Rapid Visible Detection of African Swine Fever Virus Using Hybridization Chain Reaction‐Sensitized Magnetic Nanoclusters and Affinity Chromatography

Author:

Lee Hyo1,Lee Sojeong1,Park Chaewon1,Yeom Minjoo2,Lim Jong‐Woo2,Vu Thi Thu Hang3,Kim Eunjung45ORCID,Song Daesub2,Haam Seungjoo1ORCID

Affiliation:

1. Department of Chemical and Biomolecular Engineering Yonsei University Seoul 03722 Republic of Korea

2. Department of Veterinary Medicine Virology Laboratory College of Veterinary Medicine and Research Institute for Veterinary Science, Seoul National University Seoul 08826 Republic of Korea

3. Department of Preclinical Science College of Pharmacy Korea University Sejong Campus Sejong City 30019 Republic of Korea

4. Division of Bioengineering Incheon National University Incheon 22012 Republic of Korea

5. Department of Bioengineering & Nano‐Bioengineering Research Center for Bio Materials and Process Development Incheon National University Incheon 22012 Republic of Korea

Abstract

AbstractAfrican swine fever virus (ASFV) is a severe and persistent threat to the global swine industry. As there are no vaccines against ASFV, there is an immense need to develop easy‐to‐use, cost‐effective, and rapid point‐of‐care (POC) diagnostic platforms to detect and prevent ASFV outbreaks. Here, a novel POC diagnostic system based on affinity column chromatography for the optical detection of ASFV is presented. This system employs an on‐particle hairpin chain reaction to sensitize magnetic nanoclusters with long DNA strands in a target‐selective manner, which is subsequently fed into a column chromatography device to produce quantitatively readable and colorimetric signals. The detection approach does not require expensive analytical apparatus or immobile instrumentation. The system can detect five genes constituting the ASFV whole genome with a detection limit of ≈19.8 pm in swine serum within 30 min at laboratory room temperature. With an additional pre‐amplification step using polymerase chain reaction (PCR), the assay is successfully applied to detect the presence of ASFV in 30 suspected swine samples with 100% sensitivity and specificity, similar to quantitative PCR. Thus, this simple, inexpensive, portable, robust, and customizable platform for the early detection of ASFV can facilitate the timely surveillance and implementation of control measures.

Funder

National Research Foundation of Korea

Publisher

Wiley

Subject

Biomaterials,Biotechnology,General Materials Science,General Chemistry

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