TT virus: preferential distribution in CD19(+) peripheral blood mononuclear cells and lack of viral integration

J Med Virol. 2002 Feb;66(2):276-84. doi: 10.1002/jmv.2142.

Abstract

In order to determine whether peripheral blood mononuclear cells (PBMC) contain proviral DNA or double-stranded replicative forms of TT virus (TTV) and to define which cell subset harbors TTV, we analyzed 126 PBMC DNA samples by PCR, using the NG059/NG061/NG063 and the T801/T935 primer sets. TTV sequences were detected in nearly 20% (25/126) of PBMC DNA samples. Analysis of PBMC subsets revealed that TTV was preferentially distributed in CD19(+) cells. TTV DNA was also detected in CD3(+)/CD19(+) double-depleted cells but was undetectable in CD3(+) cells. After degradation of single-stranded DNA using mung bean nuclease (MBN), TTV could not be detected in previously TTV-positive PBMC DNA samples nor in DNA from CD19(+) cells, CD3(+)-depleted, and CD3(+)/CD19(+) double-depleted cells, indicating the lack of TTV DNA integration and the absence of viral double-stranded replicative intermediates in PBMC or PBMC subset cells. Our data indicate that PBMC and PBMC subsets are not the major sites of TTV replication.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Antigens, CD19 / metabolism*
  • Base Sequence
  • CD3 Complex / metabolism
  • Child
  • Child, Preschool
  • DNA Virus Infections / virology*
  • DNA, Viral / analysis
  • Humans
  • Infant
  • Leukocytes, Mononuclear / virology*
  • Molecular Sequence Data
  • Prevalence
  • Sequence Analysis, DNA
  • Torque teno virus / genetics
  • Torque teno virus / isolation & purification*
  • Torque teno virus / physiology
  • Virus Integration*
  • Virus Replication

Substances

  • Antigens, CD19
  • CD3 Complex
  • DNA, Viral