# Bacterial biosurfactant-reinforced chitooligosaccharide/polyvinyl alcohol hydrogels accelerate methicillin-resistant Staphylococcus aureus-infected wound healing by attenuating its virulence factors

**Authors:** Geum-Jae Jeong, Dong-Joo Park, Ju-Hong Kang, Se-Chang Kim, Yu-Jin Ahn, Kyung-Jin Cho, Fazlurrahman Khan, Won-Kyo Jung, Young-Mog Kim

PMC · DOI: 10.1016/j.ajps.2026.101118 · Asian Journal of Pharmaceutical Sciences · 2026-01-10

## TL;DR

A new hydrogel made with a bacterial biosurfactant helps heal MRSA-infected wounds by reducing the bacteria's harmful effects and promoting tissue repair.

## Contribution

A novel hydrogel combining a biosurfactant from Bacillus rugosus with chitooligosaccharide and polyvinyl alcohol is developed for MRSA-infected wound healing.

## Key findings

- The hydrogel significantly enhanced cell proliferation, migration, and extracellular matrix deposition in wound healing.
- It exhibited strong antibacterial, antibiofilm, and anti-virulence effects against MRSA.
- In vivo tests showed accelerated wound healing and reduced MRSA burden with the hydrogel.

## Abstract

Methicillin-resistant Staphylococcus aureus (MRSA) causes widespread infections and poses serious public health concerns. Its high level of resistance to multiple antibiotics has garnered growing interest in identifying and applying novel antibacterial compounds derived from natural sources. In this study, we purified a biosurfactant (BS) from Bacillus rugosus HH2 to develop a natural antibacterial agent. This agent was then reinforced with chitooligosaccharide (COS) and polyvinyl alcohol (PVA) to create a hydrogel that promoted healing in MRSA-infected wounds. The COS/PVA/BS hydrogel was readily fabricated via the freeze-thaw method and demonstrated excellent mechanical strength, biological activity, and biocompatibility. In vitro assays confirmed that the hydrogel significantly enhanced the proliferation, migration, angiogenesis, and extracellular matrix deposition of fibroblasts, keratinocytes, and endothelial cells. Moreover, it exhibited strong bacteriostatic and bactericidal activities against MRSA, along with potent antibiofilm activity and inhibition of virulence factors relevant to MRSA-induced wound infections. Its anti-virulence effects have been linked to the downregulation of quorum sensing and virulence-related genes in MRSA. In an in vivo model of MRSA-induced infection, the COS/PVA/BS hydrogel significantly accelerated wound healing and markedly reduced the MRSA burden. Immunofluorescence staining confirmed enhanced neovascularization and regulated macrophage responses, underscoring the angiogenic and immunomodulatory effects of the hydrogel. Overall, the COS/PVA/BS hydrogel represents a promising therapeutic strategy for addressing antibiotic-resistant bacterial infections and promoting wound repair, supported by the use of common raw materials, a simple fabrication process, and high-yield production of natural antibacterial agents.

This study presents the Bacillus rugosus HH2-derived biosurfactant-reinforced chitooligosaccharide/polyvinyl alcohol hydrogel dressing designed to accelerate the healing of methicillin-resistant Staphylococcus aureus-infected wounds.Image, graphical abstract

## Linked entities

- **Chemicals:** chitooligosaccharide (PubChem CID 90265172)
- **Species:** Bacillus rugosus (taxon 2715209), Staphylococcus aureus (taxon 1280)

