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Phylogenomics and Diversification of the Schistosomatidae Based on Targeted Sequence Capture of Ultra-Conserved Elements

Schistosomatidae Stiles and Hassall 1898 is a medically significant family of digenetic trematodes (Trematoda: Digenea), members of which infect mammals or birds as definitive hosts and aquatic or amphibious gastropods as intermediate hosts. Currently, there are 17 named genera, for many of which ev...

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Autores principales: Ebbs, Erika T., Loker, Eric S., Bu, Lijing, Locke, Sean A., Tkach, Vasyl V., Devkota, Ramesh, Flores, Veronica R., Pinto, Hudson A., Brant, Sara V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9321907/
https://www.ncbi.nlm.nih.gov/pubmed/35890014
http://dx.doi.org/10.3390/pathogens11070769
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author Ebbs, Erika T.
Loker, Eric S.
Bu, Lijing
Locke, Sean A.
Tkach, Vasyl V.
Devkota, Ramesh
Flores, Veronica R.
Pinto, Hudson A.
Brant, Sara V.
author_facet Ebbs, Erika T.
Loker, Eric S.
Bu, Lijing
Locke, Sean A.
Tkach, Vasyl V.
Devkota, Ramesh
Flores, Veronica R.
Pinto, Hudson A.
Brant, Sara V.
author_sort Ebbs, Erika T.
collection PubMed
description Schistosomatidae Stiles and Hassall 1898 is a medically significant family of digenetic trematodes (Trematoda: Digenea), members of which infect mammals or birds as definitive hosts and aquatic or amphibious gastropods as intermediate hosts. Currently, there are 17 named genera, for many of which evolutionary interrelationships remain unresolved. The lack of a resolved phylogeny has encumbered our understanding of schistosomatid evolution, specifically patterns of host-use and the role of host-switching in diversification. Here, we used targeted sequence capture of ultra-conserved elements (UCEs) from representatives of 13 of the 17 named genera and 11 undescribed lineages that are presumed to represent either novel genera or species to generate a phylogenomic dataset for the estimation of schistosomatid interrelationships. This study represents the largest phylogenetic effort within the Schistosomatidae in both the number of loci and breadth of taxon sampling. We present a near-comprehensive family-level phylogeny providing resolution to several clades of long-standing uncertainty within Schistosomatidae, including resolution for the placement of the North American mammalian schistosomes, implying a second separate capture of mammalian hosts. Additionally, we present evidence for the placement of Macrobilharzia at the base of the Schistosoma + Bivitellobilharzia radiation. Patterns of definitive and intermediate host use and a strong role for intermediate host-switching are discussed relative to schistosomatid diversification.
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spelling pubmed-93219072022-07-27 Phylogenomics and Diversification of the Schistosomatidae Based on Targeted Sequence Capture of Ultra-Conserved Elements Ebbs, Erika T. Loker, Eric S. Bu, Lijing Locke, Sean A. Tkach, Vasyl V. Devkota, Ramesh Flores, Veronica R. Pinto, Hudson A. Brant, Sara V. Pathogens Article Schistosomatidae Stiles and Hassall 1898 is a medically significant family of digenetic trematodes (Trematoda: Digenea), members of which infect mammals or birds as definitive hosts and aquatic or amphibious gastropods as intermediate hosts. Currently, there are 17 named genera, for many of which evolutionary interrelationships remain unresolved. The lack of a resolved phylogeny has encumbered our understanding of schistosomatid evolution, specifically patterns of host-use and the role of host-switching in diversification. Here, we used targeted sequence capture of ultra-conserved elements (UCEs) from representatives of 13 of the 17 named genera and 11 undescribed lineages that are presumed to represent either novel genera or species to generate a phylogenomic dataset for the estimation of schistosomatid interrelationships. This study represents the largest phylogenetic effort within the Schistosomatidae in both the number of loci and breadth of taxon sampling. We present a near-comprehensive family-level phylogeny providing resolution to several clades of long-standing uncertainty within Schistosomatidae, including resolution for the placement of the North American mammalian schistosomes, implying a second separate capture of mammalian hosts. Additionally, we present evidence for the placement of Macrobilharzia at the base of the Schistosoma + Bivitellobilharzia radiation. Patterns of definitive and intermediate host use and a strong role for intermediate host-switching are discussed relative to schistosomatid diversification. MDPI 2022-07-05 /pmc/articles/PMC9321907/ /pubmed/35890014 http://dx.doi.org/10.3390/pathogens11070769 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
Ebbs, Erika T.
Loker, Eric S.
Bu, Lijing
Locke, Sean A.
Tkach, Vasyl V.
Devkota, Ramesh
Flores, Veronica R.
Pinto, Hudson A.
Brant, Sara V.
Phylogenomics and Diversification of the Schistosomatidae Based on Targeted Sequence Capture of Ultra-Conserved Elements
title Phylogenomics and Diversification of the Schistosomatidae Based on Targeted Sequence Capture of Ultra-Conserved Elements
title_full Phylogenomics and Diversification of the Schistosomatidae Based on Targeted Sequence Capture of Ultra-Conserved Elements
title_fullStr Phylogenomics and Diversification of the Schistosomatidae Based on Targeted Sequence Capture of Ultra-Conserved Elements
title_full_unstemmed Phylogenomics and Diversification of the Schistosomatidae Based on Targeted Sequence Capture of Ultra-Conserved Elements
title_short Phylogenomics and Diversification of the Schistosomatidae Based on Targeted Sequence Capture of Ultra-Conserved Elements
title_sort phylogenomics and diversification of the schistosomatidae based on targeted sequence capture of ultra-conserved elements
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9321907/
https://www.ncbi.nlm.nih.gov/pubmed/35890014
http://dx.doi.org/10.3390/pathogens11070769
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