# Metabolomic Analysis of Phytophthora parasitica Growth in the Presence of β‐sitosterol Indicates Adaptive Mechanisms Modulated by Sterols

**Authors:** Pâmela Ponce Martins, Evandro Silva, Marcus Vinicius Fernandes Prior, João Marcos Martins Ferreira, Marina Erê Pimenta Santos, Flavia Rodrigues Alves Patrício, Taicia Pacheco Fill, Jorge Maurício Costa Mondego

PMC · DOI: 10.1002/jobm.70149 · 2026-02-04

## TL;DR

This study explores how β-sitosterol affects the metabolism of the plant pathogen Phytophthora parasitica, revealing adaptive changes that could influence its growth and pathogenicity.

## Contribution

The study reveals novel metabolic reprogramming in Phytophthora parasitica in response to β-sitosterol, highlighting potential roles in environmental adaptation.

## Key findings

- Mycelial growth was not significantly affected by β-sitosterol concentrations.
- Differential production of sphinganine, histidine, and methylthioadenosine was observed in the presence of β-sitosterol.
- Metabolic reprogramming suggests adaptive mechanisms linked to sterol modulation in the oomycete.

## Abstract

Phytophthora parasitica is a generalist phytopathogenic oomycete that infects a series of crops with great economic interest, including tomato, tobacco, and citrus species. Sterols are essential lipids in eukaryotic organisms, playing a fundamental role in the structure and function of the cell membrane. Oomycete from Peronosporales order, including Phytophthora spp., are known for their inability to synthesize sterols, a characteristic that distinguishes them from many other organisms and influences their biology and pathogenicity. This dependence is not only crucial for zoospore sporulation but also for vegetative growth. Following the scenario at which sterol auxotrophy can interfere in the metabolism of such important phytopathogen, in this study we investigate whether β‐sitosterol modulates the metabolome of P. parasitica and its vegetative growth. For that, we used liquid chromatography–mass spectrometry LC‐HRMS combined with chemometric tools, to assess the metabolite profile of P. parasitica under different concentrations of β‐sitosterol in the culture media. Even though mycelial growth was not significantly affected by different sterol concentrations, an evident metabolic reprogramming of the oomycete was detected. Among the metabolites differentially produced in the sterol presence are the sphingolipid sphinganine, histidine and the nucleoside methylthioadenosine. We discuss the influence of these metabolites in vegetative growth of the oomycete and infer possible roles in environmental adaptation and pathogenicity.

## Linked entities

- **Chemicals:** β-sitosterol (PubChem CID 222284), sphinganine (PubChem CID 91486), histidine (PubChem CID 773), methylthioadenosine (PubChem CID 439176)

## Full-text entities

- **Diseases:** fungal (MESH:D009181), root rot (MESH:D005535), FBTs (MESH:C567791), plant (MESH:D010939), infection (MESH:D007239)
- **Chemicals:** H2O (MESH:D014867), L-histidine (MESH:D006639), beta-sitosterol (MESH:C025473), nucleotide (MESH:D009711), H (MESH:D006859), folate (MESH:D005492), glycosphingolipids (MESH:D006028), membrane lipid (MESH:D008563), 2,3-oxidosqualene (MESH:C002821), agar (MESH:D000362), copper (MESH:D003300), ROS (MESH:D017382), 5'-methylthioadenosine (MESH:C008500), serine (MESH:D012694), nucleoside (MESH:D009705), Sterol (MESH:D013261), DIM (MESH:C076154), CHCl3 (MESH:D002725), carbon (MESH:D002244), purine (MESH:C030985), benzylpenicillinpotassium (MESH:D010400), metal (MESH:D008670), GlcCer (MESH:D005963), zinc (MESH:D015032), SP (MESH:C000604007), ceramide (MESH:D002518), iron (MESH:D007501), sulfur (MESH:D013455), sulfate (MESH:D013431), phytosterol (MESH:D010840), acetonitrile (MESH:C032159), sphingolipid (MESH:D013107), C - aminobenzoic acid (-), methionine (MESH:D008715), squalene (MESH:D013185), PTFE (MESH:D011138), benzylpenicillinprocaine (MESH:D010402), amino acid (MESH:D000596), phosphoinositide (MESH:D010716), methanol (MESH:D000432), oxathiapiprolin (MESH:C000592431), PYM (MESH:C108337), glyceryl monostearate (MESH:C048159), formic acid (MESH:C030544), sugar (MESH:D000073893), nitrogen (MESH:D009584), dipeptides (MESH:D004151), Sphinganine (MESH:C005682), sphingosine (MESH:D013110), histamine (MESH:D006632), polyamine (MESH:D011073), lipid (MESH:D008055), S-adenosylmethionine (MESH:D012436), CaCO3 (MESH:D002119)
- **Species:** Citrus trifoliata (hardy orange, species) [taxon 37690], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Nicotiana tabacum (American tobacco, species) [taxon 4097], Salmonella enterica subsp. enterica serovar Typhimurium (no rank) [taxon 90371], Citrus sunki (sunki mandarin, species) [taxon 237574], Solanum lycopersicum (tomato, species) [taxon 4081], Phytophthora sojae (species) [taxon 67593], Phytophthora nicotianae (black shank of tobacco agent, species) [taxon 4792]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12873457/full.md

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Source: https://tomesphere.com/paper/PMC12873457