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The effective rate of influenza reassortment is limited during human infection.
Sobel Leonard, Ashley; McClain, Micah T; Smith, Gavin J D; Wentworth, David E; Halpin, Rebecca A; Lin, Xudong; Ransier, Amy; Stockwell, Timothy B; Das, Suman R; Gilbert, Anthony S; Lambkin-Williams, Rob; Ginsburg, Geoffrey S; Woods, Christopher W; Koelle, Katia; Illingworth, Christopher J R.
Afiliação
  • Sobel Leonard A; Department of Biology, Duke University, Durham, North Carolina, United States of America.
  • McClain MT; Duke Center for Applied Genomics and Precision Medicine, Durham, North Carolina, United States of America.
  • Smith GJ; Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore.
  • Wentworth DE; J. Craig Venter Institute, Rockville, Maryland, United States of America.
  • Halpin RA; J. Craig Venter Institute, Rockville, Maryland, United States of America.
  • Lin X; J. Craig Venter Institute, Rockville, Maryland, United States of America.
  • Ransier A; J. Craig Venter Institute, Rockville, Maryland, United States of America.
  • Stockwell TB; J. Craig Venter Institute, Rockville, Maryland, United States of America.
  • Das SR; J. Craig Venter Institute, Rockville, Maryland, United States of America.
  • Gilbert AS; hVivo PLC, The QMB Innovation Centre, Queen Mary, University of London, London, United Kingdom.
  • Lambkin-Williams R; hVivo PLC, The QMB Innovation Centre, Queen Mary, University of London, London, United Kingdom.
  • Ginsburg GS; Duke Center for Applied Genomics and Precision Medicine, Durham, North Carolina, United States of America.
  • Woods CW; Duke Center for Applied Genomics and Precision Medicine, Durham, North Carolina, United States of America.
  • Koelle K; Department of Biology, Duke University, Durham, North Carolina, United States of America.
  • Illingworth CJ; Department of Genetics, University of Cambridge, Cambridge, United Kingdom.
PLoS Pathog ; 13(2): e1006203, 2017 02.
Article em En | MEDLINE | ID: mdl-28170438
ABSTRACT
We characterise the evolutionary dynamics of influenza infection described by viral sequence data collected from two challenge studies conducted in human hosts. Viral sequence data were collected at regular intervals from infected hosts. Changes in the sequence data observed across time show that the within-host evolution of the virus was driven by the reversion of variants acquired during previous passaging of the virus. Treatment of some patients with oseltamivir on the first day of infection did not lead to the emergence of drug resistance variants in patients. Using an evolutionary model, we inferred the effective rate of reassortment between viral segments, measuring the extent to which randomly chosen viruses within the host exchange genetic material. We find strong evidence that the rate of effective reassortment is low, such that genetic associations between polymorphic loci in different segments are preserved during the course of an infection in a manner not compatible with epistasis. Combining our evidence with that of previous studies we suggest that spatial heterogeneity in the viral population may reduce the extent to which reassortment is observed. Our results do not contradict previous findings of high rates of viral reassortment in vitro and in small animal studies, but indicate that in human hosts the effective rate of reassortment may be substantially more limited.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Orthomyxoviridae / Influenza Humana / Modelos Genéticos Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Orthomyxoviridae / Influenza Humana / Modelos Genéticos Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article