# Antimicrobial Activity of Aurisin A Against Streptococcus suis and Its Protective Effect on Epithelial Cells

**Authors:** Thotsaporn Bunthiang, Siriwan Sunontarat, Nattamol Phetburom, Ruethaithip Dulyasucharit, Orapan Intharaksa, Thidarut Boonmars, Somdej Kanokmedhakul, Ratsami Lekphrom, Peechanika Chopjitt, Anusak Kerdsin, Parichart Boueroy

PMC · DOI: 10.3390/ijms27041798 · International Journal of Molecular Sciences · 2026-02-13

## TL;DR

A new compound from a mushroom shows strong antibacterial effects against a dangerous pig and human pathogen, protecting cells from damage.

## Contribution

Aurisin A, a natural compound, is shown to inhibit Streptococcus suis growth and protect epithelial cells from its harmful effects.

## Key findings

- Aurisin A inhibits biofilm formation and degrades preformed biofilms of Streptococcus suis at low concentrations.
- Aurisin A protects lung epithelial cells by reducing adhesion, cell death, and cytotoxicity caused by S. suis.
- Aurisin A reduces the hemolytic effect of S. suis on sheep blood, indicating protective activity against the pathogen.

## Abstract

Streptococcus suis is one of the most important zoonotic pathogens threatening the lives of pigs and humans. Increasingly severe antimicrobial resistance in S. suis is becoming a global issue. Therefore, there is an urgent need to discover novel antibacterial alternatives for the treatment of S. suis infections. The current study investigated aurisin A, an aristolane dimer sesquiterpene isolated from the luminescent mushroom Neonothopanus nambi Speg. (Marasmiaceae), against S. suis. The minimal inhibitory concentrations (MICs) and minimal bactericidal concentrations (MBCs) of aurisin A against S. suis strains were in the range of 1.94–62.5 μg/mL. Scanning electron microscopy showed that aurisin A induced alterations in the cellular structure of S. suis, including a significantly wrinkled surface, intracellular content leakage, and cell lysis. The crystal violet staining assay illustrated that aurisin A significantly inhibited biofilm formation of S. suis strains at sub-MICs and exhibited strong degrading activity against the preformed biofilms. Aurisin A significantly inhibited the adhesion, cell death, and cytotoxic activities of S. suis in lung epithelial cells in a concentration-dependent manner. Additionally, aurisin A significantly reduced the hemolytic effect of S. suis on defibrillated sheep blood, indicating protective activity of aurisin A against this bacteria. Taken together, these findings highlight aurisin A as a promising therapeutic candidate for the treatment of S. suis infections, with key roles in inhibiting biofilm formation and hemolytic activity, as well as providing protective effects to epithelial cells, including anti-adhesion, anti-cytotoxicity, and anti-cell death activities.

## Linked entities

- **Species:** Streptococcus suis (taxon 1307)

## Full-text entities

- **Diseases:** cholangiocarcinoma (MESH:D018281), epidermoid carcinoma (MESH:D002294), Hemolysis (MESH:D006461), inflammatory (MESH:D007249), injury to (MESH:D014947), meningitis (MESH:D008580), lung cancer (MESH:D008175), cancer (MESH:D009369), breast cancer (MESH:D001943), MRSA (MESH:D013203), septicemia (MESH:D018805), septic shock (MESH:D012772), subarachnoid infection (MESH:D013345), Cytotoxicity (MESH:D064420), S. suis infections (MESH:D007239)
- **Chemicals:** paeoniflorin (MESH:C015423), Penicillin G (MESH:D010400), vancomycin (MESH:D014640), terpenoids (MESH:D013729), tetracyclines (MESH:D013754), water (MESH:D014867), CCK-8 (MESH:D012844), cholesterol (MESH:D002784), methicillin (MESH:D008712), ethanol (MESH:D000431), fusidic acid (MESH:D005672), tobramycin (MESH:D014031), acetic acid (MESH:D019342), PI (MESH:D010716), Calcein AM (MESH:C085925), sodium chloride (MESH:D012965), gold (MESH:D006046), methanol (MESH:D000432), agar (MESH:D000362), Triton X-100 (MESH:D017830), carbon (MESH:D002244), streptomycin (MESH:D013307), AP (MESH:C030419), sulfonamides (MESH:D013449), quercetin (MESH:D011794), N. (MESH:D009584), sesquiterpene (MESH:D012717), CO2 (MESH:D002245), diterpenoids (MESH:D004224), baicalein (MESH:C006680), syringopicroside (MESH:C038066), beta-lactams (MESH:D047090), penicillin (MESH:D010406), aluminum (MESH:D000535), Aurisin A (-), Crystal Violet (MESH:D005840), triterpenoids (MESH:D014315), phillyrin (MESH:C075528), FQs (MESH:D024841), macrolides (MESH:D018942)
- **Species:** Ovis aries (domestic sheep, species) [taxon 9940], Streptococcus suis (species) [taxon 1307], Sus scrofa (pig, species) [taxon 9823], Plasmodium falciparum (malaria parasite P. falciparum, species) [taxon 5833], Homo sapiens (human, species) [taxon 9606], Staphylococcus aureus (species) [taxon 1280], Neonothopanus nambi (species) [taxon 71958], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Mycobacterium tuberculosis (species) [taxon 1773]
- **Mutations:** A51119500C
- **Cell lines:** KKU-100 — Homo sapiens (Human), Hilar cholangiocarcinoma, Cancer cell line (CVCL_3996), BC1 — Homo sapiens (Human), Primary effusion lymphoma, Cancer cell line (CVCL_1079), KKU-213 — Homo sapiens (Human), Intrahepatic cholangiocarcinoma, Cancer cell line (CVCL_M261), NCI-H187 — Homo sapiens (Human), Lung small cell carcinoma, Cancer cell line (CVCL_1501), SC19 — Mus musculus (Mouse), Hybridoma (CVCL_C4GD), A549 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_0023), KKU-139 — Homo sapiens (Human), Intrahepatic cholangiocarcinoma, Cancer cell line (CVCL_M259), KKU-156 — Homo sapiens (Human), Intrahepatic cholangiocarcinoma, Cancer cell line (CVCL_M260), S. suis — Homo sapiens (Human), Colorectal adenoma, Cancer cell line (CVCL_8754), KB — Homo sapiens (Human), Human papillomavirus-related endocervical adenocarcinoma, Cancer cell line (CVCL_0372)

## Full text

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## Figures

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## References

46 references — full list in the complete paper: https://tomesphere.com/paper/PMC12941304/full.md

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Source: https://tomesphere.com/paper/PMC12941304