# Characterizing Gene-Level Adaptations in the Gut Microbiome During Viral Infections: The Role of a Fucoidan-Rich Extract

**Authors:** Gissel García, Josanne Soto, Carmen Valenzuela, Raul De Jesús Cano

PMC · DOI: 10.3390/genes16070740 · 2025-06-26

## TL;DR

This study shows that a Fucoidan-rich extract can reduce gut inflammation and restore microbiome balance in people infected with Dengue or Oropouche virus.

## Contribution

The study introduces new insights into how Fucoidan modulates gut microbiome gene expression during viral infections.

## Key findings

- Infected participants had lower Lachnospiraceae-to-Enterobacteriaceae ratios, indicating gut inflammation.
- High-dose Fucoidan reduced inflammation and shifted the microbiome toward a balanced composition.
- Pro-inflammatory taxa like Fusobacterium decreased, while beneficial species like Akkermansia muciniphila increased.

## Abstract

Background/Objectives: This study aimed to examine the effects of a Fucoidan-rich extract from Saccharina latissima (SLE-F) on differential gut microbiota composition, intestinal inflammation status, and microbial functional gene expression in participants infected with Dengue or Oropouche virus at the Hermanos Ameijeiras Hospital in Havana, Cuba. Methods: Fecal samples were collected at baseline, day 28, and day 90 from 90 healthy adults, some of whom contracted the virus during the study period. Functional gene analysis was conducted using two approaches—the Kruskal–Wallis H test and linear discriminant analysis effect size—applied to ortholog-level data normalized by read count and gene copy number. Results: Infected participants exhibited significantly lower Lachnospiraceae-to-Enterobacteriaceae (LE) ratios, indicating increased intestinal inflammation. High-dose SLE-F treatment led to a significant reduction in the LE ratio (p = 0.006), suggesting a strong anti-inflammatory effect. Microbiome analysis revealed a shift from dysbiosis to a more balanced composition by the end of the study, characterized by increased abundances of Akkermansia muciniphila, Bifidobacterium adolescentis, and B. longum, along with decreased pro-inflammatory taxa such as Fusobacterium. Conclusions: Genetic analysis provided distinct yet complementary insights into the microbiome’s functional responses to infection and therapeutic modulation by Fucoidan. These findings highlight the therapeutic potential of high-dose Fucoidan in reducing gut inflammation and promoting microbiome recovery following viral infections.

## Linked entities

- **Diseases:** Dengue (MONDO:0005502)
- **Species:** Saccharina latissima (taxon 309358), Akkermansia muciniphila (taxon 239935), Bifidobacterium adolescentis (taxon 1680), Fusobacterium (taxon 848)

## Full-text entities

- **Diseases:** Infected (MESH:D007239), gut inflammation (MESH:D007249), Dengue (MESH:D003715), Viral Infections (MESH:D014777)
- **Chemicals:** Fucoidan (MESH:C007789), SLE-F (-)
- **Species:** Bifidobacterium longum (species) [taxon 216816], Oropouche virus (no rank) [taxon 118655], Akkermansia muciniphila (species) [taxon 239935], Bifidobacterium adolescentis (species) [taxon 1680], Fusobacterium (genus) [taxon 848]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12296014/full.md

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Source: https://tomesphere.com/paper/PMC12296014