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Epichloë seed transmission efficiency is influenced by plant defense response mechanisms

Asexual Epichloë are endophytic fungi that form mutualistic symbioses with cool-season grasses, conferring to their hosts protection against biotic and abiotic stresses. Symbioses are maintained between grass generations as hyphae are vertically transmitted from parent to progeny plants through seed...

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Autores principales: Zhang, Wei, Forester, Natasha T., Moon, Christina D., Maclean, Paul H., Gagic, Milan, Arojju, Sai Krishna, Card, Stuart D., Matthew, Cory, Johnson, Richard D., Johnson, Linda J., Faville, Marty J., Voisey, Christine R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635450/
https://www.ncbi.nlm.nih.gov/pubmed/36340377
http://dx.doi.org/10.3389/fpls.2022.1025698
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author Zhang, Wei
Forester, Natasha T.
Moon, Christina D.
Maclean, Paul H.
Gagic, Milan
Arojju, Sai Krishna
Card, Stuart D.
Matthew, Cory
Johnson, Richard D.
Johnson, Linda J.
Faville, Marty J.
Voisey, Christine R.
author_facet Zhang, Wei
Forester, Natasha T.
Moon, Christina D.
Maclean, Paul H.
Gagic, Milan
Arojju, Sai Krishna
Card, Stuart D.
Matthew, Cory
Johnson, Richard D.
Johnson, Linda J.
Faville, Marty J.
Voisey, Christine R.
author_sort Zhang, Wei
collection PubMed
description Asexual Epichloë are endophytic fungi that form mutualistic symbioses with cool-season grasses, conferring to their hosts protection against biotic and abiotic stresses. Symbioses are maintained between grass generations as hyphae are vertically transmitted from parent to progeny plants through seed. However, endophyte transmission to the seed is an imperfect process where not all seeds become infected. The mechanisms underpinning the varying efficiencies of seed transmission are poorly understood. Host gene expression in response to Epichloë sp. LpTG-3 strain AR37 was examined within inflorescence primordia and ovaries of high and low endophyte transmission genotypes within a single population of perennial ryegrass. A genome-wide association study was conducted to identify population-level single nucleotide polymorphisms (SNPs) and associated genes correlated with vertical transmission efficiency. For low transmitters of AR37, upregulation of perennial ryegrass receptor-like kinases and resistance genes, typically associated with phytopathogen detection, comprised the largest group of differentially expressed genes (DEGs) in both inflorescence primordia and ovaries. DEGs involved in signaling and plant defense responses, such as cell wall modification, secondary metabolism, and reactive oxygen activities were also abundant. Transmission-associated SNPs were associated with genes for which gene ontology analysis identified “response to fungus” as the most significantly enriched term. Moreover, endophyte biomass as measured by quantitative PCR of Epichloë non-ribosomal peptide synthetase genes, was significantly lower in reproductive tissues of low-transmission hosts compared to high-transmission hosts. Endophyte seed-transmission efficiency appears to be influenced primarily by plant defense responses which reduce endophyte colonization of host reproductive tissues.
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spelling pubmed-96354502022-11-05 Epichloë seed transmission efficiency is influenced by plant defense response mechanisms Zhang, Wei Forester, Natasha T. Moon, Christina D. Maclean, Paul H. Gagic, Milan Arojju, Sai Krishna Card, Stuart D. Matthew, Cory Johnson, Richard D. Johnson, Linda J. Faville, Marty J. Voisey, Christine R. Front Plant Sci Plant Science Asexual Epichloë are endophytic fungi that form mutualistic symbioses with cool-season grasses, conferring to their hosts protection against biotic and abiotic stresses. Symbioses are maintained between grass generations as hyphae are vertically transmitted from parent to progeny plants through seed. However, endophyte transmission to the seed is an imperfect process where not all seeds become infected. The mechanisms underpinning the varying efficiencies of seed transmission are poorly understood. Host gene expression in response to Epichloë sp. LpTG-3 strain AR37 was examined within inflorescence primordia and ovaries of high and low endophyte transmission genotypes within a single population of perennial ryegrass. A genome-wide association study was conducted to identify population-level single nucleotide polymorphisms (SNPs) and associated genes correlated with vertical transmission efficiency. For low transmitters of AR37, upregulation of perennial ryegrass receptor-like kinases and resistance genes, typically associated with phytopathogen detection, comprised the largest group of differentially expressed genes (DEGs) in both inflorescence primordia and ovaries. DEGs involved in signaling and plant defense responses, such as cell wall modification, secondary metabolism, and reactive oxygen activities were also abundant. Transmission-associated SNPs were associated with genes for which gene ontology analysis identified “response to fungus” as the most significantly enriched term. Moreover, endophyte biomass as measured by quantitative PCR of Epichloë non-ribosomal peptide synthetase genes, was significantly lower in reproductive tissues of low-transmission hosts compared to high-transmission hosts. Endophyte seed-transmission efficiency appears to be influenced primarily by plant defense responses which reduce endophyte colonization of host reproductive tissues. Frontiers Media S.A. 2022-10-21 /pmc/articles/PMC9635450/ /pubmed/36340377 http://dx.doi.org/10.3389/fpls.2022.1025698 Text en Copyright © 2022 Zhang, Forester, Moon, Maclean, Gagic, Arojju, Card, Matthew, Johnson, Johnson, Faville and Voisey https://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 Plant Science
Zhang, Wei
Forester, Natasha T.
Moon, Christina D.
Maclean, Paul H.
Gagic, Milan
Arojju, Sai Krishna
Card, Stuart D.
Matthew, Cory
Johnson, Richard D.
Johnson, Linda J.
Faville, Marty J.
Voisey, Christine R.
Epichloë seed transmission efficiency is influenced by plant defense response mechanisms
title Epichloë seed transmission efficiency is influenced by plant defense response mechanisms
title_full Epichloë seed transmission efficiency is influenced by plant defense response mechanisms
title_fullStr Epichloë seed transmission efficiency is influenced by plant defense response mechanisms
title_full_unstemmed Epichloë seed transmission efficiency is influenced by plant defense response mechanisms
title_short Epichloë seed transmission efficiency is influenced by plant defense response mechanisms
title_sort epichloë seed transmission efficiency is influenced by plant defense response mechanisms
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635450/
https://www.ncbi.nlm.nih.gov/pubmed/36340377
http://dx.doi.org/10.3389/fpls.2022.1025698
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