Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request

Interferon lambda 4 impacts the genetic diversity of hepatitis C virus

Item request has been placed! ×
Item request cannot be made. ×
loading   Processing Request
  • معلومة اضافية
    • Contributors:
      University of Oxford; University of Glasgow; University of Glascow; Nuffield Department of Medicine Oxford, UK (Big Data Institute); Queen Mary University of London (QMUL); University of Nottingham, UK (UON); King's College Hospital (KCH); Maladies infectieuses et vecteurs : écologie, génétique, évolution et contrôle (MIVEGEC); Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD France-Sud )
    • بيانات النشر:
      HAL CCSD
      eLife Sciences Publication
    • الموضوع:
      2019
    • Collection:
      Université de Montpellier: HAL
    • نبذة مختصرة :
      International audience ; Hepatitis C virus (HCV) is a highly variable pathogen that frequently establishes chronic infection. This genetic variability is affected by the adaptive immune response but the contribution of other host factors is unclear. Here, we examined the role played by interferon lambda-4 (IFN-λ4) on HCV diversity; IFN-λ4 plays a crucial role in spontaneous clearance or establishment of chronicity following acute infection. We performed viral genome-wide association studies using human and viral data from 485 patients of white ancestry infected with HCV genotype 3a. We demonstrate that combinations of host genetic variants, which determine IFN-λ4 protein production and activity, influence amino acid variation across the viral polyprotein - not restricted to specific viral proteins or HLA restricted epitopes - and modulate viral load. We also observed an association with viral di-nucleotide proportions. These results support a direct role for IFN-λ4 in exerting selective pressure across the viral genome, possibly by a novel mechanism.
    • Relation:
      info:eu-repo/semantics/altIdentifier/pmid/31478835; hal-03684509; https://hal.umontpellier.fr/hal-03684509; https://hal.umontpellier.fr/hal-03684509/document; https://hal.umontpellier.fr/hal-03684509/file/Ansari_eLife_2019.pdf; PUBMED: 31478835; PUBMEDCENTRAL: PMC6721795
    • الرقم المعرف:
      10.7554/eLife.42463
    • Rights:
      http://creativecommons.org/licenses/by/ ; info:eu-repo/semantics/OpenAccess
    • الرقم المعرف:
      edsbas.7587D17B