Data from: Genome-wide support for incipient Tula orthohantavirus species within a single rodent host lineage ...

Evolutionary divergence of viruses is most commonly driven by co-divergence with their hosts or through isolation of transmission after host-shifts. It remains mostly unknown, however, whether divergent phylogenetic clades within named virus species represent functionally equivalent byproducts of hi...

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Main Authors: Labutin, Anton, Heckel, Gerald
Format: Dataset
Language:English
Published: Dryad 2024
Subjects:
Online Access:https://dx.doi.org/10.5061/dryad.w0vt4b905
https://datadryad.org/dataset/doi:10.5061/dryad.w0vt4b905
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author Labutin, Anton
Heckel, Gerald
author_facet Labutin, Anton
Heckel, Gerald
author_sort Labutin, Anton
collection DataCite
description Evolutionary divergence of viruses is most commonly driven by co-divergence with their hosts or through isolation of transmission after host-shifts. It remains mostly unknown, however, whether divergent phylogenetic clades within named virus species represent functionally equivalent byproducts of high evolutionary rates or rather incipient virus species. Here, we test these alternatives with genomic data from two widespread phylogenetic clades in Tula orthohantavirus (TULV) within a single evolutionary lineage of their natural rodent host, the common vole Microtus arvalis. We examined voles from 42 locations in the contact region between clades for TULV infection by RT-PCR. Sequencing yielded 23 TULV Central North and 21 TULV Central South genomes which differed by 14.9-18.5% at the nucleotide and 2.2-3.7% at the amino acid level without evidence of recombination or reassortment. Geographic cline analyses demonstrated an abrupt (<1 km wide) transition between the parapatric TULV clades in continuous ... : Genotyping of host nuclear DNA Genome-wide nuclear DNA (nucDNA) was used to infer the genetic structure of hosts via Genotyping by Sequencing (GBS) (Elshire et al., 2011). We sequenced at least five individuals per sampling site across the Central transect whenever possible, for a total of 200 individuals. Sequencing was carried out by LGC Biosearch Technologies (Berlin, Germany) using Illumina NovaSeq 6000 and PstI/MspI as restriction enzymes. We combined our dataset with GBS data of 216 additional individuals from the Porcelain transect (Saxenhofer et al., 2022) processed under the same conditions. This separate dataset consisted of voles from the Central and Eastern lineage as well as admixed individuals and served as a reference for the assignment of the newly genotyped 200 individuals to the evolutionary lineages. SNP calling was performed for all 416 individuals together using the GBS v2 pipeline (Tassel 5) (Glaubitz et al., 2014) with the M. arvalis genome (BioProject ID: PRJNA737461, Gouy et al., ...
format Dataset
genre Common vole
Microtus arvalis
genre_facet Common vole
Microtus arvalis
geographic Tula
geographic_facet Tula
id ftdatacite:10.5061/dryad.w0vt4b905
institution Open Polar
language English
long_lat ENVELOPE(-65.650,-65.650,-65.517,-65.517)
op_collection_id ftdatacite
op_doi https://doi.org/10.5061/dryad.w0vt4b90510.1093/ve/veae002
op_relation https://dx.doi.org/10.1093/ve/veae002
op_rights Creative Commons Zero v1.0 Universal
https://creativecommons.org/publicdomain/zero/1.0/legalcode
cc0-1.0
publishDate 2024
publisher Dryad
record_format openpolar
