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Complete genomic sequencing of canine distemper virus with nanopore technology during an epizootic event

Canine distemper virus (CDV) endangers a wide range of wild animal populations, can cross species barriers and therefore representing a significant conservational and animal health risk around the globe. During spring to autumn 2021, according to our current estimates a minimum of 50 red foxes (Vulp...

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Autores principales: Lanszki, Zsófia, Tóth, Gábor E., Schütz, Éva, Zeghbib, Safia, Rusvai, Miklós, Jakab, Ferenc, Kemenesi, Gábor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8904823/
https://www.ncbi.nlm.nih.gov/pubmed/35260784
http://dx.doi.org/10.1038/s41598-022-08183-3
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author Lanszki, Zsófia
Tóth, Gábor E.
Schütz, Éva
Zeghbib, Safia
Rusvai, Miklós
Jakab, Ferenc
Kemenesi, Gábor
author_facet Lanszki, Zsófia
Tóth, Gábor E.
Schütz, Éva
Zeghbib, Safia
Rusvai, Miklós
Jakab, Ferenc
Kemenesi, Gábor
author_sort Lanszki, Zsófia
collection PubMed
description Canine distemper virus (CDV) endangers a wide range of wild animal populations, can cross species barriers and therefore representing a significant conservational and animal health risk around the globe. During spring to autumn 2021, according to our current estimates a minimum of 50 red foxes (Vulpes vulpes) died of CDV in Hungary, with CDV lesions. Oral, nasal and rectal swab samples were RT-PCR screened for Canine Distemper Virus from red fox carcasses. To investigate in more detail the origins of these CDV strains, 19 complete genomes were sequenced with a pan-genotype CDV-specific amplicon-based sequencing method developed by our laboratory and optimized for the Oxford Nanopore Technologies platform. Phylogenetic analysis of the complete genomic sequences and separately the hemagglutinin gene sequences revealed the role of the Europe lineage of CDV as a causative agent for the current epizootic. Here we highlight the growing importance of fast developing rapid sequencing technologies to aid rapid response activities during epidemics or epizootic events. We also emphasize the urgent need for improved surveillance of CDV, considering the epizootic capability of enzootic strains as reported in the current study. For such future efforts, we provide a novel NGS protocol to facilitate future genomic surveillance studies.
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spelling pubmed-89048232022-03-10 Complete genomic sequencing of canine distemper virus with nanopore technology during an epizootic event Lanszki, Zsófia Tóth, Gábor E. Schütz, Éva Zeghbib, Safia Rusvai, Miklós Jakab, Ferenc Kemenesi, Gábor Sci Rep Article Canine distemper virus (CDV) endangers a wide range of wild animal populations, can cross species barriers and therefore representing a significant conservational and animal health risk around the globe. During spring to autumn 2021, according to our current estimates a minimum of 50 red foxes (Vulpes vulpes) died of CDV in Hungary, with CDV lesions. Oral, nasal and rectal swab samples were RT-PCR screened for Canine Distemper Virus from red fox carcasses. To investigate in more detail the origins of these CDV strains, 19 complete genomes were sequenced with a pan-genotype CDV-specific amplicon-based sequencing method developed by our laboratory and optimized for the Oxford Nanopore Technologies platform. Phylogenetic analysis of the complete genomic sequences and separately the hemagglutinin gene sequences revealed the role of the Europe lineage of CDV as a causative agent for the current epizootic. Here we highlight the growing importance of fast developing rapid sequencing technologies to aid rapid response activities during epidemics or epizootic events. We also emphasize the urgent need for improved surveillance of CDV, considering the epizootic capability of enzootic strains as reported in the current study. For such future efforts, we provide a novel NGS protocol to facilitate future genomic surveillance studies. Nature Publishing Group UK 2022-03-08 /pmc/articles/PMC8904823/ /pubmed/35260784 http://dx.doi.org/10.1038/s41598-022-08183-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Lanszki, Zsófia
Tóth, Gábor E.
Schütz, Éva
Zeghbib, Safia
Rusvai, Miklós
Jakab, Ferenc
Kemenesi, Gábor
Complete genomic sequencing of canine distemper virus with nanopore technology during an epizootic event
title Complete genomic sequencing of canine distemper virus with nanopore technology during an epizootic event
title_full Complete genomic sequencing of canine distemper virus with nanopore technology during an epizootic event
title_fullStr Complete genomic sequencing of canine distemper virus with nanopore technology during an epizootic event
title_full_unstemmed Complete genomic sequencing of canine distemper virus with nanopore technology during an epizootic event
title_short Complete genomic sequencing of canine distemper virus with nanopore technology during an epizootic event
title_sort complete genomic sequencing of canine distemper virus with nanopore technology during an epizootic event
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8904823/
https://www.ncbi.nlm.nih.gov/pubmed/35260784
http://dx.doi.org/10.1038/s41598-022-08183-3
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