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dc.contributor.authorAdhikari, Bishwo Nen
dc.contributor.authorBandyopadhyay, Ranajiten
dc.contributor.authorCotty, Peter Jen
dc.date.accessioned2016-11-03T02:39:30Z
dc.date.available2016-11-03T02:39:30Z
dc.date.issued2016-12
dc.identifier.citationDegeneration of aflatoxin gene clusters in Aspergillus flavus from Africa and North America. 2016, 6 (1):62 AMB Expressen
dc.identifier.issn2191-0855
dc.identifier.pmid27576895
dc.identifier.doi10.1186/s13568-016-0228-6
dc.identifier.urihttp://hdl.handle.net/10150/621249
dc.description.abstractAspergillus flavus is the most common causal agent of aflatoxin contamination of food and feed. However, aflatoxin-producing potential varies widely among A. flavus genotypes with many producing no aflatoxins. Some non-aflatoxigenic genotypes are used as biocontrol agents to prevent contamination. Aflatoxin biosynthesis genes are tightly clustered in a highly conserved order. Gene deletions and presence of single nucleotide polymorphisms (SNPs) in aflatoxin biosynthesis genes are often associated with A. flavus inability to produce aflatoxins. In order to identify mechanisms of non-aflatoxigenicity in non-aflatoxigenic genotypes of value in aflatoxin biocontrol, complete cluster sequences of 35 A. flavus genotypes from Africa and North America were analyzed. Inability of some genotypes to produce aflatoxin resulted from deletion of biosynthesis genes. In other genotypes, non-aflatoxigenicity originated from SNP formation. The process of degeneration differed across the gene cluster; genes involved in early biosynthesis stages were more likely to be deleted while genes involved in later stages displayed high frequencies of SNPs. Comparative analyses of aflatoxin gene clusters provides insight into the diversity of mechanisms of non-aflatoxigenicity in A. flavus genotypes used as biological control agents. The sequences provide resources for both diagnosis of non-aflatoxigenicity and monitoring of biocontrol genotypes during biopesticide manufacture and in the environment.
dc.description.sponsorshipAgricultural Research Service, US Department of Agriculture, CRIS [5347-42000-019-00D]en
dc.language.isoenen
dc.publisherBioMed Central Ltden
dc.relation.urlhttp://link.springer.com/article/10.1186/s13568-016-0228-6en
dc.rights© 2016 The Author(s). This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/).en
dc.subjectAspergillus flavusen
dc.subjectAflatoxin gene clusteren
dc.subjectNon-aflatoxigenicen
dc.subjectCluster degenerationen
dc.subjectBiocontrolen
dc.subjectEvolutionen
dc.titleDegeneration of aflatoxin gene clusters in Aspergillus flavus from Africa and North America.en
dc.typeArticleen
dc.contributor.departmentUniv Arizona, USDA ARS, Sch Plant Scien
dc.identifier.journalAMB Expressen
dc.description.noteOpen access journal.en
dc.description.collectioninformationThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.en
dc.eprint.versionFinal published versionen
refterms.dateFOA2018-06-24T10:35:50Z
html.description.abstractAspergillus flavus is the most common causal agent of aflatoxin contamination of food and feed. However, aflatoxin-producing potential varies widely among A. flavus genotypes with many producing no aflatoxins. Some non-aflatoxigenic genotypes are used as biocontrol agents to prevent contamination. Aflatoxin biosynthesis genes are tightly clustered in a highly conserved order. Gene deletions and presence of single nucleotide polymorphisms (SNPs) in aflatoxin biosynthesis genes are often associated with A. flavus inability to produce aflatoxins. In order to identify mechanisms of non-aflatoxigenicity in non-aflatoxigenic genotypes of value in aflatoxin biocontrol, complete cluster sequences of 35 A. flavus genotypes from Africa and North America were analyzed. Inability of some genotypes to produce aflatoxin resulted from deletion of biosynthesis genes. In other genotypes, non-aflatoxigenicity originated from SNP formation. The process of degeneration differed across the gene cluster; genes involved in early biosynthesis stages were more likely to be deleted while genes involved in later stages displayed high frequencies of SNPs. Comparative analyses of aflatoxin gene clusters provides insight into the diversity of mechanisms of non-aflatoxigenicity in A. flavus genotypes used as biological control agents. The sequences provide resources for both diagnosis of non-aflatoxigenicity and monitoring of biocontrol genotypes during biopesticide manufacture and in the environment.


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