Cargando…
Arteriviruses
The family Arteriviridae, which consists of four small, enveloped, positive-strand RNA viruses, was established in 1996. The current members are Equine arteritis virus (EAV), Lactate dehydrogenase-elevating virus (LDV), Porcine reproductive and respiratory syndrome virus (PRRSV), and Simian hemorrha...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2008
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7149349/ http://dx.doi.org/10.1016/B978-012374410-4.00537-9 |
_version_ | 1783520793562447872 |
---|---|
author | Brinton, M.A. Snijder, E.J. |
author_facet | Brinton, M.A. Snijder, E.J. |
author_sort | Brinton, M.A. |
collection | PubMed |
description | The family Arteriviridae, which consists of four small, enveloped, positive-strand RNA viruses, was established in 1996. The current members are Equine arteritis virus (EAV), Lactate dehydrogenase-elevating virus (LDV), Porcine reproductive and respiratory syndrome virus (PRRSV), and Simian hemorrhagic fever virus (SHFV). Because arteriviruses share with coronaviruses a similar genome organization, conserved replicase motifs, and a common genome expression strategy, which includes a mechanism of discontinuous RNA synthesis to generate multiple subgenomic RNAs, they have been joined in the order Nidovirales. However, arteriviruses differ from coronaviruses in the smaller size of their genomes, the smaller size and morphology of their virions, and the properties of their structural proteins. The arteriviruses each have distinct narrow host ranges but are widely distributed geographically. Transmission of arteriviruses occurs via the respiratory route or via bodily fluids and in all cases their primary target cells are macrophages. The outcomes of infections with the different arteriviruses range from asymptomatic infections that can be either persistent or acute, to abortion, respiratory disease, arteritis, fatal hemorrhagic fever, and poliomyelitis. Mechanisms that are thought to contribute to persistence include masking of the primary neutralization epitope by glycosylation, the generation of neutralization escape variants, infection of macrophages by immune complexes via Fc receptors, and the presence of an immunodominant decoy epitope near the primary neutralizing epitope. |
format | Online Article Text |
id | pubmed-7149349 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
record_format | MEDLINE/PubMed |
spelling | pubmed-71493492020-04-13 Arteriviruses Brinton, M.A. Snijder, E.J. Encyclopedia of Virology Article The family Arteriviridae, which consists of four small, enveloped, positive-strand RNA viruses, was established in 1996. The current members are Equine arteritis virus (EAV), Lactate dehydrogenase-elevating virus (LDV), Porcine reproductive and respiratory syndrome virus (PRRSV), and Simian hemorrhagic fever virus (SHFV). Because arteriviruses share with coronaviruses a similar genome organization, conserved replicase motifs, and a common genome expression strategy, which includes a mechanism of discontinuous RNA synthesis to generate multiple subgenomic RNAs, they have been joined in the order Nidovirales. However, arteriviruses differ from coronaviruses in the smaller size of their genomes, the smaller size and morphology of their virions, and the properties of their structural proteins. The arteriviruses each have distinct narrow host ranges but are widely distributed geographically. Transmission of arteriviruses occurs via the respiratory route or via bodily fluids and in all cases their primary target cells are macrophages. The outcomes of infections with the different arteriviruses range from asymptomatic infections that can be either persistent or acute, to abortion, respiratory disease, arteritis, fatal hemorrhagic fever, and poliomyelitis. Mechanisms that are thought to contribute to persistence include masking of the primary neutralization epitope by glycosylation, the generation of neutralization escape variants, infection of macrophages by immune complexes via Fc receptors, and the presence of an immunodominant decoy epitope near the primary neutralizing epitope. 2008 2008-07-30 /pmc/articles/PMC7149349/ http://dx.doi.org/10.1016/B978-012374410-4.00537-9 Text en Copyright © 2008 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Brinton, M.A. Snijder, E.J. Arteriviruses |
title | Arteriviruses |
title_full | Arteriviruses |
title_fullStr | Arteriviruses |
title_full_unstemmed | Arteriviruses |
title_short | Arteriviruses |
title_sort | arteriviruses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7149349/ http://dx.doi.org/10.1016/B978-012374410-4.00537-9 |
work_keys_str_mv | AT brintonma arteriviruses AT snijderej arteriviruses |