Restricted replication of xenotropic murine leukemia virus-related virus in pigtailed macaques

Gregory Q. Del Prete, Mary F. Kearney, Jon Spindler, Ann Wiegand, Elena Chertova, James D. Roser, Jacob D. Estes, Xing Pei Hao, Charles M. Trubey, Abigail Lara, Kyeong Eun Lee, Chawaree Chaipan, Julian W. Bess, Kunio Nagashima, Brandon F. Keele, Rhonda Macallister, Jeremy Smedley, Vinay K. Pathak, Vineet N. KewalRamani, John M. CoffinJeffrey D. Lifson

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

Although xenotropic murine leukemia virus-related virus (XMRV) has been previously linked to prostate cancer and myalgic encephalomyelitis/chronic fatigue syndrome, recent data indicate that results interpreted as evidence of human XMRV infection reflect laboratory contamination rather than authentic in vivo infection. Nevertheless, XMRV is a retrovirus of undefined pathogenic potential that is able to replicate in human cells. Here we describe a comprehensive analysis of two male pigtailed macaques (Macaca nemestrina) experimentally infected with XMRV. Following intravenous inoculation with>1010 RNA copy equivalents of XMRV, viral replication was limited and transient, peaking at<2,200 viral RNA (vRNA) copies/ml plasma and becoming undetectable by 4 weeks postinfection, though viral DNA (vDNA) in peripheral blood mononuclear cells remained detectable through 119 days of follow-up. Similarly, vRNA was not detectable in lymph nodes by in situ hybridization despite detectable vDNA. Sequencing of cell-associated vDNA revealed extensive G-to-A hypermutation, suggestive of APOBECmediated viral restriction. Consistent with limited viral replication, we found transient upregulation of type I interferon responses that returned to baseline by 2 weeks postinfection, no detectable cellular immune responses, and limited or no spread to prostate tissue. Antibody responses, including neutralizing antibodies, however, were detectable by 2 weeks postinfection and maintained throughout the study. Both animals were healthy for the duration of follow-up. These findings indicate that XMRV replication and spread were limited in pigtailed macaques, predominantly by APOBEC-mediated hypermutation. Given that human APOBEC proteins restrict XMRV infection in vitro, human XMRV infection, if it occurred, would be expected to be characterized by similarly limited viral replication and spread.

Original languageEnglish (US)
Pages (from-to)3152-3166
Number of pages15
JournalJournal of virology
Volume86
Issue number6
DOIs
StatePublished - Mar 2012
Externally publishedYes

ASJC Scopus subject areas

  • Microbiology
  • Immunology
  • Insect Science
  • Virology

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