4.8 Article

Development of antibody against drug-resistant respiratory syncytial virus: Rapid detection of mutant virus using split superfolder green fluorescent protein-antibody system

Journal

BIOSENSORS & BIOELECTRONICS
Volume 194, Issue -, Pages -

Publisher

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2021.113593

Keywords

Antibody; Drug-resistance; S275F mutation; Respiratory syncytial virus; Green fluorescent protein

Funding

  1. National Research Foundation (NRF) of Korea - Ministry of Science and ICT (MSIT) of Korea [NRF-2020R1A2C1010453, NRF-2021M3E5E3080844, NRF-2019R1C1C1006867, NRF-2021M3H4A1A0 2051048, NRF-2021M3E5E3080379, NRF-2018M3A9E2022821]
  2. Global Frontier Program through Center for BioNano Health-Guard - MSIT of Korea [H-GUARD_2014M3A6B2060507, H-GUARD_2013M3A6B2078950]
  3. Technology Development Program for Biological Hazards Management in Indoor Air through Korea Environ-ment Industry & Technology Institute (KEITI) - Ministry of Environment (ME) of Korea [2021003370003]
  4. Ministry of Trade, Industry, and Energy (MOTIE) of Korea [20012435]
  5. KRIBB Research Initiative Program [1711134081, 1711134038]
  6. Nanomedical Devices Development Program of National Nano Fab Center [CSM2105M101]

Ask authors/readers for more resources

RSV infections can cause severe diseases, and the emergence of drug-resistant RSV strains is concerning. We studied an antibody that can specifically detect palivizumab-resistant RSV strains and developed a rapid detection method for the S275F RSV antigen.
Respiratory syncytial virus (RSV) infections are associated with severe bronchiolitis or pneumonia. Although palivizumab is used to prevent RSV infections, the occurrence of palivizumab-resistant RSV strains is increasing, and these strains pose a threat to public health. Herein, we report an antibody with affinity to the S275F RSV antigen, enabling the specific detection of palivizumab-resistant RSV strains. Experimental and simulation results confirmed the affinity of the antibody to the S275F RSV antigen. Furthermore, we developed a rapid S275F RSV antigen detection method using a split superfolder green fluorescent protein (ssGFP) that can interact with the antibody. In the presence of the mutant virus antigen, ssGFP emitted fluorescence within 1 min, allowing the rapid identification of S275F RSV. We anticipate that the developed antibody would be useful for the precise diagnosis of antiviral drug-resistant RSV strains and help treat patients with RSV infections.

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