Resultado da pesquisa (4)
Termo utilizado na pesquisa adenovírus
#1 - Detection of bluetongue virus in Brazilian cervids in São Paulo state
Abstract in English:
Viral hemorrhagic diseases in cervids occur worldwide and include epizootic hemorrhagic disease (EHD), bluetongue (BT), and adenoviral hemorrhagic disease (AHD). Since gross lesions in all three hemorrhagic diseases are identical (hemorrhagic enteropathy, pulmonary edema, systemic petechial and suffusion hemorrhages), it is necessary to use accurate techniques for a definitive etiologic diagnosis. Archival material (paraffin blocks) at the Department of Veterinary Pathology of FCAV – Unesp was reviewed for lesions of hemorrhagic disease and 42 captive and free-living Brazilian deer were selected to include in this study. Paraffin-embedded tissues were evaluated using immunohistochemistry and tested negative for adenovirus. Using real time RT-PCR, EHD virus was not detected in paraffin-embedded tissues in any of the cases evaluated. The same technique was used for detection of BT virus and seven positive animals (16,66%) were confirmed after agarose 4% gel electrophoresis and gene sequencing. The main macroscopic changes observed in the positive animals were hemorrhagic intestinal contents, reddish mucous membrane of the gastrointestinal tract, ulcers on tongue and petechiae in various organs. Microscopic changes observed were lymphocytic inflammatory infiltrate in liver, kidney and lungs, hemorrhage, and congestion in various organs. All positive cases were from captive animals, three females (two young and one adult), and four young males. This study demonstrates that the bluetongue virus is involved in hemorrhagic disease outbreaks of deer in Brazil.
Abstract in Portuguese:
Doenças hemorrágicas virais em cervídeos ocorrem no mundo todo e incluem a doença epizoótica hemorrágica (DEH), língua azul (LA), e doença hemorrágica por adenovírus (DHA). Uma vez que as lesões nas três doenças hemorrágicas são idênticas (enteropatia hemorrágica, edema pulmonar, petéquias sistêmicas e sufusões hemorrágicas), é necessário utilizar técnicas precisas para um diagnóstico etiológico definitivo. Material de arquivo (blocos de parafina) do Departamento de Patologia Veterinária da FCAV - Unesp foi revisado para lesões de doenças hemorrágicas e 42 cervídeos brasileiros de cativeiro e de vida livre foram selecionados e incluídos neste estudo. Tecidos embebidos em parafina foram avaliados usando imunohistoquímica e foram negativos para adenovírus. Usando o RT-PCR em tempo real, o vírus da DEH não foi detectado nos tecidos de nenhum dos casos avaliados. A mesma técnica foi utilizada para detecção do vírus da LA e sete animais positivos (16,66%) foram confirmados após eletroforese em gel de agarose a 4% e sequenciamento genético. As principais alterações macroscópicas observadas nos animais positivos foram conteúdo intestinal hemorrágico, mucosa do trato gastrointestinal avermelhada, úlceras na língua e petéquias em vários órgãos. As alterações microscópicas observadas foram infiltrado inflamatório linfocítico em fígado, rins e pulmões, e hemorragia e congestão em vários órgãos. Todos os casos positivos foram de animais de cativeiro, três fêmeas (dois jovens e um adulto), e quatro jovens do sexo masculino. Este estudo demonstra que o vírus da lingual azul está envolvido nos surtos de doença hemorrágica em veados no Brasil.
