methods for initial or secondary confirmation of contamination.
- The assays show promise for rapid food safety testing and public health surveillance.
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