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Cell-mimetic biosensors to detect avian influenza virus via viral fusion.
Park, Geunseon; Lim, Jong-Woo; Park, Chaewon; Yeom, Minjoo; Lee, Sojeong; Lyoo, Kwang-Soo; Song, Daesub; Haam, Seungjoo.
Affiliation
  • Park G; Department of Chemical and Biomolecular Engineering, Yonsei University, Seoul, 03722, Republic of Korea.
  • Lim JW; Department of Veterinary Medicine Virology Laboratory, College of Veterinary Medicine and Research Institute for Veterinary Science, Seoul National University, Seoul, 08826, Republic of Korea.
  • Park C; Department of Chemical and Biomolecular Engineering, Yonsei University, Seoul, 03722, Republic of Korea.
  • Yeom M; Department of Veterinary Medicine Virology Laboratory, College of Veterinary Medicine and Research Institute for Veterinary Science, Seoul National University, Seoul, 08826, Republic of Korea.
  • Lee S; Department of Chemical and Biomolecular Engineering, Yonsei University, Seoul, 03722, Republic of Korea.
  • Lyoo KS; College of Veterinary Medicine, Jeonbuk National University, Iksan, 54596, Republic of Korea.
  • Song D; Department of Veterinary Medicine Virology Laboratory, College of Veterinary Medicine and Research Institute for Veterinary Science, Seoul National University, Seoul, 08826, Republic of Korea. Electronic address: sds@snu.ac.kr.
  • Haam S; Department of Chemical and Biomolecular Engineering, Yonsei University, Seoul, 03722, Republic of Korea. Electronic address: haam@yonsei.ac.kr.
Biosens Bioelectron ; 212: 114407, 2022 Sep 15.
Article in En | MEDLINE | ID: mdl-35623252
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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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Influenza A virus / Biosensing Techniques / Influenza in Birds Type of study: Diagnostic_studies Limits: Animals Language: En Journal: Biosens Bioelectron Journal subject: BIOTECNOLOGIA Year: 2022 Document type: Article Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Influenza A virus / Biosensing Techniques / Influenza in Birds Type of study: Diagnostic_studies Limits: Animals Language: En Journal: Biosens Bioelectron Journal subject: BIOTECNOLOGIA Year: 2022 Document type: Article Country of publication: United kingdom