ISSN: 0973-7510

E-ISSN: 2581-690X

Research Article | Open Access
Aarya Harshal Suryawanshi, Sai Sree Thanay Allam, Satwik Korukonda, Satyashila Kamble, Bhavithavya Kumar Machavarapu, Nagavenkat Sriperambuduru and Praveen Kumar Vemuri
Department of Biotechnology, Koneru Lakshmaiah Education Foundation, Green Fields, Vaddeswaram, Andhra Pradesh, India.
Article Number: 9400 | © The Author(s). 2024
J Pure Appl Microbiol. 2024;18(3):1627-1631. https://doi.org/10.22207/JPAM.18.3.12
Received: 22 March 2024 | Accepted: 25 June 2024 | Published online: 22 July 2024
Issue online: September 2024
Abstract

Food is the primary cause for diseases in humans and carries high risk pathogens. Assessment of the safety in foods is needed to validate the presence of pathogenic bacteria. We used colony PCR for this approach to detect foodborne pathogens such as Escherichia coli, Lactobacillus and Bacillus cereus. Suitable primers were selected based on specific gene 1040 for Escherichia coli, gene S2 for Lactobacillus, and gene NVF for Bacillus cereus. Agarose gel electrophoresis is used for the detection of amplified products against a suitable marker. ImageJ is used for DNA band analysis, enabling precise quantification, normalization, and statistical comparisons. These studies have established a promising role in the detection of pathogens in various environmental samples. The insights gained from this study may serve as the foundation for rapid detection of foodborne diseases in the food industry.

Keywords

Colony PCR, Primers, Escherichia coli, Lactobacillus, Bacillus cereus

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© The Author(s) 2024. Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License which permits unrestricted use, sharing, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.