Abstract

BackgroundHuman T-cell leukemia virus types 1 and 2 (HTLV-1 and HTLV-2) are delta retroviruses with similar genetic organization. Although both viruses immortalize T-cells in vitro, they exhibit distinct pathogenic potential in vivo. To search for possible differences in its expression strategy with respect to HTLV-1, we investigated the pattern of HTLV-2 expression in infected cell lines and peripheral blood mononuclear cells (PBMCs) from infected patients using splice site-specific quantitative RT-PCR.FindingsA novel alternative splice acceptor site for exon 2 was identified; its usage in env transcripts was found to be subtype-specific. Time-course analysis revealed a two-phase expression kinetics in an infected cell line and in PBMCs of two of the three patients examined; this pattern was reminiscent of HTLV-1. In addition, the minus-strand APH2 transcript was mainly detected in the nucleus, a feature that was similar to its HTLV-1 orthologue HBZ. In contrast to HTLV-1, expression of the mRNA encoding the main regulatory proteins Tax and Rex and that of the mRNAs encoding the p28 and truncated Rex inhibitors is skewed towards p28/truncated Rex inhibitors in HTLV-2.ConclusionOur data suggest a general converging pattern of expression of HTLV-2 and HTLV-1 and highlight peculiar differences in the expression of regulatory proteins that might influence the pathobiology of these viruses.

Highlights

  • Human T-cell leukemia virus types 1 and 2 (HTLV-1 and HTLV-2) are delta retroviruses with similar genetic organization

  • Our data suggest a general converging pattern of expression of HTLV-2 and Human T-cell leukaemia virus type 1 (HTLV-1) and highlight peculiar differences in the expression of regulatory proteins that might influence the pathobiology of these viruses

  • Like HTLV-1, HTLV-2 produces plus- and minusstrand alternatively spliced transcripts that code for virion components and non-structural proteins, including Tax and Rex that regulate viral expression at the transcriptional and post-transcriptional levels, respectively [8,9]

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Summary

Introduction

Human T-cell leukemia virus types 1 and 2 (HTLV-1 and HTLV-2) are delta retroviruses with similar genetic organization. We employed splice site-specific quantitative RT-PCR (qRT-PCR) to measure individual HTLV-2 mRNAs (Figure 1) and their expression kinetics in chronically infected cell lines and in peripheral blood mononuclear cells (PBMCs) obtained from HTLV-2-infected individuals. Identification of a novel HTLV-2 splice acceptor-site We first analyzed the pattern of viral mRNAs in the HTLV-2-infected cell lines Mo-T (infected with subtype A) and BJAB-Gu (infected with subtype B).

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