# Synergistic effects of antibiotics and fucoidan on dual-species Staphylococcus aureus and Acinetobacter baumannii biofilm in diabetic rat wound models

**Authors:** Mohsen Nazari, Mohammad Taheri, Fatemeh Nouri, Maryam Bahmanzadeh, Mohammad Yousef Alikhani

PMC · DOI: 10.1371/journal.pone.0342905 · PLOS One · 2026-02-19

## TL;DR

Combining antibiotics with fucoidan improves healing in diabetic wounds infected with antibiotic-resistant bacteria by reducing biofilms and inflammation.

## Contribution

Fucoidan synergizes with gentamicin and imipenem to combat dual-species biofilms in diabetic wound models.

## Key findings

- Triple therapy reduced bacterial load by over 4 log₁₀ CFU/g compared to controls.
- Fucoidan significantly downregulated biofilm-related genes icaA and bap.
- Triple therapy accelerated wound healing with complete re-epithelialization by day 14.

## Abstract

Chronic diabetic wounds are often complicated by biofilm-forming, antibiotic-resistant pathogens such as Staphylococcus aureus and Acinetobacter baumannii, which delay healing. This study evaluated the synergistic effects of gentamicin and imipenem in combination with fucoidan, a sulfated polysaccharide from brown seaweed, against dual-species biofilms in a diabetic rat wound model.

Methicillin-resistant S. aureus (MRSA) strain 6 and A. baumannii strain 1, isolated from diabetic foot ulcers, were used to establish dual-species biofilms in vitro and in vivo. Excisional wounds were created in male Wistar rats with streptozocin-induced type II diabetes and infected with the biofilms. Rats received daily treatments of gentamicin, imipenem, their combination, or the triple combination with fucoidan. Outcomes assessed included bacterial load (CFU/g), biofilm formation, expression of biofilm-related genes (icaA and bap by real-time PCR), wound size, and histological healing parameters.

The triple therapy demonstrated the strongest antibacterial effect, reducing bacterial load by more than 4 log₁₀ CFU/g compared to controls (p < 0.005). Real-time PCR revealed significant downregulation of icaA in S. aureus (threefold decrease) and bap in A. baumannii (fourfold decrease) relative to antibiotic-only groups (p < 0.005). Histology showed accelerated wound contraction and complete re-epithelialization by day 14 with the triple combination, whereas monotherapy or dual antibiotics led to delayed healing and persistent inflammation.

Fucoidan enhances the efficacy of gentamicin and imipenem against biofilm-associated infections and promotes diabetic wound healing. This combinatorial approach offers a promising strategy for managing chronic, biofilm-infected wounds and combating antibiotic resistance.

## Linked entities

- **Genes:** icaA (N-acetylglucosaminyltransferase) [NCBI Gene 11640150], PHB2 (prohibitin 2) [NCBI Gene 11331]
- **Chemicals:** gentamicin (PubChem CID 3467), imipenem (PubChem CID 104838)
- **Diseases:** diabetes (MONDO:0005015)
- **Species:** Staphylococcus aureus (taxon 1280), Acinetobacter baumannii (taxon 470), Mus musculus (taxon 10090)

## Full-text entities

- **Diseases:** wound infection (MESH:D014946), weight loss (MESH:D015431), biofilm infections (MESH:D007239), hyperglycemic (MESH:D006944), deaths (MESH:D003643), DFUs (MESH:D017719), amputation (MESH:C565682), overdose (MESH:D062787), MRSA (MESH:D013203), Type II diabetes (MESH:D003924), irritation (MESH:D001523), Diabetic (MESH:D003920), pain (MESH:D010146), Chronic wounds (MESH:D014947), inflammation (MESH:D007249), hyperglycemia (MESH:D006943), fibroplasia (MESH:D012178), bleeding (MESH:D006470)
- **Chemicals:** PVC (MESH:D011143), glycosaminoglycans (MESH:D006025), hematoxylin (MESH:D006416), Luria-Bertani (LB) (-), crystal violet (MESH:D005840), H&amp;E (MESH:D006371), glucose (MESH:D005947), formalin (MESH:D005557), glutaraldehyde (MESH:D005976), eosin (MESH:D004801), ampicillin (MESH:D000667), IMP (MESH:D015378), oxacillin (MESH:D010068), agar (MESH:D000362), polysaccharide (MESH:D011134), FUC (MESH:C007789), xylazine (MESH:D014991), potassium phosphate (MESH:C013216), osmium tetroxide (MESH:D009993), paraffin (MESH:D010232), gold (MESH:D006046), Methicillin (MESH:D008712), ethanol (MESH:D000431), Blood glucose (MESH:D001786), polyvinyl (MESH:D011145), copper (MESH:D003300), GEN (MESH:D005839), Streptozocin (MESH:D013311), water (MESH:D014867), nicotinamide (MESH:D009536)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116], Staphylococcus aureus (species) [taxon 1280], Acinetobacter baumannii (species) [taxon 470]

## Full text

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## Figures

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## References

44 references — full list in the complete paper: https://tomesphere.com/paper/PMC12919824/full.md

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Source: https://tomesphere.com/paper/PMC12919824