LITERATUR REVIEW: APLIKASI MOLEKULER BERBASIS PCR DALAM DETEKSI  DAN KARAKTERISASI Escherichia coli PADA SEKTOR LINGKUNGAN, PANGAN, DAN KLINIS

Authors

  • Diva Yunavita Universitas Negri Padang
  • Dwi Hilda Putri State University of Padang image/svg+xml

DOI:

https://doi.org/10.30605/jcp1q263

Keywords:

Quality of service for cadres, toddlers, maternal visits

Abstract

Escherichia coli is a gram-negative bacterium and a key indicator of water and food contamination. Conventional PCR is a widely used molecular method for specific, rapid, and sensitive E. coli detection. This literature review systematically examines the application of conventional PCR in E. coli detection across water, food, and clinical sample matrices from 2017 to 2025. Thirteen scientific articles were reviewed regarding research objects, PCR methods, research stages, and findings. Conventional PCR using primers 16E1/16E2 (584 bp), Afa FP/RP (480 bp), and ESS (825 bp) effectively detected E. coli in diverse samples. PCR showed superior sensitivity (100%) and specificity (94.34%) compared to culture methods (Hariri, 2022). Direct PCR offered a cost-effective alternative without DNA extraction (JKG, 2025). Multiplex PCR enabled simultaneous detection of multiple virulence genes (Ekawati et al.; Microbiology Spectrum, 2024). Conventional PCR remains a reliable, specific, and rapid tool for E. coli detection across diverse sample types.

References

Arai, et al. (2025). An Optimized PCR Assay to Detect E. coli Harboring the astA Gene (EAST1) in Various Food Matrices. Food Safety (FSCJ). DOI: 10.14252/foodsafetyfscj.D-25-00013

Bioma: Jurnal Biologi Makassar. (2021). Deteksi Molekuler Bakteri Escherichia coli sebagai Penyebab Penyakit Diare dengan Menggunakan Teknik PCR. journal.unhas.ac.id/index.php/bioma/article/view/13194

CIHAMS: Conference on Innovation in Health, Accounting and Management Sciences. (2020). Deteksi Escherichia coli dengan Metode Polimerase Chain Reaction (PCR): Literature Review. cihams.setiabudi.ac.id/index.php/proceeding/article/view/24

Ekawati, et al. Deteksi Escherichia coli Patogen pada Pangan Menggunakan Metode Konvensional dan Multiplex PCR. Jurnal SainHealth, 1(2), 23–31.

Hariri, S. (2022). Detection of Escherichia coli in Food Samples Using Culture and Polymerase Chain Reaction Methods. Cureus, 14(12): e32808. DOI: 10.7759/cureus.32808

JIFI: Jurnal Ilmiah Farmasi Imelda. (2023). Identifikasi Bakteri Escherichia coli pada Saus Makanan Jajanan Cilok di Sekolah Dasar Kecamatan Indralaya Selatan. 7(1). jurnal.uimedan.ac.id/index.php/JURNALFARMASI/article/view/1505

Jurnal Kesmas dan Gizi (JKG). (2025). Direct PCR for Escherichia coli: A Straightforward and Cost-Effective Method. Mediastra. ejournal.medistra.ac.id/index.php/JKG/article/view/2606

Jurnal Wiyata: Penelitian Sains dan Kesehatan. (2025). Desain Primer dan Pemurnian Ganda untuk Deteksi PCR Gen 16S rRNA pada Escherichia coli. IIK Kediri. ojs.iik.ac.id/index.php/wiyata/article/view/1007

Makara Sains, 14(1): 39–43. Deteksi Cepat Bakteri Escherichia coli dalam Sampel Air dengan Metode PCR Menggunakan Primer 16E1 dan 16E2. researchgate.net/publication/47416691

Microbiology Spectrum / PMC. (2024). Novel Multiplex-PCR Test for Escherichia coli Detection Using Genes cydA, lacY, and ydiV. DOI: 10.1128/spectrum.03773-23. PMC11237426

PMC / Cureus. (2025). Detection of Virulence Determinants of Uropathogenic Escherichia coli (UPEC). PMC11923561

Putri, et al. (2022). Deteksi Bakteri Escherichia coli dengan Metode PCR pada Sampel Makanan Takjil. Prosiding Semnas Biologi FMIPA UNP, 2(1), 405–413. DOI: 10.24036/prosemnasbio/vol2/404

Putri & Achyar. (2024). Optimasi Isolasi DNA Bakteri Patogen (E. coli) pada Sampel Air Sungai Berbasis PCR. Jurnal Serambi Biologi, UNP. serambibiologi.ppj.unp.ac.id/index.php/srmb/article/view/241

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Published

2026-05-11

How to Cite

LITERATUR REVIEW: APLIKASI MOLEKULER BERBASIS PCR DALAM DETEKSI  DAN KARAKTERISASI Escherichia coli PADA SEKTOR LINGKUNGAN, PANGAN, DAN KLINIS. (2026). Jurnal Biogenerasi, 11(2), 717-722. https://doi.org/10.30605/jcp1q263