# Detection of Penicillium-Toxins in Nuts Commercialized in Italy Through LC-MS/MS Analyses

**Authors:** Fabio Buonsenso, Giovanna Roberta Meloni, Davide Spadaro

PMC · DOI: 10.3390/toxins18010012 · Toxins · 2025-12-24

## TL;DR

This study detects Penicillium-produced toxins in commercially available Italian nuts, highlighting potential food safety risks.

## Contribution

The study introduces a comprehensive LC-MS/MS method to detect multiple Penicillium-toxins in nuts, revealing their prevalence.

## Key findings

- 37% of nut samples contained at least one Penicillium-toxin, with 9% containing two or more.
- Peanuts showed the highest contamination rate (60%), and patulin was the most commonly detected toxin.
- Viridicatin was the highest-concentrated toxin found in a walnut sample at 151.40 ± 64.30 µg/kg.

## Abstract

The consumption of nuts is widespread globally and constitutes a significant component of the human diet due to its nutritional value. However, the presence of mycotoxins in food products, including nuts, is a global public health concern. Mycotoxins are toxic metabolites produced by contaminating fungi such as Aspergillus spp. and Penicillium spp., which can contaminate crops during growth, harvesting, storage, or transport. The aim of this study was to conduct monitoring for the presence of mycotoxins in nuts already on the market. Specifically, secondary metabolites produced by Penicillium spp., including ochratoxin A, patulin, citrinin, cyclopiazonic acid, citreoviridin, griseofulvin, meleagrin, mycophenolic acid, penitrem A, roquefortine C, penicillins G and V, sulochrin, andrastin A, asterriquinone, chaetoglobosin A, cyclopenin, cyclopenol, and viridicatin, were investigated. Commercial products were purchased from various retail outlets in different formats, origins, and cultivation methods to assess potential influences of these factors on mycotoxin presence. Regarding Penicillium-toxins, 37% of the samples showed the presence of at least one of them, and 9% showed the simultaneous presence of two or more Penicillium-toxins. Peanuts had the highest incidence of Penicillium-toxin contamination, with at least one metabolite detected in 60% of the analyzed samples. The most common secondary metabolite among the samples was patulin (14%), while the secondary metabolite with the highest concentration was viridicatin in a walnut sample (151.40 ± 64.30 µg/kg). Besides Penicillium-toxins, aflatoxins were also analyzed with another validated LC-MS/MS method, but they were not detected in any sample. Although most Penicillium-toxins, and in particular patulin in nuts, are not currently regulated in the international legislation, they exert toxic effects on humans and animals, and their occurrence can represent a food safety risk.

## Linked entities

- **Chemicals:** ochratoxin A (PubChem CID 442530), patulin (PubChem CID 4696), citrinin (PubChem CID 54680783), cyclopiazonic acid (PubChem CID 54682463), citreoviridin (PubChem CID 6436023), griseofulvin (PubChem CID 441140), meleagrin (PubChem CID 23728435), mycophenolic acid (PubChem CID 446541), penitrem A (PubChem CID 6610243), roquefortine C (PubChem CID 21608802), sulochrin (PubChem CID 160505), andrastin A (PubChem CID 6712564), asterriquinone (PubChem CID 100329), chaetoglobosin A (PubChem CID 6438437), cyclopenin (PubChem CID 73525), cyclopenol (PubChem CID 101201), viridicatin (PubChem CID 67206)

## Full-text entities

- **Chemicals:** chaetoglobosin A (MESH:C019290), ochratoxin A (MESH:C025589), griseofulvin (MESH:D006118), aflatoxins (MESH:D000348), cyclopiazonic acid (MESH:C000543), andrastin A (MESH:C100395), asterriquinone (MESH:C035746), viridicatin (MESH:C009673), patulin (MESH:D010365), roquefortine C (MESH:C012536), cyclopenol (MESH:C044418), mycophenolic acid (MESH:D009173), citreoviridin (MESH:C014416), cyclopenin (MESH:C007200), citrinin (MESH:D002953), sulochrin (MESH:C111298), penicillins G and V (-)
- **Species:** Penicillium (genus) [taxon 5073], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

53 references — full list in the complete paper: https://tomesphere.com/paper/PMC12845813/full.md

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Source: https://tomesphere.com/paper/PMC12845813