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The steady increase in commercialization of genetically modified organisms (GMOs) demands low-cost, rapid and portable GMO-detection methods that are technically and economically sustainable. Traditional nucleic acid detection platforms are still expensive, immobile and generate complex read-outs to be analyzed by experienced personal. Herein, we report the development of a portable, rapid and user-friendly GMO-detection biosensor, DaimonDNA. The system specifically amplifies the target DNA using loop-mediated isothermal amplification (LAMP) and provides real-time, naked-eye detection with Hydroxynaphthol blue reagent in less than 30 min. The construction of the platform relies on 3D printing and off-the-shelf electronic components that makes it extremely low-cost (<25 Euro), light weight (108 g), mobile (6 × 6 × 3 cm) and suitable for field deployment. We present the detection of the soybean lectin gene as a species control, and P35S as a transgene element found in many GMO varieties. We confirmed specificity of the DaimonDNA biosensor using" RoundUp Ready (RRS)" and MON89788 soybean genomic DNA with P35S and lectin primer sets. We characterized sensitivity of our system using 76.92, 769.2 and 7692 copies of RRS soybean genomic DNA in a non-GMO background. We benchmarked the DNA amplification and detection efficiency of our system against a thermocycling machine by quantifying the images obtained from gel electrophoresis and showed that our system is comparable to most other reported isothermal amplification techniques. This system can also be used for widespread point-of-care or field-based testing that is infrequently performed due to the lack of rapid, inexpensive, user-friendly and portable methods.
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http://dx.doi.org/10.1016/j.bios.2019.111409 | DOI Listing |
J Vet Diagn Invest
September 2025
Biology Department; Faculty of Sciences, Umm Al-Qura University, Makkah, Saudi Arabia.
Lumpy skin disease (LSD) is a viral disease that affects livestock and is caused by the lumpy skin disease virus (LSDV). An outbreak of LSD in any country can lead to acute economic damage for livestock owners. The significance of prompt and accurate diagnosis in managing this viral disease cannot be overstated.
View Article and Find Full Text PDFPlant Dis
September 2025
Jiangsu Academy of Agricultural Sciences, Nanjing, Jiangsu, China;
Grape white rot, caused by Coniella vitis, is a devastating disease that affects grape production in China and worldwide, resulting in substantial yield and quality losses. Early and accurate detection of C. vitis is critical for effective disease management.
View Article and Find Full Text PDFAnalyst
September 2025
Department of Bioengineering, University of Washington, Seattle, WA 98105, USA.
Curable sexually transmitted infections (STIs) caused by the bacteria (CT) and (NG) are widespread globally. These infections are particularly dangerous for female patients, causing pelvic inflammatory disease, infertility, and increased risk of HIV acquisition. Vaginal self-swab sampling can improve access to STI screening but is still subject to treatment delays due to centralized processing.
View Article and Find Full Text PDFJ AOAC Int
September 2025
Office of Laboratory Operations and Applied Science, Human Foods Program, U.S. Food and Drug Administration, College Park, Maryland.
Background: As a leading cause of foodborne illness worldwide, detection of Salmonella enterica subsp. enterica serovar Typhimurium is essential for food safety and public health.
Objective: This study aimed to develop a loop-mediated isothermal amplification (LAMP) assay for the rapid and sensitive detection of Salmonella ser.
Anal Chim Acta
October 2025
Instituto de Química, Universidade Federal de Goiás, 74690-900, Goiânia, GO, Brazil. Electronic address:
Background: The increasing prevalence of methicillin-resistant Staphylococcus aureus (MRSA), particularly due to the presence of the mecA gene, emphasizes the need for decentralized, rapid, and accurate molecular diagnostics. While qPCR remains the gold standard method, its dependence on expensive equipment and centralized labs limits accessibility in field or point-of-care (POC) settings. To address this limitation, we developed an Electrochemical Loop-Mediated Isothermal Amplification (E-LAMP) platform for rapid, low-cost, and highly sensitive detection of the mecA gene, using 3D-printed electrodes and a smartphone-controlled potentiostat.
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