spelling ftdatacite:10.5061/dryad.w0vt4b905 2025-03-30T15:09:20+00:00 Data from: Genome-wide support for incipient Tula orthohantavirus species within a single rodent host lineage ... Labutin, Anton Heckel, Gerald 2024 https://dx.doi.org/10.5061/dryad.w0vt4b905 https://datadryad.org/dataset/doi:10.5061/dryad.w0vt4b905 en eng Dryad https://dx.doi.org/10.1093/ve/veae002 Creative Commons Zero v1.0 Universal https://creativecommons.org/publicdomain/zero/1.0/legalcode cc0-1.0 FOS: Biological sciences Genome-wide association studies genomic admixture Host-pathogen co-evolution Microtus arvalis Tula orthohantavirus virus speciation RNA virus Hantavirus dataset Dataset 2024 ftdatacite https://doi.org/10.5061/dryad.w0vt4b90510.1093/ve/veae002 2025-03-03T20:26:48Z Evolutionary divergence of viruses is most commonly driven by co-divergence with their hosts or through isolation of transmission after host-shifts. It remains mostly unknown, however, whether divergent phylogenetic clades within named virus species represent functionally equivalent byproducts of high evolutionary rates or rather incipient virus species. Here, we test these alternatives with genomic data from two widespread phylogenetic clades in Tula orthohantavirus (TULV) within a single evolutionary lineage of their natural rodent host, the common vole Microtus arvalis. We examined voles from 42 locations in the contact region between clades for TULV infection by RT-PCR. Sequencing yielded 23 TULV Central North and 21 TULV Central South genomes which differed by 14.9-18.5% at the nucleotide and 2.2-3.7% at the amino acid level without evidence of recombination or reassortment. Geographic cline analyses demonstrated an abrupt (<1 km wide) transition between the parapatric TULV clades in continuous ... : Genotyping of host nuclear DNA Genome-wide nuclear DNA (nucDNA) was used to infer the genetic structure of hosts via Genotyping by Sequencing (GBS) (Elshire et al., 2011). We sequenced at least five individuals per sampling site across the Central transect whenever possible, for a total of 200 individuals. Sequencing was carried out by LGC Biosearch Technologies (Berlin, Germany) using Illumina NovaSeq 6000 and PstI/MspI as restriction enzymes. We combined our dataset with GBS data of 216 additional individuals from the Porcelain transect (Saxenhofer et al., 2022) processed under the same conditions. This separate dataset consisted of voles from the Central and Eastern lineage as well as admixed individuals and served as a reference for the assignment of the newly genotyped 200 individuals to the evolutionary lineages. SNP calling was performed for all 416 individuals together using the GBS v2 pipeline (Tassel 5) (Glaubitz et al., 2014) with the M. arvalis genome (BioProject ID: PRJNA737461, Gouy et al., ... Dataset Common vole Microtus arvalis DataCite Tula ENVELOPE(-65.650,-65.650,-65.517,-65.517)
spellingShingle FOS: Biological sciences
Genome-wide association studies
genomic admixture
Host-pathogen co-evolution
Microtus arvalis
Tula orthohantavirus
virus speciation
RNA virus
Hantavirus
Labutin, Anton
Heckel, Gerald
Data from: Genome-wide support for incipient Tula orthohantavirus species within a single rodent host lineage ...
title Data from: Genome-wide support for incipient Tula orthohantavirus species within a single rodent host lineage ...
title_full Data from: Genome-wide support for incipient Tula orthohantavirus species within a single rodent host lineage ...
title_fullStr Data from: Genome-wide support for incipient Tula orthohantavirus species within a single rodent host lineage ...
title_full_unstemmed Data from: Genome-wide support for incipient Tula orthohantavirus species within a single rodent host lineage ...
title_short Data from: Genome-wide support for incipient Tula orthohantavirus species within a single rodent host lineage ...
title_sort data from: genome-wide support for incipient tula orthohantavirus species within a single rodent host lineage ...
topic FOS: Biological sciences
Genome-wide association studies
genomic admixture
Host-pathogen co-evolution
Microtus arvalis
Tula orthohantavirus
virus speciation
RNA virus
Hantavirus
topic_facet FOS: Biological sciences
Genome-wide association studies
genomic admixture
Host-pathogen co-evolution
Microtus arvalis
Tula orthohantavirus
virus speciation
RNA virus
Hantavirus
url https://dx.doi.org/10.5061/dryad.w0vt4b905
https://datadryad.org/dataset/doi:10.5061/dryad.w0vt4b905