| Literature DB >> 30012850 |
Heather D Hickman1, Jacqueline W Mays1, James Gibbs1, Ivan Kosik1, Javier G Magadán1, Kazuyo Takeda2, Suman Das1, Glennys V Reynoso1, Barbara F Ngudiankama1, JiaJie Wei1, John P Shannon1, Daniel McManus1, Jonathan W Yewdell3.
Abstract
Probing the limits of CD8+ T cell immunosurveillance, we inserted the SIINFEKL peptide into influenza A virus (IAV)-negative strand gene segments. Although IAV genomic RNA is considered noncoding, there is a conserved, relatively long open reading frame present in segment 8, encoding a potential protein termed NEG8. The biosynthesis of NEG8 from IAV has yet to be demonstrated. Although we failed to detect NEG8 protein expression in IAV-infected mouse cells, cell surface Kb-SIINFEKL complexes are generated when SIINFEKL is genetically appended to the predicted C terminus of NEG8, as shown by activation of OT-I T cells in vitro and in vivo. Moreover, recombinant IAV encoding of SIINFEKL embedded in the negative strand of the neuraminidase-stalk coding sequence also activates OT-I T cells in mice. Together, our findings demonstrate both the translation of sequences on the negative strand of a single-stranded RNA virus and its relevance in antiviral immunosurveillance.Entities:
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Year: 2018 PMID: 30012850 PMCID: PMC6082381 DOI: 10.4049/jimmunol.1800586
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422