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Updated: Aug 6, 2026

Visual Detection of Multiple Nucleic Acids in a Capillary Array
Published on: November 15, 2017
Advances in Nucleic Acid-Based Amplification Strategies for Dual-Mode Biosensing of Pathogenic Bacteria: From
Salah Tofik Jalal Balaky1,2, Ban Hussein Alwash3, Faisal Faruq Sadiq Zamzamokey4,5
1Medical Microbiology Department, College of Health Sciences, Hawler Medical University, Erbil, Iraq.
Abstract:
Rapid, accurate, and reliable detection of pathogenic bacteria remains a critical need in clinical, food, and environmental monitoring. In today's context, nucleic acid amplification-mediated biosensing have emerged as a prominent approach to improve detection sensitivity, whereas dual-mode signal readout approaches have more enhanced analytical robustness and reliability. This review outlines recent advances in nucleic acid signal amplification strategies, including enzyme-based methods like LAMP, RPA, and RCA, as well as enzyme-free approaches like HCR, CHA, and EDR. Special attention is given to incorporating these amplification methods into dual-mode biosensing systems that combine both optical and electrochemical transduction mechanisms. This integration enables complementary signal generation and improves detection accuracy by reducing false-positive and false-negative results. This study critically examines the advancement of nucleic acid signal amplification strategies (NASAS)-mediated dual-mode sensing systems for detecting major pathogenic bacteria, including Escherichia coli, Salmonella, Listeria monocytogenes, Staphylococcus aureus, and Vibrio species, focusing on selectivity, sensitivity, assay design, and real-sample applicability. Finally, the review highlights present challenges related to system integration, standardization, and point-of-care applications. Additionally, it outlines potential future directions for rendering nucleic acid amplification-based dual-mode probes into practical diagnostic devices. Overall, this study affords a comprehensive synthesis of emerging approaches and design mechanisms for next-generation diagnostic scaffold for pathogen analysis.
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