A Phylogenetic Estimation of Trophic Transition Networks for Ascomycetous Fungi: Are Lichens Cradles of Symbiotrophic Fungal Diversification?

Fungi associated with photosynthetic organisms are major determinants of terrestrial biomass, nutrient cycling, and ecosystem productivity from the poles to the equator. Whereas most fungi are known because of their fruit bodies (e.g., saprotrophs), symptoms (e.g., pathogens), or emergent properties...

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Published in:Systematic Biology
Main Authors: Arnold, A. Elizabeth, Miadlikowska, Jolanta, Higgins, K. Lindsay, Sarvate, Snehal D., Gugger, Paul, Way, Amanda, Hofstetter, Valérie, Kauff, Frank, Lutzoni, François
Format: Text
Language:English
Published: Oxford University Press 2009
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Online Access:http://sysbio.oxfordjournals.org/cgi/content/short/syp001v1
https://doi.org/10.1093/sysbio/syp001
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spelling fthighwire:oai:open-archive.highwire.org:sysbio:syp001v1 2023-05-15T15:13:01+02:00 A Phylogenetic Estimation of Trophic Transition Networks for Ascomycetous Fungi: Are Lichens Cradles of Symbiotrophic Fungal Diversification? Arnold, A. Elizabeth Miadlikowska, Jolanta Higgins, K. Lindsay Sarvate, Snehal D. Gugger, Paul Way, Amanda Hofstetter, Valérie Kauff, Frank Lutzoni, François 2009-07-11 04:09:42.0 text/html http://sysbio.oxfordjournals.org/cgi/content/short/syp001v1 https://doi.org/10.1093/sysbio/syp001 en eng Oxford University Press http://sysbio.oxfordjournals.org/cgi/content/short/syp001v1 http://dx.doi.org/10.1093/sysbio/syp001 Copyright (C) 2009, Society of Systematic Biologists Article TEXT 2009 fthighwire https://doi.org/10.1093/sysbio/syp001 2015-03-01T00:33:20Z Fungi associated with photosynthetic organisms are major determinants of terrestrial biomass, nutrient cycling, and ecosystem productivity from the poles to the equator. Whereas most fungi are known because of their fruit bodies (e.g., saprotrophs), symptoms (e.g., pathogens), or emergent properties as symbionts (e.g., lichens), the majority of fungal diversity is thought to occur among species that rarely manifest their presence with visual cues on their substrate (e.g., the apparently hyperdiverse fungal endophytes associated with foliage of plants). Fungal endophytes are ubiquitous among all lineages of land plants and live within overtly healthy tissues without causing disease, but the evolutionary origins of these highly diverse symbionts have not been explored. Here, we show that a key to understanding both the evolution of endophytism and the diversification of the most species-rich phylum of Fungi (Ascomycota) lies in endophyte-like fungi that can be isolated from the interior of apparently healthy lichens. These “endolichenic” fungi are distinct from lichen mycobionts or any other previously recognized fungal associates of lichens, represent the same major lineages of Ascomycota as do endophytes, largely parallel the high diversity of endophytes from the arctic to the tropics, and preferentially associate with green algal photobionts in lichen thalli. Using phylogenetic analyses that incorporate these newly recovered fungi and ancestral state reconstructions that take into account phylogenetic uncertainty, we show that endolichenism is an incubator for the evolution of endophytism. In turn, endophytism is evolutionarily transient, with endophytic lineages frequently transitioning to and from pathogenicity. Although symbiotrophic lineages frequently give rise to free-living saprotrophs, reversions to symbiosis are rare. Together, these results provide the basis for estimating trophic transition networks in the Ascomycota and provide a first set of hypotheses regarding the evolution of symbiotrophy and ... Text Arctic HighWire Press (Stanford University) Arctic Systematic Biology 58 3 283 297
institution Open Polar
collection HighWire Press (Stanford University)
op_collection_id fthighwire
language English
topic Article
spellingShingle Article
Arnold, A. Elizabeth
Miadlikowska, Jolanta
Higgins, K. Lindsay
Sarvate, Snehal D.
