| Literature DB >> 33489936 |
Biana Bernshtein1, Aharon Nachshon1, Miri Shnayder1, Lauren Stern2, Selmir Avdic3, Emily Blyth3,4,5,6, David Gottlieb4,5,6, Allison Abendroth2, Barry Slobedman2, Noam Stern-Ginossar1, Michal Schwartz1.
Abstract
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.Entities:
Keywords: blood compartment; hematopoietic stem cell transplantation; human cytomegalovirus; peripheral blood mononuclear cell; reactivation
Year: 2021 PMID: 33489936 PMCID: PMC7820775 DOI: 10.3389/fcimb.2020.607470
Source DB: PubMed Journal: Front Cell Infect Microbiol ISSN: 2235-2988 Impact factor: 5.293