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Effect of hot water extracts of Arthrospira maxima (spirulina) against respiratory syncytial virus

  • Wei Chen
  • , Yi Hsiang Chen
  • , Ya Chun Liao
  • , Xin Wen Huang
  • , Ting Jang Lu*
  • , Shin Ru Shih
  • *Corresponding author for this work
  • Chang Gung University
  • National Taiwan University
  • Chang Gung Memorial Hospital

Research output: Contribution to journalJournal Article peer-review

13 Scopus citations

Abstract

Background: Spirulina (Arthrospira maxima) hot water extracts such as calcium spirulan (Ca-SP) have demonstrated antiviral effects against herpes simplex virus (HSV), human immunodeficiency virus-1 (HIV-1), and influenza virus infections. There is no prior evidence suggesting the anti-viral activity of the spirulina hot water extract against respiratory syncytial virus (RSV). Purpose: There are currently no effective antivirals available to treat RSV infection. Therefore, the development of safe and novel anti-RSV drugs is urgent and necessary. The aim of this work was to demonstrate the anti-RSV activity of spirulina hot water extracts and determine the potential mechanism of action. Methods: Cytotoxicity and anti-RSV activity of spirulina hot water extracts were measured using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and neutralization assays, respectively. Potential mechanisms and components were assessed using time of addition, attachment, internalization, pull-down assays, and composition analysis. Results: The polysaccharide-enriched high-molecular weight fraction (>100 kDa, SHD1) had a high total sugar content, with rhamnose accounting for approximately 60 mol% of total monosaccharides. The main glycosyl linkages included 3-, 4-, and 2,3-rhamnopyranosyl linkages. All spirulina hot water extracts showed no toxicity toward human epithelial type 2 (HEp-2) cells but demonstrated anti-RSV activity. The SHD1 had a half maximal effective concentration (EC50) of 0.0915 mg/ml and a selective index (SI) of >261.5 against RSV. SHD1 significantly reduced viral yield in a dose-dependent manner during the RSV attachment stage. SHD1 disrupted RSV internalization and inhibited RSV attachment (G) protein binding to heparan sulfate receptors on the host cell surface, thus preventing RSV attachment and entry. Conclusion: SHD1 serves as an effective candidate for novel drug development against RSV infection.

Original languageEnglish
Article number154611
Pages (from-to)154611
JournalPhytomedicine
Volume110
DOIs
StatePublished - 02 2023

Bibliographical note

Copyright © 2022. Published by Elsevier GmbH.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Antiviral activity
  • Arthrospira maxima
  • Respiratory syncytial virus
  • Water extract
  • Respiratory Syncytial Viruses
  • Spirulina
  • Respiratory Syncytial Virus Infections/drug therapy
  • Humans
  • Antiviral Agents/pharmacology

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