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1.
Braz. j. microbiol ; 45(1): 231-234, 2014. ilus, tab, graf
Artigo em Inglês | LILACS, VETINDEX | ID: biblio-1469606

Resumo

Canarypox viruses (CNPV) carrying the coding sequence of VP2 protein from infectious bursal disease virus (IBDV) were obtained. These viruses were able to express VP2 protein in vitro and to induce IBDV-neutralizing antibodies when inoculated in specific pathogen-free chickens demonstrating that CNPV platform is usefulness to develop immunogens for chickens.


Assuntos
Animais , Galinhas/virologia , Proteínas Virais , Vírus da Doença Infecciosa da Bursa , Vírus da Varíola dos Canários
2.
Braz. J. Microbiol. ; 45(1): 231-234, 2014. ilus, tab, graf
Artigo em Inglês | VETINDEX | ID: vti-27321

Resumo

Canarypox viruses (CNPV) carrying the coding sequence of VP2 protein from infectious bursal disease virus (IBDV) were obtained. These viruses were able to express VP2 protein in vitro and to induce IBDV-neutralizing antibodies when inoculated in specific pathogen-free chickens demonstrating that CNPV platform is usefulness to develop immunogens for chickens.(AU)


Assuntos
Animais , Galinhas/virologia , Vírus da Varíola dos Canários , Proteínas Virais , Vírus da Doença Infecciosa da Bursa
3.
Rev. bras. ciênc. avic ; 14(2): 109-113, 2012. tab
Artigo em Inglês | VETINDEX | ID: biblio-1400474

Resumo

This study was designed to investigate the effects of a probiotic plus an immunomodulatory product on the growth performance, immune response and net economic returns of broiler chicks vaccinated against Infectious bursal diseases virus (IBDV). A flock of 350 day-old chicks were equally and randomly distributed in seven groups, each comprising 50 birds. A mixture of microorganisms (¹Probiotic) or Cyclophosphamide (immune suppressor) was offered through feed supplementation to different groups. The Probiotic, consisting of Lactobacillus species, Bifidobacterium, Streptococcus salivarius and Enterococcus faecium, in addition to Aspergillus oryza and Candida pintolopessii. Compared with control treatment group, the probiotic-supplemented chicks had better feed conversion ratio (FCR) (1.938 and 1.959), with significantly heavier live body weight 2141.0±34.2 and 2120.3±33.2, respectively. Similarly, their antibody titers against IBDV were significantly higher (941 and 832) on day 35. No morbidity and mortality were observed in these groups. This study suggests that a product composed of a probiotic and cyclophosphamide enhanced the growth rate as well as the immunity against infectious bursal disease virus of broilers chicks.(AU)


Assuntos
Animais , Galinhas/imunologia , Probióticos/química , Fatores Imunológicos/efeitos adversos , Fenômenos Fisiológicos da Nutrição Animal/fisiologia , Bursite/veterinária , Infecções por Birnaviridae/veterinária , Vírus da Doença Infecciosa da Bursa/imunologia
4.
Artigo em Inglês | VETINDEX | ID: vti-717983

Resumo

This study was designed to investigate the effects of a probiotic plus an immunomodulatory product on the growth performance, immune response and net economic returns of broiler chicks vaccinated against Infectious bursal diseases virus (IBDV). A flock of 350 day-old chicks were equally and randomly distributed in seven groups, each comprising 50 birds. A mixture of microorganisms (¹Probiotic) or Cyclophosphamide (immune suppressor) was offered through feed supplementation to different groups. The Probiotic, consisting of Lactobacillus species, Bifidobacterium, Streptococcus salivarius and Enterococcus faecium, in addition to Aspergillus oryza and Candida pintolopessii. Compared with control treatment group, the probiotic-supplemented chicks had better feed conversion ratio (FCR) (1.938 and 1.959), with significantly heavier live body weight 2141.0±34.2 and 2120.3±33.2, respectively. Similarly, their antibody titers against IBDV were significantly higher (941 and 832) on day 35. No morbidity and mortality were observed in these groups. This study suggests that a product composed of a probiotic and cyclophosphamide enhanced the growth rate as well as the immunity against infectious bursal disease virus of broilers chicks.

