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A Putative Zn(2)Cys(6) Transcription Factor Is Associated With Isoprothiolane Resistance in Magnaporthe oryzae

Isoprothiolane (IPT), a systemic fungicide, has been applied to control rice blast since the 1970s. Although resistance to IPT has been observed, the mechanism of resistance still has not been fully elucidated. In this study, nucleotide polymorphisms were detected between two IPT-resistant mutants g...

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Autores principales: Wang, Zuo-Qian, Meng, Fan-Zhu, Zhang, Ming-Ming, Yin, Liang-Fen, Yin, Wei-Xiao, Lin, Yang, Hsiang, Tom, Peng, You-Liang, Wang, Zong-Hua, Luo, Chao-Xi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6220061/
https://www.ncbi.nlm.nih.gov/pubmed/30429837
http://dx.doi.org/10.3389/fmicb.2018.02608
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author Wang, Zuo-Qian
Meng, Fan-Zhu
Zhang, Ming-Ming
Yin, Liang-Fen
Yin, Wei-Xiao
Lin, Yang
Hsiang, Tom
Peng, You-Liang
Wang, Zong-Hua
Luo, Chao-Xi
author_facet Wang, Zuo-Qian
Meng, Fan-Zhu
Zhang, Ming-Ming
Yin, Liang-Fen
Yin, Wei-Xiao
Lin, Yang
Hsiang, Tom
Peng, You-Liang
Wang, Zong-Hua
Luo, Chao-Xi
author_sort Wang, Zuo-Qian
collection PubMed
description Isoprothiolane (IPT), a systemic fungicide, has been applied to control rice blast since the 1970s. Although resistance to IPT has been observed, the mechanism of resistance still has not been fully elucidated. In this study, nucleotide polymorphisms were detected between two IPT-resistant mutants generated in the lab, and their parental wild type isolates using a whole-genome sequencing approach. In the genomes of the two resistant mutants, single point mutations were identified in a gene encoding a Zn(2)Cys(6) transcription factor-like protein. Notably, either knocking out the gene or replacing the wild type allele with the mutant allele (R343W) in a wild type isolate resulted in resistance to IPT, indicating that the gene is associated with IPT resistance, and thus was designated as MoIRR (Magnaporthe oryzae isoprothiolane resistance related). Along with point mutations R343W in mutant 1a_mut, and R345C in 1c_mut, a 16 bp insertion in 6c_mut was also located in the Fungal_TF_MHR domain of MoIRR, revealing that this domain may be the core element for IPT resistance. In addition, IPT-resistant mutants and transformants showed cross-resistance with iprobenfos (IBP), which was consistent with previous observations. These results indicated that MoIRR is strongly connected to resistance to choline biosynthesis inhibitor (CBI), and further work should focus on investigating downstream effects of MoIRR.
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spelling pubmed-62200612018-11-14 A Putative Zn(2)Cys(6) Transcription Factor Is Associated With Isoprothiolane Resistance in Magnaporthe oryzae Wang, Zuo-Qian Meng, Fan-Zhu Zhang, Ming-Ming Yin, Liang-Fen Yin, Wei-Xiao Lin, Yang Hsiang, Tom Peng, You-Liang Wang, Zong-Hua Luo, Chao-Xi Front Microbiol Microbiology Isoprothiolane (IPT), a systemic fungicide, has been applied to control rice blast since the 1970s. Although resistance to IPT has been observed, the mechanism of resistance still has not been fully elucidated. In this study, nucleotide polymorphisms were detected between two IPT-resistant mutants generated in the lab, and their parental wild type isolates using a whole-genome sequencing approach. In the genomes of the two resistant mutants, single point mutations were identified in a gene encoding a Zn(2)Cys(6) transcription factor-like protein. Notably, either knocking out the gene or replacing the wild type allele with the mutant allele (R343W) in a wild type isolate resulted in resistance to IPT, indicating that the gene is associated with IPT resistance, and thus was designated as MoIRR (Magnaporthe oryzae isoprothiolane resistance related). Along with point mutations R343W in mutant 1a_mut, and R345C in 1c_mut, a 16 bp insertion in 6c_mut was also located in the Fungal_TF_MHR domain of MoIRR, revealing that this domain may be the core element for IPT resistance. In addition, IPT-resistant mutants and transformants showed cross-resistance with iprobenfos (IBP), which was consistent with previous observations. These results indicated that MoIRR is strongly connected to resistance to choline biosynthesis inhibitor (CBI), and further work should focus on investigating downstream effects of MoIRR. Frontiers Media S.A. 2018-10-31 /pmc/articles/PMC6220061/ /pubmed/30429837 http://dx.doi.org/10.3389/fmicb.2018.02608 Text en Copyright © 2018 Wang, Meng, Zhang, Yin, Yin, Lin, Hsiang, Peng, Wang and Luo. 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) and the copyright owner(s) 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
Wang, Zuo-Qian
Meng, Fan-Zhu
Zhang, Ming-Ming
Yin, Liang-Fen
Yin, Wei-Xiao
Lin, Yang
Hsiang, Tom
Peng, You-Liang
Wang, Zong-Hua
Luo, Chao-Xi
A Putative Zn(2)Cys(6) Transcription Factor Is Associated With Isoprothiolane Resistance in Magnaporthe oryzae
title A Putative Zn(2)Cys(6) Transcription Factor Is Associated With Isoprothiolane Resistance in Magnaporthe oryzae
title_full A Putative Zn(2)Cys(6) Transcription Factor Is Associated With Isoprothiolane Resistance in Magnaporthe oryzae
title_fullStr A Putative Zn(2)Cys(6) Transcription Factor Is Associated With Isoprothiolane Resistance in Magnaporthe oryzae
title_full_unstemmed A Putative Zn(2)Cys(6) Transcription Factor Is Associated With Isoprothiolane Resistance in Magnaporthe oryzae
title_short A Putative Zn(2)Cys(6) Transcription Factor Is Associated With Isoprothiolane Resistance in Magnaporthe oryzae
title_sort putative zn(2)cys(6) transcription factor is associated with isoprothiolane resistance in magnaporthe oryzae
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6220061/
https://www.ncbi.nlm.nih.gov/pubmed/30429837
http://dx.doi.org/10.3389/fmicb.2018.02608
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