Outbreaks of Aujeszky’s Disease in Pigs from Panama

Obaldía, Nicanor

doi:10.1007/s11250-005-5081-6

Cited by 3 publications

(1 citation statement)

References 3 publications

(3 reference statements)

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“…Aujeszky's disease is caused by the Pseudorabies virus (PRV) (Mettenleiter, 2000) with domestic pigs and wild boar as principal hosts (Christensen et al, 1993;Ruiz-Fons et al, 2008). Outbreaks have occurred in countries including Denmark, Germany, Ireland, Poland, the United Kingdom, and the United States (Christensen et al, 1993;Gloster et al, 1984;Henderson et al, 1995;Müller et al, 2003;Obaldía, 2005;Salwa, 2004;Scheidt et al, 1991).…”

Section: Pseudorabies Virusmentioning

confidence: 99%

Atmospheric dispersion modelling of bioaerosols that are pathogenic to humans and livestock – A review to inform risk assessment studies

Leuken

Swart

Havelaar

et al. 2016

Microbial Risk Analysis

112

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Section: Pseudorabies Virusmentioning

confidence: 99%

Atmospheric dispersion modelling of bioaerosols that are pathogenic to humans and livestock – A review to inform risk assessment studies

Leuken

Swart

Havelaar

et al. 2016

Microbial Risk Analysis

112

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Identification of linear B cell epitope on gB, gC, and gE proteins of porcine pseudorabies virus using monoclonal antibodies

Zhang

Sun

et al. 2019

Veterinary Microbiology

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Development of Real-Time Polymerase Chain Reaction Assays for Rapid Detection and Differentiation of Wild-Type Pseudorabies and Gene-Deleted Vaccine Viruses

Lager

Richt

et al. 2008

J VET Diagn Invest

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The successful eradication of pseudorabies in U.S. domestic swine was accomplished through the use of glycoprotein E (gE) deleted modified live virus vaccines and an accompanying gE differential enzyme-linked immunosorbent assay (ELISA). Yet, pseudorabies virus (PRV) was established in feral swine in the United States, becoming a potential reservoir of PRV for infection of domestic swine and other native wildlife. A critical need for the current PRV surveillance program in the United States is the rapid detection of PRV infection. For this reason, a set of 2 real-time polymerase chain reaction (PCR) assays by using TaqMan chemistry was developed and evaluated for their capability in the detection and differentiation of field and vaccine strains of PRV. PCR primers and probes were designed for gB and gE genes of PRV, respectively. The newly developed PRV-specific real-time PCR assays could detect all wild-type PRV isolates from diagnostic submissions and differentiate them from vaccine strains. The analytical sensitivity of the assays was approximately 0.1 plaque-forming units per reaction. The assays were highly specific for PRV, because no positive results were obtained from testing other common swine viral pathogens and other animal herpesviruses. The results of testing samples from domestic and feral swine and from bovine showed that the real-time PCR assays are more sensitive than gel-based PCR. These results demonstrated the potential application of the developed real-time PCR assays as a differential test for rapid and specific detection of PRV in domestic and feral swine, as well as nonporcine species that can be infected with PRV and serve as carriers.

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Outbreaks of Aujeszky’s Disease in Pigs from Panama

Cited by 3 publications

References 3 publications

Atmospheric dispersion modelling of bioaerosols that are pathogenic to humans and livestock – A review to inform risk assessment studies

Atmospheric dispersion modelling of bioaerosols that are pathogenic to humans and livestock – A review to inform risk assessment studies

Identification of linear B cell epitope on gB, gC, and gE proteins of porcine pseudorabies virus using monoclonal antibodies

Development of Real-Time Polymerase Chain Reaction Assays for Rapid Detection and Differentiation of Wild-Type Pseudorabies and Gene-Deleted Vaccine Viruses

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