5.
Tese em Português | VETTESES | ID: vtt-206854

Resumo

O Brasil é o segundo produtor mundial de carne de frango, com produção de 13,14 milhões de toneladas em 2015, sendo em torno de 4 milhões de toneladas destinadas à exportação. Aves silvestres de vida livre, devido as suas características biológicas, são capazes de carrear microrganismos patogênicos de forma biológica ou mecânica, podendo atuar como disseminadores de diferentes enfermidades na produção industrial, comercial ou doméstica de aves. O objetivo deste estudo é investigar a exposição aos vírus da Doença de Newcastle (NDV), Doença de Marek e Doença Infecciosa da Bolsa de Fabrício (IBDV) em aves silvestres residentes próximo a uma criação de aves coloniais, e em aves migratórias (Calidris fuscicollis e Thalassarche melanophris) que ocorrem no litoral do Rio Grande do Sul. A metodologia empregada foi a detecção de material genético viral por RT-PCR e PCR em suabes de orofaringe e cloaca, e pesquisa de anticorpos por ELISA em amostras de soro e sangue total colhido em papel filtro. Não foi detectada a presença de NDV e vírus da Doença de Marek por métodos moleculares nas aves silvestres pesquisadas (n=24), nem anticorpos contra NDV e IBDV nos ensaios imunoenzimáticos (n=30). Todas as amostras de soro de Calidris fuscicollis testadas (n=58) mostraram resultados negativos para anticorpos contra NDV e IBDV. No entanto, 50% (4/8) apresentaram positividade para anticorpos contra vírus da Doença de Marek. Em Thalassarche melanophris, 100% das amostras foram negativas para IBVD e positivas para o vírus da Doença de Marek. Os resultados obtidos reforçam a importância da vigilância contínua dos vírus potencialmente patogênicos aos plantéis avícolas através do monitoramento de aves migratórias, dada a importante posição do Brasil no mercado produtor e exportador de frangos de corte.


Brazil is the second largest producer of chicken meat, with a 13.14 millions of tons production in 2015 and, about 4 millions of tons were for export. Wild birds, of free life, due to its biological characteristics are capable of carrying pathogenic microorganisms both biologically or mechanically, may thus act as disseminators of several different diseases in industrial, commercial and even domestic poultry production. This study aims at investigating the exposure to Newcastle Disease Virus (NDV), Mareks Disease and Infectious Bursal Disease (IBDV) in wild birds living near a colonial poultry breeding and, in migratory birds (Calidris fuscicollis and Thalassarche melanophris) that are present on the coast of Rio Grande do Sul. The methodology used was the viral genetic material detection using RT-PCR and PCR in cloacal and oropharynx swabs and, ELISA serology in total blood samples collected in filter paper. It was not detected the presence of NDV or Mareks Disease Virus by molecular methods in the wild birds investigated (n=24), NDV and IBDV antibodies were also not detect in immunoenzymatic assays (n=30). All serum samples of Calidris fuscicollis tested (n=58) were negative for NDV and IBDV antibodies. However, 50% (4/8) presented positive results for Mareks Disease virus antibodies. In Thalassarche melanophris, 100% of the samples returned negative for IBDV and positive for Mareks Disease Virus. The findings reinforce the importance of continuous surveillance of viruses potentially pathogenic to poultry breeding flock by monitoring migratory birds, especially considering the important position Brazil has in chicken meat production and export market.

