Gluten Detection by Real-Time PCR: an Alternative for Tracking Processed Foods

Abstract This work reports a real-time PCR assay to specifically detect the presence of gluten in complex food matrices and to carry out an in-silico prospection of primers used in scientific research. The primers used were “tritprglut” and “Planta 18S” (reference gene), which had mean quantificatio...

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Main Authors: Wemerson de Castro Oliveira, Hans Fröder, Eléia Righi
Format: Article
Language:English
Published: Instituto de Tecnologia do Paraná (Tecpar) 2025-02-01
Series:Brazilian Archives of Biology and Technology
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132025000100500&lng=en&tlng=en
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author Wemerson de Castro Oliveira
Hans Fröder
Eléia Righi
author_facet Wemerson de Castro Oliveira
Hans Fröder
Eléia Righi
author_sort Wemerson de Castro Oliveira
collection DOAJ
description Abstract This work reports a real-time PCR assay to specifically detect the presence of gluten in complex food matrices and to carry out an in-silico prospection of primers used in scientific research. The primers used were “tritprglut” and “Planta 18S” (reference gene), which had mean quantification cycle values (Cq) of 34.30 and 16.98, respectively. The real-time PCR protocol was validated in different meats (beef, chicken, pork, horse and lamb) with an average Cq of 25.69. Tests to verify fraud in industrialized foods were carried out with the following products: cereal bars, chocolate, crackers and two types of snacks. All foods complied with the information contained on the label, except for the cereal bar that was identified as “may contain gluten” and had a “high content” concentration (1,925 mg/kg). The LD value was 36 cycles and the LQ was 60 mg/kg, being within the “low content” classification range. The in-silico tests were performed using two software, MFE and NETprimer, and the content parameters GC, Tm (°C), ∆G (kcal/mol), dimer formation and hairpins. The “Wheat-w-Gliadin” primer showed the best average parameters: size= 24 bp; GC= 44%; Tm = 62.5 °C; ∆G= -32.25 kcal/mol; no dimer or hairpin formation; and a maximum primer rating (100). There were differences in results between the software used. The results highlight the potential of the real-time PCR technique in detecting gluten and/or allergens in foods with a complex matrix, such as chocolate and cereal bars tested in this study, proving to be sensitive and robust to detect the presence of potentially high gluten concentrations. harmful for celiac consumers.
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publishDate 2025-02-01
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spelling doaj-art-a29a6886c39f4587a0d7a0554849d1f22025-02-04T07:40:10ZengInstituto de Tecnologia do Paraná (Tecpar)Brazilian Archives of Biology and Technology1678-43242025-02-016810.1590/1678-4324-2025230869Gluten Detection by Real-Time PCR: an Alternative for Tracking Processed FoodsWemerson de Castro Oliveirahttps://orcid.org/0000-0001-7256-265XHans Fröderhttps://orcid.org/0000-0003-1551-236XEléia Righihttps://orcid.org/0000-0002-2766-8719Abstract This work reports a real-time PCR assay to specifically detect the presence of gluten in complex food matrices and to carry out an in-silico prospection of primers used in scientific research. The primers used were “tritprglut” and “Planta 18S” (reference gene), which had mean quantification cycle values (Cq) of 34.30 and 16.98, respectively. The real-time PCR protocol was validated in different meats (beef, chicken, pork, horse and lamb) with an average Cq of 25.69. Tests to verify fraud in industrialized foods were carried out with the following products: cereal bars, chocolate, crackers and two types of snacks. All foods complied with the information contained on the label, except for the cereal bar that was identified as “may contain gluten” and had a “high content” concentration (1,925 mg/kg). The LD value was 36 cycles and the LQ was 60 mg/kg, being within the “low content” classification range. The in-silico tests were performed using two software, MFE and NETprimer, and the content parameters GC, Tm (°C), ∆G (kcal/mol), dimer formation and hairpins. The “Wheat-w-Gliadin” primer showed the best average parameters: size= 24 bp; GC= 44%; Tm = 62.5 °C; ∆G= -32.25 kcal/mol; no dimer or hairpin formation; and a maximum primer rating (100). There were differences in results between the software used. The results highlight the potential of the real-time PCR technique in detecting gluten and/or allergens in foods with a complex matrix, such as chocolate and cereal bars tested in this study, proving to be sensitive and robust to detect the presence of potentially high gluten concentrations. harmful for celiac consumers.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132025000100500&lng=en&tlng=engluten screeningallergenmolecular biologyvegetable proteinin-silico
spellingShingle Wemerson de Castro Oliveira
Hans Fröder
Eléia Righi
Gluten Detection by Real-Time PCR: an Alternative for Tracking Processed Foods
Brazilian Archives of Biology and Technology
gluten screening
allergen
molecular biology
vegetable protein
in-silico
title Gluten Detection by Real-Time PCR: an Alternative for Tracking Processed Foods
title_full Gluten Detection by Real-Time PCR: an Alternative for Tracking Processed Foods
title_fullStr Gluten Detection by Real-Time PCR: an Alternative for Tracking Processed Foods
title_full_unstemmed Gluten Detection by Real-Time PCR: an Alternative for Tracking Processed Foods
title_short Gluten Detection by Real-Time PCR: an Alternative for Tracking Processed Foods
title_sort gluten detection by real time pcr an alternative for tracking processed foods
topic gluten screening
allergen
molecular biology
vegetable protein
in-silico
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132025000100500&lng=en&tlng=en
work_keys_str_mv AT wemersondecastrooliveira glutendetectionbyrealtimepcranalternativefortrackingprocessedfoods
AT hansfroder glutendetectionbyrealtimepcranalternativefortrackingprocessedfoods
AT eleiarighi glutendetectionbyrealtimepcranalternativefortrackingprocessedfoods