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Targeting the Host Mitochondria as a Novel Human Cytomegalovirus Antiviral Strategy
Human cytomegalovirus (HCMV) exploits host mitochondrial function to promote viral replication. HCMV gene products have been described to directly interact and alter functional or structural aspects of host mitochondria. Current antivirals against HCMV, such as ganciclovir and letermovir, are design...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10223864/ https://www.ncbi.nlm.nih.gov/pubmed/37243170 http://dx.doi.org/10.3390/v15051083 |
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author | Bachman, Lauryn O. Zwezdaryk, Kevin J. |
author_facet | Bachman, Lauryn O. Zwezdaryk, Kevin J. |
author_sort | Bachman, Lauryn O. |
collection | PubMed |
description | Human cytomegalovirus (HCMV) exploits host mitochondrial function to promote viral replication. HCMV gene products have been described to directly interact and alter functional or structural aspects of host mitochondria. Current antivirals against HCMV, such as ganciclovir and letermovir, are designed against viral targets. Concerns with the current antivirals include toxicity and viral resistance. Targeting host mitochondrial function is a promising alternative or complimentary antiviral approach as (1) drugs targeting host mitochondrial function interact with host targets, minimizing viral resistance, and (2) host mitochondrial metabolism plays key roles in HCMV replication. This review describes how HCMV alters mitochondrial function and highlights pharmacological targets that can be exploited for novel antiviral development. |
format | Online Article Text |
id | pubmed-10223864 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102238642023-05-28 Targeting the Host Mitochondria as a Novel Human Cytomegalovirus Antiviral Strategy Bachman, Lauryn O. Zwezdaryk, Kevin J. Viruses Review Human cytomegalovirus (HCMV) exploits host mitochondrial function to promote viral replication. HCMV gene products have been described to directly interact and alter functional or structural aspects of host mitochondria. Current antivirals against HCMV, such as ganciclovir and letermovir, are designed against viral targets. Concerns with the current antivirals include toxicity and viral resistance. Targeting host mitochondrial function is a promising alternative or complimentary antiviral approach as (1) drugs targeting host mitochondrial function interact with host targets, minimizing viral resistance, and (2) host mitochondrial metabolism plays key roles in HCMV replication. This review describes how HCMV alters mitochondrial function and highlights pharmacological targets that can be exploited for novel antiviral development. MDPI 2023-04-28 /pmc/articles/PMC10223864/ /pubmed/37243170 http://dx.doi.org/10.3390/v15051083 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Bachman, Lauryn O. Zwezdaryk, Kevin J. Targeting the Host Mitochondria as a Novel Human Cytomegalovirus Antiviral Strategy |
title | Targeting the Host Mitochondria as a Novel Human Cytomegalovirus Antiviral Strategy |
title_full | Targeting the Host Mitochondria as a Novel Human Cytomegalovirus Antiviral Strategy |
title_fullStr | Targeting the Host Mitochondria as a Novel Human Cytomegalovirus Antiviral Strategy |
title_full_unstemmed | Targeting the Host Mitochondria as a Novel Human Cytomegalovirus Antiviral Strategy |
title_short | Targeting the Host Mitochondria as a Novel Human Cytomegalovirus Antiviral Strategy |
title_sort | targeting the host mitochondria as a novel human cytomegalovirus antiviral strategy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10223864/ https://www.ncbi.nlm.nih.gov/pubmed/37243170 http://dx.doi.org/10.3390/v15051083 |
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