Gugger, Paul
Way, Amanda
Hofstetter, Valérie
Kauff, Frank
Lutzoni, François
A Phylogenetic Estimation of Trophic Transition Networks for Ascomycetous Fungi: Are Lichens Cradles of Symbiotrophic Fungal Diversification?
topic_facet Article
description Fungi associated with photosynthetic organisms are major determinants of terrestrial biomass, nutrient cycling, and ecosystem productivity from the poles to the equator. Whereas most fungi are known because of their fruit bodies (e.g., saprotrophs), symptoms (e.g., pathogens), or emergent properties as symbionts (e.g., lichens), the majority of fungal diversity is thought to occur among species that rarely manifest their presence with visual cues on their substrate (e.g., the apparently hyperdiverse fungal endophytes associated with foliage of plants). Fungal endophytes are ubiquitous among all lineages of land plants and live within overtly healthy tissues without causing disease, but the evolutionary origins of these highly diverse symbionts have not been explored. Here, we show that a key to understanding both the evolution of endophytism and the diversification of the most species-rich phylum of Fungi (Ascomycota) lies in endophyte-like fungi that can be isolated from the interior of apparently healthy lichens. These “endolichenic” fungi are distinct from lichen mycobionts or any other previously recognized fungal associates of lichens, represent the same major lineages of Ascomycota as do endophytes, largely parallel the high diversity of endophytes from the arctic to the tropics, and preferentially associate with green algal photobionts in lichen thalli. Using phylogenetic analyses that incorporate these newly recovered fungi and ancestral state reconstructions that take into account phylogenetic uncertainty, we show that endolichenism is an incubator for the evolution of endophytism. In turn, endophytism is evolutionarily transient, with endophytic lineages frequently transitioning to and from pathogenicity. Although symbiotrophic lineages frequently give rise to free-living saprotrophs, reversions to symbiosis are rare. Together, these results provide the basis for estimating trophic transition networks in the Ascomycota and provide a first set of hypotheses regarding the evolution of symbiotrophy and ...
format Text
author Arnold, A. Elizabeth
Miadlikowska, Jolanta
Higgins, K. Lindsay
Sarvate, Snehal D.
Gugger, Paul
Way, Amanda
Hofstetter, Valérie
Kauff, Frank
Lutzoni, François
author_facet Arnold, A. Elizabeth
Miadlikowska, Jolanta
Higgins, K. Lindsay
Sarvate, Snehal D.
Gugger, Paul
Way, Amanda
Hofstetter, Valérie
Kauff, Frank
Lutzoni, François
author_sort Arnold, A. Elizabeth
title A Phylogenetic Estimation of Trophic Transition Networks for Ascomycetous Fungi: Are Lichens Cradles of Symbiotrophic Fungal Diversification?
title_short A Phylogenetic Estimation of Trophic Transition Networks for Ascomycetous Fungi: Are Lichens Cradles of Symbiotrophic Fungal Diversification?
title_full A Phylogenetic Estimation of Trophic Transition Networks for Ascomycetous Fungi: Are Lichens Cradles of Symbiotrophic Fungal Diversification?
title_fullStr A Phylogenetic Estimation of Trophic Transition Networks for Ascomycetous Fungi: Are Lichens Cradles of Symbiotrophic Fungal Diversification?
title_full_unstemmed A Phylogenetic Estimation of Trophic Transition Networks for Ascomycetous Fungi: Are Lichens Cradles of Symbiotrophic Fungal Diversification?
title_sort phylogenetic estimation of trophic transition networks for ascomycetous fungi: are lichens cradles of symbiotrophic fungal diversification?
publisher Oxford University Press
publishDate 2009
url http://sysbio.oxfordjournals.org/cgi/content/short/syp001v1
https://doi.org/10.1093/sysbio/syp001
geographic Arctic
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genre Arctic
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op_relation http://sysbio.oxfordjournals.org/cgi/content/short/syp001v1
http://dx.doi.org/10.1093/sysbio/syp001
op_rights Copyright (C) 2009, Society of Systematic Biologists
op_doi https://doi.org/10.1093/sysbio/syp001
container_title Systematic Biology
container_volume 58
container_issue 3
container_start_page 283
op_container_end_page 297
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