Development of a DIVA ELISA for diagnosis of Aujeszky's disease using recombinant gE fused to thioredoxin as antigen.

The major control methods for Aujeszky's Disease (AD) involve SHV1 gE gene-deleted vaccines and ELISA for detection of specific gE antibodies in infected animals, distinguishing infected animals from vaccinated animals (DIVA). This work aimed to develop a DIVA ELISA recombinant gE (gErec) for AD diagnosis using recombinant gE fused to thioredoxin protein. The analytical sensitivity and specificity were assessed with World Organisation for Animal Health (OIE) AD serum and sera from specific pathogen free (SPF), vaccinated SPF and AD-vaccinated SPF animals. The OIE serum reacted up to the recommended limit of detection and the other sera presented negative results. The cut-off point, diagnostic sensitivity and diagnostic specificity were determined by receiver operating curve analysis. This cut-off value corresponded to a diagnostic sensitivity of 97.60% and diagnostic specificity of 96.42%. Furthermore, two other cut-off points were chosen to discuss the ELISAgErec as a screening test in AD-endemic and free areas.

Production of pseudorabies virus recombinant glycoprotein B and its use in an agar gel immunodiffusion (AGID) test for detection of antibodies with sensitivity and specificity equal to the virus neutralization assay.

Pseudorabies virus (PrV) causes Aujeszky's disease (AD), which affects mainly swine, but also cattle, sheep, and wild animals, resulting in substantial economic losses due to animal mortality and lost productivity worldwide. To combat PrV, eradication programs using PrV strains lacking the gene encoding glycoprotein E (gE) are ongoing in several countries. These eradication programs have generated a currently unmet demand for affordable, easy-to-use, and sensitive tests that can detect PrV infection in pigs infected with either wild-type virus or vaccine strain (gE-deleted) virus. To meet this demand, we used the baculovirus-insect cell system to produce recombinant glycoprotein B (gB) as antigen for an immune assay. The high GC-content (70% average) of the gB gene from the Argentinian PrV CL15 strain necessitated the use of betaine as a PCR enhancer to amplify the extracellular domain. Recombinant gB was expressed at high levels and reacted strongly with sera from PrV infected pigs. We used the recombinant gB to develop an agar gel immunodiffusion (AGID) test for detection of PrV antibodies. Compared to the gold standard virus neutralization (VN) assay, the AGID sensitivity and specificity were 95% and 96.6% respectively. Thus, recombinant gB produced in the baculovirus-insect cell system is a viable source of antigen for the detection of PrV antibodies in AGID tests. Considering its relatively lower cost, simplicity of use and result interpretation, our AGID is a valuable alternative tool to the VN assay.

Descrição das ações de vigilância em focos da doença de Aujeszky / Description of surveillance actions in outbreaks of Aujeszky´s disease

Aujeszkys disease (AD) is known for causing huge productive and economical losses in the swine industry. This study focused on describing the actions of the official animal health protection used on identification of AD outbreaks. Two outbreaks that occurred in Cerqueira César city were selected, a case presenting only seropositive animals (outbreak 1) and  another one where there were animals with clinical signs of the disease (outbreak 2). The methods used to identify the outbreaks in surveillance actions and to diagnose the epidemiological situation were described. The measures implemented to eliminate the outbreaks in infected pig production systems were appointed in animal health protection laws and were able to eliminated all outbreaks identified. In conclusion, the official animal health protection measures and the appliance of the sanitary legislation were effective in eradicating AD, reassuring that notifications of suspicous cases of AD facilitate animal health surveillance activities.

A doença de Aujeszky (DA) é conhecida na suinocultura pelo seu grande impacto produtivo e econômico. Este trabalho teve como objetivo a descrição das ações de defesa sanitária animal utilizadas na identificação de focos dessa enfermidade. Foram selecionadas duas situações de foco de DA que ocorreram no Município de Cerqueira César, um caso apresentando somente animais sororreagentes (Foco 1) e outro em que havia animais com sinais clínicos da enfermidade (Foco 2). Estão descritos os métodos de identificação de focos utilizados nas ações de vigilância e o diagnóstico da situação epidemiológica encontrada. As medidas aplicadas na erradicação dos focos nos sistemas de produção de suínos infectados foram as prescritas na legislação de defesa sanitária animal e  todos os focos identificados foram eliminados. Ao final, concluiu-se que as ações de defesa sanitária e a legislação em vigor foram eficazes, demonstrando que os sistemas de notificações das suspeitas da enfermidade são facilitadores das ações de vigilância.

