Influenza A gradual and epochal evolution: insights from simple models.
The recurrence of influenza A epidemics has originally been explained by a "continuous antigenic drift" scenario. Recently, it has been shown that if genetic drift is gradual, the evolution of influenza A main antigen, the haemagglutinin, is punctuated. As a consequence, it has been sugges...
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doaj-ca01f5d5f6c54b138b94346aa21db3d72021-03-03T22:34:20ZengPublic Library of Science (PLoS)PLoS ONE1932-62032009-10-01410e742610.1371/journal.pone.0007426Influenza A gradual and epochal evolution: insights from simple models.Sébastien BallesterosElisabeta VerguBernard CazellesThe recurrence of influenza A epidemics has originally been explained by a "continuous antigenic drift" scenario. Recently, it has been shown that if genetic drift is gradual, the evolution of influenza A main antigen, the haemagglutinin, is punctuated. As a consequence, it has been suggested that influenza A dynamics at the population level should be approximated by a serial model. Here, simple models are used to test whether a serial model requires gradual antigenic drift within groups of strains with the same antigenic properties (antigenic clusters). We compare the effect of status based and history based frameworks and the influence of reduced susceptibility and infectivity assumptions on the transient dynamics of antigenic clusters. Our results reveal that the replacement of a resident antigenic cluster by a mutant cluster, as observed in data, is reproduced only by the status based model integrating the reduced infectivity assumption. This combination of assumptions is useful to overcome the otherwise extremely high model dimensionality of models incorporating many strains, but relies on a biological hypothesis not obviously satisfied. Our findings finally suggest the dynamical importance of gradual antigenic drift even in the presence of punctuated immune escape. A more regular renewal of susceptible pool than the one implemented in a serial model should be part of a minimal theory for influenza at the population level.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/19841740/?tool=EBI |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Sébastien Ballesteros Elisabeta Vergu Bernard Cazelles |
spellingShingle |
Sébastien Ballesteros Elisabeta Vergu Bernard Cazelles Influenza A gradual and epochal evolution: insights from simple models. PLoS ONE |
author_facet |
Sébastien Ballesteros Elisabeta Vergu Bernard Cazelles |
author_sort |
Sébastien Ballesteros |
title |
Influenza A gradual and epochal evolution: insights from simple models. |
title_short |
Influenza A gradual and epochal evolution: insights from simple models. |
title_full |
Influenza A gradual and epochal evolution: insights from simple models. |
title_fullStr |
Influenza A gradual and epochal evolution: insights from simple models. |
title_full_unstemmed |
Influenza A gradual and epochal evolution: insights from simple models. |
title_sort |
influenza a gradual and epochal evolution: insights from simple models. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2009-10-01 |
description |
The recurrence of influenza A epidemics has originally been explained by a "continuous antigenic drift" scenario. Recently, it has been shown that if genetic drift is gradual, the evolution of influenza A main antigen, the haemagglutinin, is punctuated. As a consequence, it has been suggested that influenza A dynamics at the population level should be approximated by a serial model. Here, simple models are used to test whether a serial model requires gradual antigenic drift within groups of strains with the same antigenic properties (antigenic clusters). We compare the effect of status based and history based frameworks and the influence of reduced susceptibility and infectivity assumptions on the transient dynamics of antigenic clusters. Our results reveal that the replacement of a resident antigenic cluster by a mutant cluster, as observed in data, is reproduced only by the status based model integrating the reduced infectivity assumption. This combination of assumptions is useful to overcome the otherwise extremely high model dimensionality of models incorporating many strains, but relies on a biological hypothesis not obviously satisfied. Our findings finally suggest the dynamical importance of gradual antigenic drift even in the presence of punctuated immune escape. A more regular renewal of susceptible pool than the one implemented in a serial model should be part of a minimal theory for influenza at the population level. |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/19841740/?tool=EBI |
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