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Digital PCR for Genotype Quantification: A Case Study in a Pasta Production Chain
Caterina Morcia1, Valeria Terzi1, Roberta Ghizzoni1
1Consiglio per la ricerca in agricoltura e l'analisi dell'economia agraria-Centro di Ricerca Genomica e Bioinformatica (CREA-GB), Via San Protaso 302, 29017 Fiorenzuola d'Arda, Italy.
Biology
|June 2, 2021
Summary
Digital polymerase chain reaction (dPCR) precisely quantifies specific plant genotypes in raw materials and transformed products. This breakthrough technology offers a reliable method for variety confirmation and quantification in food supply chains.
Area of Science:
- Agricultural Science
- Biotechnology
- Molecular Biology
Background:
- Digital polymerase chain reaction (dPCR) offers high precision for mutation detection.
- Plant genotype quantification is crucial for agricultural supply chains.
Purpose of the Study:
- To evaluate the applicability of dPCR for quantifying specific plant genotypes in raw materials and transformed products.
- To assess dPCR's utility in confirming and quantifying a durum wheat variety using a private point mutation.
Main Methods:
- Development and evaluation of a dPCR assay targeting a specific point mutation in durum wheat.
- Analysis of supply-chain samples, including commercial grain lots and pasta.
- Comparison of dPCR performance, costs, and applicability against SSR and DArTseq methods.
Main Results:
- The dPCR assay successfully confirmed the presence of the target durum wheat variety.
- Quantification of the target variety in both raw materials and transformed food products was achieved.
- The dPCR assay demonstrated high precision and applicability for variety tracking.
Conclusions:
- dPCR is a suitable and precise analytical technique for plant genotype quantification in agricultural supply chains.
- The developed dPCR assay can reliably identify and quantify specific varieties, aiding in quality control and traceability.
- dPCR presents a competitive alternative to traditional methods like SSR and DArTseq for varietal analysis.
Keywords:
allelic discriminationdigital PCR (dPCR)durum wheatgenotype-by-sequencing (GBS)molecular traceabilitypastaprivate allelequantification of varietysimple sequence repeats (SSRs)varietal confirmation