Descrição das ações de vigilância em focos da doença de Aujeszky / Description of surveillance actions in outbreaks of Aujeszky´s disease

Aujeszkys disease (AD) is known for causing huge productive and economical losses in the swine industry. This study focused on describing the actions of the official animal health protection used on identification of AD outbreaks. Two outbreaks that occurred in Cerqueira César city were selected, a case presenting only seropositive animals (outbreak 1) and  another one where there were animals with clinical signs of the disease (outbreak 2). The methods used to identify the outbreaks in surveillance actions and to diagnose the epidemiological situation were described. The measures implemented to eliminate the outbreaks in infected pig production systems were appointed in animal health protection laws and were able to eliminated all outbreaks identified. In conclusion, the official animal health protection measures and the appliance of the sanitary legislation were effective in eradicating AD, reassuring that notifications of suspicous cases of AD facilitate animal health surveillance activities.(AU)

A doença de Aujeszky (DA) é conhecida na suinocultura pelo seu grande impacto produtivo e econômico. Este trabalho teve como objetivo a descrição das ações de defesa sanitária animal utilizadas na identificação de focos dessa enfermidade. Foram selecionadas duas situações de foco de DA que ocorreram no Município de Cerqueira César, um caso apresentando somente animais sororreagentes (Foco 1) e outro em que havia animais com sinais clínicos da enfermidade (Foco 2). Estão descritos os métodos de identificação de focos utilizados nas ações de vigilância e o diagnóstico da situação epidemiológica encontrada. As medidas aplicadas na erradicação dos focos nos sistemas de produção de suínos infectados foram as prescritas na legislação de defesa sanitária animal e  todos os focos identificados foram eliminados. Ao final, concluiu-se que as ações de defesa sanitária e a legislação em vigor foram eficazes, demonstrando que os sistemas de notificações das suspeitas da enfermidade são facilitadores das ações de vigilância.(AU)

Soroprevalência de pseudorraiva, peste suína clássica e brucelose em suínos do estado do Piauí / Seroprevalence of pseudorabies, classical swine fever and brucellosis in swine in the state of Piauí

Este trabalho teve como objetivo determinar a soroprevalência de pseudorraiva, peste suína clássica (PSC) e brucelose suína em suínos do estado do Piauí, Brasil. Foram coletadas amostras sanguíneas de 384 suínos de criações intensivas e extensivas do estado. Anticorpos anti-Brucella spp. foram detectados pelo teste do antígeno acidificado tamponado e confirmados pelo teste 2-mercaptoetanol, enquanto a detecção de anticorpos contra os vírus da PSC e pseudorraiva foi realizada por ensaio imunoenzimático (ELISA), utilizando-se kits comerciais específicos. Anticorpos anti-Brucella spp. foram detectados em 1,04% (2/192) dos suínos de criações intensivas. Dos rebanhos avaliados, 0,78% (3/384) dos animais exibiram anticorpos contra o vírus da PSC, sendo 1,04% (2/192) de criações intensivas e 0,52% (1/192) de criações extensivas. Anticorpos contra o vírus da pseudorraiva foram detectados apenas em suínos de criação extensiva, com prevalência de 5,2% (10/192). Esses são os primeiros dados sobre a soroprevalência da brucelose suína, pseudorraiva e PSC em rebanhos do Piauí. A detecção de 10 amostras positivas para pseudorraiva causa preocupação sobre a possibilidade da circulação viral na população suídea desse estado e revela uma necessidade premente de realização de estudos mais extensos para melhor compreender a importância dessas enfermidades de notificação obrigatória em estados da região Nordeste brasileira.

