For the first time, mushroom products sold on the Italian market were authenticated using DNA barcoding. The analysis was performed on 71 market products (MPs) of different types (canned, dried, frozen, ready-to-cook-dishes) collected in supermarket chains. The ITS complete region was amplified and sequenced. The obtained sequences were then submitted to a BLAST analysis against both an internal dataset developed in a previous study and GenBank for species identification. Issues during amplification and sequencing were especially highlighted for canned products, plausibly due to the processing. The internal dataset was able to support the identification at species level. However, the need to improve it with sequences of commercially relevant species it is essential to increase its identification capability. Cases of suspected mislabeling were observed, with Agaricus bisporus and Bjerkandera adusta respectively found in two products labeled as Boletus edulis and its group. The presence of B. adusta, a not edible plant pathogen, also highlighted a scarce attention in the application of good hygiene and manufacturing practices. Since only 1 or 2 sequence/s were produced from each MP, we cannot exclude that mislabeling rate (2.8%) may be under-estimated. Specific guidelines on sampling strategy should be therefore fixed for mislabeling assessment purposes. Also, the use of alternative DNA based methods, such as metabarcoding, able to identify all the species present in a sample, should be considered.

Molecular authentication of mushroom products: First survey on the Italian market

Giusti, Alice
Primo
Writing – Original Draft Preparation
;
Tinacci, Lara;Armani, Andrea
Writing – Review & Editing
2023-01-01

Abstract

For the first time, mushroom products sold on the Italian market were authenticated using DNA barcoding. The analysis was performed on 71 market products (MPs) of different types (canned, dried, frozen, ready-to-cook-dishes) collected in supermarket chains. The ITS complete region was amplified and sequenced. The obtained sequences were then submitted to a BLAST analysis against both an internal dataset developed in a previous study and GenBank for species identification. Issues during amplification and sequencing were especially highlighted for canned products, plausibly due to the processing. The internal dataset was able to support the identification at species level. However, the need to improve it with sequences of commercially relevant species it is essential to increase its identification capability. Cases of suspected mislabeling were observed, with Agaricus bisporus and Bjerkandera adusta respectively found in two products labeled as Boletus edulis and its group. The presence of B. adusta, a not edible plant pathogen, also highlighted a scarce attention in the application of good hygiene and manufacturing practices. Since only 1 or 2 sequence/s were produced from each MP, we cannot exclude that mislabeling rate (2.8%) may be under-estimated. Specific guidelines on sampling strategy should be therefore fixed for mislabeling assessment purposes. Also, the use of alternative DNA based methods, such as metabarcoding, able to identify all the species present in a sample, should be considered.
2023
Giusti, Alice; Ricci, Enrica; Tinacci, Lara; Verdigi, Francesco; Narducci, Roberto; Gasperetti, Laura; Armani, Andrea
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/1175945
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