6.
Braz. j. vet. pathol ; 2(2): 75-79, 2009. ilus
Artigo em Inglês | VETINDEX | ID: biblio-1435690

Resumo

We exposed chicken embryos at embryonating day (ED18) to a cell-adapted very virulent strain of IBDV (ca-vvIBDV) and original vvIBDV and examined the apoptosis from infected bursa of Fabricius (BF) and thymus organs. Following ca-vvIBDV exposure, embryonic bursa showed mild cellular destruction, lower rate of apoptosis and presence of viral proteins detectable by immunohistochemistry. In contrary, original vvIBDV exposed embryos had an enhanced detectable changes in the bursa associated to an increase apoptotic events, and most of the times, total destruction of BF follicles. In thymus, viral antigen was detectable until after hatch. Positives cell signals to activated caspase-3 were intensively detect in embryos lymphoid tissues exposed to original vvIBDV observed in BF and less in thymus. No immunoreactive thymocytes were visualized in embryos exposed to ca-vvIBDV. Apoptosis changes, such as chromatin condensation, DNA fragmentation, and the appearance of apoptotic nuclear bodies, were observed in both organs. TUNEL-detected DNA was more intense in original vvIBDV infected lymphoid cells, and less apoptotic cells were detectable in attenuated strain. By sequencing analysis, e attenuation presented amino acid changes at position 222 (A→→P), 256 (I→V) and 279 (D→N). One serine in the serine-rich heptapeptide (position 333) was substituted into other amino acid which is similar to the IBDV vaccine strain. Taken together our results indicate that virus attenuation interferes with caspase-3 apoptotic pathway and may play an important role in switch viral pathogenesis.


Assuntos
Animais , Galinhas/virologia , Apoptose , Vírus da Doença Infecciosa da Bursa , Caspase 3 , Tecido Linfoide/virologia
7.
Artigo em Inglês | LILACS-Express | VETINDEX | ID: biblio-1489851

Resumo

The interference of low or high maternal antibodies titers on the attenuated infectious bursal disease (IBD) virus (IBDV) vaccine infection and its effects on the performance of broilers vaccinated at the 18th day of incubation (in ovo), at one day of age (subcutaneously-SC), or at 15 days of age (drinking water-DW) were investigated. After a series of three live vaccinations, breeders were given or not an IBD oil emulsion vaccine (IBD-OEV) prior to sexual maturity. At day 18 of incubation (in ovo), a commercial vaccine containing HVT and an intermediate IBDV strain or the single HVT vaccine was given. An intermediate IBDV vaccine was given SC at one day of age, or at 15 days of age via DW. The progeny of unvaccinated breeders presented higher neutralizing IBDVspecific antibody (IBDVab) titers at 25 and 40 days of age than those of the progeny of IBD-OEV breeders (p 0.05) at any broilers vaccination age and route. The lower IBDV RNA detection by RT-PCR in the bursa of Fabricius (BF) and the lower IBDV antibody titers in the serum of the groups vaccinated at one and 15 days of age derived from IBD-OEV breeders may indicate antibody-mediated IBDV neutralization. The inovo and one-day vaccinations did not interfere with performance, both in low and high antibody-titered progenies. The in-ovo vaccination against IBD is considered convenient and safe for industrial chickens, irrespective their maternal antibody levels.

8.
Artigo em Inglês | VETINDEX | ID: vti-717865

Resumo

The interference of low or high maternal antibodies titers on the attenuated infectious bursal disease (IBD) virus (IBDV) vaccine infection and its effects on the performance of broilers vaccinated at the 18th day of incubation (in ovo), at one day of age (subcutaneously-SC), or at 15 days of age (drinking water-DW) were investigated. After a series of three live vaccinations, breeders were given or not an IBD oil emulsion vaccine (IBD-OEV) prior to sexual maturity. At day 18 of incubation (in ovo), a commercial vaccine containing HVT and an intermediate IBDV strain or the single HVT vaccine was given. An intermediate IBDV vaccine was given SC at one day of age, or at 15 days of age via DW. The progeny of unvaccinated breeders presented higher neutralizing IBDVspecific antibody (IBDVab) titers at 25 and 40 days of age than those of the progeny of IBD-OEV breeders (p 0.05) at any broilers vaccination age and route. The lower IBDV RNA detection by RT-PCR in the bursa of Fabricius (BF) and the lower IBDV antibody titers in the serum of the groups vaccinated at one and 15 days of age derived from IBD-OEV breeders may indicate antibody-mediated IBDV neutralization. The inovo and one-day vaccinations did not interfere with performance, both in low and high antibody-titered progenies. The in-ovo vaccination against IBD is considered convenient and safe for industrial chickens, irrespective their maternal antibody levels.

