Human Cytomegalovirus Primary Infection and Reactivation: Insights From Virion-Carried Molecules

Human cytomegalovirus (HCMV), a ubiquitous beta-herpesvirus, is able to establish lifelong latency after initial infection. Periodical reactivation occurs after immunosuppression, remaining a major cause of death in immunocompromised patients. HCMV has to reach a structural and functional balance wi...

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Main Authors: Yu-Qing Wang, Xiang-Yu Zhao
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-07-01
Series:Frontiers in Microbiology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fmicb.2020.01511/full
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spelling doaj-9df0df9212104c228807a98318fcbd252020-11-25T02:37:15ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2020-07-011110.3389/fmicb.2020.01511547050Human Cytomegalovirus Primary Infection and Reactivation: Insights From Virion-Carried MoleculesYu-Qing Wang0Yu-Qing Wang1Xiang-Yu Zhao2Peking University People’s Hospital, Peking University Institute of Hematology, National Clinical Research Center for Hematologic Disease, Key Laboratory of Hematopoietic Stem Cell Transplantation, Beijing, ChinaPKU-THU Center for Life Sciences, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, ChinaPeking University People’s Hospital, Peking University Institute of Hematology, National Clinical Research Center for Hematologic Disease, Key Laboratory of Hematopoietic Stem Cell Transplantation, Beijing, ChinaHuman cytomegalovirus (HCMV), a ubiquitous beta-herpesvirus, is able to establish lifelong latency after initial infection. Periodical reactivation occurs after immunosuppression, remaining a major cause of death in immunocompromised patients. HCMV has to reach a structural and functional balance with the host at its earliest entry. Virion-carried mediators are considered to play pivotal roles in viral adaptation into a new cellular environment upon entry. Additionally, one clear difference between primary infection and reactivation is the idea that virion-packaged factors are already formed such that those molecules can be used swiftly by the virus. In contrast, virion-carried mediators have to be transcribed and translated; thus, they are not readily available during reactivation. Hence, understanding virion-carried molecules helps to elucidate HCMV reactivation. In this article, the impact of virion-packaged molecules on viral structure, biological behavior, and viral life cycle will be reviewed.https://www.frontiersin.org/article/10.3389/fmicb.2020.01511/fullHCMVvirion-carried moleculesprimary infectionreactivationtegumentenvelope
collection DOAJ
language English
format Article
sources DOAJ
author Yu-Qing Wang
Yu-Qing Wang
Xiang-Yu Zhao
spellingShingle Yu-Qing Wang
Yu-Qing Wang
Xiang-Yu Zhao
Human Cytomegalovirus Primary Infection and Reactivation: Insights From Virion-Carried Molecules
Frontiers in Microbiology
HCMV
virion-carried molecules
primary infection
reactivation
tegument
envelope
author_facet Yu-Qing Wang
Yu-Qing Wang
Xiang-Yu Zhao
author_sort Yu-Qing Wang
title Human Cytomegalovirus Primary Infection and Reactivation: Insights From Virion-Carried Molecules
title_short Human Cytomegalovirus Primary Infection and Reactivation: Insights From Virion-Carried Molecules
title_full Human Cytomegalovirus Primary Infection and Reactivation: Insights From Virion-Carried Molecules
title_fullStr Human Cytomegalovirus Primary Infection and Reactivation: Insights From Virion-Carried Molecules
title_full_unstemmed Human Cytomegalovirus Primary Infection and Reactivation: Insights From Virion-Carried Molecules
title_sort human cytomegalovirus primary infection and reactivation: insights from virion-carried molecules
publisher Frontiers Media S.A.
series Frontiers in Microbiology
issn 1664-302X
publishDate 2020-07-01
description Human cytomegalovirus (HCMV), a ubiquitous beta-herpesvirus, is able to establish lifelong latency after initial infection. Periodical reactivation occurs after immunosuppression, remaining a major cause of death in immunocompromised patients. HCMV has to reach a structural and functional balance with the host at its earliest entry. Virion-carried mediators are considered to play pivotal roles in viral adaptation into a new cellular environment upon entry. Additionally, one clear difference between primary infection and reactivation is the idea that virion-packaged factors are already formed such that those molecules can be used swiftly by the virus. In contrast, virion-carried mediators have to be transcribed and translated; thus, they are not readily available during reactivation. Hence, understanding virion-carried molecules helps to elucidate HCMV reactivation. In this article, the impact of virion-packaged molecules on viral structure, biological behavior, and viral life cycle will be reviewed.
topic HCMV
virion-carried molecules
primary infection
reactivation
tegument
envelope
url https://www.frontiersin.org/article/10.3389/fmicb.2020.01511/full
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