A dynamic nomenclature proposal for SARS-CoV-2 lineages to assist genomic epidemiology

The ongoing pandemic spread of a new human coronavirus, SARS-CoV-2, which is associated with severe pneumonia/disease (COVID-19), has resulted in the generation of tens of thousands of virus genome sequences. The rate of genome generation is unprecedented, yet there is currently no coherent nor acce...

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Published inNature microbiology Vol. 5; no. 11; pp. 1403 - 1407
Main Authors Rambaut, Andrew, Holmes, Edward C., O’Toole, Áine, Hill, Verity, McCrone, John T., Ruis, Christopher, du Plessis, Louis, Pybus, Oliver G.
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.11.2020
Nature Publishing Group
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Abstract The ongoing pandemic spread of a new human coronavirus, SARS-CoV-2, which is associated with severe pneumonia/disease (COVID-19), has resulted in the generation of tens of thousands of virus genome sequences. The rate of genome generation is unprecedented, yet there is currently no coherent nor accepted scheme for naming the expanding phylogenetic diversity of SARS-CoV-2. Here, we present a rational and dynamic virus nomenclature that uses a phylogenetic framework to identify those lineages that contribute most to active spread. Our system is made tractable by constraining the number and depth of hierarchical lineage labels and by flagging and delabelling virus lineages that become unobserved and hence are probably inactive. By focusing on active virus lineages and those spreading to new locations, this nomenclature will assist in tracking and understanding the patterns and determinants of the global spread of SARS-CoV-2. The authors propose a nomenclature of SARS-CoV-2 lineages to assist research on epidemiology and decision-making during the COVID-19 pandemic. This nomenclature is based on the SARS-CoV-2 phylogeny and designed to provide a real-time bird’s-eye view of the diversity of the hundreds of thousands of genome sequences collected worldwide. The authors develop a set of rules to produce a hierarchical four-level nomenclature of labels that is flexible and dynamic.
AbstractList The ongoing pandemic spread of a new human coronavirus, SARS-CoV-2, which is associated with severe pneumonia/disease (COVID-19), has resulted in the generation of tens of thousands of virus genome sequences. The rate of genome generation is unprecedented, yet there is currently no coherent nor accepted scheme for naming the expanding phylogenetic diversity of SARS-CoV-2. Here, we present a rational and dynamic virus nomenclature that uses a phylogenetic framework to identify those lineages that contribute most to active spread. Our system is made tractable by constraining the number and depth of hierarchical lineage labels and by flagging and delabelling virus lineages that become unobserved and hence are probably inactive. By focusing on active virus lineages and those spreading to new locations, this nomenclature will assist in tracking and understanding the patterns and determinants of the global spread of SARS-CoV-2.The ongoing pandemic spread of a new human coronavirus, SARS-CoV-2, which is associated with severe pneumonia/disease (COVID-19), has resulted in the generation of tens of thousands of virus genome sequences. The rate of genome generation is unprecedented, yet there is currently no coherent nor accepted scheme for naming the expanding phylogenetic diversity of SARS-CoV-2. Here, we present a rational and dynamic virus nomenclature that uses a phylogenetic framework to identify those lineages that contribute most to active spread. Our system is made tractable by constraining the number and depth of hierarchical lineage labels and by flagging and delabelling virus lineages that become unobserved and hence are probably inactive. By focusing on active virus lineages and those spreading to new locations, this nomenclature will assist in tracking and understanding the patterns and determinants of the global spread of SARS-CoV-2.
The ongoing pandemic spread of a new human coronavirus, SARS-CoV-2, which is associated with severe pneumonia/disease (COVID-19), has resulted in the generation of tens of thousands of virus genome sequences. The rate of genome generation is unprecedented, yet there is currently no coherent nor accepted scheme for naming the expanding phylogenetic diversity of SARS-CoV-2. Here, we present a rational and dynamic virus nomenclature that uses a phylogenetic framework to identify those lineages that contribute most to active spread. Our system is made tractable by constraining the number and depth of hierarchical lineage labels and by flagging and delabelling virus lineages that become unobserved and hence are probably inactive. By focusing on active virus lineages and those spreading to new locations, this nomenclature will assist in tracking and understanding the patterns and determinants of the global spread of SARS-CoV-2.
