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Development of PCR, LAMP and qPCR Assays for the Detection of Aflatoxigenic Strains of Aspergillus flavus and A. parasiticus in Hazelnut
Aspergillus flavus and A. parasiticus are two species able to produce aflatoxins in foodstuffs, and in particular in hazelnuts, at harvest and during postharvest phase. As not all the strains of these species are aflatoxin producers, it is necessary to develop techniques that can detect aflatoxigeni...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7761073/ https://www.ncbi.nlm.nih.gov/pubmed/33266343 http://dx.doi.org/10.3390/toxins12120757 |
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author | Ortega, Sara Franco Siciliano, Ilenia Prencipe, Simona Gullino, Maria Lodovica Spadaro, Davide |
author_facet | Ortega, Sara Franco Siciliano, Ilenia Prencipe, Simona Gullino, Maria Lodovica Spadaro, Davide |
author_sort | Ortega, Sara Franco |
collection | PubMed |
description | Aspergillus flavus and A. parasiticus are two species able to produce aflatoxins in foodstuffs, and in particular in hazelnuts, at harvest and during postharvest phase. As not all the strains of these species are aflatoxin producers, it is necessary to develop techniques that can detect aflatoxigenic from not aflatoxigenic strains. Two assays, a LAMP (loop-mediated isothermal amplification) and a real time PCR with TaqMan(®) probe were designed and validated in terms of specificity, sensitivity, reproducibility, and repeatability. The capability of the strains to produce aflatoxins was measured in vitro and both assays showed to be specific for the aflatoxigenic strains of A. flavus and A. parasiticus. The limit of detection of the LAMP assay was 100–999 picograms of DNA, while the qPCR detected 160 femtograms of DNA in hazelnuts. Both techniques were validated using artificially inoculated hazelnuts and naturally infected hazelnuts. The qPCR was able to detect as few as eight cells of aflatoxigenic Aspergillus in naturally infected hazelnut. The combination of the LAMP assay, which can be performed in less than an hour, as screening method, with the high sensitivity of the qPCR, as confirmation assay, is able to detect aflatoxigenic strains already in field, helping to preserve the food safety of hazelnuts. |
format | Online Article Text |
id | pubmed-7761073 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77610732020-12-26 Development of PCR, LAMP and qPCR Assays for the Detection of Aflatoxigenic Strains of Aspergillus flavus and A. parasiticus in Hazelnut Ortega, Sara Franco Siciliano, Ilenia Prencipe, Simona Gullino, Maria Lodovica Spadaro, Davide Toxins (Basel) Article Aspergillus flavus and A. parasiticus are two species able to produce aflatoxins in foodstuffs, and in particular in hazelnuts, at harvest and during postharvest phase. As not all the strains of these species are aflatoxin producers, it is necessary to develop techniques that can detect aflatoxigenic from not aflatoxigenic strains. Two assays, a LAMP (loop-mediated isothermal amplification) and a real time PCR with TaqMan(®) probe were designed and validated in terms of specificity, sensitivity, reproducibility, and repeatability. The capability of the strains to produce aflatoxins was measured in vitro and both assays showed to be specific for the aflatoxigenic strains of A. flavus and A. parasiticus. The limit of detection of the LAMP assay was 100–999 picograms of DNA, while the qPCR detected 160 femtograms of DNA in hazelnuts. Both techniques were validated using artificially inoculated hazelnuts and naturally infected hazelnuts. The qPCR was able to detect as few as eight cells of aflatoxigenic Aspergillus in naturally infected hazelnut. The combination of the LAMP assay, which can be performed in less than an hour, as screening method, with the high sensitivity of the qPCR, as confirmation assay, is able to detect aflatoxigenic strains already in field, helping to preserve the food safety of hazelnuts. MDPI 2020-11-30 /pmc/articles/PMC7761073/ /pubmed/33266343 http://dx.doi.org/10.3390/toxins12120757 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ortega, Sara Franco Siciliano, Ilenia Prencipe, Simona Gullino, Maria Lodovica Spadaro, Davide Development of PCR, LAMP and qPCR Assays for the Detection of Aflatoxigenic Strains of Aspergillus flavus and A. parasiticus in Hazelnut |
title | Development of PCR, LAMP and qPCR Assays for the Detection of Aflatoxigenic Strains of Aspergillus
flavus and A. parasiticus in Hazelnut |
title_full | Development of PCR, LAMP and qPCR Assays for the Detection of Aflatoxigenic Strains of Aspergillus
flavus and A. parasiticus in Hazelnut |
title_fullStr | Development of PCR, LAMP and qPCR Assays for the Detection of Aflatoxigenic Strains of Aspergillus
flavus and A. parasiticus in Hazelnut |
title_full_unstemmed | Development of PCR, LAMP and qPCR Assays for the Detection of Aflatoxigenic Strains of Aspergillus
flavus and A. parasiticus in Hazelnut |
title_short | Development of PCR, LAMP and qPCR Assays for the Detection of Aflatoxigenic Strains of Aspergillus
flavus and A. parasiticus in Hazelnut |
title_sort | development of pcr, lamp and qpcr assays for the detection of aflatoxigenic strains of aspergillus
flavus and a. parasiticus in hazelnut |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7761073/ https://www.ncbi.nlm.nih.gov/pubmed/33266343 http://dx.doi.org/10.3390/toxins12120757 |
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