A dose-effect relationship for deltaretrovirus-dependent leukemogenesis in sheep

<p>Abstract</p> <p>Background</p> <p>Retrovirus-induced tumors develop in a broad range of frequencies and after extremely variable periods of time, from only a few days to several decades, depending mainly on virus type. For hitherto unexplained reasons, deltaretroviru...

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Main Authors: Wattel Eric, Willems Lucas, Kerkhofs Pierre, Lançon Agnes, Debacq Christophe, Alcaraz Maria, Pomier Carole, Mortreux Franck
Format: Article
Language:English
Published: BMC 2009-04-01
Series:Retrovirology
Online Access:http://www.retrovirology.com/content/6/1/30
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spelling doaj-203da2f2d5714b34a4984f1cd43b56662020-11-24T22:02:58ZengBMCRetrovirology1742-46902009-04-01613010.1186/1742-4690-6-30A dose-effect relationship for deltaretrovirus-dependent leukemogenesis in sheepWattel EricWillems LucasKerkhofs PierreLançon AgnesDebacq ChristopheAlcaraz MariaPomier CaroleMortreux Franck<p>Abstract</p> <p>Background</p> <p>Retrovirus-induced tumors develop in a broad range of frequencies and after extremely variable periods of time, from only a few days to several decades, depending mainly on virus type. For hitherto unexplained reasons, deltaretroviruses cause hematological malignancies only in a minority of naturally infected organisms and after a very prolonged period of clinical latency.</p> <p>Results</p> <p>Here we demonstrate that the development of malignancies in sheep experimentally infected with the deltaretrovirus bovine leukemia virus (BLV) depends only on the level of BLV replication. Animals were experimentally infected with leukemogenic or attenuated, but infectious, BLV molecular clones and monitored prospectively through 8 months for viral replication. As early as 2 weeks after infection and subsequently at any time during follow-up, leukemogenic viruses produced significantly higher absolute levels of reverse transcription (RT), clonal expansion of infected cells, and circulating proviruses with RT- and somatic-dependent mutations than attenuated viruses. These differences were only quantitative, and both kinds of viruses triggered parallel temporal fluctuations of host lymphoid cells, viral loads, infected cell clonality and proliferation.</p> <p>Conclusion</p> <p>Deltaretrovirus-associated leukemogenesis in sheep appears to be a two-hit process over time depending on the amounts of first horizontally and then vertically expanded viruses.</p> http://www.retrovirology.com/content/6/1/30
collection DOAJ
language English
format Article
sources DOAJ
author Wattel Eric
Willems Lucas
Kerkhofs Pierre
Lançon Agnes
Debacq Christophe
Alcaraz Maria
Pomier Carole
Mortreux Franck
spellingShingle Wattel Eric
Willems Lucas
Kerkhofs Pierre
Lançon Agnes
Debacq Christophe
Alcaraz Maria
Pomier Carole
Mortreux Franck
A dose-effect relationship for deltaretrovirus-dependent leukemogenesis in sheep
Retrovirology
author_facet Wattel Eric
Willems Lucas
Kerkhofs Pierre
Lançon Agnes
Debacq Christophe
Alcaraz Maria
Pomier Carole
Mortreux Franck
author_sort Wattel Eric
title A dose-effect relationship for deltaretrovirus-dependent leukemogenesis in sheep
title_short A dose-effect relationship for deltaretrovirus-dependent leukemogenesis in sheep
title_full A dose-effect relationship for deltaretrovirus-dependent leukemogenesis in sheep
title_fullStr A dose-effect relationship for deltaretrovirus-dependent leukemogenesis in sheep
title_full_unstemmed A dose-effect relationship for deltaretrovirus-dependent leukemogenesis in sheep
title_sort dose-effect relationship for deltaretrovirus-dependent leukemogenesis in sheep
publisher BMC
series Retrovirology
issn 1742-4690
publishDate 2009-04-01
description <p>Abstract</p> <p>Background</p> <p>Retrovirus-induced tumors develop in a broad range of frequencies and after extremely variable periods of time, from only a few days to several decades, depending mainly on virus type. For hitherto unexplained reasons, deltaretroviruses cause hematological malignancies only in a minority of naturally infected organisms and after a very prolonged period of clinical latency.</p> <p>Results</p> <p>Here we demonstrate that the development of malignancies in sheep experimentally infected with the deltaretrovirus bovine leukemia virus (BLV) depends only on the level of BLV replication. Animals were experimentally infected with leukemogenic or attenuated, but infectious, BLV molecular clones and monitored prospectively through 8 months for viral replication. As early as 2 weeks after infection and subsequently at any time during follow-up, leukemogenic viruses produced significantly higher absolute levels of reverse transcription (RT), clonal expansion of infected cells, and circulating proviruses with RT- and somatic-dependent mutations than attenuated viruses. These differences were only quantitative, and both kinds of viruses triggered parallel temporal fluctuations of host lymphoid cells, viral loads, infected cell clonality and proliferation.</p> <p>Conclusion</p> <p>Deltaretrovirus-associated leukemogenesis in sheep appears to be a two-hit process over time depending on the amounts of first horizontally and then vertically expanded viruses.</p>
url http://www.retrovirology.com/content/6/1/30
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