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      Arteriviruses

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          Abstract

          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.

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          The molecular biology of arteriviruses.

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            Nidovirus transcription: how to make sense...?

            Many positive-stranded RNA viruses use subgenomic mRNAs to express part of their genetic information. To produce structural and accessory proteins, members of the order Nidovirales (corona-, toro-, arteri- and roniviruses) generate a 3' co-terminal nested set of at least three and often seven to nine mRNAs. Coronavirus and arterivirus subgenomic transcripts are not only 3' co-terminal but also contain a common 5' leader sequence, which is derived from the genomic 5' end. Their synthesis involves a process of discontinuous RNA synthesis that resembles similarity-assisted RNA recombination. Most models proposed over the past 25 years assume co-transcriptional fusion of subgenomic RNA leader and body sequences, but there has been controversy over the question of whether this occurs during plus- or minus-strand synthesis. In the latter model, which has now gained considerable support, subgenomic mRNA synthesis takes place from a complementary set of subgenome-size minus-strand RNAs, produced by discontinuous minus-strand synthesis. Sense-antisense base-pairing interactions between short conserved sequences play a key regulatory role in this process. In view of the presumed common ancestry of nidoviruses, the recent finding that ronivirus and torovirus mRNAs do not contain a common 5' leader sequence is surprising. Apparently, major mechanistic differences must exist between nidoviruses, which raises questions about the functions of the common leader sequence and nidovirus transcriptase proteins and the evolution of nidovirus transcription. In this review, nidovirus transcription mechanisms are compared, the experimental systems used are critically assessed and, in particular, the impact of recently developed reverse genetic systems is discussed.
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              Immunological responses of swine to porcine reproductive and respiratory syndrome virus infection.

              The immunology of porcine reproductive and respiratory syndrome virus (PRRS) begins with an initial encounter of PRRSV with the pig. Regardless of the route of entry of PRRSV--via inhalation, intramuscular vaccination, insemination, or other routes--productive infection occurs predominately in alveolar macrophages of the lung. Thus, innate responses of the lung and the alveolar macrophage comprise the initial defense against PRRSV. The virus appears not to elicit innate interferon and cytokine responses characteristic of other strongly immunogenic viral pathogens, and its effects are consistent with induction of a weak adaptive immune response. Humoral and cell-mediated immunity is induced in due course, and results in clearance of virus from the circulation but not from lymphoid tissues, where the infection becomes persistent. Subsequent reexposure to PRRSV elicits an anamnestic response that is partially to completely protective. Within this unconventional picture of anti-PRRSV immunity lie a variety of unresolved issues, including the nature of protective immunity within individual pigs and among pigs in commercial populations, the efficacy of protective immunity against genetically different PRRSV isolates, the effects of developmental age, sex, genetics, and other host factors on the immune response to PRRSV, and the possible suppression of host immunity to other pathogens.
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                Author and article information

                Journal
                Encyclopedia of Virology
                Encyclopedia of Virology
                30 July 2008
                2008
                30 July 2008
                : 176-186
                Affiliations
                Georgia State University, Atlanta, GA, USA
                Leiden University Medical Center, Leiden, The Netherlands
                Senior Scientific Advisor, Division of Emerging Infections and Surveillance Services, Centers for Disease Control and Prevention, Atlanta GA, USA
                Emeritus Director at the CNRS, French National Center for Scientific Research, Biotechnology School of the University of Strasbourg, Illkirch, France
                Article
                B978-0-12-374410-4.00537-9
                10.1016/B978-012374410-4.00537-9
                7149349
                6208edba-1b8d-4491-b9b1-49fc057e5520
                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.

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                Article

                discontinuous transcription,eav,enveloped virus,equine arteritis virus,icosahedral capsid,lactate dehydrogenase-elevating virus,ldv,leader sequence,macrophages,persistent infections,porcine respiratory,reproductive syndrome,prrsv,shfv,simian hemorrhagic fever virus,subgenomic mrnas

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