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A polymorphic residue that attenuates the antiviral potential of interferon lambda 4 in hominid lineages.
Bamford, Connor G G; Aranday-Cortes, Elihu; Filipe, Ines Cordeiro; Sukumar, Swathi; Mair, Daniel; Filipe, Ana da Silva; Mendoza, Juan L; Garcia, K Christopher; Fan, Shaohua; Tishkoff, Sarah A; McLauchlan, John.
Affiliation
  • Bamford CGG; MRC-University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
  • Aranday-Cortes E; MRC-University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
  • Filipe IC; MRC-University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
  • Sukumar S; MRC-University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
  • Mair D; MRC-University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
  • Filipe ADS; MRC-University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
  • Mendoza JL; Howard Hughes Medical Institute, Department of Molecular and Cellular Physiology and Department of Structural Biology, Stanford University School of Medicine, Stanford, CA, United States of America.
  • Garcia KC; Howard Hughes Medical Institute, Department of Molecular and Cellular Physiology and Department of Structural Biology, Stanford University School of Medicine, Stanford, CA, United States of America.
  • Fan S; Departments of Genetics and Biology, University of Pennsylvania, Philadelphia PA, United States of America.
  • Tishkoff SA; Departments of Genetics and Biology, University of Pennsylvania, Philadelphia PA, United States of America.
  • McLauchlan J; MRC-University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
PLoS Pathog ; 14(10): e1007307, 2018 10.
Article in En | MEDLINE | ID: mdl-30308076
ABSTRACT
As antimicrobial signalling molecules, type III or lambda interferons (IFNλs) are critical for defence against infection by diverse pathogens, including bacteria, fungi and viruses. Counter-intuitively, expression of one member of the family, IFNλ4, is associated with decreased clearance of hepatitis C virus (HCV) in the human population; by contrast, a natural frameshift mutation that abrogates IFNλ4 production improves HCV clearance. To further understand how genetic variation between and within species affects IFNλ4 function, we screened a panel of all known extant coding variants of human IFNλ4 for their antiviral potential and identify three that substantially affect activity P70S, L79F and K154E. The most notable variant was K154E, which was found in African Congo rainforest 'Pygmy' hunter-gatherers. K154E greatly enhanced in vitro activity in a range of antiviral (HCV, Zika virus, influenza virus and encephalomyocarditis virus) and gene expression assays. Remarkably, E154 is the ancestral residue in mammalian IFNλ4s and is extremely well conserved, yet K154 has been fixed throughout evolution of the hominid genus Homo, including Neanderthals. Compared to chimpanzee IFNλ4, the human orthologue had reduced activity due to amino acid K154. Comparison of published gene expression data from humans and chimpanzees showed that this difference in activity between K154 and E154 in IFNλ4 correlates with differences in antiviral gene expression in vivo during HCV infection. Mechanistically, our data show that the human-specific K154 negatively affects IFNλ4 activity through a novel means by reducing its secretion and potency. We thus demonstrate that attenuated activity of IFNλ4 is conserved among humans and postulate that differences in IFNλ4 activity between species contribute to distinct host-specific responses to-and outcomes of-infection, such as HCV infection. The driver of reduced IFNλ4 antiviral activity in humans remains unknown but likely arose between 6 million and 360,000 years ago in Africa.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antiviral Agents / Interleukins / Hepatitis C / Cardiovirus Infections / Polymorphism, Single Nucleotide / Zika Virus Infection Limits: Animals / Humans Language: En Journal: PLoS Pathog Year: 2018 Document type: Article Affiliation country: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antiviral Agents / Interleukins / Hepatitis C / Cardiovirus Infections / Polymorphism, Single Nucleotide / Zika Virus Infection Limits: Animals / Humans Language: En Journal: PLoS Pathog Year: 2018 Document type: Article Affiliation country: United kingdom