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Comparing genotype and chemotype of Fusarium graminearum from cereals in Ontario, Canada
Fusarium graminearum is responsible for production of the mycotoxin deoxynivalenol (DON) on maize and wheat in Ontario, Canada. It has been understood since the early 1980s that in most parts of Canada, the predominant chemotype of F. graminearum is 15ADON, and not the 3ADON chemotype mainly found i...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6508712/ https://www.ncbi.nlm.nih.gov/pubmed/31071188 http://dx.doi.org/10.1371/journal.pone.0216735 |
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author | Crippin, Trinda Renaud, Justin B. Sumarah, Mark W. Miller, J. David |
author_facet | Crippin, Trinda Renaud, Justin B. Sumarah, Mark W. Miller, J. David |
author_sort | Crippin, Trinda |
collection | PubMed |
description | Fusarium graminearum is responsible for production of the mycotoxin deoxynivalenol (DON) on maize and wheat in Ontario, Canada. It has been understood since the early 1980s that in most parts of Canada, the predominant chemotype of F. graminearum is 15ADON, and not the 3ADON chemotype mainly found in Europe and Asia. The discovery of F. graminearum strains that did not produce DON but the structurally related 7-α hydroxy, 15-deacetylcalonectrin (3ANX) and its hydrolysis product 7-α hydroxy, 3,15-dideacetylcalonectrin to (NX) demonstrated that we still have a lot to learn about this well studied but complicated fungus. We conducted a survey of maize and wheat samples from Ontario farms. In the 2015 crop year, we isolated 86 strains and tested a representative subset of 20 using the published genetic probes for assessing genotype. We also developed a targeted LC-MS/MS method for the identification and quantitation of known toxins from this species to determine chemotype. The results showed that 80% of our strains produced some 3ANX in addition to 15ADON and one strain produced 3ANX and no 15ADON. Comparison of chemical data with genotyping revealed that in more than 50% of the cases there was no clear agreement. These data demonstrate the importance of chemical analysis for understanding the toxigenic potential of strains, especially using a LC-MS method that is capable of differentiating 3ADON and 15ADON. For this collection, genotyping of isolates did not produce reliable information on the chemotype. This is the first report of 3ANX toxin production concurrently with 15ADON and suggests that the 3ANX producers in North America likely originated from the 15ADON background. |
format | Online Article Text |
id | pubmed-6508712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-65087122019-05-23 Comparing genotype and chemotype of Fusarium graminearum from cereals in Ontario, Canada Crippin, Trinda Renaud, Justin B. Sumarah, Mark W. Miller, J. David PLoS One Research Article Fusarium graminearum is responsible for production of the mycotoxin deoxynivalenol (DON) on maize and wheat in Ontario, Canada. It has been understood since the early 1980s that in most parts of Canada, the predominant chemotype of F. graminearum is 15ADON, and not the 3ADON chemotype mainly found in Europe and Asia. The discovery of F. graminearum strains that did not produce DON but the structurally related 7-α hydroxy, 15-deacetylcalonectrin (3ANX) and its hydrolysis product 7-α hydroxy, 3,15-dideacetylcalonectrin to (NX) demonstrated that we still have a lot to learn about this well studied but complicated fungus. We conducted a survey of maize and wheat samples from Ontario farms. In the 2015 crop year, we isolated 86 strains and tested a representative subset of 20 using the published genetic probes for assessing genotype. We also developed a targeted LC-MS/MS method for the identification and quantitation of known toxins from this species to determine chemotype. The results showed that 80% of our strains produced some 3ANX in addition to 15ADON and one strain produced 3ANX and no 15ADON. Comparison of chemical data with genotyping revealed that in more than 50% of the cases there was no clear agreement. These data demonstrate the importance of chemical analysis for understanding the toxigenic potential of strains, especially using a LC-MS method that is capable of differentiating 3ADON and 15ADON. For this collection, genotyping of isolates did not produce reliable information on the chemotype. This is the first report of 3ANX toxin production concurrently with 15ADON and suggests that the 3ANX producers in North America likely originated from the 15ADON background. Public Library of Science 2019-05-09 /pmc/articles/PMC6508712/ /pubmed/31071188 http://dx.doi.org/10.1371/journal.pone.0216735 Text en © 2019 Crippin et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Crippin, Trinda Renaud, Justin B. Sumarah, Mark W. Miller, J. David Comparing genotype and chemotype of Fusarium graminearum from cereals in Ontario, Canada |
title | Comparing genotype and chemotype of Fusarium graminearum from cereals in Ontario, Canada |
title_full | Comparing genotype and chemotype of Fusarium graminearum from cereals in Ontario, Canada |
title_fullStr | Comparing genotype and chemotype of Fusarium graminearum from cereals in Ontario, Canada |
title_full_unstemmed | Comparing genotype and chemotype of Fusarium graminearum from cereals in Ontario, Canada |
title_short | Comparing genotype and chemotype of Fusarium graminearum from cereals in Ontario, Canada |
title_sort | comparing genotype and chemotype of fusarium graminearum from cereals in ontario, canada |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6508712/ https://www.ncbi.nlm.nih.gov/pubmed/31071188 http://dx.doi.org/10.1371/journal.pone.0216735 |
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