9.
Artigo em Inglês | VETINDEX | ID: vti-444366

Resumo

Sequencing and phylogenetic analysis based on the nucleotide sequence of the gene encoding VP2 protein was carried out in order to characterize the agent of two outbreaks of infectious bursal disease in layer flocks in the state of Minas Gerais in 2004. The results indicate the outbreaks could be related to the vaccinal virus.


O sequenciamento e a análise filogenética a partir da seqüência nucleotídica do gene que codifica a proteína VP2 foram realizados com o intuito de caracterizar os agentes causadores de dois surtos da doença infecciosa bursal em lotes de poedeiras do estado Minas Gerais, em 2004. Os resultados indicam que os surtos analisados podem estar relacionados com o vírus de origem vacinal.

10.
Ci. Rural ; 38(7)2008.
Artigo em Português | VETINDEX | ID: vti-705569

Resumo

The backyard poultry are not included in the biosecurity system applied in commercial flocks in Brazil. To investigate the presence of antibodies to specific viral pathogens in this population, blood samples were collected from 867 non-vaccinated birds, from 60 flocks in 22 counties of the Rio Grande do Sul State, Brazil. The samples were tested to detect antibodies against infectious bronchitis virus (IBV), avian reovirus (ARV) and infectious bursal disease virus (IBDV), through the virus neutralization test. Antibodies to IBV were detected in 65% (564/867), against ARV in 21.6% (187/867), and against IBDV in 80.2% (695/867) of the samples. All the flocks had chickens positive to IBV and IBDV antibodies, and 88.3% of them harbored antibodies to ARV. The results show the presence of these viruses in backyard poultry from the central region of the State. It also indicates the need for additional studies aimed to evaluate the real importance of these infections for this type of flocks.


No Brasil, a população de aves conhecida como galinhas de terreiro encontra-se fora do sistema de biosseguridade aplicada às criações comerciais. Para investigar a presença de anticorpos contra alguns vírus específicos nesta população, foram coletadas amostras de sangue de 867 aves não-vacinadas em 60 propriedades de 22 municípios do Estado do Rio Grande do Sul, Brasil. O soro foi testado para a presença de anticorpos contra o vírus da bronquite infecciosa das galinhas (IBV), reovírus aviário (ARV) e o vírus da doença infecciosa da bolsa (IBDV) pela técnica de soroneutralização. Anticorpos contra IBV foram detectados em 65% (564/867) das amostras, contra ARV em 21,6% (187/867) e contra IBDV em 80,2% (695/867) das aves. Todas as propriedades avaliadas apresentavam uma ave positiva para anticorpos contra IBV e IBDV e 88,3% delas eram positivas para ARV. Os resultados demonstram que esses vírus estão presentes em galinhas de terreiro nas criações avícolas não-industriais da região central do Estado. Os resultados indicam a necessidade de um programa de vigilância permanente nessa população e ainda indicam a necessidade de avaliar o impacto destas infecções nos próprios plantéis e o risco associado à transmissão destas às criações comerciais.

11.
Artigo em Português | LILACS-Express | VETINDEX | ID: biblio-1477319

Resumo

The backyard poultry are not included in the biosecurity system applied in commercial flocks in Brazil. To investigate the presence of antibodies to specific viral pathogens in this population, blood samples were collected from 867 non-vaccinated birds, from 60 flocks in 22 counties of the Rio Grande do Sul State, Brazil. The samples were tested to detect antibodies against infectious bronchitis virus (IBV), avian reovirus (ARV) and infectious bursal disease virus (IBDV), through the virus neutralization test. Antibodies to IBV were detected in 65% (564/867), against ARV in 21.6% (187/867), and against IBDV in 80.2% (695/867) of the samples. All the flocks had chickens positive to IBV and IBDV antibodies, and 88.3% of them harbored antibodies to ARV. The results show the presence of these viruses in backyard poultry from the central region of the State. It also indicates the need for additional studies aimed to evaluate the real importance of these infections for this type of flocks.