#2 - Fowl adenovirus Group I as a causal agent of inclusion body hepatitis/hydropericardium syndrome (IBH/HPS) outbreak in brazilian broiler flocks, 34(8):733-737
Abstract in English:
ABSTRACT.- Mettifogo E., Nuñez L.F.N., Santander Parra S.H., Astolfi-Ferreira C.S. & Ferreira A.J.P. 2014. Fowl adenovirus Group I as a causal agent of inclusion body hepatitis/hydropericardium syndrome (IBH/HPS) outbreak in brazilian broiler flocks. Pesquisa Veterinária Brasileira 34(8):733-737. Departamento de Patologia, Faculdade de Medicina Veterinária e Zootecnia, Universidade de São Paulo, Av. Prof. Dr. Orlando Marques de Paiva 87, São Paulo, SP 05508-270, Brazil. E-mail: ajpferr@usp.br
Commercial broiler flocks from a farm located in the State of São Paulo, Brazil, presented diarrhea, depression, increased mortality and poor weight gain. Upon post-mortem examination, classical signs of Inclusion Body Hepatitis/Hydropericardium Syndrome (IBH/HPS) were observed, including enlarged pale yellow-colored livers and straw-colored liquid in the pericardial sac. In addition, gross lesions were also observed in the kidneys, pancreas, thymus, intestines and gallbladder. Samples of these organs were analyzed by PCR for the detection of the hexon gene of the Fowl Adenovirus (FAdVs) Group I. The results were positive for both flocks (A and B) assayed by PCR. The macroscopic lesions associated with the detection of FAdV Group I by PCR in several of these affected organs allowed for the identification of IBH/HPS. In fact, this is the first report in Brazil of IBH/HPS in broilers, which identifies FAdVs group I as a causal agent of the disease. These findings may contribute to the worldwide epidemiology of the adenovirus-mediated hepatitis/hydropericardium syndrome.
Abstract in Portuguese:
RESUMO.- Mettifogo E., Nuñez L.F.N., Santander Parra S.H., Astolfi-Ferreira C.S. & Ferreira A.J.P. 2014. Fowl adenovirus Group I as a causal agent of inclusion body hepatitis/hydropericardium syndrome (IBH/HPS) outbreak in brazilian broiler flocks. [Adenovirus aviário Ggrupo I como um agente causal da síndrome da hepatite por corpúsculo de inclusão/hidropericárdio (IBH/HPS) em lotes de frangos de corte.] Pesquisa Veterinária Brasileira 34(8):733-737. Departamento de Patologia, Faculdade de Medicina Veterinária e Zootecnia, Universidade de São Paulo, Av. Prof. Dr. Orlando Marques de Paiva 87, São Paulo, SP 05508-270, Brazil. E-mail: ajpferr@usp.br
Lotes comerciais de frangos de uma granja localizada no Estado de São Paulo, Brasil, apresentavam diarreia, depressão, aumento de mortalidade e baixo ganho de peso. Após o exame post-mortem, sinais clássicos da síndrome de hepatite por corpúsculo de inclusão/hidropericárdio (IBH/HPS) foram observados incluindo hepatomegalia com aspecto amarelado pálido e líquido de coloração amarelo palha no saco pericárdio. Além disso, as alterações macroscópicas foram também observadas nos rins, pâncreas, timo, intestinos e vesícula biliar. Amostras destes órgãos foram analisadas pela técnica de PCR para detectar o adenovírus aviário do grupo I através do gene Hexon. Os resultados foram positivos para ambos os lotes (A e B) utilizando-se a técnica de PCR. As lesões macroscópicas associadas à detecção do adenovírus aviário do grupo I pela técnica de PCR em vários destes órgãos acometidos permitiu a identificação da síndrome de hepatite/hidropericárdio em frangos no Brasil. Ao nosso conhecimento, este é a primeira descrição da síndrome de hepatite/hidropericárdio causado por adenovírus aviário do grupo I, no Brasil. Estes achados podem contribuir com a epidemiologia mundial do adenovírus mediando a síndrome de hepatite/hidropericárdio.
