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Intrinsic Immune Mechanisms Restricting Human Cytomegalovirus Replication

Cellular restriction factors (RFs) act as important constitutive innate immune barriers against viruses. In 2006, the promyelocytic leukemia protein was described as the first RF against human cytomegalovirus (HCMV) infection which is antagonized by the viral immediate early protein IE1. Since then,...

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Autores principales: Schilling, Eva-Maria, Scherer, Myriam, Stamminger, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7911179/
https://www.ncbi.nlm.nih.gov/pubmed/33530304
http://dx.doi.org/10.3390/v13020179
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author Schilling, Eva-Maria
Scherer, Myriam
Stamminger, Thomas
author_facet Schilling, Eva-Maria
Scherer, Myriam
Stamminger, Thomas
author_sort Schilling, Eva-Maria
collection PubMed
description Cellular restriction factors (RFs) act as important constitutive innate immune barriers against viruses. In 2006, the promyelocytic leukemia protein was described as the first RF against human cytomegalovirus (HCMV) infection which is antagonized by the viral immediate early protein IE1. Since then, at least 15 additional RFs against HCMV have been identified, including the chromatin regulatory protein SPOC1, the cytidine deaminase APOBEC3A and the dNTP triphosphohydrolase SAMHD1. These RFs affect distinct steps of the viral replication cycle such as viral entry, gene expression, the synthesis of progeny DNA or egress. This review summarizes our current knowledge on intrinsic immune mechanisms restricting HCMV replication as well as on the viral strategies to counteract the inhibitory effects of RFs. Detailed knowledge on the interplay between host RFs and antagonizing viral factors will be fundamental to develop new approaches to combat HCMV infection.
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spelling pubmed-79111792021-02-28 Intrinsic Immune Mechanisms Restricting Human Cytomegalovirus Replication Schilling, Eva-Maria Scherer, Myriam Stamminger, Thomas Viruses Review Cellular restriction factors (RFs) act as important constitutive innate immune barriers against viruses. In 2006, the promyelocytic leukemia protein was described as the first RF against human cytomegalovirus (HCMV) infection which is antagonized by the viral immediate early protein IE1. Since then, at least 15 additional RFs against HCMV have been identified, including the chromatin regulatory protein SPOC1, the cytidine deaminase APOBEC3A and the dNTP triphosphohydrolase SAMHD1. These RFs affect distinct steps of the viral replication cycle such as viral entry, gene expression, the synthesis of progeny DNA or egress. This review summarizes our current knowledge on intrinsic immune mechanisms restricting HCMV replication as well as on the viral strategies to counteract the inhibitory effects of RFs. Detailed knowledge on the interplay between host RFs and antagonizing viral factors will be fundamental to develop new approaches to combat HCMV infection. MDPI 2021-01-26 /pmc/articles/PMC7911179/ /pubmed/33530304 http://dx.doi.org/10.3390/v13020179 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Schilling, Eva-Maria
Scherer, Myriam
Stamminger, Thomas
Intrinsic Immune Mechanisms Restricting Human Cytomegalovirus Replication
title Intrinsic Immune Mechanisms Restricting Human Cytomegalovirus Replication
title_full Intrinsic Immune Mechanisms Restricting Human Cytomegalovirus Replication
title_fullStr Intrinsic Immune Mechanisms Restricting Human Cytomegalovirus Replication
title_full_unstemmed Intrinsic Immune Mechanisms Restricting Human Cytomegalovirus Replication
title_short Intrinsic Immune Mechanisms Restricting Human Cytomegalovirus Replication
title_sort intrinsic immune mechanisms restricting human cytomegalovirus replication
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7911179/
https://www.ncbi.nlm.nih.gov/pubmed/33530304
http://dx.doi.org/10.3390/v13020179
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