The ongoing pandemic spread of a novel human coronavirus, SARS-COV-2, associated with severe pneumonia disease (COVID-19), has resulted in the generation of tens of thousands of virus genome sequences. The rate of genome generation is unprecedented, yet there is currently no coherent nor accepted scheme for naming the expanding phylogenetic diversity of SARS-CoV-2. We present a rational and dynamic virus nomenclature that uses a phylogenetic framework to identify those lineages that contribute most to active spread. Our system is made tractable by constraining the number and depth of hierarchical lineage labels and by flagging and de-labelling virus lineages that become unobserved and hence are likely inactive. By focusing on active virus lineages and those spreading to new locations this nomenclature will assist in tracking and understanding the patterns and determinants of the global spread of SARS-CoV-2.
The ongoing pandemic spread of a new human coronavirus, SARS-CoV-2, which is associated with severe pneumonia/disease (COVID-19), has resulted in the generation of tens of thousands of virus genome sequences. The rate of genome generation is unprecedented, yet there is currently no coherent nor accepted scheme for naming the expanding phylogenetic diversity of SARS-CoV-2. Here, we present a rational and dynamic virus nomenclature that uses a phylogenetic framework to identify those lineages that contribute most to active spread. Our system is made tractable by constraining the number and depth of hierarchical lineage labels and by flagging and delabelling virus lineages that become unobserved and hence are probably inactive. By focusing on active virus lineages and those spreading to new locations, this nomenclature will assist in tracking and understanding the patterns and determinants of the global spread of SARS-CoV-2. The authors propose a nomenclature of SARS-CoV-2 lineages to assist research on epidemiology and decision-making during the COVID-19 pandemic. This nomenclature is based on the SARS-CoV-2 phylogeny and designed to provide a real-time bird’s-eye view of the diversity of the hundreds of thousands of genome sequences collected worldwide. The authors develop a set of rules to produce a hierarchical four-level nomenclature of labels that is flexible and dynamic.
The ongoing pandemic spread of a new human coronavirus, SARS-CoV-2, which is associated with severe pneumonia/disease (COVID-19), has resulted in the generation of tens of thousands of virus genome sequences. The rate of genome generation is unprecedented, yet there is currently no coherent nor accepted scheme for naming the expanding phylogenetic diversity of SARS-CoV-2. Here, we present a rational and dynamic virus nomenclature that uses a phylogenetic framework to identify those lineages that contribute most to active spread. Our system is made tractable by constraining the number and depth of hierarchical lineage labels and by flagging and delabelling virus lineages that become unobserved and hence are probably inactive. By focusing on active virus lineages and those spreading to new locations, this nomenclature will assist in tracking and understanding the patterns and determinants of the global spread of SARS-CoV-2.The authors propose a nomenclature of SARS-CoV-2 lineages to assist research on epidemiology and decision-making during the COVID-19 pandemic. This nomenclature is based on the SARS-CoV-2 phylogeny and designed to provide a real-time bird’s-eye view of the diversity of the hundreds of thousands of genome sequences collected worldwide. The authors develop a set of rules to produce a hierarchical four-level nomenclature of labels that is flexible and dynamic.
Author Ruis, Christopher
McCrone, John T.
du Plessis, Louis
Rambaut, Andrew
Pybus, Oliver G.
Holmes, Edward C.