#3 - Granulocyte-macrophage colony-stimulating factor does not increase the potency or efficacy of a foot-and-mouth disease virus subunit vaccine, p.150-158
Abstract in English:
Caron L., Brum M.C.S., Moraes M.P., Golde W.T., Arns C.W. & Grubman M.J. 2005. Granulocyte-macrophage colony-stimulating factor does not increase the potency or efficacy of a foot-and-mouth disease virus subunit vaccine. Pesquisa Veterinária Brasileira 25(3):150-158. USDA, ARS, PIADC-FMD Research Unit, PO.Box 848, Greenport, NY 11944 0848, USA. E-mail: mgrubman@piadc.ars.usda.gov
Foot-and-mouth disease (FMD) is one of the most feared diseases of livestock worldwide. Vaccination has been a very effective weapon in controlling the disease, however a number of concerns with the current vaccine including the inability of approved diagnostic tests to reliably distinguish vaccinated from infected animals and the need for high containment facilities for vaccine production, have limited its use during outbreaks in countries previously free of the disease. A number of FMD vaccine candidates have been tested and a replication-defective human adenovirus type 5 (Ad5) vector containing the FMDV capsid (P1-2A) and 3C protease coding regions has been shown to completely protect pigs against challenge with the homologous virus (FMDV A12 and A24). An Ad5-P1-2A+3C vaccine for FMDV O1 Campos (Ad5-O1C), however, only induced a low FMDV-specific neutralizing antibody response in swine potency tests. Granulocyte-macrophage colony-stimulating factor (GM-CSF) has been successfully used to stimulate the immune response in vaccine formulations against a number of diseases, including HIV, hepatitis C and B. To attempt to improve the FMDV-specific immune response induced by Ad5-O1C, we inoculated swine with Ad5-O1C and an Ad5 vector containing the gene for porcine GM-CSF (pGM-CSF). However, in the conditions used in this trial, pGM-CSF did not improve the immune response to Ad5-O1C and adversely affected the level of protection of swine challenged with homologous FMDV.
Abstract in Portuguese:
Caron L., Brum M.C.S., Moraes M.P., Golde W.T., Arns C.W. & Grubman M.J. 2005. Granulocyte-macrophage colony-stimulating factor does not increase the potency or efficacy of a foot-and-mouth disease virus subunit vaccine. Pesquisa Veterinária Brasileira 25(3):150-158. USDA, ARS, PIADC-FMD Research Unit, PO.Box 848, Greenport, NY 11944 0848, USA. E-mail: mgrubman@piadc.ars.usda.gov
Foot-and-mouth disease (FMD) is one of the most feared diseases of livestock worldwide. Vaccination has been a very effective weapon in controlling the disease, however a number of concerns with the current vaccine including the inability of approved diagnostic tests to reliably distinguish vaccinated from infected animals and the need for high containment facilities for vaccine production, have limited its use during outbreaks in countries previously free of the disease. A number of FMD vaccine candidates have been tested and a replication-defective human adenovirus type 5 (Ad5) vector containing the FMDV capsid (P1-2A) and 3C protease coding regions has been shown to completely protect pigs against challenge with the homologous virus (FMDV A12 and A24). An Ad5-P1-2A+3C vaccine for FMDV O1 Campos (Ad5-O1C), however, only induced a low FMDV-specific neutralizing antibody response in swine potency tests. Granulocyte-macrophage colony-stimulating factor (GM-CSF) has been successfully used to stimulate the immune response in vaccine formulations against a number of diseases, including HIV, hepatitis C and B. To attempt to improve the FMDV-specific immune response induced by Ad5-O1C, we inoculated swine with Ad5-O1C and an Ad5 vector containing the gene for porcine GM-CSF (pGM-CSF). However, in the conditions used in this trial, pGM-CSF did not improve the immune response to Ad5-O1C and adversely affected the level of protection of swine challenged with homologous FMDV.
