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Post-transplant Replication of Torque Teno Virus in Granulocytes

Torque Teno virus (TTV) in humans is characterized by ubiquitous occurrence in peripheral blood (PB), without any related disease described to date. Several studies reported a significant increase of TTV plasma DNA levels in allogeneic transplant recipients, and suggested a correlation of elevated v...

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Autores principales: Kosulin, Karin, Kernbichler, Silvia, Pichler, Herbert, Lawitschka, Anita, Geyeregger, René, Witt, Volker, Lion, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6281686/
https://www.ncbi.nlm.nih.gov/pubmed/30555452
http://dx.doi.org/10.3389/fmicb.2018.02956
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author Kosulin, Karin
Kernbichler, Silvia
Pichler, Herbert
Lawitschka, Anita
Geyeregger, René
Witt, Volker
Lion, Thomas
author_facet Kosulin, Karin
Kernbichler, Silvia
Pichler, Herbert
Lawitschka, Anita
Geyeregger, René
Witt, Volker
Lion, Thomas
author_sort Kosulin, Karin
collection PubMed
description Torque Teno virus (TTV) in humans is characterized by ubiquitous occurrence in peripheral blood (PB), without any related disease described to date. Several studies reported a significant increase of TTV plasma DNA levels in allogeneic transplant recipients, and suggested a correlation of elevated virus titers with immunosuppression and transplant-related complications. However, the site of viral replication in this setting has remained unclear. We have studied TTV in serial plasma specimens derived from 43 pediatric allogeneic hematopoietic stem cell transplantation (HSCT) recipients by RQ-PCR, and found increasing TTV-DNA levels in all patients post-transplant, with a peak around day +100 and maximum virus copy numbers reaching 4 × 10E9/ml. To assess whether the virus replicates in PB-cells, leukocyte subsets including granulocytes, monocytes, NK-cells, T- and B-lymphocytes were serially isolated by flow-sorting for TTV analysis in 19 patients. The virus was undetectable in most cell types, but was identified in granulocytes in all instances, revealing a median DNA copy number increase of 1.8 logs between days +30–100 post-transplant. Our data therefore provide evidence for TTV replication in granulocytes in this setting. In a control cohort of immunocompetent children and in HSCT recipients before day +30, TTV positivity in granulocytes was less common (33%), and the copy numbers were considerably lower. However, rising TTV replication about 2 weeks after granulocyte engraftment (>500 cells/μl) was observed suggesting that granulocyte recovery might be required for TTV expansion in severely immunosuppressed transplant recipients.
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spelling pubmed-62816862018-12-14 Post-transplant Replication of Torque Teno Virus in Granulocytes Kosulin, Karin Kernbichler, Silvia Pichler, Herbert Lawitschka, Anita Geyeregger, René Witt, Volker Lion, Thomas Front Microbiol Microbiology Torque Teno virus (TTV) in humans is characterized by ubiquitous occurrence in peripheral blood (PB), without any related disease described to date. Several studies reported a significant increase of TTV plasma DNA levels in allogeneic transplant recipients, and suggested a correlation of elevated virus titers with immunosuppression and transplant-related complications. However, the site of viral replication in this setting has remained unclear. We have studied TTV in serial plasma specimens derived from 43 pediatric allogeneic hematopoietic stem cell transplantation (HSCT) recipients by RQ-PCR, and found increasing TTV-DNA levels in all patients post-transplant, with a peak around day +100 and maximum virus copy numbers reaching 4 × 10E9/ml. To assess whether the virus replicates in PB-cells, leukocyte subsets including granulocytes, monocytes, NK-cells, T- and B-lymphocytes were serially isolated by flow-sorting for TTV analysis in 19 patients. The virus was undetectable in most cell types, but was identified in granulocytes in all instances, revealing a median DNA copy number increase of 1.8 logs between days +30–100 post-transplant. Our data therefore provide evidence for TTV replication in granulocytes in this setting. In a control cohort of immunocompetent children and in HSCT recipients before day +30, TTV positivity in granulocytes was less common (33%), and the copy numbers were considerably lower. However, rising TTV replication about 2 weeks after granulocyte engraftment (>500 cells/μl) was observed suggesting that granulocyte recovery might be required for TTV expansion in severely immunosuppressed transplant recipients. Frontiers Media S.A. 2018-11-29 /pmc/articles/PMC6281686/ /pubmed/30555452 http://dx.doi.org/10.3389/fmicb.2018.02956 Text en Copyright © 2018 Kosulin, Kernbichler, Pichler, Lawitschka, Geyeregger, Witt and Lion. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Kosulin, Karin
Kernbichler, Silvia
Pichler, Herbert
Lawitschka, Anita
Geyeregger, René
Witt, Volker
Lion, Thomas
Post-transplant Replication of Torque Teno Virus in Granulocytes
title Post-transplant Replication of Torque Teno Virus in Granulocytes
title_full Post-transplant Replication of Torque Teno Virus in Granulocytes
title_fullStr Post-transplant Replication of Torque Teno Virus in Granulocytes
title_full_unstemmed Post-transplant Replication of Torque Teno Virus in Granulocytes
title_short Post-transplant Replication of Torque Teno Virus in Granulocytes
title_sort post-transplant replication of torque teno virus in granulocytes
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6281686/
https://www.ncbi.nlm.nih.gov/pubmed/30555452
http://dx.doi.org/10.3389/fmicb.2018.02956
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