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Profiling the Blood Compartment of Hematopoietic Stem Cell Transplant Patients During Human Cytomegalovirus Reactivation

Human cytomegalovirus (HCMV) is a widespread pathogen establishing a latent infection in its host. HCMV reactivation is a major health burden in immunocompromised individuals, and is a major cause of morbidity and mortality following hematopoietic stem cell transplantation (HSCT). Here we determined...

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Autores principales: Bernshtein, Biana, Nachshon, Aharon, Shnayder, Miri, Stern, Lauren, Avdic, Selmir, Blyth, Emily, Gottlieb, David, Abendroth, Allison, Slobedman, Barry, Stern-Ginossar, Noam, Schwartz, Michal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7820775/
https://www.ncbi.nlm.nih.gov/pubmed/33489936
http://dx.doi.org/10.3389/fcimb.2020.607470
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author Bernshtein, Biana
Nachshon, Aharon
Shnayder, Miri
Stern, Lauren
Avdic, Selmir
Blyth, Emily
Gottlieb, David
Abendroth, Allison
Slobedman, Barry
Stern-Ginossar, Noam
Schwartz, Michal
author_facet Bernshtein, Biana
Nachshon, Aharon
Shnayder, Miri
Stern, Lauren
Avdic, Selmir
Blyth, Emily
Gottlieb, David
Abendroth, Allison
Slobedman, Barry
Stern-Ginossar, Noam
Schwartz, Michal
author_sort Bernshtein, Biana
collection PubMed
description Human cytomegalovirus (HCMV) is a widespread pathogen establishing a latent infection in its host. HCMV reactivation is a major health burden in immunocompromised individuals, and is a major cause of morbidity and mortality following hematopoietic stem cell transplantation (HSCT). Here we determined HCMV genomic levels using droplet digital PCR in different peripheral blood mononuclear cell (PBMC) populations in HCMV reactivating HSCT patients. This high sensitivity approach revealed that all PBMC populations harbored extremely low levels of viral DNA at the peak of HCMV DNAemia. Transcriptomic analysis of PBMCs from high-DNAemia samples revealed elevated expression of genes typical of HCMV specific T cells, while regulatory T cell enhancers as well as additional genes related to immune response were downregulated. Viral transcript levels in these samples were extremely low, but remarkably, the detected transcripts were mainly immediate early viral genes. Overall, our data indicate that HCMV DNAemia is associated with distinct signatures of immune response in the blood compartment, however it is not necessarily accompanied by substantial infection of PBMCs and the residual infected PBMCs are not productively infected.
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spelling pubmed-78207752021-01-23 Profiling the Blood Compartment of Hematopoietic Stem Cell Transplant Patients During Human Cytomegalovirus Reactivation Bernshtein, Biana Nachshon, Aharon Shnayder, Miri Stern, Lauren Avdic, Selmir Blyth, Emily Gottlieb, David Abendroth, Allison Slobedman, Barry Stern-Ginossar, Noam Schwartz, Michal Front Cell Infect Microbiol Cellular and Infection Microbiology Human cytomegalovirus (HCMV) is a widespread pathogen establishing a latent infection in its host. HCMV reactivation is a major health burden in immunocompromised individuals, and is a major cause of morbidity and mortality following hematopoietic stem cell transplantation (HSCT). Here we determined HCMV genomic levels using droplet digital PCR in different peripheral blood mononuclear cell (PBMC) populations in HCMV reactivating HSCT patients. This high sensitivity approach revealed that all PBMC populations harbored extremely low levels of viral DNA at the peak of HCMV DNAemia. Transcriptomic analysis of PBMCs from high-DNAemia samples revealed elevated expression of genes typical of HCMV specific T cells, while regulatory T cell enhancers as well as additional genes related to immune response were downregulated. Viral transcript levels in these samples were extremely low, but remarkably, the detected transcripts were mainly immediate early viral genes. Overall, our data indicate that HCMV DNAemia is associated with distinct signatures of immune response in the blood compartment, however it is not necessarily accompanied by substantial infection of PBMCs and the residual infected PBMCs are not productively infected. Frontiers Media S.A. 2021-01-08 /pmc/articles/PMC7820775/ /pubmed/33489936 http://dx.doi.org/10.3389/fcimb.2020.607470 Text en Copyright © 2021 Bernshtein, Nachshon, Shnayder, Stern, Avdic, Blyth, Gottlieb, Abendroth, Slobedman, Stern-Ginossar and Schwartz 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 Cellular and Infection Microbiology
Bernshtein, Biana
Nachshon, Aharon
Shnayder, Miri
Stern, Lauren
Avdic, Selmir
Blyth, Emily
Gottlieb, David
Abendroth, Allison
Slobedman, Barry
Stern-Ginossar, Noam
Schwartz, Michal
Profiling the Blood Compartment of Hematopoietic Stem Cell Transplant Patients During Human Cytomegalovirus Reactivation
title Profiling the Blood Compartment of Hematopoietic Stem Cell Transplant Patients During Human Cytomegalovirus Reactivation
title_full Profiling the Blood Compartment of Hematopoietic Stem Cell Transplant Patients During Human Cytomegalovirus Reactivation
title_fullStr Profiling the Blood Compartment of Hematopoietic Stem Cell Transplant Patients During Human Cytomegalovirus Reactivation
title_full_unstemmed Profiling the Blood Compartment of Hematopoietic Stem Cell Transplant Patients During Human Cytomegalovirus Reactivation
title_short Profiling the Blood Compartment of Hematopoietic Stem Cell Transplant Patients During Human Cytomegalovirus Reactivation
title_sort profiling the blood compartment of hematopoietic stem cell transplant patients during human cytomegalovirus reactivation
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7820775/
https://www.ncbi.nlm.nih.gov/pubmed/33489936
http://dx.doi.org/10.3389/fcimb.2020.607470
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