Identification of Sources of Resistance for Peanut Aspergillus flavus Colonization and Aflatoxin Contamination

Peanut aflatoxin contamination caused by Aspergillus flavus is a serious constraint for food safety and human health in Senegal. The present study aimed to identify sources of resistance for A. flavus colonization and aflatoxin contamination. Thus, seeds from 67 peanut genotypes were tested under la...

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Main Authors: Richard Moise Alansou Dieme, Issa Faye, Yedomon Ange Bovys Zoclanclounon, Daniel Fonceka, Ousmane Ndoye, Papa Madiallacke Diedhiou
Format: Article
Language:English
Published: Wiley 2018-01-01
Series:International Journal of Agronomy
Online Access:http://dx.doi.org/10.1155/2018/5468602
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author Richard Moise Alansou Dieme
Issa Faye
Yedomon Ange Bovys Zoclanclounon
Daniel Fonceka
Ousmane Ndoye
Papa Madiallacke Diedhiou
author_facet Richard Moise Alansou Dieme
Issa Faye
Yedomon Ange Bovys Zoclanclounon
Daniel Fonceka
Ousmane Ndoye
Papa Madiallacke Diedhiou
author_sort Richard Moise Alansou Dieme
collection DOAJ
description Peanut aflatoxin contamination caused by Aspergillus flavus is a serious constraint for food safety and human health in Senegal. The present study aimed to identify sources of resistance for A. flavus colonization and aflatoxin contamination. Thus, seeds from 67 peanut genotypes were tested under laboratory conditions. Aqueous conidial suspension of an aflatoxinogenic strain of A. flavus was used for inoculation in Petri dishes containing ten seeds of each genotype, and data on incidence and severity were recorded. Total aflatoxin concentration in seeds was determined on 15th day after inoculation using mReader® method. Results showed a significant (p<0.001) variation of aflatoxin, incidence and severity among the tested peanut genotypes. Incidence ranged from 0 to 70% with a mean of 20.36 ± 0.8%. Out of the 67 genotypes, eight showed incidence less than 10%. Severity ranged from 0 to 44% with a mean value of 8.82 ± 0.45%. The genotype 12CS_104 showed aflatoxin concentration level in conformity with the European standard (4 ppb). Out of three clusters revealed by hierarchical classification based on disease incidence and severity, the cluster 1 contained 33 genotypes characterised by low incidence and severity values. These genotypes can be tested under field conditions to confirm their resistance to A flavus.
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spelling doaj-art-da8f0bdb90fe47d9b0625c4bd4c689c52025-02-03T05:58:25ZengWileyInternational Journal of Agronomy1687-81591687-81672018-01-01201810.1155/2018/54686025468602Identification of Sources of Resistance for Peanut Aspergillus flavus Colonization and Aflatoxin ContaminationRichard Moise Alansou Dieme0Issa Faye1Yedomon Ange Bovys Zoclanclounon2Daniel Fonceka3Ousmane Ndoye4Papa Madiallacke Diedhiou5Université Gaston Berger, BP 211 Saint-Louis, SenegalCentre National de Recherches Agronomiques de Bambey, Institut Sénégalais de Recherches Agricoles, BP 211 Bambey, SenegalCentre d’Etudes Régional pour l’Amélioration de l’Adaptation à la Sécheresse, Route de Khombole, BP 3320 Thiès, SenegalCentre d’Etudes Régional pour l’Amélioration de l’Adaptation à la Sécheresse, Route de Khombole, BP 3320 Thiès, SenegalConseil Ouest et centre Africain pour la Recherche et le Développement Agricoles, Avenue Bourguiba, BP 48 Dakar RP, SenegalUniversité Gaston Berger, BP 211 Saint-Louis, SenegalPeanut aflatoxin contamination caused by Aspergillus flavus is a serious constraint for food safety and human health in Senegal. The present study aimed to identify sources of resistance for A. flavus colonization and aflatoxin contamination. Thus, seeds from 67 peanut genotypes were tested under laboratory conditions. Aqueous conidial suspension of an aflatoxinogenic strain of A. flavus was used for inoculation in Petri dishes containing ten seeds of each genotype, and data on incidence and severity were recorded. Total aflatoxin concentration in seeds was determined on 15th day after inoculation using mReader® method. Results showed a significant (p<0.001) variation of aflatoxin, incidence and severity among the tested peanut genotypes. Incidence ranged from 0 to 70% with a mean of 20.36 ± 0.8%. Out of the 67 genotypes, eight showed incidence less than 10%. Severity ranged from 0 to 44% with a mean value of 8.82 ± 0.45%. The genotype 12CS_104 showed aflatoxin concentration level in conformity with the European standard (4 ppb). Out of three clusters revealed by hierarchical classification based on disease incidence and severity, the cluster 1 contained 33 genotypes characterised by low incidence and severity values. These genotypes can be tested under field conditions to confirm their resistance to A flavus.http://dx.doi.org/10.1155/2018/5468602
spellingShingle Richard Moise Alansou Dieme
Issa Faye
Yedomon Ange Bovys Zoclanclounon
Daniel Fonceka
Ousmane Ndoye
Papa Madiallacke Diedhiou
Identification of Sources of Resistance for Peanut Aspergillus flavus Colonization and Aflatoxin Contamination
International Journal of Agronomy
title Identification of Sources of Resistance for Peanut Aspergillus flavus Colonization and Aflatoxin Contamination
title_full Identification of Sources of Resistance for Peanut Aspergillus flavus Colonization and Aflatoxin Contamination
title_fullStr Identification of Sources of Resistance for Peanut Aspergillus flavus Colonization and Aflatoxin Contamination
title_full_unstemmed Identification of Sources of Resistance for Peanut Aspergillus flavus Colonization and Aflatoxin Contamination
title_short Identification of Sources of Resistance for Peanut Aspergillus flavus Colonization and Aflatoxin Contamination
title_sort identification of sources of resistance for peanut aspergillus flavus colonization and aflatoxin contamination
url http://dx.doi.org/10.1155/2018/5468602
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