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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Main Author: Nora M. Chapman
Format: Article
Language:English
Published: MDPI AG 2022-05-01
Series:Vaccines
Subjects:
Online Access:https://www.mdpi.com/2076-393X/10/5/770
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author Nora M. Chapman
author_facet Nora M. Chapman
author_sort Nora M. Chapman
collection DOAJ
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 doaj.art-8e1e61bc53be471194a5f22c456d65892023-11-23T13:26:58ZengMDPI AGVaccines2076-393X2022-05-0110577010.3390/vaccines10050770Persistent Enterovirus Infection: Little Deletions, Long InfectionsNora M. Chapman0Department of Pathology & Microbiology, University of Nebraska Medical Center, Omaha, NE 68198, USAEnteroviruses 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.https://www.mdpi.com/2076-393X/10/5/770enterovirusterminal deletioncoxsackievirus Bpersistent infectionpositive-strand initiationnegative-strand initiation
spellingShingle Nora M. Chapman
Persistent Enterovirus Infection: Little Deletions, Long Infections
Vaccines
enterovirus
terminal deletion
coxsackievirus B
persistent infection
positive-strand initiation
negative-strand initiation
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 enterovirus
terminal deletion
coxsackievirus B
persistent infection
positive-strand initiation
negative-strand initiation
url https://www.mdpi.com/2076-393X/10/5/770
work_keys_str_mv AT noramchapman persistententerovirusinfectionlittledeletionslonginfections