One hundred years of influenza A evolution

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One hundred years of influenza A evolution. / Nielsen, Bjarke Frost; Berrig, Christian; Grenfell, Bryan T.; Andreasen, Viggo.

In: Theoretical Population Biology, Vol. 159, 31.07.2024, p. 25-34.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Nielsen, BF, Berrig, C, Grenfell, BT & Andreasen, V 2024, 'One hundred years of influenza A evolution', Theoretical Population Biology, vol. 159, pp. 25-34. https://doi.org/10.1016/j.tpb.2024.07.005

APA

Nielsen, B. F., Berrig, C., Grenfell, B. T., & Andreasen, V. (2024). One hundred years of influenza A evolution. Theoretical Population Biology, 159, 25-34. https://doi.org/10.1016/j.tpb.2024.07.005

Vancouver

Nielsen BF, Berrig C, Grenfell BT, Andreasen V. One hundred years of influenza A evolution. Theoretical Population Biology. 2024 Jul 31;159:25-34. https://doi.org/10.1016/j.tpb.2024.07.005

Author

Nielsen, Bjarke Frost ; Berrig, Christian ; Grenfell, Bryan T. ; Andreasen, Viggo. / One hundred years of influenza A evolution. In: Theoretical Population Biology. 2024 ; Vol. 159. pp. 25-34.

Bibtex

@article{cce0ead9a8c04793b73126a5eb1cd299,
title = "One hundred years of influenza A evolution",
abstract = "Leveraging the simplicity of nucleotide mismatch distributions, we provide an intuitive window into the evolution of the human influenza A {\textquoteleft}nonstructural{\textquoteright} (NS) gene segment. In an analysis suggested by the eminent Danish biologist Freddy B. Christiansen, we illustrate the existence of a continuous genetic “backbone” of influenza A NS sequences, steadily increasing in nucleotide distance to the 1918 root over more than a century. The 2009 influenza A/H1N1 pandemic represents a clear departure from this enduring genetic backbone. Utilizing nucleotide distance maps and phylogenetic analyses, we illustrate remaining uncertainties regarding the origin of the 2009 pandemic, highlighting the complexity of influenza evolution. The NS segment is interesting precisely because it experiences less pervasive positive selection, and departs less strongly from neutral evolution than e.g. the HA antigen. Consequently, sudden deviations from neutral diversification can indicate changes in other genes via the hitchhiking effect. Our approach employs two measures based on nucleotide mismatch counts to analyze the evolutionary dynamics of the NS gene segment. The rooted Hamming map of distances between a reference sequence and all other sequences over time, and the unrooted temporal Hamming distribution which captures the distribution of genotypic distances between simultaneously circulating viruses, thereby revealing patterns of nucleotide diversity and epi-evolutionary dynamics.",
keywords = "Hamming distance, Influenza evolution, Nonstructural gene, NS gene, Nucleotide distance, Viral diversity, Viral evolution",
author = "Nielsen, {Bjarke Frost} and Christian Berrig and Grenfell, {Bryan T.} and Viggo Andreasen",
note = "Publisher Copyright: {\textcopyright} 2024",
year = "2024",
month = jul,
day = "31",
doi = "10.1016/j.tpb.2024.07.005",
language = "English",
volume = "159",
pages = "25--34",
journal = "Theoretical Population Biology",
issn = "0040-5809",
publisher = "Academic Press",

}

RIS

TY - JOUR

T1 - One hundred years of influenza A evolution

AU - Nielsen, Bjarke Frost

AU - Berrig, Christian

AU - Grenfell, Bryan T.

AU - Andreasen, Viggo

N1 - Publisher Copyright: © 2024

PY - 2024/7/31

Y1 - 2024/7/31

N2 - Leveraging the simplicity of nucleotide mismatch distributions, we provide an intuitive window into the evolution of the human influenza A ‘nonstructural’ (NS) gene segment. In an analysis suggested by the eminent Danish biologist Freddy B. Christiansen, we illustrate the existence of a continuous genetic “backbone” of influenza A NS sequences, steadily increasing in nucleotide distance to the 1918 root over more than a century. The 2009 influenza A/H1N1 pandemic represents a clear departure from this enduring genetic backbone. Utilizing nucleotide distance maps and phylogenetic analyses, we illustrate remaining uncertainties regarding the origin of the 2009 pandemic, highlighting the complexity of influenza evolution. The NS segment is interesting precisely because it experiences less pervasive positive selection, and departs less strongly from neutral evolution than e.g. the HA antigen. Consequently, sudden deviations from neutral diversification can indicate changes in other genes via the hitchhiking effect. Our approach employs two measures based on nucleotide mismatch counts to analyze the evolutionary dynamics of the NS gene segment. The rooted Hamming map of distances between a reference sequence and all other sequences over time, and the unrooted temporal Hamming distribution which captures the distribution of genotypic distances between simultaneously circulating viruses, thereby revealing patterns of nucleotide diversity and epi-evolutionary dynamics.

AB - Leveraging the simplicity of nucleotide mismatch distributions, we provide an intuitive window into the evolution of the human influenza A ‘nonstructural’ (NS) gene segment. In an analysis suggested by the eminent Danish biologist Freddy B. Christiansen, we illustrate the existence of a continuous genetic “backbone” of influenza A NS sequences, steadily increasing in nucleotide distance to the 1918 root over more than a century. The 2009 influenza A/H1N1 pandemic represents a clear departure from this enduring genetic backbone. Utilizing nucleotide distance maps and phylogenetic analyses, we illustrate remaining uncertainties regarding the origin of the 2009 pandemic, highlighting the complexity of influenza evolution. The NS segment is interesting precisely because it experiences less pervasive positive selection, and departs less strongly from neutral evolution than e.g. the HA antigen. Consequently, sudden deviations from neutral diversification can indicate changes in other genes via the hitchhiking effect. Our approach employs two measures based on nucleotide mismatch counts to analyze the evolutionary dynamics of the NS gene segment. The rooted Hamming map of distances between a reference sequence and all other sequences over time, and the unrooted temporal Hamming distribution which captures the distribution of genotypic distances between simultaneously circulating viruses, thereby revealing patterns of nucleotide diversity and epi-evolutionary dynamics.

KW - Hamming distance

KW - Influenza evolution

KW - Nonstructural gene

KW - NS gene

KW - Nucleotide distance

KW - Viral diversity

KW - Viral evolution

U2 - 10.1016/j.tpb.2024.07.005

DO - 10.1016/j.tpb.2024.07.005

M3 - Journal article

C2 - 39094981

AN - SCOPUS:85200597103

VL - 159

SP - 25

EP - 34

JO - Theoretical Population Biology

JF - Theoretical Population Biology

SN - 0040-5809

ER -

ID: 402399404