#4 - Occurrence of antibodies for avian viruses in broilers in a region of high density poultry production
Abstract in English:
Blood samples were obtained at slaughter from sixty 43 to 56 day old broilers, from each of 60 healthy flocks located in a region of high density poultry production. The flocks tested corresponded to approximately 10% of the total number existing in the region and were located within a radius of 50 km. All broilers had been vaccinated against Marek's disease atone day of age. Sera were tested in the immunodiffusion test for antibodies to avian reovirus (ARV), infectious bursal disease vírus (IBDV), fowl poxvirus (FPV), herpes virus of turkeys (HVT), avian adenovirus of groups 1 (AAV-1) and 2 (AAV-2). The sarne sera were tested in the micro serum neutralization test in plates for antibodies to infectious bronchitis virus (IBV) and infectious laryngotracheitis virus (ILTV), and for hemagglutination inhibition antibodies to Newcastle disease virus (NDV). Antibodies to ARV, detected in 2172 (63.6%) of 3418 sera, and to AAV-1, in 2701 (78.2%) of 3456 sera, were found in all 60 flocks, while antibodies to IBDV, in 3086 (89.4%) of 3452 sera, were found in only 57 of the sarne flocks. These results indicated that the three viruses are ubiquitous in broilers. Antibodies to FPV in 14 (0.5%) of 2935 sera, and to NDV in 6 (0.2%) of 3320 sera, were demonstrated in five of 59 and in one of 60 flocks, respectively, indicating that these two viruses occur only rarely. Antibodies to HVT, in 315 (9.0%) of 3384 sera, were detected in 39 of 60 flocks tested, suggesting poor serological response to vaccination and low field exposure to MDV. Antibodies to IBV, in 61 (2.1 %) of 2925 sera, were found in 12 of 57 flocks tested. However, in only one flock was the percentage of reactors significant (41 %); in the 11 flocks the percentage of broilers with antibody ranged from 1.7 to 16.1 %. Finally, no antibodies were found in 3491 sera from 60 flocks tested for AAV-2, nor in 3035 sera from 59 flocks when tested for ILTV, indicating that these two viruses do not exist in the geographical area tested. The significance of these findings is discussed.
Abstract in Portuguese:
Amostras de sangue foram obtidas ao abate de 60 frangos de corte, de 43 a 56 dias de idade, de cada uma de 60 granjas sem problemas sanitários aparentes localizadas em uma região de alta densidade de produção avícola. As granjas correspondiam a 10% do número total que existe na região e estavam localizadas em um raio de 50 km. Todos os frangos tinham sido vacinados contra a doença de Marek no primeiro dia de vida. Os soros foram avaliados no teste de imunodifusão para anticorpos para reovírus aviário (R V A), vírus da doença infecciosa da bursa (VDIB), vírus da bouba aviária (VBA), vírus herpes de perus (HVT), adenovírus aviário do grupo 1 (AVA-1) e do grupo 2 (A VA-2). Os mesmos soros foram examinados no microteste de soroneutralização em placas para anticorpos para o vírus da bronquite infecciosa (VBI) e o vírus da laringotraqueíte infecciosa (VLTI), bem como anticorpos inibidores da hemoaglutinação para o vírus da doença de Newcastle (VDN). Anticorpos para RVA, detectados em 2172 (63,6%) de 3418 soros, e para AVA-1, em 2701 (78,2%) de 3456 soros, foram demonstrados em todas as 60 granjas, enquanto que, anticorpos para o VDIB, em 3086 (89,4%) de 3452 soros, foram encontrados em somente 57 destas granjas. Estes resultados indicam que os três vírus são ubíquos em frangos de corte da região estudada. Anticorpos para o VBA em 14 (0,5%) de 2935 soros, para o VDN em seis (0,2%) de 3320 soros, foram encontrados em cinco de 59 e em uma de 60 granjas, respectivamente, indicando que esses dois vírus ocorrem apenas raramente. Anticorpos para HVT, em 315 (9,0%) de 3484 soros, foram detectados em 39 de 60 granjas testadas, sugerindo resposta sorológica pobre à vacinação e baixa exposição de campo ao vírus da doença de Marek. Anticorpos para o VBI, em 61 (2,1%) de 2925 soros, foram encontrados em 12 de 57 granjas testadas. Porém, em apenas uma granja a percentagem de reagentes era significativa (41 %); nas outras 11 granjas a percentagem de frangos com anticorpos variava de 1,7 a 16,1%. Finalmente, não foram detectados anticorpos em 3491 soros de 60 granjas testada para A VA-2, nem em 3035 soros de 59 granjas testadas para o VLTI, indicando que esses vírus não existem na área geográficas estudada. O significado de todos os achados é discutido.
