Validation of isolation and polymerase chain reaction of Salmonella species and Escherichia coli bacteria for developing a prototype kit for detecting foodborne pathogens diseases

• Main Authors: Muktiningsih Nurjayadi, Muktiningsih Nurjayadi, Irvan Maulana, Irvan Maulana, Nabila Alya Pramudiyasih, Nabila Alya Pramudiyasih, Ratna Nur Kusumawati, Ratna Nur Kusumawati, Maharaniaska Azzahra, Maharaniaska Azzahra, Niken Kurnia Liman, Niken Kurnia Liman, Muhammad Arkent Sangkara, Muhammad Arkent Sangkara, Esnawan Wibisono, Esnawan Wibisono, Fera Kurniadewi, Fera Kurniadewi, Vira Saamia, Vira Saamia, Dwi Anna Oktaviani Saputro, Dwi Anna Oktaviani Saputro, I. Made Wiranatha, I. Made Wiranatha, El-Enshasy, Hesham Ali
• Format: Conference or Workshop Item
• Published: 2023
• Subjects: TP Chemical technology
• Online Access: http://eprints.utm.my/108178/; http://dx.doi.org/10.1063/5.0126314
• Institution: Universiti Teknologi Malaysia

Gram-negative bacteria that cause food poisoning became an important focus of attention in both developed and developing countries. These bacteria include Salmonella spp and Escherichia coli. In the previous stage, the conditions and reaction formula for the prototype rapid kit detections of foodborne pathogens were obtained using the Real Time PCR method. This research is a stage of validating the conditions and reaction formulas found in the previous stage, to obtain a consistent and reproducible prototype product. Validation of the isolation stage of Salmonella spp (Salmonella typhi, Salmonella typhimurium, Salmonella enteritidis) and Escherichia coli bacteria were carried out by cultivating cultures at 250 rpm aeration conditions, and temperature 37oC. A total of three mL of cultures was centrifuged at 5000 rpm and yielded each cell weight of 0.25-0.6 grams. The results of the isolation of genomic DNA with Qiaprep were 200 microliters with the amount of DNA 10600-11700 nanograms. The concentrations were 23-58.5 ng/mL, and the purities were 1.809-2.084. Furthermore, the resulting genomic DNA is used as a template for the PCR process. The validation of the PCR stage of Salmonella spp using annealing temperature of 60oC and template concentration of 50 ng resulted in the Salmonella typhi fim-C gene amplicons, Salmonella typhimurium pef gene and Salmonella enteritidis prot6E gene measuring 95 bp, 139 bp and 170 bp, respectively. PCR validation of the E. coli DNA template at 60oC with the same concentration resulted in an amplicon measuring 121 bp. Based on the data obtained, it can be concluded that the validation of the isolation stage and confirmed PCR produced data that were consistent with previous studies and were reproducible. With the result that the development of a detection kit prototype can be continued to the validation stage with Real Time PCR and laboratory-scale trials for artificially contaminated food samples and food samples from products on the market.