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There Is Always Another Way! Cytomegalovirus’ Multifaceted Dissemination Schemes

Human cytomegalovirus (HCMV) is a β-herpes virus that is a significant pathogen within immune compromised populations. HCMV morbidity is induced through viral dissemination and inflammation. Typically, viral dissemination is thought to follow Fenner’s hypothesis where virus replicates at the site of...

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Autores principales: Jackson, Joseph W., Sparer, Tim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6071125/
https://www.ncbi.nlm.nih.gov/pubmed/30037007
http://dx.doi.org/10.3390/v10070383
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author Jackson, Joseph W.
Sparer, Tim
author_facet Jackson, Joseph W.
Sparer, Tim
author_sort Jackson, Joseph W.
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description Human cytomegalovirus (HCMV) is a β-herpes virus that is a significant pathogen within immune compromised populations. HCMV morbidity is induced through viral dissemination and inflammation. Typically, viral dissemination is thought to follow Fenner’s hypothesis where virus replicates at the site of infection, followed by replication in the draining lymph nodes, and eventually replicating within blood filtering organs. Although CMVs somewhat follow Fenner’s hypothesis, they deviate from it by spreading primarily through innate immune cells as opposed to cell-free virus. Also, in vivo CMVs infect new cells via cell-to-cell spread and disseminate directly to secondary organs through novel mechanisms. We review the historic and recent literature pointing to CMV’s direct dissemination to secondary organs and the genes that it has evolved for increasing its ability to disseminate. We also highlight aspects of CMV infection for studying viral dissemination when using in vivo animal models.
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spelling pubmed-60711252018-08-09 There Is Always Another Way! Cytomegalovirus’ Multifaceted Dissemination Schemes Jackson, Joseph W. Sparer, Tim Viruses Review Human cytomegalovirus (HCMV) is a β-herpes virus that is a significant pathogen within immune compromised populations. HCMV morbidity is induced through viral dissemination and inflammation. Typically, viral dissemination is thought to follow Fenner’s hypothesis where virus replicates at the site of infection, followed by replication in the draining lymph nodes, and eventually replicating within blood filtering organs. Although CMVs somewhat follow Fenner’s hypothesis, they deviate from it by spreading primarily through innate immune cells as opposed to cell-free virus. Also, in vivo CMVs infect new cells via cell-to-cell spread and disseminate directly to secondary organs through novel mechanisms. We review the historic and recent literature pointing to CMV’s direct dissemination to secondary organs and the genes that it has evolved for increasing its ability to disseminate. We also highlight aspects of CMV infection for studying viral dissemination when using in vivo animal models. MDPI 2018-07-20 /pmc/articles/PMC6071125/ /pubmed/30037007 http://dx.doi.org/10.3390/v10070383 Text en © 2018 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
Jackson, Joseph W.
Sparer, Tim
There Is Always Another Way! Cytomegalovirus’ Multifaceted Dissemination Schemes
title There Is Always Another Way! Cytomegalovirus’ Multifaceted Dissemination Schemes
title_full There Is Always Another Way! Cytomegalovirus’ Multifaceted Dissemination Schemes
title_fullStr There Is Always Another Way! Cytomegalovirus’ Multifaceted Dissemination Schemes
title_full_unstemmed There Is Always Another Way! Cytomegalovirus’ Multifaceted Dissemination Schemes
title_short There Is Always Another Way! Cytomegalovirus’ Multifaceted Dissemination Schemes
title_sort there is always another way! cytomegalovirus’ multifaceted dissemination schemes
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6071125/
https://www.ncbi.nlm.nih.gov/pubmed/30037007
http://dx.doi.org/10.3390/v10070383
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