# Transcriptomic and metabolomic insights from functionalized V-shaped Lactiplantibacillus plantarum towards mitigating Candida albicans virulence

**Authors:** Satish Kumar Rajasekharan, Athira Venugopal, Hamitha Chinganadi Hameed, Jennessa Jacob, Vinothkannan Ravichandran, Doron Steinberg, Adi Faigenboim, Chaitany Jayprakash Raorane, Moshe Shemesh

PMC · DOI: 10.1016/j.bioflm.2025.100321 · Biofilm · 2025-10-01

## TL;DR

This study explores how a probiotic bacterium, Lactiplantibacillus plantarum, can inhibit the harmful yeast Candida albicans through unique structures and bioactive metabolites.

## Contribution

The study identifies two novel metabolites from V-shaped L. plantarum that inhibit Candida albicans virulence pathways.

## Key findings

- V-shaped L. plantarum structures produce antibiofilm metabolites effective against Candida albicans.
- Transcriptomic analysis shows upregulated genes related to aromatic amino acid biosynthesis in VSLP.
- Two new metabolites, bluensomycin and majoroside F6, inhibit the Ras-adenylate cyclase pathway in yeast.

## Abstract

The genomic capacity of probiotic Lactobacilli enables producing bioactive metabolites that represent promising alternatives to antibiotics for combating food-borne and multi drug-resistant pathogens. The current study characterizes a global antagonistic potential of the probiotic bacterium Lactiplantibacillus plantarum, which demonstrates unique multicellular structuring triggered in response to acidic environments. We demonstrate the inhibitory potential of postbiotics derived from the V-shaped structured L. plantarum (VSLP) against Candida albicans. Using the liquid chromatography-mass spectrometry (LC-MS) profiling, we further identify different antibiofilm metabolites secreted during the VSLP formation. Transcriptomic studies reveal a notable upregulation of genes associated with the biosynthesis of aromatic amino acids such as serD, ywqE2, trpB, trpA. Furthermore, significant differential expressions were observed in genes within the biosynthetic gene cluster (BGCs) identified through antiSMASH analysis of L. plantarum genome. In addition, two novel VSLP metabolites (bluensomycin and majoroside F6) functioned as inhibitors of Ras-adenylate cyclase pathway that control biofilms and hyphae in yeast. We suggest that functionalized probiotic cells, such as VSLP, may effectively control the pathogenic microorganisms that provide a staple basis for developing future therapeutic probiotics.

## Linked entities

- **Genes:** trpB (tryptophan synthase subunit beta) [NCBI Gene 879212], TPSG1 (tryptase gamma 1) [NCBI Gene 25823]
- **Chemicals:** bluensomycin (PubChem CID 20055290), majoroside F6 (PubChem CID 131751089)
- **Species:** Lactiplantibacillus plantarum (taxon 1590), Candida albicans (taxon 5476)

## Full-text entities

- **Chemicals:** bluensomycin (MESH:C006786), aromatic amino acids (MESH:D024322), postbiotics (-), majoroside F6 (MESH:C062686)
- **Species:** Lactiplantibacillus plantarum (species) [taxon 1590], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Candida albicans (species) [taxon 5476]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12549387/full.md

## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC12549387/full.md

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Source: https://tomesphere.com/paper/PMC12549387