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Cell-mimetic biosensors to detect avian influenza virus via viral fusion

Authors
GEUNSEON PARKLim J.-W.CHAEWON PARKYeom M.SOJEONG LEELyoo K.-S.Song D.SEUNGJOO HAAM
Issue Date
Sep-2022
Publisher
ELSEVIER ADVANCED TECHNOLOGY
Keywords
Avian influenza; Pathogenicity; Viral fusion; Enzymatic activation; Cell-mimetic nanostructure
Citation
BIOSENSORS & BIOELECTRONICS, v.212, pp 114407-1 - 114407-8
Journal Title
BIOSENSORS & BIOELECTRONICS
Volume
212
Start Page
114407-1
End Page
114407-8
URI
https://yscholarhub.yonsei.ac.kr/handle/2021.sw.yonsei/22924
DOI
10.1016/j.bios.2022.114407
ISSN
0956-5663
1873-4235
Abstract
Avian influenza virus (AIV) causes acute infectious diseases in poultry, critically impacting food supply. Highly pathogenic avian influenza viruses (HPAIVs), in particular, cause morbidity and mortality, resulting in significant economic losses in the poultry industry. To prevent the spread of HPAIVs, detection at early stages is critical to implement effective countermeasures such as quarantine and isolation. Through a viral fusion mechanism, cell-mimetic nanoparticles (CMPs), developed in the current study, can rapidly detect HPAIV and low pathogenic AIV (LPAIV). The CMPs comprise polymeric nanoparticles, which are constructed using sialic acid and fluorescence resonance energy transfer (FRET) dye pairs that expose the FRET off signal in response to LPAIV and HPAIV, after activation by enzymatic cleavage in the endosomal environment. The CMPs detect a wide variety of LPAIVs and HPAIVs in biological environments. Additionally, the cross-reactivity of CMPs is determined by testing their function with different viral species. Therefore, these findings demonstrate the significant potential of the proposed strategy for mimicking viral infection in vitro and using them as a highly effective diagnostic assay to rapidly detect LPAIV and HPAIV, preventing economic losses associated with viral outbreaks.
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