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First genome-scale insights into the virulence of the snow mold causal fungus Microdochium nivale

Pink snow mold, caused by a phytopathogenic and psychrotolerant fungus, Microdochium nivale, is a severe disease of winter cereals and grasses that predominantly occurs under snow cover or shortly after its melt. Snow mold has significantly progressed during the past decade, often reaching epiphytot...

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Autores principales: Tsers, Ivan, Marenina, Ekaterina, Meshcherov, Azat, Petrova, Olga, Gogoleva, Olga, Tkachenko, Alexander, Gogoleva, Natalia, Gogolev, Yuri, Potapenko, Evgenii, Muraeva, Olga, Ponomareva, Mira, Korzun, Viktor, Gorshkov, Vladimir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9830731/
https://www.ncbi.nlm.nih.gov/pubmed/36627722
http://dx.doi.org/10.1186/s43008-022-00107-0
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author Tsers, Ivan
Marenina, Ekaterina
Meshcherov, Azat
Petrova, Olga
Gogoleva, Olga
Tkachenko, Alexander
Gogoleva, Natalia
Gogolev, Yuri
Potapenko, Evgenii
Muraeva, Olga
Ponomareva, Mira
Korzun, Viktor
Gorshkov, Vladimir
author_facet Tsers, Ivan
Marenina, Ekaterina
Meshcherov, Azat
Petrova, Olga
Gogoleva, Olga
Tkachenko, Alexander
Gogoleva, Natalia
Gogolev, Yuri
Potapenko, Evgenii
Muraeva, Olga
Ponomareva, Mira
Korzun, Viktor
Gorshkov, Vladimir
author_sort Tsers, Ivan
collection PubMed
description Pink snow mold, caused by a phytopathogenic and psychrotolerant fungus, Microdochium nivale, is a severe disease of winter cereals and grasses that predominantly occurs under snow cover or shortly after its melt. Snow mold has significantly progressed during the past decade, often reaching epiphytotic levels in northern countries and resulting in dramatic yield losses. In addition, M. nivale gradually adapts to a warmer climate, spreading to less snowy territories and causing different types of plant diseases throughout the growing period. Despite its great economic importance, M. nivale is poorly investigated; its genome has not been sequenced and its crucial virulence determinants have not been identified or even predicted. In our study, we applied a hybrid assembly based on Oxford Nanopore and Illumina reads to obtain the first genome sequence of M. nivale. 11,973 genes (including 11,789 protein-encoding genes) have been revealed in the genome assembly. To better understand the genetic potential of M. nivale and to obtain a convenient reference for transcriptomic studies on this species, the identified genes were annotated and split into hierarchical three-level functional categories. A file with functionally classified M. nivale genes is presented in our study for general use. M. nivale gene products that best meet the criteria for virulence factors have been identified. The genetic potential to synthesize human-dangerous mycotoxins (fumonisin, ochratoxin B, aflatoxin, and gliotoxin) has been revealed for M. nivale. The transcriptome analysis combined with the assays for extracellular enzymatic activities (conventional virulence factors of many phytopathogens) was carried out to assess the effect of host plant (rye) metabolites on the M. nivale phenotype. In addition to disclosing plant-metabolite-upregulated M. nivale functional gene groups (including those related to host plant protein destruction and amino acid metabolism, xenobiotic detoxication (including phytoalexins benzoxazinoids), cellulose destruction (cellulose monooxygenases), iron transport, etc.), the performed analysis pointed to a crucial role of host plant lipid destruction and fungal lipid metabolism modulation in plant-M. nivale interactions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s43008-022-00107-0.
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spelling pubmed-98307312023-01-11 First genome-scale insights into the virulence of the snow mold causal fungus Microdochium nivale Tsers, Ivan Marenina, Ekaterina Meshcherov, Azat Petrova, Olga Gogoleva, Olga Tkachenko, Alexander Gogoleva, Natalia Gogolev, Yuri Potapenko, Evgenii Muraeva, Olga Ponomareva, Mira Korzun, Viktor Gorshkov, Vladimir IMA Fungus Research Pink snow mold, caused by a phytopathogenic and psychrotolerant fungus, Microdochium nivale, is a severe disease of winter cereals and grasses that predominantly occurs under snow cover or shortly after its melt. Snow mold has significantly progressed during the past decade, often reaching epiphytotic levels in northern countries and resulting in dramatic yield losses. In addition, M. nivale gradually adapts to a warmer climate, spreading to less snowy territories and causing different types of plant diseases throughout the growing period. Despite its great economic importance, M. nivale is poorly investigated; its genome has not been sequenced and its crucial virulence determinants have not been identified or even predicted. In our study, we applied a hybrid assembly based on Oxford Nanopore and Illumina reads to obtain the first genome sequence of M. nivale. 11,973 genes (including 11,789 protein-encoding genes) have been revealed in the genome assembly. To better understand the genetic potential of M. nivale and to obtain a convenient reference for transcriptomic studies on this species, the identified genes were annotated and split into hierarchical three-level functional categories. A file with functionally classified M. nivale genes is presented in our study for general use. M. nivale gene products that best meet the criteria for virulence factors have been identified. The genetic potential to synthesize human-dangerous mycotoxins (fumonisin, ochratoxin B, aflatoxin, and gliotoxin) has been revealed for M. nivale. The transcriptome analysis combined with the assays for extracellular enzymatic activities (conventional virulence factors of many phytopathogens) was carried out to assess the effect of host plant (rye) metabolites on the M. nivale phenotype. In addition to disclosing plant-metabolite-upregulated M. nivale functional gene groups (including those related to host plant protein destruction and amino acid metabolism, xenobiotic detoxication (including phytoalexins benzoxazinoids), cellulose destruction (cellulose monooxygenases), iron transport, etc.), the performed analysis pointed to a crucial role of host plant lipid destruction and fungal lipid metabolism modulation in plant-M. nivale interactions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s43008-022-00107-0. BioMed Central 2023-01-10 /pmc/articles/PMC9830731/ /pubmed/36627722 http://dx.doi.org/10.1186/s43008-022-00107-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research
Tsers, Ivan
Marenina, Ekaterina
Meshcherov, Azat
Petrova, Olga
Gogoleva, Olga
Tkachenko, Alexander
Gogoleva, Natalia
Gogolev, Yuri
Potapenko, Evgenii
Muraeva, Olga
Ponomareva, Mira
Korzun, Viktor
Gorshkov, Vladimir
First genome-scale insights into the virulence of the snow mold causal fungus Microdochium nivale
title First genome-scale insights into the virulence of the snow mold causal fungus Microdochium nivale
title_full First genome-scale insights into the virulence of the snow mold causal fungus Microdochium nivale
title_fullStr First genome-scale insights into the virulence of the snow mold causal fungus Microdochium nivale
title_full_unstemmed First genome-scale insights into the virulence of the snow mold causal fungus Microdochium nivale
title_short First genome-scale insights into the virulence of the snow mold causal fungus Microdochium nivale
title_sort first genome-scale insights into the virulence of the snow mold causal fungus microdochium nivale
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9830731/
https://www.ncbi.nlm.nih.gov/pubmed/36627722
http://dx.doi.org/10.1186/s43008-022-00107-0
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