Determination of foodborne pathogens in minced beef by real-time PCR without culture enrichment.

J Microbiol Methods

Department of Molecular Biology and Genetics, Faculty of Science, Ataturk University, Erzurum, Turkey. Electronic address:

Published: April 2024

AI Article Synopsis

  • Meat provides an ideal environment for foodborne pathogens like Listeria monocytogenes, Salmonella enterica, and Escherichia coli O157:H7, which can lead to serious health issues.
  • A study surveyed 100 minced beef samples from different butchers in Erzurum province and used Real-Time PCR for pathogen detection, finding Listeria in 45 samples, E. coli in 30, and Salmonella in 29.
  • The Real-Time PCR method showed higher efficiency and reliability compared to traditional techniques, allowing for quicker, more cost-effective, and less labor-intensive detection of these harmful bacteria.

Article Abstract

Meat provides the necessary environment for the growth of foodborne pathogens due to its features such as being rich in protein and having sufficient water activity. Listeria monocytogenes, Salmonella enterica, and Escherichia coli O157:H7, which can be transmitted through many foods, including water, and cause serious diseases, are among the significant pathogens. In the current study. Detection of Listeria monocytogenes, Escherichia coli and Salmonella enterica in 100 minced beef samples collected from different butchers and markets situated in the central districts of Erzurum province was performed by Real-Time PCR without pre-enrichment and DNA isolation. Linear regression equations of Ct values of standard pathogenic bacteria were created. Ct values of minced beef samples obtained as a result of Real-Time PCR analysis were substituted in the equations, and the amounts of pathogenic bacteria in the samples were determined. Listeria monocytogenes, Escherichia coli, and Salmonella enterica were detected in 45, 30, and 29 of 100 minced beef samples, respectively. It is known that the Real-Time PCR method, which is used to detect pathogenic bacteria, is more specific, fast, and reliable than conventional methods. According to the results obtained, it has been clearly observed that with our new approach, pathogenic bacteria growing on foods can be detected sensitively with less cost, shorter amount of time, and minimized workload without pre-enrichment and DNA isolation.

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Source
http://dx.doi.org/10.1016/j.mimet.2024.106896DOI Listing

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