This study aimed to determine the prevalence of Pseudorabies, Classical Swine Fever (CSF) and Swine Brucellosis in swine in the state of Piauí, Brazil. Blood samples were collected from 384 pigs from intensive and small outdoor systems in the state. Anti-Brucella spp. antibodies were detected by Buffered Acidified Antigen Test and positive results confirmed by 2-Mercaptoethanol Test. Detection of antibodies against CSF and Pseudorabies virus were performed by Enzyme-Linked Immunosorbent Assay (ELISA) using specific commercial kits. Only two samples (1.04% - 2/192) from the intensive system were seropositive to Brucella spp. In the evaluated herds, 0.78% (3/384) of animals had antibodies against CSF virus, two from outdoor pigs (1.04% - 2/192) and one from intensive systems (0.52% - 1/192). Antibodies against the Pseudorabies virus were detected only in outdoor pigs, with seroprevalence of 5.2% (10/192). This is the first report on seroprevalence of Pseudorabies, CSF and Brucellosis in hog farms in Piauí, Brazil. The detection of 10 positive cases raises a concern regarding Pseudorabies virus circulation in the swine population in the state and reveals a need for further studies to better understand the real situation and status of obligatory notified diseases in the swine herds in the Northestern states of Brazil.

Soroprevalência de pseudorraiva, peste suína clássica e brucelose em suínos do estado do Piauí / Seroprevalence of pseudorabies, classical swine fever and brucellosis in swine in the state of Piauí

Este trabalho teve como objetivo determinar a soroprevalência de pseudorraiva, peste suína clássica (PSC) e brucelose suína em suínos do estado do Piauí, Brasil. Foram coletadas amostras sanguíneas de 384 suínos de criações intensivas e extensivas do estado. Anticorpos anti-Brucella spp. foram detectados pelo teste do antígeno acidificado tamponado e confirmados pelo teste 2-mercaptoetanol, enquanto a detecção de anticorpos contra os vírus da PSC e pseudorraiva foi realizada por ensaio imunoenzimático (ELISA), utilizando-se kits comerciais específicos. Anticorpos anti-Brucella spp. foram detectados em 1,04% (2/192) dos suínos de criações intensivas. Dos rebanhos avaliados, 0,78% (3/384) dos animais exibiram anticorpos contra o vírus da PSC, sendo 1,04% (2/192) de criações intensivas e 0,52% (1/192) de criações extensivas. Anticorpos contra o vírus da pseudorraiva foram detectados apenas em suínos de criação extensiva, com prevalência de 5,2% (10/192). Esses são os primeiros dados sobre a soroprevalência da brucelose suína, pseudorraiva e PSC em rebanhos do Piauí. A detecção de 10 amostras positivas para pseudorraiva causa preocupação sobre a possibilidade da circulação viral na população suídea desse estado e revela uma necessidade premente de realização de estudos mais extensos para melhor compreender a importância dessas enfermidades de notificação obrigatória em estados da região Nordeste brasileira.(AU)

This study aimed to determine the prevalence of Pseudorabies, Classical Swine Fever (CSF) and Swine Brucellosis in swine in the state of Piauí, Brazil. Blood samples were collected from 384 pigs from intensive and small outdoor systems in the state. Anti-Brucella spp. antibodies were detected by Buffered Acidified Antigen Test and positive results confirmed by 2-Mercaptoethanol Test. Detection of antibodies against CSF and Pseudorabies virus were performed by Enzyme-Linked Immunosorbent Assay (ELISA) using specific commercial kits. Only two samples (1.04% - 2/192) from the intensive system were seropositive to Brucella spp. In the evaluated herds, 0.78% (3/384) of animals had antibodies against CSF virus, two from outdoor pigs (1.04% - 2/192) and one from intensive systems (0.52% - 1/192). Antibodies against the Pseudorabies virus were detected only in outdoor pigs, with seroprevalence of 5.2% (10/192). This is the first report on seroprevalence of Pseudorabies, CSF and Brucellosis in hog farms in Piauí, Brazil. The detection of 10 positive cases raises a concern regarding Pseudorabies virus circulation in the swine population in the state and reveals a need for further studies to better understand the real situation and status of obligatory notified diseases in the swine herds in the Northestern states of Brazil.(AU)

Expression and purification of Suid Herpesvirus-1 glycoprotein E in the baculovirus system and its use to diagnose Aujeszky's disease in infected pigs.

