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May 26, 2026Viruses0 citationsOpen Access

Stage-of-Action Characterization of a Non-Sulfated Heteropolysaccharide from Gracilaria lemaneiformis Against Dengue Virus Serotype 2

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JDJiaxin DaiYLYingfang LiuJLJingshu Li

Key Points

  • This research examines the antiviral potential of a non-sulfated heteropolysaccharide from Gracilaria lemaneiformis against dengue virus serotype 2.
  • Characterized heteropolysaccharide GLHP from Gracilaria lemaneiformis using Fourier-transform infrared (FT-IR) spectroscopy.
  • Conducted time-of-addition analyses in Huh7 and BHK-21 cells to determine the stage-specific antiviral activity.
  • Tested cytotoxicity with CC50 values confirming low toxicity levels.
  • Co-inoculation with GLHP showed the strongest inhibition of intracellular viral RNA compared to pre-inoculation (p<0.05).
  • GLHP significantly reduced extracellular virus output under post-inoculation conditions (p<0.01), indicating dual antiviral effects.
  • GLHP attenuation of virus-induced cytopathic effects supports its potential as an antiviral agent against DENV-2.

Abstract

Marine algal polysaccharides have been widely investigated as antiviral candidates, yet nearly all anti-dengue studies have focused on sulfated species. Whether algal polysaccharides lacking prominent sulfation can inhibit dengue virus (DENV) remains unexplored. Here, we profiled the stage-specific antiviral activity of a heteropolysaccharide (GLHP) from Gracilaria lemaneiformis, whose Fourier-transform infrared (FT-IR) spectrum lacks characteristic sulfate ester absorption bands, against DENV serotype 2 (DENV-2) in Huh7 and BHK-21 cells. GLHP exhibited low cytotoxicity (CC50 exceeding 1000 μg/mL in Huh7 cells and approximately 950 μg/mL in BHK-21 cells). Time-of-addition analysis revealed that co-inoculation GLHP treatment (Co-inoc.) produced the strongest and most consistent inhibition of intracellular viral RNA, whereas pre-inoculation GLHP treatment (Pre-inoc.) was ineffective, indicating that the antiviral activity is predominantly associated with the virus–cell contact and entry stage. GLHP additionally reduced extracellular progeny virus output under post-inoculation GLHP treatment (Post-inoc.) conditions, and this reduction exceeded the corresponding change in intracellular viral RNA levels, suggesting an additional effect that may involve either a late replication step or secondary entry blockade of progeny virions. Attenuation of virus-induced cytopathic effects under Co-inoc. conditions further supported the antiviral activity. To our knowledge, these findings identify GLHP as the first non-sulfated marine polysaccharide shown to exhibit stage-defined antiviral activity against DENV-2 and support further investigation of its antiviral potential and structural determinants.

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Cite This Study

Dai et al. (2026) studied this question.

synapsesocial.com/papers/6a153bdfb5d9c58d83e8d492https://doi.org/10.3390/v18060594
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