No Brasil, a população de aves conhecida como galinhas de terreiro encontra-se fora do sistema de biosseguridade aplicada às criações comerciais. Para investigar a presença de anticorpos contra alguns vírus específicos nesta população, foram coletadas amostras de sangue de 867 aves não-vacinadas em 60 propriedades de 22 municípios do Estado do Rio Grande do Sul, Brasil. O soro foi testado para a presença de anticorpos contra o vírus da bronquite infecciosa das galinhas (IBV), reovírus aviário (ARV) e o vírus da doença infecciosa da bolsa (IBDV) pela técnica de soroneutralização. Anticorpos contra IBV foram detectados em 65% (564/867) das amostras, contra ARV em 21,6% (187/867) e contra IBDV em 80,2% (695/867) das aves. Todas as propriedades avaliadas apresentavam uma ave positiva para anticorpos contra IBV e IBDV e 88,3% delas eram positivas para ARV. Os resultados demonstram que esses vírus estão presentes em galinhas de terreiro nas criações avícolas não-industriais da região central do Estado. Os resultados indicam a necessidade de um programa de vigilância permanente nessa população e ainda indicam a necessidade de avaliar o impacto destas infecções nos próprios plantéis e o risco associado à transmissão destas às criações comerciais.

12.
Arq. bras. med. vet. zootec ; 59(2): 313-320, abr. 2007. graf, ilus, tab
Artigo em Português | VETINDEX | ID: vti-7356

Resumo

Vinte e nove pintos SPF de um dia foram inoculados com o vírus da doença infecciosa da bursa de Fabricius (VDIB) para avaliar a ocorrência precoce de apoptose e a expressão da proteína viral 2 (VP2) e da enzima gliceraldeído fosfato dehidrogenase (GAPDH). Os animais foram distribuídos em cinco grupos: 1-controle; e 2 a 5- com 24, 48, 72 e 96 horas pós-inoculação, respectivamente. Fragmentos da bursa de Fabricius foram colhidos para processamento histológico e extração de RNA. Lâminas coradas em HE e TUNEL (marcação in situ da fragmentação do genoma com transferase terminal de deoxinucleotídeo) foram utilizadas na morfometria do índice apoptótico. Amostras de mRNA foram testadas para a expressão dos genes VP2 e GAPDH utilizando-se transcrição reversa e RT-PCR. Utilizou-se um kit SYBR GREEN PCR, e a reação foi desenvolvida em ABI Prism 7000 SDS. Os índices apoptóticos cresceram progressivamente indicando uma relação na atrofia bursal causada pelo VDIB. Paralelamente, os resultados da PCR em tempo real demonstraram queda da carga viral nas células linfóides da bursa nos diferentes intervalos de tempo do experimento. Esses resultados sugerem um papel protetor da apoptose na diminuição da replicação viral.(AU)


Twenty-nine SPF 1-day-old chicks were inoculated with infectious bursal disease virus (IBDV) to evaluate early apoptosis and the expression of viral protein 2 (VP2) and glyceraldehyde-3-phosphate dehydrogenease (GAPDH). Five groups were formed: G1-control -and G2 to G5, - 24, 48, 72 and 96 hours post inoculation, respectively. Half of each BF was fixed and processed by routine techniques. To quantify apoptosis, 5µm-thick sections were stained with HE and submitted to TUNEL (terminal transferase UDP nick end labeling) technique. mRNA was extracted from pooled samples of 3 animals/group and used for the expression of VP2 and GADPH genes using the reverse transcription and real-time polymerase chain reaction (RT-PCR). A SYBR GREEN PCR kit was used and the reaction was carried out in an ABI Prism 7000 SDS. Apoptotic indexes progressively increased indicating a role of IBDV in inducing hypotrophy of the BF. Also, it was showed that as long as apoptosis increased, viral protein expression decreased, which suggests that apoptosis plays a role as a defense mechanism against viral replication.(AU)


Assuntos
Apoptose/fisiologia , Bolsa de Fabricius/metabolismo , Proteínas Virais/efeitos adversos , Gliceraldeído-3-Fosfato Desidrogenases/efeitos adversos , Reação em Cadeia da Polimerase Via Transcriptase Reversa/métodos , Aves Domésticas
13.
Artigo em Inglês | VETINDEX | ID: vti-443859