Suid Herpesvirus 1 (SHV-1) is the etiological agent of Aujeszky's disease (AD), which affects swine herds worldwide and causes substantial economic losses due to animal mortality and lost productivity. In order to eradicate SHV-1, vaccination programs using viruses lacking the gene encoding glycoprotein E (gE) are ongoing in several countries. These eradication programs have generated a currently unmet demand for affordable and sensitive tests that can detect SHV-1 infection, yet distinguish between infected and vaccinated pigs. To meet this demand, we used the baculovirus-insect cell system to produce immunologically authentic full-length recombinant gE protein for use in a serum ELISA assay. As previous efforts to clone the gE gene had failed due to its extremely high GC-content (75% average), we used betaine as a PCR enhancer to facilitate amplification of the entire gE gene from the Argentinian CL15 strain of SHV-1. The cloned gE gene was expressed at high levels in recombinant baculovirus-infected insect cells and reacted strongly with sera from SHV-1 infected pigs. We used the recombinant gE protein to develop a local indirect ELISA test with sensitivity and specificity comparable to currently available commercial tests. Thus, recombinant gE produced in baculovirus-infected insect cells is a viable source of antigen for the detection of SHV-1 in ELISA tests. We also provide evidence supporting a potential application of this recombinant form of gE as a SHV-1 subunit vaccine.

A differential ELISA based on recombinant immunodominant epitopes of the gE gene of SHV-1 in a baculovirus-insect cell system to discriminate between pigs infected naturally with pseudorabies and vaccinated pigs.

In the present study, the fragment corresponding to the immunodominant epitopes of the gE gene (gEpi) from the CL15 Argentinean strain of pseudorabies virus was expressed successfully in a baculovirus-insect cell system that contained the M6 gene of Bluetongue virus, which encodes the NS1 nonstructural protein. This protein has the ability to polymerize into highly immunogenic tubules inside infected cells that can be purified at large quantities by ultracentrifugation. Previously, the NS1 protein has been expressed by fusing it to sequences derived from viruses, such as human immunodeficiency virus type 1, hepatitis B virus, bovine leukemia virus, foot-and-mouth disease virus and influenza A virus. In the present study, a recombinant protein was obtained containing the gEpi fused to NS1 (NS1-gEpi) and used it as ELISA antigen for detection of anti-gE antibodies in order to discriminate between infected and vaccinated animals. This is the first report where gEpi was expressed in this particular baculovirus-insect cell system.

Antibodies against pseudorabies virus in feral swine in southeast Brazil / Anticorpos contra o vírus da doença de Aujeszky em javalis no estado de São Paulo

Serum samples collected from 358 wild boars (Sus scrofa) in breeding farms in São Paulo, southeast Brazil, from 1998 to 2001, were tested for antibodies against pseudorabies virus (PRV) by means of serum neutralization (SN) and enzyme-linked immunobsorbent assay (ELISA). Seropositive animals were detected in three of seven herds analyzed. Overall seroprevalence as assessed by SN was 30.7%, ranging from 25.2% to 100% for the herds that presented seropositive animals. Indirect ELISA detected lower seroprevalence (19.3%). Sensitivity and specificity of ELISA were equal to 57.3% and 97.6%, respectively. Agreement was equal to 85.2% (P<0.0001). These results showed that PRV infections occurred in farmed feral swine in southeast Brazil, and affect pseudorabies eradication program.(AU)

Soros de 358 javalis (Sus scrofa), criados em sistema de semiconfinamento em propriedades do estado de São Paulo, foram coletados entre 1998 e 2000 e testados para anticorpos contra o vírus da doença de Aujeszky (VDA), pela técnica de soroneutralização (SN) e ensaio imunoenzimático (ELISA). Foram detectados animais soropositivos em três das sete propriedades analisadas. Do total de javalis testados, 30,7% apresentaram anticorpos neutralizantes contra o VDA, com variação de 25,2% a 100% nas propriedades com animais sororreagentes. O ELISA detectou menor número de sororeagentes (19,3%), sendo a sensibilidade e a especificidade 57,3% e 97,6%, respectivamente, e a correlação observada de 85,2% (P<0,0001). Os resultados mostram que a infecção pelo vírus da doença de Aujeszky ocorre em criações de javalis no estado de São Paulo, e compromete o sucesso de um futuro programa de erradicação da doença na região.(AU)

Risk factors for Aujeszky's disease in pig herds and detection of field virus antibodies in fattening pigs in the state of Yucatan, Mexico.

