The Utilization of the SaLux19-Based Loop-Mediated Isothermal Amplification (LAMP) Assay for the Rapid and Sensitive Identification of Minute Amounts of a Biological Specimen

Author:

Ruszova Ema12ORCID,Vanek Daniel1234ORCID,Stühmer Walter5ORCID,Khaznadar Ziad1,Subhashini Nidhi6ORCID

Affiliation:

1. Bulovka University Hospital, 180 81 Prague, Czech Republic

2. Forensic DNA Service, Budinova 2, 180 81 Prague, Czech Republic

3. Institute for Environmental Sciences, Charles University, 110 00 Prague, Czech Republic

4. Department of Forensic Medicine, Second Faculty of Medicine, Charles University, 110 00 Prague, Czech Republic

5. Max Planck Institute of Multidisciplinary Sciences, Hermann-Rein-Str. 3, 37075 Göttingen, Germany

6. Seratec GmbH, Ernst-Ruhstrat-Str. 5, 37079 Göttingen, Germany

Abstract

Our research has developed a highly sensitive and simple assay to detect small amounts of animal and human biological material in less than 40 min. The handheld SaLux19 device developed at the Max Planck Institute of Experimental Medicine in Göttingen, Germany, was used to validate our concept. The proposed system uses isothermal amplification of DNA in a rapid assay format. Our results show that the assay can detect Sus scrofa nucleic acids with very high sensitivity and specificity. This detection system has potential for forensic scenarios.

Publisher

MDPI AG

Reference34 articles.

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2. Recent advances in loop-mediated isothermal amplification (LAMP) for rapid and efficient detection of pathogens;Garg;Curr. Res. Microb. Sci.,2022

3. Scott, A.C.T., Layne, T.R., and Landers, J.P. (2023, November 23). Low-Cost Isothermal Amplification Microdevice for Rapid Colorimetric Detection Applied to Body Fluid Identification and Y-Screening, Available online: https://ojp.gov/pdffiles1/nij/grants/256090.pdf.

4. Loop-mediated Isothermal Amplification of DNA;Notomi;Nucleic Acids Res.,2000

5. Khan, M., Wang, R., Li, B., Liu, P., Weng, Q., and Chen, Q. (2018). Comparative Evaluation of the LAMP Assay and PCR-Based Assays for the Rapid Detection of Alternaria Solani. Front. Microbiol., 9.

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