The Kynurenine 3-Monooxygenase Encoding Gene, BcKMO, Is Involved in the Growth, Development, and Pathogenicity of Botrytis cinerea

A pathogenic mutant, BCG183, was obtained by screening the T-DNA insertion library of Botrytis cinerea. A novel pathogenicity-related gene BcKMO, which encodes kynurenine 3-monooxygenase (KMO), was isolated and identified via thermal asymmetric interlaced PCR, bioinformatics analyses, and KMO activi...

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Main Authors: Kang Zhang, Xuemei Yuan, Jinping Zang, Min Wang, Fuxin Zhao, Peifen Li, Hongzhe Cao, Jianmin Han, Jihong Xing, Jingao Dong
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-05-01
Series:Frontiers in Microbiology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fmicb.2018.01039/full
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author Kang Zhang
Kang Zhang
Xuemei Yuan
Xuemei Yuan
Jinping Zang
Jinping Zang
Min Wang
Min Wang
Fuxin Zhao
Fuxin Zhao
Peifen Li
Peifen Li
Hongzhe Cao
Hongzhe Cao
Jianmin Han
Jianmin Han
Jihong Xing
Jihong Xing
Jingao Dong
Jingao Dong
author_facet Kang Zhang
Kang Zhang
Xuemei Yuan
Xuemei Yuan
Jinping Zang
Jinping Zang
Min Wang
Min Wang
Fuxin Zhao
Fuxin Zhao
Peifen Li
Peifen Li
Hongzhe Cao
Hongzhe Cao
Jianmin Han
Jianmin Han
Jihong Xing
Jihong Xing
Jingao Dong
Jingao Dong
author_sort Kang Zhang
collection DOAJ
description A pathogenic mutant, BCG183, was obtained by screening the T-DNA insertion library of Botrytis cinerea. A novel pathogenicity-related gene BcKMO, which encodes kynurenine 3-monooxygenase (KMO), was isolated and identified via thermal asymmetric interlaced PCR, bioinformatics analyses, and KMO activity measurement. The mutant BCG183 grew slowly, did not produce conidia and sclerotia, had slender hyphae, and presented enhanced pathogenicity. The phenotype and pathogenicity of the BcKMO-complementing mutant (BCG183/BcKMO) were similar to those of the wild-type (WT) strain. The activities of polymethylgalacturonase, polygalacturonase, and toxins were significantly higher, whereas acid production was significantly decreased in the mutant BCG183, when compared with those in the WT and BCG183/BcKMO. Moreover, the sensitivity of mutant BCG183 to NaCl and KCl was remarkably increased, whereas that to fluconazole, Congo Red, menadione, H2O2, and SQ22536 and U0126 [cAMP-dependent protein kinase (cAMP) and mitogen-activated protein kinase (MAPK) signaling pathways inhibitors, respectively] were significantly decreased compared with the other strains. Furthermore, the key genes involved in the cAMP and MAPK signaling pathways, Pka1, Pka2, PkaR, Bcg2, Bcg3, bmp1, and bmp3, were significantly upregulated or downregulated in the mutant BCG183. BcKMO expression levels were also upregulated or downregulated in the RNAi mutants of the key genes involved in the cAMP and MAPK signaling pathways. These findings indicated that BcKMO positively regulates growth and development, but negatively regulates pathogenicity of B. cinerea. Furthermore, BcKMO was found to be involved in controlling cell wall degrading enzymes activity, toxins activity, acid production, and cell wall integrity, and participate in cAMP and MAPK signaling pathways of B. cinerea.
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spelling doaj.art-2c3f1cf47c5149ac8c3def99696a2e6e2022-12-21T18:20:40ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2018-05-01910.3389/fmicb.2018.01039361386The Kynurenine 3-Monooxygenase Encoding Gene, BcKMO, Is Involved in the Growth, Development, and Pathogenicity of Botrytis cinereaKang Zhang0Kang Zhang1Xuemei Yuan2Xuemei Yuan3Jinping Zang4Jinping Zang5Min Wang6Min Wang7Fuxin Zhao8Fuxin Zhao9Peifen Li10Peifen Li11Hongzhe Cao12Hongzhe Cao13Jianmin Han14Jianmin Han15Jihong Xing16Jihong Xing17Jingao Dong18Jingao Dong19Key Laboratory of Hebei Province for Plant Physiology and Molecular Pathology, Hebei Agricultural University, Baoding, ChinaMycotoxin and Molecular Plant Pathology Laboratory, Hebei Agricultural University, Baoding, ChinaKey Laboratory of Hebei Province for Plant Physiology and Molecular Pathology, Hebei Agricultural University, Baoding, ChinaMycotoxin and Molecular Plant Pathology Laboratory, Hebei Agricultural University, Baoding, ChinaKey Laboratory of Hebei Province for Plant Physiology and Molecular Pathology, Hebei Agricultural University, Baoding, ChinaMycotoxin and Molecular Plant Pathology Laboratory, Hebei Agricultural University, Baoding, ChinaKey Laboratory of Hebei Province for Plant Physiology and Molecular Pathology, Hebei Agricultural University, Baoding, ChinaMycotoxin and Molecular Plant Pathology Laboratory, Hebei Agricultural University, Baoding, ChinaKey Laboratory of Hebei Province for Plant Physiology and Molecular Pathology, Hebei