## Full-text entities

- **Genes:** Lipase [NCBI Gene 17374477], Acta2 (actin alpha 2, smooth muscle, aorta) [NCBI Gene 11475] {aka 0610041G09Rik, Actvs, SMAalpha, SMalphaA, a-SMA, alphaSMA}, RELA (RELA proto-oncogene, NF-kB subunit) [NCBI Gene 5970] {aka AIF3BL3, CMCU, NFKB3, p65}, MAPK8 (mitogen-activated protein kinase 8) [NCBI Gene 5599] {aka JNK, JNK-46, JNK1, JNK1A2, JNK21B1/2, PRKM8}, alpha-hemolysin [NCBI Gene 28381283]
- **Diseases:** Hemolysis (MESH:D006461), metabolic dysfunction (MESH:D008659), skin lesions (MESH:D012871), KCCM 40510 (MESH:D006480), pain (MESH:D010146), malodor (MESH:C536561), fibrosis (MESH:D005355), abscess (MESH:D000038), inflammation (MESH:D007249), wounds (MESH:D014947), Swelling (MESH:D004487), bacterial infections (MESH:D001424), infectious (MESH:D003141), sepsis (MESH:D018805), MRSA (MESH:D013203), HDF (MESH:D016136), necrosis (MESH:D009336), deaths (MESH:D003643), cytotoxicity (MESH:D064420), weight loss (MESH:D015431), infected wounds (MESH:D014946), infected (MESH:D007239)
- **Chemicals:** Staphyloxanthin (MESH:C031841), Water (MESH:D014867), sodium hydroxide (MESH:D012972), Methicillin (MESH:D008712), ethanol (MESH:D000431), hydrochloric acid (MESH:D006851), isopropyl alcohol (MESH:D019840), formazan (MESH:D005562), FDA (MESH:C018506), CS (MESH:D048271), gold (MESH:D006046), sodium deoxycholate (MESH:D003840), methanol (MESH:D000432), nylon (MESH:D009757), paraffin (MESH:D010232), picric acid (MESH:C005858), polymer (MESH:D011108), streptomycin (MESH:D013307), HOCl (MESH:D006997), Triton X-100 (MESH:D017830), nitrogen (MESH:D009584), polysaccharides (MESH:D011134), sodium carbonate (MESH:C005686), Lipid (MESH:D008055), paraformaldehyde (MESH:C003043), Chloroform (MESH:D002725), surfactin A (MESH:C000706152), CO2 (MESH:D002245), ROS (MESH:D017382), 4',6-diamidino-2-phenylindole (MESH:C007293), DMSO (MESH:D004121), Formaldehyde (MESH:D005557), Mn (MESH:D008345), Hydrogen (MESH:D006859), Tween 20 (MESH:D011136), glutaraldehyde (MESH:D005976), eosin (MESH:D004801), beta-lactam (MESH:D047090), disodium hydrogen phosphate (MESH:C018279), SYTO 9 (MESH:C103389), Hematoxylin (MESH:D006416), penicillin (MESH:D010406), 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MESH:C022616), H&amp;E (MESH:D006371), COS (MESH:C493484), crystal violet (MESH:D005840), BS hydrogel (-), PI (MESH:D011419), H2O2 (MESH:D006861), Alexa Fluor 488 (MESH:C000711379), Congo Red (MESH:D003224), gum arabic (MESH:D006170), polyvinyl alcohol hydrogel (MESH:C062364), amine (MESH:D000588), MTT (MESH:C070243), PVA (MESH:D011142)
- **Species:** Ovis aries (domestic sheep, species) [taxon 9940], Raphanus sativus (radish, species) [taxon 3726], Escherichia coli (E. coli, species) [taxon 562], Pseudomonas aeruginosa (species) [taxon 287], Mus musculus (house mouse, species) [taxon 10090], Senegalia senegal (gum-arabic, species) [taxon 138043], Homo sapiens (human, species) [taxon 9606], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Staphylococcus aureus (species) [taxon 1280]
- **Cell lines:** HDF — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_U509), KCCM 40510 — Homo sapiens (Human), Induced pluripotent stem cell (CVCL_E031), ATCC 6538 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_0023), HaCaT — Homo sapiens (Human), Spontaneously immortalized cell line (CVCL_0038), HUVEC — Homo sapiens (Human), Finite cell line (CVCL_3722)

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12887791/full.md

## References

88 references — full list in the complete paper: https://tomesphere.com/paper/PMC12887791/full.md

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Source: https://tomesphere.com/paper/PMC12887791