TY - JOUR
T1 - Predicting Antigenicity of Influenza A Viruses Using biophysical ideas
AU - Degoot, Abdoelnaser M.
AU - Adabor, Emmanuel S.
AU - Chirove, Faraimunashe
AU - Ndifon, Wilfred
N1 - Publisher Copyright:
© 2019, The Author(s).
PY - 2019/12/1
Y1 - 2019/12/1
N2 - Antigenic variations of influenza A viruses are induced by genomic mutation in their trans-membrane protein HA1, eliciting viral escape from neutralization by antibodies generated in prior infections or vaccinations. Prediction of antigenic relationships among influenza viruses is useful for designing (or updating the existing) influenza vaccines, provides important insights into the evolutionary mechanisms underpinning viral antigenic variations, and helps to understand viral epidemiology. In this study, we present a simple and physically interpretable model that can predict antigenic relationships among influenza A viruses, based on biophysical ideas, using both genomic amino acid sequences and experimental antigenic data. We demonstrate the applicability of the model using a benchmark dataset of four subtypes of influenza A (H1N1, H3N2, H5N1, and H9N2) viruses and report on its performance profiles. Additionally, analysis of the model’s parameters confirms several observations that are consistent with the findings of other previous studies, for which we provide plausible explanations.
AB - Antigenic variations of influenza A viruses are induced by genomic mutation in their trans-membrane protein HA1, eliciting viral escape from neutralization by antibodies generated in prior infections or vaccinations. Prediction of antigenic relationships among influenza viruses is useful for designing (or updating the existing) influenza vaccines, provides important insights into the evolutionary mechanisms underpinning viral antigenic variations, and helps to understand viral epidemiology. In this study, we present a simple and physically interpretable model that can predict antigenic relationships among influenza A viruses, based on biophysical ideas, using both genomic amino acid sequences and experimental antigenic data. We demonstrate the applicability of the model using a benchmark dataset of four subtypes of influenza A (H1N1, H3N2, H5N1, and H9N2) viruses and report on its performance profiles. Additionally, analysis of the model’s parameters confirms several observations that are consistent with the findings of other previous studies, for which we provide plausible explanations.
UR - http://www.scopus.com/inward/record.url?scp=85069505522&partnerID=8YFLogxK
U2 - 10.1038/s41598-019-46740-5
DO - 10.1038/s41598-019-46740-5
M3 - Article
C2 - 31308446
AN - SCOPUS:85069505522
SN - 2045-2322
VL - 9
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 10218
ER -