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Phenylpyrroles: 30 Years, Two Molecules and (Nearly) No Resistance
Phenylpyrroles are chemical analogs of the natural antifungal compound pyrrolnitrin. Fenpiclonil, but mainly fludioxonil are registered against multiple fungal crop diseases since over 25 years for seed or foliar treatment. They have severe physiological impacts on the pathogen, including membrane h...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5159414/ https://www.ncbi.nlm.nih.gov/pubmed/28018333 http://dx.doi.org/10.3389/fmicb.2016.02014 |
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author | Kilani, Jaafar Fillinger, Sabine |
author_facet | Kilani, Jaafar Fillinger, Sabine |
author_sort | Kilani, Jaafar |
collection | PubMed |
description | Phenylpyrroles are chemical analogs of the natural antifungal compound pyrrolnitrin. Fenpiclonil, but mainly fludioxonil are registered against multiple fungal crop diseases since over 25 years for seed or foliar treatment. They have severe physiological impacts on the pathogen, including membrane hyperpolarization, changes in carbon metabolism and the accumulation of metabolites leading to hyphal swelling and burst. The selection and characterization of mutants resistant to phenylpyrroles have revealed that these fungicides activate the fungal osmotic signal transduction pathway through their perception by a typical fungal hybrid histidine kinase (HHK). The HHK is prone to point mutations that confer fungicide resistance and affect its sensor domain, composed of tandem repeats of HAMP motifs. Fludioxonil resistant mutants have been selected in many fungal species under laboratory conditions. Generally they present severe impacts on fitness parameters. Since only few cases of field resistance specific to phenylpyrroles have been reported one may suspect that the fitness penalty of phenylpyrrole resistance is the reason for the lack of field resistance. |
format | Online Article Text |
id | pubmed-5159414 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-51594142016-12-23 Phenylpyrroles: 30 Years, Two Molecules and (Nearly) No Resistance Kilani, Jaafar Fillinger, Sabine Front Microbiol Microbiology Phenylpyrroles are chemical analogs of the natural antifungal compound pyrrolnitrin. Fenpiclonil, but mainly fludioxonil are registered against multiple fungal crop diseases since over 25 years for seed or foliar treatment. They have severe physiological impacts on the pathogen, including membrane hyperpolarization, changes in carbon metabolism and the accumulation of metabolites leading to hyphal swelling and burst. The selection and characterization of mutants resistant to phenylpyrroles have revealed that these fungicides activate the fungal osmotic signal transduction pathway through their perception by a typical fungal hybrid histidine kinase (HHK). The HHK is prone to point mutations that confer fungicide resistance and affect its sensor domain, composed of tandem repeats of HAMP motifs. Fludioxonil resistant mutants have been selected in many fungal species under laboratory conditions. Generally they present severe impacts on fitness parameters. Since only few cases of field resistance specific to phenylpyrroles have been reported one may suspect that the fitness penalty of phenylpyrrole resistance is the reason for the lack of field resistance. Frontiers Media S.A. 2016-12-16 /pmc/articles/PMC5159414/ /pubmed/28018333 http://dx.doi.org/10.3389/fmicb.2016.02014 Text en Copyright © 2016 Kilani and Fillinger. http://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) or licensor 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 Kilani, Jaafar Fillinger, Sabine Phenylpyrroles: 30 Years, Two Molecules and (Nearly) No Resistance |
title | Phenylpyrroles: 30 Years, Two Molecules and (Nearly) No Resistance |
title_full | Phenylpyrroles: 30 Years, Two Molecules and (Nearly) No Resistance |
title_fullStr | Phenylpyrroles: 30 Years, Two Molecules and (Nearly) No Resistance |
title_full_unstemmed | Phenylpyrroles: 30 Years, Two Molecules and (Nearly) No Resistance |
title_short | Phenylpyrroles: 30 Years, Two Molecules and (Nearly) No Resistance |
title_sort | phenylpyrroles: 30 years, two molecules and (nearly) no resistance |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5159414/ https://www.ncbi.nlm.nih.gov/pubmed/28018333 http://dx.doi.org/10.3389/fmicb.2016.02014 |
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