Resumo

In order to identify and characterize the agent of a suggestive clinical case of Gumboro disease (GD) that affected a 34-day-old broiler flock in Buriti Alegre (Goias State, Midwestern Brazil) in the year 2001, we carried out a combination of classic and modern virological methods. Histopathological analysis of the bursa revealed necrosis, presence of depleted follicles, some infiltration of heterophils, edema and formation of cystic cavities that are compatible with lesions observed in GD. Inoculation of embryonated eggs of specific pathogen-free (SPF) chickens with macerated bursa suspension resulted in embryo mortality and lesions which were also compatible with those caused by IBDV. A sample of bursa was submitted to a nested reverse transcriptase-polymerase chain reaction (RT-PCR) procedure to amplify the hypervariable region of the VP2 gene. The amplicon that was obtained from this sample (BR-GO) was digested with the restriction enzymes TaqI, StyI and SspI, but not with SacI, a pattern similar to that observed with very virulent IBDV (vvIBDV) strains. Furthermore, nucleotide sequence analysis revealed alanine, isoleucine, and isoleucine at amino acid positions 222, 256, and 294, respectively, which are also found in vvIBDV strains. Finally, phylogenetic analysis grouped BR-GO isolate with other vvIBDV strains.


Para identificar e caracterizar o agente causador de um quadro clínico sugestivo de doença de Gumboro (DG) que afetou um plantel de frangos de corte com 34 dias de idade, em Buriti Alegre (estado de Goiás, centro-oeste do Brasil), no ano de 2001, procedeu-se uma combinação de métodos virológicos clássicos e modernos. Análises histopatológicas de bursas revelaram necrose, depleção de folículos linfóides, infiltração de heterófilos, edema e formação de cistos, lesões compatíveis com DG. A inoculação em ovos embrionados de galinhas SPF (specific pathogen-free) de uma suspensão de macerado de amostras de bursas resultou em mortalidade embrionária e lesões macroscópicas compatíveis com aquelas provocadas pelo VDIB. Amostras de bursas foram submetidas à técnica de transcrição reversa-reação em cadeia da polimerase (RT-PCR), utilizando-se oligonucleotídeos específicos para amplificação da região hipervariável do gene da VP2. Essa reação produziu um fragmento do tamanho esperado, que foi digerido pelas enzimas de restrição TaqI, StyI e SspI, mas não foi digerido com SacI. Este padrão foi o mesmo observado com cepas de VDIB hipervirulentas (vvVDIB). Análise da seqüência nucleotídica revelou a presença dos aminoácidos alanina, isoleucina e isoleucina nas posições 222, 256 e 294, respectivamente, característica dessas cepas. Além disso, análise filogenética realizada agrupou a cepa encontrada, denominada de BR-GO, com outras cepas de vvVDIB.

14.
Braz. J. Vet. Pathol. ; 2(2): 75-79, 2009.
Artigo em Inglês | VETINDEX | ID: vti-683702

Resumo

We exposed chicken embryos at embryonating day (ED18) to a cell-adapted very virulent strain of IBDV (ca-vvIBDV) and original vvIBDV and examined the apoptosis from infected bursa of Fabricius (BF) and thymus organs. Following ca-vvIBDV exposure, embryonic bursa showed mild cellular destruction, lower rate of apoptosis and presence of viral proteins detectable by immunohistochemistry. In contrary, original vvIBDV exposed embryos had an enhanced detectable changes in the bursa associated to an increase apoptotic events, and most of the times, total destruction of BF follicles. In thymus, viral antigen was detectable until after hatch. Positives cell signals to activated caspase-3 were intensively detect in embryos lymphoid tissues exposed to original vvIBDV observed in BF and less in thymus. No immunoreactive thymocytes were visualized in embryos exposed to ca-vvIBDV. Apoptosis changes, such as chromatin condensation, DNA fragmentation, and the appearance of apoptotic nuclear bodies, were observed in both organs. TUNEL-detected DNA was more intense in original vvIBDV infected lymphoid cells, and less apoptotic cells were detectable in attenuated strain. By sequencing analysis, the attenuation presented amino acid changes at position 222 (AP), 256 (IV) and 279 (DN). One serine in the serine-rich heptapeptide (position 333) was substituted into other amino acid which is similar

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