Two epidemiological studies were conducted from August 1997 to May 1998: a case-control study to identify herd level risk factors for antibodies to Aujeszky's disease virus (ADV) in sows in the state of Yucatan, Mexico and a cross-sectional study to determine the prevalence of antibodies against ADV in fattening pigs. In the case-control study, data on herd management and biosecurity were obtained from all the 27 ADV known field-virus-seropositive farms (cases) and 62 randomly selected seronegative farms (controls) by questionnaire. Breeding animals of these seropositive farms had received a gE-deletion vaccine. In the cross-sectional study, 26 farrow-to-finish farms of the 27 seropositive farms were used and blood samples taken from 60 fattening pigs per herd (15 pigs for each stage of production). Serum samples were analyzed by the screening-ELISA and gE-ELISA tests. In the case-control study, three of the 15 risk factors were significant. Odds ratios for distance to the nearest farm (< or = 2.5km), not sampling for the detection of ADV and herds with origin of breeding animals within the state were 9.5, 18.1 and 8.7. In the cross-sectional study, 11 (42.3%) of the 26 sampled farms were seropositive to vaccine antibodies. None of the piglets were positive to antibodies against field virus risk--suggesting that the strategy of vaccinating only the breeding animals reduced the ADV infection of the piglets.

Rapid diagnosis of pseudorabies virus infection in swine tissues using the polymerase chain reaction (PCR).

In Argentina pseudorabies is an endemic disease. Routine diagnosis is made by virus isolation. It is a very long procedure to carry out and gives variable results depending on the quality of sample, hence the need for effective techniques, which are rapid and not dependent on the isolation of infectious virus. The polymerase chain reaction (PCR) technique has provided a sensitive, specific and rapid mean to detect DNA sequences. This study describes a PCR method for detection of pseudorabies virus sequences in swine tissues. In order to determine the presence of suid herpesvirus-1 DNA and antigens, 36 tissue samples collected from 19 dead pigs, with signs of pseudorabies infection, were examined by PCR, virus isolation and indirect immunofluorescence, respectively. Fifteen out of 19 pigs were positive at least for one tissue by PCR (15/19) while only three pseudorabies virus strains were isolated (3/19). All the amplified products were identified by digestion with Sa/l and hybridization. The method described herein circumvents tedious viral isolation and DNA purification and would be a valuable tool for rapid diagnosis, since it would take less than 5 h to reach an accurate result even in poorly preserved tissue samples.

Rapid diagnosis of pseudorabies virus infection in swine tissues using the polymerase chain reaction (PCR)

In Argentina pseudorabies is an endemic disease. Routine diagnosis is made by virus isolation. It is a very long procedure to carry out and gives variable results depending on the quality of sample, hence the need for effective techniques, which are rapid and not dependent on the isolation of infectious virus. The polymerase chain reaction (PCR) technique has provided a sensitive, specific and rapid mean to detect DNA sequences. This study describes a PCR method for detection of pseudorabies virus sequences in swine tissues. In order to determine the presence of suid herpesvirus-1 DNA and antigens, 36 tissue samples collected from 19 dead pigs, with signs of pseudorabies infection, were examined by PCR, virus isolation and indirect immunofluorescence, respectively. Fifteen out of 19 pigs were positive at least for one tissue by PCR (15/19) while only three pseudorabies virus strains were isolated (3/19). All the amplified products were identified by digestion with Sa/l and hybridization. The method described herein circumvents tedious viral isolation and DNA purification and would be a valuable tool for rapid diagnosis, since it would take less than 5 h to reach an accurate result even in poorly preserved tissue samples.(AU)

Evaluation of a blocking ELISA using a urease conjugate for the detection of antibodies to pseudorabies virus.

A blocking enzyme-linked immunosorbent assay (ELISA) using a urease conjugate (U-B-ELISA) was evaluated for screening sera for antibodies to pseudorabies virus under field conditions. A total of 764 serum samples were analyzed by U-B-ELISA. Of these, 264 were evaluated by both virus neutralization and U-B-ELISA, and the results were compared. U-B-ELISA showed 98.5% and 98.9% sensitivity and specificity, respectively. This test combines the sensitivity and specificity of the blocking ELISA format while allowing visual assessment of results.

Pseudorabies (Aujeszky's disease) in Argentina.

Various methods have been employed for the diagnosis of pseudorabies in Argentina. A large serological survey was carried out by means of enzyme-linked immunosorbent assay (blocking ELISA) and virus neutralisation (VN). An outbreak was studied by virological and immunohistochemical methods and in situ nucleic acid hybridisation.