Antibody selection and amino acid reversions

dc.contributor.authorDa Silva, J.
dc.date.issued2012
dc.description.abstractPathogens adapt to antibody surveillance through amino acid replacements in targeted protein regions, or epitopes, that interfere with antibody binding. However, such escape mutations may exact a fitness cost due to impaired protein function. Here, it is hypothesized that the recurring generation of specific neutralizing antibodies to an epitope region as it evolves in response to antibody selection will cause amino acid reversions by releasing early escape mutations from immune selection. The plausibility of this hypothesis was tested with stochastic simulation of adaptation at the molecular sequence level in finite populations. Under the conditions of strong selection and weak mutation, the rates of allele fixation and amino acid reversion increased with population size and selection coefficients. These rates decreased with population size, however, if mutation became strong, because clonal interference reduced the rate of adaptation. The model successfully predicts the rate of reversion per allele fixation for an important human immunodeficiency virus type 1 (HIV-1) antibody epitope region. Therefore, antibody selection may generate complex adaptive dynamics.
dc.description.statementofresponsibilityJack da Silva
dc.identifier.citationEvolution, 2012; 66(10):3079-3087
dc.identifier.doi10.1111/j.1558-5646.2012.01686.x
dc.identifier.issn0014-3820
dc.identifier.issn1558-5646
dc.identifier.orcidDa Silva, J. [0000-0001-5631-5421]
dc.identifier.urihttp://hdl.handle.net/2440/74502
dc.language.isoen
dc.publisherSoc Study Evolution
dc.rights© 2012 The Author(s). Evolution © 2012 The Society for the Study of Evolution.
dc.source.urihttps://doi.org/10.1111/j.1558-5646.2012.01686.x
dc.subjectAmino acid reversion
dc.subjectantibody
dc.subjectepitope
dc.subjectescape mutation
dc.subjectHIV
dc.titleAntibody selection and amino acid reversions
dc.typeJournal article
pubs.publication-statusPublished

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