# Novel Skin- and Oral-Derived Probiotic Candidates: Functional Evaluation and Application Perspectives

**Authors:** Ivana Repić, Nina Čuljak, Matea Hrupački, Iva Čanak, Ksenija Markov, Jadranka Frece

PMC · DOI: 10.3390/microorganisms14020385 · Microorganisms · 2026-02-06

## TL;DR

This study identifies new probiotic candidates from skin and oral sources with potential health benefits beyond the gut.

## Contribution

The study evaluates novel skin- and oral-derived probiotic isolates for functional properties relevant to probiotic applications.

## Key findings

- Lcb. rhamnosus S3 showed the highest probiotic potential with strong antimicrobial activity and survival in simulated conditions.
- Limosilactobacillus sp. (S1) exhibited the strongest antimicrobial activity against C. acnes and high adhesion to skin cells.
- S. cerevisiae isolates showed strong autoaggregation and antioxidant capacity but poor freeze-drying resistance.

## Abstract

The skin and oral environment represent complex microbial ecosystems that host diverse bacterial communities with potential health-promoting properties beyond the gastrointestinal tract (GIT). In this study, four bacterial and three yeast isolates were obtained from saliva (S1, S3, S5, and S6) and human skin (A1, A2, and A3) and subjected to identification and functional characterization. Phenotypic identification by API and MALDI-TOF mass spectrometry identified bacterial isolates as Limosilactobacillus sp. (S1) and Lacticaseibacillus rhamnosus (S3, S5, and S6), while the yeasts were identified as Saccharomyces cerevisiae (A1, A2, and A3). The isolates were evaluated for their functional properties, including antimicrobial activity, autoaggregation, antioxidative potential, resistance to freeze-drying, survival in simulated saliva and GIT conditions, adhesion to Caco-2 and HaCaT cell lines, and biofilm-forming ability. Lcb. rhamnosus S3 demonstrated the highest probiotic potential, characterized by strong inhibition of S. aureus, high autoaggregation capacity, substantial survival following freeze-drying, and good tolerance to simulated saliva and GIT conditions. Limosilactobacillus sp. (S1) demonstrated the strongest antimicrobial activity against C. acnes and the highest adhesion capacity to HaCaT cells, indicating its suitability for topical dermatological applications. Although S. cerevisiae isolates did not exhibit antimicrobial activity, they showed strong autoaggregation and notable antioxidant capacity. However, their low resistance to freeze-drying limits their applicability in probiotic formulation development.

## Linked entities

- **Chemicals:** doxorubicin (PubChem CID 31703)
- **Diseases:** breast cancer (MONDO:0004989)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Diseases:** eczema (MESH:D004485), infections (MESH:D007239), cytotoxicity (MESH:D064420), AD (MESH:D003876), acne (MESH:D000152), inflammation (MESH:D007249), injury to (MESH:D014947), inflammatory skin disease (MESH:D012871), skin injuries (MESH:D000069836), oral diseases (MESH:D009059), oral cancer (MESH:D009062), diarrhea (MESH:D003967), Colonic adenocarcinoma (MESH:D003110)
- **Chemicals:** S (MESH:D013455), crystal violet (MESH:D005840), DMEM (-), hydrogen peroxide (MESH:D006861), sodium phosphate dibasic dodecahydrate (MESH:C018279), glycerol (MESH:D005990), tetracycline (MESH:D013752), K (MESH:D011188), polystyrene (MESH:D011137), glutathione (MESH:D005978), citric acid (MESH:D019343), ampicillin (MESH:D000667), KOH (MESH:C029943), lipids (MESH:D008055), CD (MESH:D002104), PBS (MESH:D007854), potassium chloride (MESH:D011189), folate (MESH:D005492), beta-glucans (MESH:D047071), DMSO (MESH:D004121), chloramphenicol (MESH:D002701), saline (MESH:D012965), methanol (MESH:D000432), TE (MESH:D013691), potassium bicarbonate (MESH:C026329), metal (MESH:D008670), potassium thiocyanate (MESH:C009941), potassium phosphate monobasic (MESH:C013216), nitrogen (MESH:D009584), lactic acid (MESH:D019344), C (MESH:D002244), streptomycin (MESH:D013307), Triton X-100 (MESH:D017830), agar (MESH:D000362), 1,1-diphenyl-2-picryl-hydrazyl (MESH:C004931), clindamycin (MESH:D002981), water (MESH:D014867), E (MESH:D004540), V (MESH:D014639), mannans (MESH:D008351), vancomycin (MESH:D014640), gentamicin (MESH:D005839), calcium chloride dihydrate (MESH:D002122), kanamycin (MESH:D007612), erythromycin (MESH:D004917), ethanol (MESH:D000431)
- **Species:** Listeria monocytogenes (species) [taxon 1639], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Staphylococcus aureus (species) [taxon 1280], Leptospira sp. AB (species) [taxon 103236], Homo sapiens (human, species) [taxon 9606], Clostridioides difficile (species) [taxon 1496], Bifidobacterium (genus) [taxon 1678], Limosilactobacillus fermentum (species) [taxon 1613], Cutibacterium acnes (species) [taxon 1747], Leeuwenhoekiella sp. LB (species) [taxon 1603302], Escherichia coli (E. coli, species) [taxon 562], Pseudomonas aeruginosa (species) [taxon 287], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], S. boulardii [taxon 252598], Lacticaseibacillus rhamnosus (species) [taxon 47715], Salmonella enterica subsp. enterica serovar Typhimurium (no rank) [taxon 90371], Limosilactobacillus sp. (species) [taxon 2773925]
- **Cell lines:** Caco-2 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0025), HaCaT — Homo sapiens (Human), Spontaneously immortalized cell line (CVCL_0038), ATCC 25923TM — Homo sapiens (Human), Finite cell line (CVCL_LK64), ATCC 23074TM — Homo sapiens (Human), Transformed cell line (CVCL_IG02), ATCC HTB-37 — Mus musculus (Mouse), Hybridoma (CVCL_A8FQ), ATCC 27853 — Homo sapiens (Human), Transformed cell line (CVCL_ZH96)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12942872/full.md

## References

79 references — full list in the complete paper: https://tomesphere.com/paper/PMC12942872/full.md

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Source: https://tomesphere.com/paper/PMC12942872