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Tertiary mutations stabilize CD8+ T lymphocyte escape-associated compensatory mutations following transmission of simian immunodeficiency virus

  • Benjamin J. Burwitz
  • , Helen L. Wu
  • , Jason S. Reed
  • , Katherine B. Hammond
  • , Laura P. Newman
  • , Benjamin N. Bimber
  • , Francesca A. Nimiyongskul
  • , Enrique J. Leon
  • , Nicholas J. Maness
  • , Thomas C. Friedrich
  • , Masaru Yokoyama
  • , Hironori Sato
  • , Tetsuro Matano
  • , David H. O'Connor
  • , Jonah B. Sacha

Research output: Contribution to journalArticlepeer-review

Abstract

Compensatory mutations offset fitness defects resulting from CD8+ T lymphocyte (CD8TL)-mediated escape, but their impact on viral evolution following transmission to naive hosts remains unclear. Here, we investigated the reversion kinetics of Gag181-189CM9 CD8TL escape-associated compensatory mutations in simian immunodeficiency virus (SIV)-infected macaques. Preexisting compensatory mutations did not result in acute-phase escape of the SIVmac239 CD8TL epitope Gag181-189CM9 and instead required a tertiary mutation for stabilization in the absence of Gag181-189CM9 escape mutations. Therefore, transmitted compensatory mutations do not necessarily predict rapid CD8TL escape.

Original languageEnglish (US)
Pages (from-to)3598-3604
Number of pages7
JournalJournal of virology
Volume88
Issue number6
DOIs
StatePublished - Mar 2014

Funding

FundersFunder number
NIH Office of the DirectorP51OD011106

    ASJC Scopus subject areas

    • Microbiology
    • Immunology
    • Insect Science
    • Virology

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