Assessing Genome-Wide Diversity in European Hantaviruses through Sequence Capture from Natural Host Samples

Research on the ecology and evolution of viruses is often hampered by the limitation of sequence information to short parts of the genomes or single genomes derived from cultures. In this study, we use hybrid sequence capture enrichment in combination with high-throughput sequencing to provide effic...

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Published in:Viruses
Main Authors: Melanie Hiltbrunner, Gerald Heckel
Format: Text
Language:English
Published: Multidisciplinary Digital Publishing Institute 2020
Subjects:
Online Access:https://doi.org/10.3390/v12070749
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spelling ftmdpi:oai:mdpi.com:/1999-4915/12/7/749/ 2023-08-20T04:05:59+02:00 Assessing Genome-Wide Diversity in European Hantaviruses through Sequence Capture from Natural Host Samples Melanie Hiltbrunner Gerald Heckel agris 2020-07-11 application/pdf https://doi.org/10.3390/v12070749 EN eng Multidisciplinary Digital Publishing Institute Animal Viruses https://dx.doi.org/10.3390/v12070749 https://creativecommons.org/licenses/by/4.0/ Viruses; Volume 12; Issue 7; Pages: 749 hybrid sequence capture virus genomes targeted enrichment high-throughput deep sequencing de novo assembly hantavirus phylogeny evolutionary history rodent-borne viruses Text 2020 ftmdpi https://doi.org/10.3390/v12070749 2023-07-31T23:45:45Z Research on the ecology and evolution of viruses is often hampered by the limitation of sequence information to short parts of the genomes or single genomes derived from cultures. In this study, we use hybrid sequence capture enrichment in combination with high-throughput sequencing to provide efficient access to full genomes of European hantaviruses from rodent samples obtained in the field. We applied this methodology to Tula (TULV) and Puumala (PUUV) orthohantaviruses for which analyses from natural host samples are typically restricted to partial sequences of their tri-segmented RNA genome. We assembled a total of ten novel hantavirus genomes de novo with very high coverage (on average >99%) and sequencing depth (average >247×). A comparison with partial Sanger sequences indicated an accuracy of >99.9% for the assemblies. An analysis of two common vole (Microtus arvalis) samples infected with two TULV strains each allowed for the de novo assembly of all four TULV genomes. Combining the novel sequences with all available TULV and PUUV genomes revealed very similar patterns of sequence diversity along the genomes, except for remarkably higher diversity in the non-coding region of the S-segment in PUUV. The genomic distribution of polymorphisms in the coding sequence was similar between the species, but differed between the segments with the highest sequence divergence of 0.274 for the M-segment, 0.265 for the S-segment, and 0.248 for the L-segment (overall 0.258). Phylogenetic analyses showed the clustering of genome sequences consistent with their geographic distribution within each species. Genome-wide data yielded extremely high node support values, despite the impact of strong mutational saturation that is expected for hantavirus sequences obtained over large spatial distances. We conclude that genome sequencing based on capture enrichment protocols provides an efficient means for ecological and evolutionary investigations of hantaviruses at an unprecedented completeness and depth. Text Common vole Microtus arvalis MDPI Open Access Publishing Tula ENVELOPE(-65.650,-65.650,-65.517,-65.517) Viruses 12 7 749
institution Open Polar
collection MDPI Open Access Publishing
op_collection_id ftmdpi
language English
topic hybrid sequence capture
virus genomes
targeted enrichment
high-throughput deep sequencing
de novo assembly
hantavirus phylogeny
evolutionary history
rodent-borne viruses
spellingShingle hybrid sequence capture
virus genomes
targeted enrichment
high-throughput deep sequencing
de novo assembly
hantavirus phylogeny
evolutionary history
rodent-borne viruses
Melanie Hiltbrunner
Gerald Heckel
Assessing Genome-Wide Diversity in European Hantaviruses through Sequence Capture from Natural Host Samples
topic_facet hybrid sequence capture
virus genomes
targeted enrichment
high-throughput deep sequencing
de novo assembly
hantavirus phylogeny
evolutionary history
rodent-borne viruses
description Research on the ecology and evolution of viruses is often hampered by the limitation of sequence information to short parts of the genomes or single genomes derived from cultures. In this study, we use hybrid sequence capture enrichment in combination with high-throughput sequencing to provide efficient access to full genomes of European hantaviruses from rodent samples obtained in the field. We applied this methodology to Tula (TULV) and Puumala (PUUV) orthohantaviruses for which analyses from natural host samples are typically restricted to partial sequences of their tri-segmented RNA genome. We assembled a total of ten novel hantavirus genomes de novo with very high coverage (on average >99%) and sequencing depth (average >247×). A comparison with partial Sanger sequences indicated an accuracy of >99.9% for the assemblies. An analysis of two common vole (Microtus arvalis) samples infected with two TULV strains each allowed for the de novo assembly of all four TULV genomes. Combining the novel sequences with all available TULV and PUUV genomes revealed very similar patterns of sequence diversity along the genomes, except for remarkably higher diversity in the non-coding region of the S-segment in PUUV. The genomic distribution of polymorphisms in the coding sequence was similar between the species, but differed between the segments with the highest sequence divergence of 0.274 for the M-segment, 0.265 for the S-segment, and 0.248 for the L-segment (overall 0.258). Phylogenetic analyses showed the clustering of genome sequences consistent with their geographic distribution within each species. Genome-wide data yielded extremely high node support values, despite the impact of strong mutational saturation that is expected for hantavirus sequences obtained over large spatial distances. We conclude that genome sequencing based on capture enrichment protocols provides an efficient means for ecological and evolutionary investigations of hantaviruses at an unprecedented completeness and depth.
format Text
author Melanie Hiltbrunner
Gerald Heckel
author_facet Melanie Hiltbrunner
Gerald Heckel
author_sort Melanie Hiltbrunner
title Assessing Genome-Wide Diversity in European Hantaviruses through Sequence Capture from Natural Host Samples
title_short Assessing Genome-Wide Diversity in European Hantaviruses through Sequence Capture from Natural Host Samples
title_full Assessing Genome-Wide Diversity in European Hantaviruses through Sequence Capture from Natural Host Samples
title_fullStr Assessing Genome-Wide Diversity in European Hantaviruses through Sequence Capture from Natural Host Samples
title_full_unstemmed Assessing Genome-Wide Diversity in European Hantaviruses through Sequence Capture from Natural Host Samples
title_sort assessing genome-wide diversity in european hantaviruses through sequence capture from natural host samples
publisher Multidisciplinary Digital Publishing Institute
publishDate 2020
url https://doi.org/10.3390/v12070749
op_coverage agris
long_lat ENVELOPE(-65.650,-65.650,-65.517,-65.517)
geographic Tula
geographic_facet Tula
genre Common vole
Microtus arvalis
genre_facet Common vole
Microtus arvalis
op_source Viruses; Volume 12; Issue 7; Pages: 749
op_relation Animal Viruses
https://dx.doi.org/10.3390/v12070749
op_rights https://creativecommons.org/licenses/by/4.0/
op_doi https://doi.org/10.3390/v12070749
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