O’Toole, Áine
Hill, Verity
AuthorAffiliation 2 Marie Bashir Institute for Infectious Diseases and Biosecurity, School of Life and Environmental Sciences and School of Medical Sciences, University of Sydney, Sydney, NSW, Australia
3 Department of Zoology, University of Oxford, Oxford, UK
1 Institute of Evolutionary Biology, University of Edinburgh, Edinburgh, UK
4 Department of Medicine, University of Cambridge, UK
AuthorAffiliation_xml – name: 4 Department of Medicine, University of Cambridge, UK
– name: 2 Marie Bashir Institute for Infectious Diseases and Biosecurity, School of Life and Environmental Sciences and School of Medical Sciences, University of Sydney, Sydney, NSW, Australia
– name: 1 Institute of Evolutionary Biology, University of Edinburgh, Edinburgh, UK
– name: 3 Department of Zoology, University of Oxford, Oxford, UK
Author_xml – sequence: 1
  givenname: Andrew
  orcidid: 0000-0003-4337-3707
  surname: Rambaut
  fullname: Rambaut, Andrew
  email: a.rambaut@ed.ac.uk
  organization: Institute of Evolutionary Biology, University of Edinburgh
– sequence: 2
  givenname: Edward C.
  orcidid: 0000-0001-9596-3552
  surname: Holmes
  fullname: Holmes, Edward C.
  email: edward.holmes@sydney.edu.au
  organization: Marie Bashir Institute for Infectious Diseases and Biosecurity, School of Life and Environmental Sciences and School of Medical Sciences, University of Sydney
– sequence: 3
  givenname: Áine
  orcidid: 0000-0001-8083-474X
  surname: O’Toole
  fullname: O’Toole, Áine
  organization: Institute of Evolutionary Biology, University of Edinburgh
– sequence: 4
  givenname: Verity
  surname: Hill
  fullname: Hill, Verity
  organization: Institute of Evolutionary Biology, University of Edinburgh
– sequence: 5
  givenname: John T.
  surname: McCrone
  fullname: McCrone, John T.
  organization: Institute of Evolutionary Biology, University of Edinburgh
– sequence: 6
  givenname: Christopher
  surname: Ruis
  fullname: Ruis, Christopher
  organization: Department of Medicine, University of Cambridge
– sequence: 7
  givenname: Louis
  surname: du Plessis
  fullname: du Plessis, Louis
  organization: Department of Zoology, University of Oxford
– sequence: 8
  givenname: Oliver G.
  orcidid: 0000-0002-8797-2667
  surname: Pybus
  fullname: Pybus, Oliver G.
  email: oliver.pybus@zoo.ox.ac.uk
  organization: Department of Zoology, University of Oxford
BackLink https://www.ncbi.nlm.nih.gov/pubmed/32669681$$D View this record in MEDLINE/PubMed
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Snippet The ongoing pandemic spread of a new human coronavirus, SARS-CoV-2, which is associated with severe pneumonia/disease (COVID-19), has resulted in the...
The ongoing pandemic spread of a novel human coronavirus, SARS-COV-2, associated with severe pneumonia disease (COVID-19), has resulted in the generation of...
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SubjectTerms 45
631/114/1386
631/114/739
631/181/757
631/326/596/2554
631/326/596/4130
Betacoronavirus - genetics
Betacoronavirus - isolation & purification
Biomedical and Life Sciences
Coronavirus Infections - epidemiology
Coronavirus Infections - virology
Coronaviruses
COVID-19
Decision making
Disease transmission
Epidemiology
Genome, Viral
Genomes
Genotype
Humans
Infectious Diseases
Life Sciences
Medical Microbiology
Microbiology
Molecular Epidemiology
Nomenclature
Pandemics
Parasitology
Phylogenetics
Phylogeny
Pneumonia, Viral - epidemiology
Pneumonia, Viral - virology
SARS-CoV-2
Severe acute respiratory syndrome coronavirus 2
Virology
Title A dynamic nomenclature proposal for SARS-CoV-2 lineages to assist genomic epidemiology
URI https://link.springer.com/article/10.1038/s41564-020-0770-5
https://www.ncbi.nlm.nih.gov/pubmed/32669681
https://www.proquest.com/docview/2471500175
https://www.proquest.com/docview/2424444359
https://pubmed.ncbi.nlm.nih.gov/PMC7610519
Volume 5
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