Статья

Allele-specific nonstationarity in evolution of influenza A virus surface proteins

A. Popova, K. Safina, V. Ptushenko, A. Stolyarova, A. Favorov, A. Neverov, G. Bazykin,
2021

Influenza A virus (IAV) is a major public health problem and a pandemic threat. Its evolution is largely driven by diversifying positive selection so that relative fitness of different amino acid variants changes with time due to changes in herd immunity or genomic context, and novel amino acid variants attain fitness advantage. Here, we hypothesize that diversifying selection also has another manifestation: the fitness associated with a particular amino acid variant should decline with time since its origin, as the herd immunity adapts to it. By tracing the evolution of antigenic sites at IAV surface proteins, we show that an amino acid variant becomes progressively more likely to become replaced by another variant with time since its origin—a phenomenon we call “senescence.” Senescence is particularly pronounced at experimentally validated antigenic sites, implying that it is largely driven by host immunity. By contrast, at internal sites, existing variants become more favorable with time, probably due to arising contingent mutations at other epistatically interacting sites. Our findings reveal a previously unde-scribed facet of adaptive evolution and suggest approaches for prediction of evolutionary dynamics of pathogens. © 2019 National Academy of Sciences. All rights reserved.

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Версии

  • 1. Version of Record от 2021-04-27

Метаданные

Об авторах
  • A. Popova
    Department of Molecular Diagnostics, Central Research Institute for Epidemiology, Moscow, 111123, Russian Federation
  • K. Safina
    Center of Life Sciences, Skolkovo Institute of Science and Technology, Skolkovo, 143028, Russian Federation
  • V. Ptushenko
    Institute for Information Transmission Problems (Kharkevich Institute), Russian Academy of Sciences, Moscow, 127051, Russian Federation
  • A. Stolyarova
    A. N. Belozersky Institute of Physical–Chemical Biology, M. V. Lomonosov Moscow State University, Moscow, 119992, Russian Federation
  • A. Favorov
    Department of Photochemistry and Photobiology, N. M. Emanuel Institute of Biochemical Physics of Russian Academy of Sciences, Moscow, 119334, Russian Federation
  • A. Neverov
    Division of Biostatistics and Bioinformatics, Department of Oncology, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins School of Medicine, Baltimore, MD 21205, United States
  • G. Bazykin
    Laboratory of System Biology and Computational Genetics, Vavilov Institute of General Genetics, Moscow, 119991, Russian Federation
Название журнала
  • Proceedings of the National Academy of Sciences of the United States of America
Том
  • 116
Выпуск
  • 42
Страницы
  • 21104-21112
Ключевые слова
  • H1 protein; H2 protein; IAV protein; membrane protein; N1 protein; N2 protein; unclassified drug; amino acid; membrane protein; viral protein; virus antigen; allele; amino acid sequence; Article; binding affinity; binding site; controlled study; evolution; genetic variability; herd immunity; host immunity; immunity; Influenza A virus; Influenza A virus (H1N1); Influenza A virus (H3N2); microbial diversity; mutation; nonhuman; nonstationary evolution; phylogeny; priority journal; senescence; trend study; validation study; allele; genetic variation; genetics; immunology; Influenza A virus; molecular evolution; pandemic; Alleles; Amino Acids; Antigens, Viral; Evolution, Molecular; Genetic Variation; Influenza A virus; Membrane Proteins; Pandemics; Viral Proteins
Издатель
  • National Academy of Sciences
Тип документа
  • journal article
Источник
  • scopus