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Authors

Muktiningsih Nurjayadi, Department of Chemistry, Faculty of Mathematics and Natural Science, Universitas Negeri Jakarta, Jakarta Timur 13220, IndonesiaFollow
Anisa Fitriyanti, Department of Chemistry, Faculty of Mathematics and Natural Science, Universitas Negeri Jakarta, Jakarta Timur 13220, Indonesia
Royna Rahma Musie, Department of Chemistry, Faculty of Mathematics and Natural Science, Universitas Negeri Jakarta, Jakarta Timur 13220, Indonesia
Gusti Angieta Putri, Department of Chemistry, Faculty of Mathematics and Natural Science, Universitas Negeri Jakarta, Jakarta Timur 13220, Indonesia
Puan Aqila Azizah, Department of Chemistry, Faculty of Mathematics and Natural Science, Universitas Negeri Jakarta, Jakarta Timur 13220, Indonesia
Helzi Angelina, Department of Chemistry, Faculty of Mathematics and Natural Science, Universitas Negeri Jakarta, Jakarta Timur 13220, Indonesia
Grace Grace, Department of Chemistry, Faculty of Mathematics and Natural Science, Universitas Negeri Jakarta, Jakarta Timur 13220, Indonesia
Ananda Indah Putri Sihombing, Department of Chemistry, Faculty of Mathematics and Natural Science, Universitas Negeri Jakarta, Jakarta Timur 13220, Indonesia
Agus Setiawan, Department of Chemistry, Faculty of Mathematics and Natural Science, Universitas Negeri Jakarta, Jakarta Timur 13220, Indonesia
Jefferson Lynford Declan, Department of Chemistry, Faculty of Mathematics and Natural Science, Universitas Negeri Jakarta, Jakarta Timur 13220, Indonesia
Gladys Indira Putri, Department of Chemistry, Faculty of Mathematics and Natural Science, Universitas Negeri Jakarta, Jakarta Timur 13220, Indonesia
Dandy Akbar Juliansyah, Department of Chemistry, Faculty of Mathematics and Natural Science, Universitas Negeri Jakarta, Jakarta Timur 13220, Indonesia
Siti Fatimah, Research Center for Detection of Pathogenic Bacteria, Lembaga Penelitian dan Pengabdian Kepada Masyarakat, Universitas Negeri Jakarta, Jakarta Timur 13220, Indonesia
Ayu Berkahingrum, Department of Chemistry, Faculty of Mathematics and Natural Science, Universitas Negeri Jakarta, Jakarta Timur 13220, Indonesia
Irma Ratna Kartika, Department of Chemistry, Faculty of Mathematics and Natural Science, Universitas Negeri Jakarta, Jakarta Timur 13220, Indonesia
Fera Kurniadewi, Department of Chemistry, Faculty of Mathematics and Natural Science, Universitas Negeri Jakarta, Jakarta Timur 13220, Indonesia
Vira Saamia, Center Forensic Laboratory of the Criminal Investigation, Police of the Republic of Indonesia, Bogor 16810, Indonesia
Shyi-Tien Chen, Department of Safety, Health and Environmental Engineering, National Kaohsiung University of Science and Technology, Kaohsiung City 82445, Taiwan
Bassam Aboemolak, Arnold Palmer Hospital Pediatric Specialty Diagnostic Laboratory, Florida 32806, USA
Hesham Ali El Enshasy, Innovation Center in Agritechnology for Advanced Bioprocessing, Universiti Teknologi Malaysia, Johor 81310, Malaysia

Abstract

Escherichia coli is a foodborne pathogenic bacterium that can cause diarrhea, while yhaV is a virulence-associated gene linked to the toxin–antitoxin system in E. coli. This study was aimed at evaluating the confirmation, specificity, and sensitivity of a yhaV gene primer using real-time polymerase chain reaction. The yhaV-targeting PCR successfully amplified a DNA fragment with an amplicon length of 207 bp (base pairs) under an annealing temperature optimized to a range of 54 °C to 62 °C via gradient PCR. The PCR using the primer pair produced a consistent Ct (cycle threshold) of 14.14 ± 0.05 and showed a single peak in the melting curve at a Tm (melting temperature) of 83.67 °C ± 0.02. The specificity test indicated that the yhaV primer effectively distinguished E. coli from nontarget bacteria on the basis of differences in Ct and Tm values. The sensitivity analysis showed that the PCR directed toward the primer pair successfully detected E. coli at a minimum concentration of 2.24 pg/µL, with a Ct value of 29.93 and a detection limit of 31.5 × 102 CFU. These results suggest that yhaV-based real-time PCR quickly and accurately identifies E. coli. Primer designs that target yhaV have the potential to be developed as components of a rapid, specific, and sensitive kit for detecting E. coli in food samples.

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