Agricultural University, Baoding, ChinaMycotoxin and Molecular Plant Pathology Laboratory, Hebei Agricultural University, Baoding, ChinaKey Laboratory of Hebei Province for Plant Physiology and Molecular Pathology, Hebei Agricultural University, Baoding, ChinaMycotoxin and Molecular Plant Pathology Laboratory, Hebei Agricultural University, Baoding, ChinaKey Laboratory of Hebei Province for Plant Physiology and Molecular Pathology, Hebei Agricultural University, Baoding, ChinaMycotoxin and Molecular Plant Pathology Laboratory, Hebei Agricultural University, Baoding, ChinaKey Laboratory of Hebei Province for Plant Physiology and Molecular Pathology, Hebei Agricultural University, Baoding, ChinaMycotoxin and Molecular Plant Pathology Laboratory, Hebei Agricultural University, Baoding, ChinaKey Laboratory of Hebei Province for Plant Physiology and Molecular Pathology, Hebei Agricultural University, Baoding, ChinaMycotoxin and Molecular Plant Pathology Laboratory, Hebei Agricultural University, Baoding, ChinaKey Laboratory of Hebei Province for Plant Physiology and Molecular Pathology, Hebei Agricultural University, Baoding, ChinaMycotoxin and Molecular Plant Pathology Laboratory, Hebei Agricultural University, Baoding, ChinaA pathogenic mutant, BCG183, was obtained by screening the T-DNA insertion library of Botrytis cinerea. A novel pathogenicity-related gene BcKMO, which encodes kynurenine 3-monooxygenase (KMO), was isolated and identified via thermal asymmetric interlaced PCR, bioinformatics analyses, and KMO activity measurement. The mutant BCG183 grew slowly, did not produce conidia and sclerotia, had slender hyphae, and presented enhanced pathogenicity. The phenotype and pathogenicity of the BcKMO-complementing mutant (BCG183/BcKMO) were similar to those of the wild-type (WT) strain. The activities of polymethylgalacturonase, polygalacturonase, and toxins were significantly higher, whereas acid production was significantly decreased in the mutant BCG183, when compared with those in the WT and BCG183/BcKMO. Moreover, the sensitivity of mutant BCG183 to NaCl and KCl was remarkably increased, whereas that to fluconazole, Congo Red, menadione, H2O2, and SQ22536 and U0126 [cAMP-dependent protein kinase (cAMP) and mitogen-activated protein kinase (MAPK) signaling pathways inhibitors, respectively] were significantly decreased compared with the other strains. Furthermore, the key genes involved in the cAMP and MAPK signaling pathways, Pka1, Pka2, PkaR, Bcg2, Bcg3, bmp1, and bmp3, were significantly upregulated or downregulated in the mutant BCG183. BcKMO expression levels were also upregulated or downregulated in the RNAi mutants of the key genes involved in the cAMP and MAPK signaling pathways. These findings indicated that BcKMO positively regulates growth and development, but negatively regulates pathogenicity of B. cinerea. Furthermore, BcKMO was found to be involved in controlling cell wall degrading enzymes activity, toxins activity, acid production, and cell wall integrity, and participate in cAMP and MAPK signaling pathways of B. cinerea.https://www.frontiersin.org/article/10.3389/fmicb.2018.01039/fullBotrytis cinereaBcKMOkynurenine 3-monooxygenasegrowthdevelopmentpathogenicity
spellingShingle Kang Zhang
Kang Zhang
Xuemei Yuan
Xuemei Yuan
Jinping Zang
Jinping Zang
Min Wang
Min Wang
Fuxin Zhao
Fuxin Zhao
Peifen Li
Peifen Li
Hongzhe Cao
Hongzhe Cao
Jianmin Han
Jianmin Han
Jihong Xing
Jihong Xing
Jingao Dong
Jingao Dong
The Kynurenine 3-Monooxygenase Encoding Gene, BcKMO, Is Involved in the Growth, Development, and Pathogenicity of Botrytis cinerea
Frontiers in Microbiology
Botrytis cinerea
BcKMO
kynurenine 3-monooxygenase
growth
development
pathogenicity
title The Kynurenine 3-Monooxygenase Encoding Gene, BcKMO, Is Involved in the Growth, Development, and Pathogenicity of Botrytis cinerea
title_full The Kynurenine 3-Monooxygenase Encoding Gene, BcKMO, Is Involved in the Growth, Development, and Pathogenicity of Botrytis cinerea
title_fullStr The Kynurenine 3-Monooxygenase Encoding Gene, BcKMO, Is Involved in the Growth, Development, and Pathogenicity of Botrytis cinerea
title_full_unstemmed The Kynurenine 3-Monooxygenase Encoding Gene, BcKMO, Is Involved in the Growth, Development, and Pathogenicity of Botrytis cinerea
title_short The Kynurenine 3-Monooxygenase Encoding Gene, BcKMO, Is Involved in the Growth, Development, and Pathogenicity of Botrytis cinerea
title_sort kynurenine 3 monooxygenase encoding gene bckmo is involved in the growth development and pathogenicity of botrytis cinerea
topic Botrytis cinerea
BcKMO
kynurenine 3-monooxygenase
growth
development
pathogenicity
url https://www.frontiersin.org/article/10.3389/fmicb.2018.01039/full
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