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Genomic signatures and insights into host niche adaptation of the entomopathogenic fungus Metarhizium humberi

The genus Metarhizium is composed of species used in biological control programs of agricultural pests worldwide. This genus includes common fungal pathogen of many insects and mites and endophytes that can increase plant growth. Metarhizium humberi was recently described as a new species. This spec...

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Autores principales: Iwanicki, Natasha Sant′Anna, Botelho, Ana Beatriz Riguetti Zanardo, Klingen, Ingeborg, Júnior, Italo Delalibera, Rossmann, Simeon, Lysøe, Erik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9210286/
https://www.ncbi.nlm.nih.gov/pubmed/34865006
http://dx.doi.org/10.1093/g3journal/jkab416
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author Iwanicki, Natasha Sant′Anna
Botelho, Ana Beatriz Riguetti Zanardo
Klingen, Ingeborg
Júnior, Italo Delalibera
Rossmann, Simeon
Lysøe, Erik
author_facet Iwanicki, Natasha Sant′Anna
Botelho, Ana Beatriz Riguetti Zanardo
Klingen, Ingeborg
Júnior, Italo Delalibera
Rossmann, Simeon
Lysøe, Erik
author_sort Iwanicki, Natasha Sant′Anna
collection PubMed
description The genus Metarhizium is composed of species used in biological control programs of agricultural pests worldwide. This genus includes common fungal pathogen of many insects and mites and endophytes that can increase plant growth. Metarhizium humberi was recently described as a new species. This species is highly virulent against some insect pests and promotes growth in sugarcane, strawberry, and soybean crops. In this study, we sequenced the genome of M. humberi, isolate ESALQ1638, and performed a functional analysis to determine its genomic signatures and highlight the genes and biological processes associated with its lifestyle. The genome annotation predicted 10633 genes in M. humberi, of which 92.0% are assigned putative functions, and ∼17% of the genome was annotated as repetitive sequences. We found that 18.5% of the M. humberi genome is similar to experimentally validated proteins associated with pathogen–host interaction. Compared to the genomes of eight Metarhizium species, the M. humberi ESALQ1638 genome revealed some unique traits that stood out, e.g., more genes functionally annotated as polyketide synthases (PKSs), overrepresended GO-terms associated to transport of ions, organic and amino acid, a higher percentage of repetitive elements, and higher levels of RIP-induced point mutations. The M. humberi genome will serve as a resource for promoting studies on genome structure and evolution that can contribute to research on biological control and plant biostimulation. Thus, the genomic data supported the broad host range of this species within the generalist PARB clade and suggested that M. humberi ESALQ1638 might be particularly good at producing secondary metabolites and might be more efficient in transporting amino acids and organic compounds.
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spelling pubmed-92102862022-06-21 Genomic signatures and insights into host niche adaptation of the entomopathogenic fungus Metarhizium humberi Iwanicki, Natasha Sant′Anna Botelho, Ana Beatriz Riguetti Zanardo Klingen, Ingeborg Júnior, Italo Delalibera Rossmann, Simeon Lysøe, Erik G3 (Bethesda) Genome Report The genus Metarhizium is composed of species used in biological control programs of agricultural pests worldwide. This genus includes common fungal pathogen of many insects and mites and endophytes that can increase plant growth. Metarhizium humberi was recently described as a new species. This species is highly virulent against some insect pests and promotes growth in sugarcane, strawberry, and soybean crops. In this study, we sequenced the genome of M. humberi, isolate ESALQ1638, and performed a functional analysis to determine its genomic signatures and highlight the genes and biological processes associated with its lifestyle. The genome annotation predicted 10633 genes in M. humberi, of which 92.0% are assigned putative functions, and ∼17% of the genome was annotated as repetitive sequences. We found that 18.5% of the M. humberi genome is similar to experimentally validated proteins associated with pathogen–host interaction. Compared to the genomes of eight Metarhizium species, the M. humberi ESALQ1638 genome revealed some unique traits that stood out, e.g., more genes functionally annotated as polyketide synthases (PKSs), overrepresended GO-terms associated to transport of ions, organic and amino acid, a higher percentage of repetitive elements, and higher levels of RIP-induced point mutations. The M. humberi genome will serve as a resource for promoting studies on genome structure and evolution that can contribute to research on biological control and plant biostimulation. Thus, the genomic data supported the broad host range of this species within the generalist PARB clade and suggested that M. humberi ESALQ1638 might be particularly good at producing secondary metabolites and might be more efficient in transporting amino acids and organic compounds. Oxford University Press 2021-12-04 /pmc/articles/PMC9210286/ /pubmed/34865006 http://dx.doi.org/10.1093/g3journal/jkab416 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Genetics Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Genome Report
Iwanicki, Natasha Sant′Anna
Botelho, Ana Beatriz Riguetti Zanardo
Klingen, Ingeborg
Júnior, Italo Delalibera
Rossmann, Simeon
Lysøe, Erik
Genomic signatures and insights into host niche adaptation of the entomopathogenic fungus Metarhizium humberi
title Genomic signatures and insights into host niche adaptation of the entomopathogenic fungus Metarhizium humberi
title_full Genomic signatures and insights into host niche adaptation of the entomopathogenic fungus Metarhizium humberi
title_fullStr Genomic signatures and insights into host niche adaptation of the entomopathogenic fungus Metarhizium humberi
title_full_unstemmed Genomic signatures and insights into host niche adaptation of the entomopathogenic fungus Metarhizium humberi
title_short Genomic signatures and insights into host niche adaptation of the entomopathogenic fungus Metarhizium humberi
title_sort genomic signatures and insights into host niche adaptation of the entomopathogenic fungus metarhizium humberi
topic Genome Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9210286/
https://www.ncbi.nlm.nih.gov/pubmed/34865006
http://dx.doi.org/10.1093/g3journal/jkab416
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