Isolation and PCR validation of Bacillus cereus and Listeria monocytogenes bacteria for the development of prototype kit detection of foodborne pathogens diseases

作     者：Muktiningsih Nurjayadi Irvan Maulana Nabila Alya Pramudiyasih Ratna Nur Kusumawati Maharaniaska Azzahra Niken Kurnia Liman Muhammad Arkent Sangkara Esnawan Wibisono Fera Kurniadewi Vira Saamia Dwi Anna Oktaviani Saputro I. Made Wiranatha Hesham Ali El-Enshasy 

作者机构：Department of Chemistry Faculty of Mathematics and Natural Science Universitas Negeri Jakarta Gedung KH. Hasjim Asj’ari 6th Floor Jl. Rawamangun Muka Jakarta Timur 13220 Indonesia Center Forensic Laboratory of the Criminal Investigation Police of the Republic of Indonesia Cipambuan Babakan Madang Bogor West Java 16810 Indonesia Institute of Bioproduct Development (IBD) Universiti Teknologi Malaysia (UTM) Skudai Johor Bahru Johor Malaysia School of Chemical and Energy Engineering Universiti Teknologi Malaysia (UTM) Skudai Johor Bahru Johor Malaysia City of Scientific Research and Technology Applications New Burg Al Arab Alexandria Egypt 

出 版 物：《AIP Conference Proceedings》 

年 卷 期：2023年第2614卷第1期

学科分类：07[理学] 0702[理学-物理学] 

摘      要：The case of foodborne disease by pathogenic bacteria is an extraordinary event whose source and route of spread occur quickly. Bacillus cereus and Listeria monocytogenes are included in the gram-positive bacteria that cause food poisoning infections in humans. In previous studies, the conditions and reaction formulas for the prototype rapid kit detections of foodborne pathogens were obtained using the Real-Time PCR method. This research validates the conditions and reaction formulas in the prior stage to obtain a consistent and reproducible prototype product. Validation of the isolation stage of Bacillus cereus and Listeria monocytogenes bacteria was carried out by culturing bacterial cultures at aeration conditions of 250 rpm and a temperature of 37oC. A total of three mL of the culture was centrifuged at 5000 rpm and yielded 0.03 and 0.02 grams of B. cereus and L. monocytogenes cells, respectively. The results of the isolation of genomic DNA with Qiaprep were 200 µL with the amount of DNA 10600-11700 nanograms; the concentration was 23-58.5 ng/μL, and the purity was 1.809-2.084. Furthermore, the resulting it is used as a template for the PCR process. The validation of the PCR stage of B. cereus and L. monocytogenes at a temperature of 60oC and template concentration of 50-60 ng resulted in an amplicon of both bacteria. The cyt-k gene B. cereus and hly L. monocytogenes are measuring respectively 114 bp and 158 bp. Based on the data obtained, it can be concluded that the validation of the isolation and PCR stages has been successfully carried out by producing data consistent with previous studies. The development of a detection kit prototype is then revealed to the Real-Time PCR stage and laboratory-scale trials for artificially contaminated food samples and food samples from products on the market.