Journal Article

Viral microRNA regulation of Akt is necessary for reactivation of Human Cytomegalovirus from latency in CD34+ hematopoietic progenitor cells and humanized mice

Turner, Rebekah, Parkins, Christopher J., Yurochko, Andrew D., Hancock, Meaghan H., Mitchell, Jennifer, Lee, Byeong-Jae, Slind, Luke, Diggins, Nicole L., Pham, Andrew H., Nelson, Jay A., Caposio, Patrizia

2024

Overview

Human cytomegalovirus (HCMV) actively manipulates cellular signaling pathways to benefit viral replication. Phosphatidyl-inositol 3-kinase (PI3K)/Akt signaling is an important negative regulator of HCMV replication, and during lytic infection the virus utilizes pUL38 to limit Akt phosphorylation and activity. During latency, PI3K/Akt signaling also limits virus replication, but how this is overcome at the time of reactivation is unknown. Virally encoded microRNAs (miRNAs) are a key component of the virus arsenal used to alter signaling during latency and reactivation. In the present study we show that three HCMV miRNAs (miR-UL36, miR-UL112 and miR-UL148D) downregulate Akt expression and attenuate downstream signaling, resulting in the activation of FOXO3a and enhanced internal promoter-driven IE transcription. A virus lacking expression of all three miRNAs is unable to reactivate from latency both in CD34 + hematopoietic progenitor cells and in a humanized mouse model of HCMV infection, however downregulating Akt restores the ability of the mutant virus to replicate. These findings highlight the negative role Akt signaling plays in HCMV replication in lytic and latent infection and how the virus has evolved miRNA-mediated countermeasures to promote successful reactivation.

• Publisher: Public Library of Science,Public Library of Science (PLoS)
• Subject: 1-Phosphatidylinositol 3-kinase / AKT protein / Animals / Antigens, CD34 - metabolism / Biology and life sciences / Bone marrow / CD34 antigen / Cells (biology) / Cytokines / Cytomegalovirus / Cytomegalovirus - genetics / Cytomegalovirus - physiology / Cytomegalovirus Infections - genetics / Cytomegalovirus Infections - metabolism / Cytomegalovirus Infections - virology / Fibroblasts / FOXO3 protein / Gene Expression Regulation, Viral / Hematopoietic stem cells / Hematopoietic Stem Cells - metabolism / Hematopoietic Stem Cells - virology / Hemopoiesis / Humans / Hypotheses / Infections / Inositol / Inositols / Kinases / Latency / Latent infection / Medicine and Health Sciences / Mice / MicroRNAs / MicroRNAs - genetics / MicroRNAs - metabolism / miRNA / Phosphorylation / Progenitor cells / Proteins / Proto-Oncogene Proteins c-akt - metabolism / Regulation / Replication / Research and Analysis Methods / RNA, Viral - genetics / RNA, Viral - metabolism / Signal Transduction / Stem cells / Virus Activation - physiology / Virus Latency - physiology / Virus Replication - physiology / Viruses