Influenza A Virus Negative Strand RNA Is Translated for CD8+ T Cell Immunosurveillance
Author(s) -
Heather D. Hickman,
Jacqueline W. Mays,
James S. Gibbs,
Ivan Košík,
Javier G. Magadán,
Kazuyo Takeda,
Suman R. Das,
Glennys V. Reynoso,
Barbara F. Ngudiankama,
Jiajie Wei,
John P. Shan,
Daniel T. McManus,
Jonathan W. Yewdell
Publication year - 2018
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1800586
Subject(s) - immunosurveillance , virology , virus , biology , cytotoxic t cell , rna virus , cd8 , influenza a virus , rna , immunology , immune system , genetics , gene , in vitro
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 K b -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.
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