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Persistent Enterovirus Infection: Little Deletions, Long Infections

Enteroviruses have now been shown to persist in cell cultures and in vivo by a novel mechanism involving the deletion of varying amounts of the 5′ terminal genomic region termed domain I (also known as the cloverleaf). Molecular clones of coxsackievirus B3 (CVB3) genomes with 5′ terminal deletions (...

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Autor principal: Chapman, Nora M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9143164/
https://www.ncbi.nlm.nih.gov/pubmed/35632526
http://dx.doi.org/10.3390/vaccines10050770
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author Chapman, Nora M.
author_facet Chapman, Nora M.
author_sort Chapman, Nora M.
collection PubMed
description Enteroviruses have now been shown to persist in cell cultures and in vivo by a novel mechanism involving the deletion of varying amounts of the 5′ terminal genomic region termed domain I (also known as the cloverleaf). Molecular clones of coxsackievirus B3 (CVB3) genomes with 5′ terminal deletions (TD) of varying length allow the study of these mutant populations, which are able to replicate in the complete absence of wildtype virus genomes. The study of TD enteroviruses has revealed numerous significant differences from canonical enteroviral biology. The deletions appear and become the dominant population when an enterovirus replicates in quiescent cell populations, but can also occur if one of the cis-acting replication elements of the genome (CRE-2C) is artificially mutated in the element’s stem and loop structures. This review discusses how the TD genomes arise, how they interact with the host, and their effects on host biology.
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spelling pubmed-91431642022-05-29 Persistent Enterovirus Infection: Little Deletions, Long Infections Chapman, Nora M. Vaccines (Basel) Review Enteroviruses have now been shown to persist in cell cultures and in vivo by a novel mechanism involving the deletion of varying amounts of the 5′ terminal genomic region termed domain I (also known as the cloverleaf). Molecular clones of coxsackievirus B3 (CVB3) genomes with 5′ terminal deletions (TD) of varying length allow the study of these mutant populations, which are able to replicate in the complete absence of wildtype virus genomes. The study of TD enteroviruses has revealed numerous significant differences from canonical enteroviral biology. The deletions appear and become the dominant population when an enterovirus replicates in quiescent cell populations, but can also occur if one of the cis-acting replication elements of the genome (CRE-2C) is artificially mutated in the element’s stem and loop structures. This review discusses how the TD genomes arise, how they interact with the host, and their effects on host biology. MDPI 2022-05-12 /pmc/articles/PMC9143164/ /pubmed/35632526 http://dx.doi.org/10.3390/vaccines10050770 Text en © 2022 by the author. 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
Chapman, Nora M.
Persistent Enterovirus Infection: Little Deletions, Long Infections
title Persistent Enterovirus Infection: Little Deletions, Long Infections
title_full Persistent Enterovirus Infection: Little Deletions, Long Infections
title_fullStr Persistent Enterovirus Infection: Little Deletions, Long Infections
title_full_unstemmed Persistent Enterovirus Infection: Little Deletions, Long Infections
title_short Persistent Enterovirus Infection: Little Deletions, Long Infections
title_sort persistent enterovirus infection: little deletions, long infections
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9143164/
https://www.ncbi.nlm.nih.gov/pubmed/35632526
http://dx.doi.org/10.3390/vaccines10050770
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