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The Aspergillus niger Major Allergen (Asp n 3) DNA-Specific Sequence Is a Reliable Marker to Identify Early Fungal Contamination and Postharvest Damage in Mangifera indica Fruit

The aim of this work was to study the value of the main allergen Asp n 3 of Aspergillus niger as a molecular marker of allergenicity and pathogenicity with the potential to be used in the identification of A. niger as a contaminant and cause of spoilage of Mangifera indica. Real-time polymerase chai...

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Autores principales: Martínez, Jorge, Nevado, Ander, Suñén, Ester, Gabriel, Marta, Vélez-del-Burgo, Ainara, Sánchez, Patricia, Postigo, Idoia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273346/
https://www.ncbi.nlm.nih.gov/pubmed/34262539
http://dx.doi.org/10.3389/fmicb.2021.663323
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author Martínez, Jorge
Nevado, Ander
Suñén, Ester
Gabriel, Marta
Vélez-del-Burgo, Ainara
Sánchez, Patricia
Postigo, Idoia
author_facet Martínez, Jorge
Nevado, Ander
Suñén, Ester
Gabriel, Marta
Vélez-del-Burgo, Ainara
Sánchez, Patricia
Postigo, Idoia
author_sort Martínez, Jorge
collection PubMed
description The aim of this work was to study the value of the main allergen Asp n 3 of Aspergillus niger as a molecular marker of allergenicity and pathogenicity with the potential to be used in the identification of A. niger as a contaminant and cause of spoilage of Mangifera indica. Real-time polymerase chain reaction (RT-PCR) was used for the amplification of Asp n 3 gene. Two pairs of primers were designed: one for the amplification of the entire sequence and another one for the amplification of the most conserved region of this peroxisomal protein. The presence of A. niger was demonstrated by the early detection of the allergenic protein Asp n 3 coding gene, which could be considered a species-specific marker. The use of primers designed based on the conserved region of the Asp n 3 encoding gene allowed us to identify the presence of the closely related fungal species Aspergillus fumigatus by detecting Asp n 3 homologous protein, which can be cross-reactive. The use of conserved segments of the Asp n 3 gene or its entire sequence allows us to detect phylogenetically closely related species within the Aspergilaceae family or to identify species-specific contaminating fungi.
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spelling pubmed-82733462021-07-13 The Aspergillus niger Major Allergen (Asp n 3) DNA-Specific Sequence Is a Reliable Marker to Identify Early Fungal Contamination and Postharvest Damage in Mangifera indica Fruit Martínez, Jorge Nevado, Ander Suñén, Ester Gabriel, Marta Vélez-del-Burgo, Ainara Sánchez, Patricia Postigo, Idoia Front Microbiol Microbiology The aim of this work was to study the value of the main allergen Asp n 3 of Aspergillus niger as a molecular marker of allergenicity and pathogenicity with the potential to be used in the identification of A. niger as a contaminant and cause of spoilage of Mangifera indica. Real-time polymerase chain reaction (RT-PCR) was used for the amplification of Asp n 3 gene. Two pairs of primers were designed: one for the amplification of the entire sequence and another one for the amplification of the most conserved region of this peroxisomal protein. The presence of A. niger was demonstrated by the early detection of the allergenic protein Asp n 3 coding gene, which could be considered a species-specific marker. The use of primers designed based on the conserved region of the Asp n 3 encoding gene allowed us to identify the presence of the closely related fungal species Aspergillus fumigatus by detecting Asp n 3 homologous protein, which can be cross-reactive. The use of conserved segments of the Asp n 3 gene or its entire sequence allows us to detect phylogenetically closely related species within the Aspergilaceae family or to identify species-specific contaminating fungi. Frontiers Media S.A. 2021-06-28 /pmc/articles/PMC8273346/ /pubmed/34262539 http://dx.doi.org/10.3389/fmicb.2021.663323 Text en Copyright © 2021 Martínez, Nevado, Suñén, Gabriel, Vélez-del-Burgo, Sánchez and Postigo. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Martínez, Jorge
Nevado, Ander
Suñén, Ester
Gabriel, Marta
Vélez-del-Burgo, Ainara
Sánchez, Patricia
Postigo, Idoia
The Aspergillus niger Major Allergen (Asp n 3) DNA-Specific Sequence Is a Reliable Marker to Identify Early Fungal Contamination and Postharvest Damage in Mangifera indica Fruit
title The Aspergillus niger Major Allergen (Asp n 3) DNA-Specific Sequence Is a Reliable Marker to Identify Early Fungal Contamination and Postharvest Damage in Mangifera indica Fruit
title_full The Aspergillus niger Major Allergen (Asp n 3) DNA-Specific Sequence Is a Reliable Marker to Identify Early Fungal Contamination and Postharvest Damage in Mangifera indica Fruit
title_fullStr The Aspergillus niger Major Allergen (Asp n 3) DNA-Specific Sequence Is a Reliable Marker to Identify Early Fungal Contamination and Postharvest Damage in Mangifera indica Fruit
title_full_unstemmed The Aspergillus niger Major Allergen (Asp n 3) DNA-Specific Sequence Is a Reliable Marker to Identify Early Fungal Contamination and Postharvest Damage in Mangifera indica Fruit
title_short The Aspergillus niger Major Allergen (Asp n 3) DNA-Specific Sequence Is a Reliable Marker to Identify Early Fungal Contamination and Postharvest Damage in Mangifera indica Fruit
title_sort aspergillus niger major allergen (asp n 3) dna-specific sequence is a reliable marker to identify early fungal contamination and postharvest damage in mangifera indica fruit
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273346/
https://www.ncbi.nlm.nih.gov/pubmed/34262539
http://dx.doi.org/10.3389/fmicb.2021.663323
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