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Cross-species transcriptomics identifies core regulatory changes differentiating the asymptomatic asexual and virulent sexual life cycles of grass-symbiotic Epichloë fungi

Fungi from the genus Epichloë form systemic endobiotic infections of cool season grasses, producing a range of host-protective natural products in return for access to nutrients. These infections are asymptomatic during vegetative host growth, with associations between asexual Epichloë spp. and thei...

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Autores principales: Berry, Daniel, Lee, Kate, Winter, David, Mace, Wade, Becker, Yvonne, Nagabhyru, Padmaja, Treindl, Artemis D, Bogantes, Esteban Valverde, Young, Carolyn A, Leuchtmann, Adrian, Johnson, Linda J, Johnson, Richard D, Cox, Murray P, Schardl, Christopher L, Scott, Barry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8982410/
https://www.ncbi.nlm.nih.gov/pubmed/35191483
http://dx.doi.org/10.1093/g3journal/jkac043
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author Berry, Daniel
Lee, Kate
Winter, David
Mace, Wade
Becker, Yvonne
Nagabhyru, Padmaja
Treindl, Artemis D
Bogantes, Esteban Valverde
Young, Carolyn A
Leuchtmann, Adrian
Johnson, Linda J
Johnson, Richard D
Cox, Murray P
Schardl, Christopher L
Scott, Barry
author_facet Berry, Daniel
Lee, Kate
Winter, David
Mace, Wade
Becker, Yvonne
Nagabhyru, Padmaja
Treindl, Artemis D
Bogantes, Esteban Valverde
Young, Carolyn A
Leuchtmann, Adrian
Johnson, Linda J
Johnson, Richard D
Cox, Murray P
Schardl, Christopher L
Scott, Barry
author_sort Berry, Daniel
collection PubMed
description Fungi from the genus Epichloë form systemic endobiotic infections of cool season grasses, producing a range of host-protective natural products in return for access to nutrients. These infections are asymptomatic during vegetative host growth, with associations between asexual Epichloë spp. and their hosts considered mutualistic. However, the sexual cycle of Epichloë spp. involves virulent growth, characterized by the envelopment and sterilization of a developing host inflorescence by a dense sheath of mycelia known as a stroma. Microscopic analysis of stromata revealed a dramatic increase in hyphal propagation and host degradation compared with asymptomatic tissues. RNAseq was used to identify differentially expressed genes in asymptomatic vs stromatized tissues from 3 diverse Epichloë–host associations. Comparative analysis identified a core set of 135 differentially expressed genes that exhibited conserved transcriptional changes across all 3 associations. The core differentially expressed genes more strongly expressed during virulent growth encode proteins associated with host suppression, digestion, adaptation to the external environment, a biosynthetic gene cluster, and 5 transcription factors that may regulate Epichloë stroma formation. An additional 5 transcription factor encoding differentially expressed genes were suppressed during virulent growth, suggesting they regulate mutualistic processes. Expression of biosynthetic gene clusters for natural products that suppress herbivory was universally suppressed during virulent growth, and additional biosynthetic gene clusters that may encode production of novel host-protective natural products were identified. A comparative analysis of 26 Epichloë genomes found a general decrease in core differentially expressed gene conservation among asexual species, and a specific decrease in conservation for the biosynthetic gene cluster expressed during virulent growth and an unusual uncharacterized gene.
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spelling pubmed-89824102022-04-05 Cross-species transcriptomics identifies core regulatory changes differentiating the asymptomatic asexual and virulent sexual life cycles of grass-symbiotic Epichloë fungi Berry, Daniel Lee, Kate Winter, David Mace, Wade Becker, Yvonne Nagabhyru, Padmaja Treindl, Artemis D Bogantes, Esteban Valverde Young, Carolyn A Leuchtmann, Adrian Johnson, Linda J Johnson, Richard D Cox, Murray P Schardl, Christopher L Scott, Barry G3 (Bethesda) Investigation Fungi from the genus Epichloë form systemic endobiotic infections of cool season grasses, producing a range of host-protective natural products in return for access to nutrients. These infections are asymptomatic during vegetative host growth, with associations between asexual Epichloë spp. and their hosts considered mutualistic. However, the sexual cycle of Epichloë spp. involves virulent growth, characterized by the envelopment and sterilization of a developing host inflorescence by a dense sheath of mycelia known as a stroma. Microscopic analysis of stromata revealed a dramatic increase in hyphal propagation and host degradation compared with asymptomatic tissues. RNAseq was used to identify differentially expressed genes in asymptomatic vs stromatized tissues from 3 diverse Epichloë–host associations. Comparative analysis identified a core set of 135 differentially expressed genes that exhibited conserved transcriptional changes across all 3 associations. The core differentially expressed genes more strongly expressed during virulent growth encode proteins associated with host suppression, digestion, adaptation to the external environment, a biosynthetic gene cluster, and 5 transcription factors that may regulate Epichloë stroma formation. An additional 5 transcription factor encoding differentially expressed genes were suppressed during virulent growth, suggesting they regulate mutualistic processes. Expression of biosynthetic gene clusters for natural products that suppress herbivory was universally suppressed during virulent growth, and additional biosynthetic gene clusters that may encode production of novel host-protective natural products were identified. A comparative analysis of 26 Epichloë genomes found a general decrease in core differentially expressed gene conservation among asexual species, and a specific decrease in conservation for the biosynthetic gene cluster expressed during virulent growth and an unusual uncharacterized gene. Oxford University Press 2022-02-22 /pmc/articles/PMC8982410/ /pubmed/35191483 http://dx.doi.org/10.1093/g3journal/jkac043 Text en © The Author(s) 2022. 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 Investigation
Berry, Daniel
Lee, Kate
Winter, David
Mace, Wade
Becker, Yvonne
Nagabhyru, Padmaja
Treindl, Artemis D
Bogantes, Esteban Valverde
Young, Carolyn A
Leuchtmann, Adrian
Johnson, Linda J
Johnson, Richard D
Cox, Murray P
Schardl, Christopher L
Scott, Barry
Cross-species transcriptomics identifies core regulatory changes differentiating the asymptomatic asexual and virulent sexual life cycles of grass-symbiotic Epichloë fungi
title Cross-species transcriptomics identifies core regulatory changes differentiating the asymptomatic asexual and virulent sexual life cycles of grass-symbiotic Epichloë fungi
title_full Cross-species transcriptomics identifies core regulatory changes differentiating the asymptomatic asexual and virulent sexual life cycles of grass-symbiotic Epichloë fungi
title_fullStr Cross-species transcriptomics identifies core regulatory changes differentiating the asymptomatic asexual and virulent sexual life cycles of grass-symbiotic Epichloë fungi
title_full_unstemmed Cross-species transcriptomics identifies core regulatory changes differentiating the asymptomatic asexual and virulent sexual life cycles of grass-symbiotic Epichloë fungi
title_short Cross-species transcriptomics identifies core regulatory changes differentiating the asymptomatic asexual and virulent sexual life cycles of grass-symbiotic Epichloë fungi
title_sort cross-species transcriptomics identifies core regulatory changes differentiating the asymptomatic asexual and virulent sexual life cycles of grass-symbiotic epichloë fungi
topic Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8982410/
https://www.ncbi.nlm.nih.gov/pubmed/35191483
http://dx.doi.org/10.1093/g3journal/jkac043
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