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Phylogenetic Revision and Patterns of Host Specificity in the Fungal Subphylum Entomophthoromycotina

The Entomophthoromycotina, a subphylum close to the root of terrestrial fungi with a bias toward insects as their primary hosts, has been notoriously difficult to categorize taxonomically for decades. Here, we reassess the phylogeny of this group based on conserved genes encoding ribosomal RNA and R...

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Autores principales: Möckel, Lars, Meusemann, Karen, Misof, Bernhard, Schwartze, Volker U., De Fine Licht, Henrik H., Voigt, Kerstin, Stielow, Benjamin, de Hoog, Sybren, Beutel, Rolf G., Buellesbach, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879804/
https://www.ncbi.nlm.nih.gov/pubmed/35208711
http://dx.doi.org/10.3390/microorganisms10020256
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author Möckel, Lars
Meusemann, Karen
Misof, Bernhard
Schwartze, Volker U.
De Fine Licht, Henrik H.
Voigt, Kerstin
Stielow, Benjamin
de Hoog, Sybren
Beutel, Rolf G.
Buellesbach, Jan
author_facet Möckel, Lars
Meusemann, Karen
Misof, Bernhard
Schwartze, Volker U.
De Fine Licht, Henrik H.
Voigt, Kerstin
Stielow, Benjamin
de Hoog, Sybren
Beutel, Rolf G.
Buellesbach, Jan
author_sort Möckel, Lars
collection PubMed
description The Entomophthoromycotina, a subphylum close to the root of terrestrial fungi with a bias toward insects as their primary hosts, has been notoriously difficult to categorize taxonomically for decades. Here, we reassess the phylogeny of this group based on conserved genes encoding ribosomal RNA and RNA polymerase II subunits, confirming their general monophyly, but challenging previously assumed taxonomic relationships within and between particular clades. Furthermore, for the prominent, partially human-pathogenic taxon Conidiobolus, a new type species C. coronatus is proposed in order to compensate for the unclear, presumably lost previous type species C. utriculosus Brefeld 1884. We also performed an exhaustive survey of the broad host spectrum of the Entomophthoromycotina, which is not restricted to insects alone, and investigated potential patterns of co-evolution across their megadiverse host range. Our results suggest multiple independent origins of parasitism within this subphylum and no apparent co-evolutionary events with any particular host lineage. However, Pterygota (i.e., winged insects) clearly constitute the most dominantly parasitized superordinate host group. This appears to be in accordance with an increased dispersal capacity mediated by the radiation of the Pterygota during insect evolution, which has likely greatly facilitated the spread, infection opportunities, and evolutionary divergence of the Entomophthoromycotina as well.
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spelling pubmed-88798042022-02-26 Phylogenetic Revision and Patterns of Host Specificity in the Fungal Subphylum Entomophthoromycotina Möckel, Lars Meusemann, Karen Misof, Bernhard Schwartze, Volker U. De Fine Licht, Henrik H. Voigt, Kerstin Stielow, Benjamin de Hoog, Sybren Beutel, Rolf G. Buellesbach, Jan Microorganisms Article The Entomophthoromycotina, a subphylum close to the root of terrestrial fungi with a bias toward insects as their primary hosts, has been notoriously difficult to categorize taxonomically for decades. Here, we reassess the phylogeny of this group based on conserved genes encoding ribosomal RNA and RNA polymerase II subunits, confirming their general monophyly, but challenging previously assumed taxonomic relationships within and between particular clades. Furthermore, for the prominent, partially human-pathogenic taxon Conidiobolus, a new type species C. coronatus is proposed in order to compensate for the unclear, presumably lost previous type species C. utriculosus Brefeld 1884. We also performed an exhaustive survey of the broad host spectrum of the Entomophthoromycotina, which is not restricted to insects alone, and investigated potential patterns of co-evolution across their megadiverse host range. Our results suggest multiple independent origins of parasitism within this subphylum and no apparent co-evolutionary events with any particular host lineage. However, Pterygota (i.e., winged insects) clearly constitute the most dominantly parasitized superordinate host group. This appears to be in accordance with an increased dispersal capacity mediated by the radiation of the Pterygota during insect evolution, which has likely greatly facilitated the spread, infection opportunities, and evolutionary divergence of the Entomophthoromycotina as well. MDPI 2022-01-24 /pmc/articles/PMC8879804/ /pubmed/35208711 http://dx.doi.org/10.3390/microorganisms10020256 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Möckel, Lars
Meusemann, Karen
Misof, Bernhard
Schwartze, Volker U.
De Fine Licht, Henrik H.
Voigt, Kerstin
Stielow, Benjamin
de Hoog, Sybren
Beutel, Rolf G.
Buellesbach, Jan
Phylogenetic Revision and Patterns of Host Specificity in the Fungal Subphylum Entomophthoromycotina
title Phylogenetic Revision and Patterns of Host Specificity in the Fungal Subphylum Entomophthoromycotina
title_full Phylogenetic Revision and Patterns of Host Specificity in the Fungal Subphylum Entomophthoromycotina
title_fullStr Phylogenetic Revision and Patterns of Host Specificity in the Fungal Subphylum Entomophthoromycotina
title_full_unstemmed Phylogenetic Revision and Patterns of Host Specificity in the Fungal Subphylum Entomophthoromycotina
title_short Phylogenetic Revision and Patterns of Host Specificity in the Fungal Subphylum Entomophthoromycotina
title_sort phylogenetic revision and patterns of host specificity in the fungal subphylum entomophthoromycotina
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879804/
https://www.ncbi.nlm.nih.gov/pubmed/35208711
http://dx.doi.org/10.3390/microorganisms10020256
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