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Open AccessJournal ArticleDOI

Molecular Biology of Pseudorabies Virus: Impact on Neurovirology and Veterinary Medicine

TLDR
Pseudorabies virus serves as a self-perpetuating transsynaptic tracer of neuronal circuitry, and it is detailed the original studies of PRV circuitry mapping, the biology underlying this application, and the development of the next generation of tracer viruses.
Abstract
Pseudorabies virus (PRV) is a herpesvirus of swine, a member of the Alphaherpesvirinae subfamily, and the etiological agent of Aujeszky's disease. This review describes the contributions of PRV research to herpesvirus biology, neurobiology, and viral pathogenesis by focusing on (i) the molecular biology of PRV, (ii) model systems to study PRV pathogenesis and neurovirulence, (iii) PRV transsynaptic tracing of neuronal circuits, and (iv) veterinary aspects of pseudorabies disease. The structure of the enveloped infectious particle, the content of the viral DNA genome, and a step-by-step overview of the viral replication cycle are presented. PRV infection is initiated by binding to cellular receptors to allow penetration into the cell. After reaching the nucleus, the viral genome directs a regulated gene expression cascade that culminates with viral DNA replication and production of new virion constituents. Finally, progeny virions self-assemble and exit the host cells. Animal models and neuronal culture systems developed for the study of PRV pathogenesis and neurovirulence are discussed. PRV serves as a self-perpetuating transsynaptic tracer of neuronal circuitry, and we detail the original studies of PRV circuitry mapping, the biology underlying this application, and the development of the next generation of tracer viruses. The basic veterinary aspects of pseudorabies management and disease in swine are discussed. PRV infection progresses from acute infection of the respiratory epithelium to latent infection in the peripheral nervous system. Sporadic reactivation from latency can transmit PRV to new hosts. The successful management of PRV disease has relied on vaccination, prevention, and testing.

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Journal ArticleDOI

Advances in swine biomedical model genomics.

TL;DR: The potential for genomic approaches to develop new alternatives for control of the most economically important disease of pigs, porcine reproductive and respiratory syndrome (PRRS), and the potential for applying knowledge gained with this virus for human viral infectious disease studies is discussed.
Journal ArticleDOI

Antiviral Activity of Graphene Oxide: How Sharp Edged Structure and Charge Matter.

TL;DR: The results showed that GO significantly suppressed the infection of PRV and PEDV for a 2 log reduction in virus titers at noncytotoxic concentrations and inactivated both viruses by structural destruction prior to viral entry.
Journal ArticleDOI

Pseudorabies Virus Variant in Bartha-K61–Vaccinated Pigs, China, 2012

TL;DR: It is suggested that Bartha-K61 vaccine does not provide effective protection against PRV HeN1 infection.
Journal ArticleDOI

Local Retinal Circuits of Melanopsin-Containing Ganglion Cells Identified by Transsynaptic Viral Tracing

TL;DR: It is shown that ipRGCs are connected by monostratified amacrine cells that provide strong inhibition from classical-photoreceptor-driven circuits, and evidence that dopaminergic interplexiform cells are synaptically connected to ipR GCs is shown.
Journal ArticleDOI

Pathogenic pseudorabies virus, China, 2012.

TL;DR: Evidence confirmed that the pathogenic pseudorabies virus was the etiologic agent of this epidemic of disease in pigs in China in 2012.
References
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Journal ArticleDOI

Induction of protective immunity and neutralizing antibodies to pseudorabies virus by immunization of anti-idiotypic antibodies.

TL;DR: Xenogenic anti-idiotypic antibodies (anti-Id) were prepared in rabbits against three murine neutralizing monoclonal antibodies directed to pseudorabies virus glycoproteins, and mice immunized with the anti-Id were protected from lethal infection of PrV.
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Multiple sets of adjacent μE1 and oct-1 binding sites upstream of the pseudorabies virus immediate-early gene promoter

TL;DR: The upstream element was necessary for efficient expression of the pseudorabies virus immediate-early gene and increased somewhat the efficiency of the herpes simplex virus thymidine kinase promoter.
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Use of a Recombinant Pseudorabies Virus to Analyze Motor Cortical Reorganization after Unilateral Facial Denervation

TL;DR: The results reveal that a peripheral nerve injury induces changes in the Ba-DupLac infection pattern in the related cortical areas, and suggest that this phenomenon may be related to the changed in the expression or to the redistribution of cell-adhesion molecules, which are known to facilitate the entrance and/or transmission of PRV into neurons.
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Acetylcholine reactivates latent pseudorabies virus in mice

TL;DR: The latency model of pseudorabies virus (PrV) wild strain, YS-81, in mice was established and latent PrV reactivated with acetylcholine and it was found that this model is useful in investigating the mechanism of latentPrV reactivation by acetylCholine.
Journal ArticleDOI

Protection from pseudorabies virus challenge in mice by a combination of purified gII, gIII and gVI antigens.

TL;DR: The results indicate that the mixture of each glycoprotein is more effective for eliciting of protective immunities in mice and that serological activity do not always correlate with protection.
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