Rafiatou Ba, B. Yehouenou, U. Hounguè, P. Agbangnan, P. Sessou, Nelly M.F. Monteiro, M. T. D. Hounsode, F. Gbaguidi, L. Baba-Moussa
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Results: Eleven (11) molds were isolated from the samples collected and three storage modes were observed. Fusarium sp, Penicillium sp and Aspergillus niger were the prevalent species with frequencies of 20.71%; 15.15% and 12.12%, respectively. Grain maize mode (55%) was the most used. Also the isolated molds have the ability to produce the toxins when the conditions are favorable. The identification of mycotoxins by Thin Layer Chromatography showed that the isolated and identified molds were producers of mycotoxins. A. parasiticus and A. flavus were not observed in technologies A and B in all the study areas. A. flavus, A. parasiticus, A. ochraceus, F. graminearum, F. oxysporum and P. roqueforti showed their ability to produce Aflatoxin B2, Aflatoxin G1, Ochratoxin A, Deoxynivalenol, moniliformin and Roquefortin C, respectively. Conclusion: These results clearly show an correlation between the technologies of storage and the contamination by the mycotoxins.","PeriodicalId":9269,"journal":{"name":"British microbiology research journal","volume":"15 1","pages":"1-10"},"PeriodicalIF":0.0000,"publicationDate":"2016-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Performance of Maize Storage Technologies in Benin: Fungal Ecology and Mycotoxin Contamination\",\"authors\":\"Rafiatou Ba, B. Yehouenou, U. Hounguè, P. Agbangnan, P. Sessou, Nelly M.F. Monteiro, M. T. D. Hounsode, F. Gbaguidi, L. Baba-Moussa\",\"doi\":\"10.9734/BMRJ/2016/26297\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Objectives: The present work was to study the fungal ecology of maize according to the various storage technologies and evaluate the ability of fungal isolates to produce mycotoxin. 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The identification of mycotoxins by Thin Layer Chromatography showed that the isolated and identified molds were producers of mycotoxins. A. parasiticus and A. flavus were not observed in technologies A and B in all the study areas. A. flavus, A. parasiticus, A. ochraceus, F. graminearum, F. oxysporum and P. roqueforti showed their ability to produce Aflatoxin B2, Aflatoxin G1, Ochratoxin A, Deoxynivalenol, moniliformin and Roquefortin C, respectively. 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引用次数: 1
摘要
目的:研究不同贮藏技术对玉米真菌生态的影响,评价不同贮藏条件下分离真菌产生霉菌毒素的能力。原研究论文Ba et al.;中国生物医学工程学报,2015 (1):1-10;文章no.BMRJ。26297材料与方法:在7个农业生态区选择A ~ G 7种玉米贮藏技术,收集198份玉米贮藏样品。在使用的所有类型的技术中,在所有预期的区域都观察到霉菌的存在。采用薄层色谱法对储藏玉米中分离的霉菌毒素进行了鉴定。结果:从采集的样品中分离出11株霉菌,并观察到3种储存方式。镰刀菌、青霉和黑曲霉是常见菌种,频率为20.71%;分别为15.15%和12.12%。以谷物玉米模式(55%)使用最多。此外,当条件有利时,分离的霉菌也有能力产生毒素。薄层色谱法对真菌毒素的鉴定表明,分离鉴定的霉菌是真菌毒素的产生菌。A、B技术在所有研究区均未发现寄生蜂和黄蚜。黄曲霉、寄生蜂、赭曲霉、禾草霉、尖孢霉和洛克福尔霉分别能产生黄曲霉毒素B2、黄曲霉毒素G1、赭曲霉毒素A、脱氧雪腐镰刀菌醇、moniliformin和洛克福尔素C。结论:真菌毒素污染与贮藏工艺有密切关系。
Performance of Maize Storage Technologies in Benin: Fungal Ecology and Mycotoxin Contamination
Objectives: The present work was to study the fungal ecology of maize according to the various storage technologies and evaluate the ability of fungal isolates to produce mycotoxin. Original Research Article Ba et al.; BMRJ, 15(1): 1-10, 2016; Article no.BMRJ.26297 2 Materials and Methods: Seven maize storage technologies (from A to G) were selected in seven agro-ecological zones and 198 samples of stored maize were collected based on storage technologies. The presence of mold was observed in all the areas prospected in all the type of technologies used. The identification of the mycotoxins produced by mildews isolated of the stored maize has been performed by Thin Layer Chromatography. Results: Eleven (11) molds were isolated from the samples collected and three storage modes were observed. Fusarium sp, Penicillium sp and Aspergillus niger were the prevalent species with frequencies of 20.71%; 15.15% and 12.12%, respectively. Grain maize mode (55%) was the most used. Also the isolated molds have the ability to produce the toxins when the conditions are favorable. The identification of mycotoxins by Thin Layer Chromatography showed that the isolated and identified molds were producers of mycotoxins. A. parasiticus and A. flavus were not observed in technologies A and B in all the study areas. A. flavus, A. parasiticus, A. ochraceus, F. graminearum, F. oxysporum and P. roqueforti showed their ability to produce Aflatoxin B2, Aflatoxin G1, Ochratoxin A, Deoxynivalenol, moniliformin and Roquefortin C, respectively. Conclusion: These results clearly show an correlation between the technologies of storage and the contamination by the mycotoxins.