Resultado da pesquisa (19)

Termo utilizado na pesquisa galinhas

#11 - Efficacy of bacterin-, outer membrane protein- and fimbriae extract-based vaccines for the control of Salmonella Enteritidis experimental infection in chickens, 33(3):326-330

Abstract in English:

ABSTRACT.- Menão M.C., Astolfi-Ferreira C.S., Knöbl T. & Ferreira A.J.P. 2013. Efficacy of bacterin-, outer membrane protein- and fimbriae extract-based vaccines for the control of Salmonella Enteritidis experimental infection in chickens. Pesquisa Veterinária Brasileira 33(3):326-330. 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 The efficacy of three vaccines was evaluated in chickens for the control of experimental infection with Salmonella Enteritidis (SE) phage type 4. The vaccines were produced with bacterin, outer membrane proteins (OMP) and fimbriae crude extract (FE). The chickens were vaccinated intramuscularly with two doses of each vaccine at 12 and 15 weeks of age. The chickens were then orally challenged with 109 CFU/chicken Salmonella Enteritidis phage type 4 at 18 weeks of age. Fecal swabs were performed for the recovery of shedding SE, and SE was recovered from the liver and spleen. Additionally, antibody titers were measured in the serum by micro-agglutination test. The results indicated that the vaccine produced with bacterin yielded better results and resulted in reduction of fecal shedding and organ invasion by SE after oral challenge, although no vaccine was 100% effective for the control of SE experimental infection.

Abstract in Portuguese:

RESUMO.- Menão M.C., Astolfi-Ferreira C.S., Knöbl T. & Ferreira A.J.P. 2013. Efficacy of bacterin-, outer membrane protein- and fimbriae extract-based vaccines for the control of Salmonella Enteritidis experimental infection in chickens. [Eficácia de bactéria inativada (bacterina), proteína da membrana externa e extrato de fimbrias no controle de infecção experimental por Salmonella Enteritidis (SE) em galinhas.] Pesquisa Veterinária Brasileira 33(3):326-330. 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 A eficácia de três vacinas de Salmonella Enteritidis fagotipo 4, produzidas na forma de bacterina, proteínas de membrana externa (OMP) e extrato bruto de fímbrias (FE) foi avaliada para proteção de aves infectadas experimentalmente. As aves foram vacinadas por via intramuscular com duas doses de cada vacina as 12 e 15 semanas de idade e desafiadas com 109 UFCs de Salmonella Enteritidis fagotipo 4 às 18 semanas de idade, por via oral. A eficácia foi determinada através do reisolamento da bactéria nas fezes e no fígado e baço, e os anticorpos foram mensurados no soro. Os resultados demonstraram que a vacina produzida com a bacterina foi mais eficaz em comparação às outras vacinas examinadas, para reduzir a excreção fecal e a invasão de órgãos após o desafio por SE.


#12 - Serologic and molecular diagnostic and bioassay in mice for detection of Toxoplasma gondii in free range chickens from Pantanal of Mato Grosso do Sul, 32(8):721-726

Abstract in English:

ABSTRACT.- Holsback L., Pena H.F.J., Ragozo A., Lopes E.G., Gennari S.M. & Soares R.M. 2012. Serologic and molecular diagnostic and bioassay in mice for detection of Toxoplasma gondii in free range chickens from Pantanal of Mato Grosso do Sul. Pesquisa Veterinária Brasileira 32(8):721-726. Setor de Veterinária e Produção Animal, Universidade Estadual do Norte do Paraná, Campus Luiz Meneghel, Rodovia BR 369 Km 54, Bandeirantes, PR 86360-000, Brazil. E-mail: lhsfertonani@uenp.edu.br The aim of this study was to investigate the occurrence of Toxoplasma gondii and compare the results obtained in the Modified Agglutination Test (MAT), Polimerase Chain Reaction (PCR) and bioassay in mice. In order to accomplish this, 40 free-range chickens from eight farms in neighboring areas to the Pantanal in Nhecolândia, Mato Grosso do Sul, were euthanized and blood samples, brain and heart were collected. The occurrence of anti-T. gondii antibodies found in chickens was 67.5% (27 samples), considering as a cutoff point the dilution 1:5. Among the samples analyzed, 7 (25.9%) were positive in the dilution 1:5, 3 (11.1%) in 1:10, 2 (7.4%) in 1:20, 3 (11.1%) in 1:320, 1 ( 3.7%) in 1:640, 3 (11.1%) in 1:1280, 2 (7.4%) in 1:2560, 4 (14.8%) in 1:5120 and 2 (7.4%) in 1:10.240. From the mixture of tissue samples (brain and heart) from the chickens analyzed, 16 (40%) presented electrophoretic bands compatible with T. gondii by PCR (gene B1). In the comparison of techniques, 59.26% positivity in PCR was revealed among animals that were seropositive in MAT (cutoff 1:5). From 141 inoculated mice, six (4.44%) died of acute toxoplasmosis between 15 and 23 days after inoculation. Surviving mice were sacrificed at 74 days after inoculation, and a total of 28 cysts were found in the brains of 10 distinct groups. From the seropositive hens, 27 bioassays were performed and 11 (40.7%) isolates were obtained. A greater number of isolations happened in mice that were inoculated with tissues from chickens that had high titers for anti-T. gondii antibodies. Chronic infection in mice was observed in nine groups (33.3%) from five different properties. Among the surviving mice, 25.6% were positive for T. gondii in MAT (1:25). From mice positive in PCR, 87.5% were also positive in MAT. Among the PCR-negative mice, 5.2% were positive for T. gondii in MAT. It can be concluded through this study that the occurrence of infecton by T. gondii in the rural properties studied was high, that PCR directed to gene B1 does not confirm the viability of the parasite, but it can be used as a screening method for the selection of chickens infected by T. gondii, that the animals with titer greater than 10 must be prioritized for the selection of animals for bioassay, since for them, the chances of isolating the parasite are greater and that seroconversion in experimentally infected mice is not a good indicator for isolating the agent.

Abstract in Portuguese:

RESUMO.- Holsback L., Pena H.F.J., Ragozo A., Lopes E.G., Gennari S.M. & Soares R.M. 2012. Serologic and molecular diagnostic and bioassay in mice for detection of Toxoplasma gondii in free range chickens from Pantanal of Mato Grosso do Sul. Pesquisa Veterinária Brasileira 32(8):721-726. Setor de Veterinária e Produção Animal, Universidade Estadual do Norte do Paraná, Campus Luiz Meneghel, Rodovia BR 369 Km 54, Bandeirantes, PR 86360-000, Brazil. E-mail: lhsfertonani@uenp.edu.br Os objetivos deste estudo foram investigar a ocorrência de Toxoplasma gondii e comparar os resultados obtidos no Teste de Aglutinação Modificada (MAT), Reação em Cadeia pela Polimerase (PCR) e o bioensaio em camundongos. Para tanto, 40 galinhas de criação livre de oito fazendas em áreas limítrofes ao Pantanal da Nhecolândia, Mato Grosso do Sul, foram eutanasiadas e amostras de sangue, o cérebro e o coração foram coletados. A frequência de anticorpos anti-T. gondii encontrada nas galinhas foi de 67,5% (27 amostras), considerando como ponto de corte a diluição 1:5. Entre as amostras analisadas, 7 (25,9%) foram positivas na diluição 1:5, 3 (11,1%) em 1:10, 2 (7,4%) em 1:20, 3 (11,1%) em 1:320, 1 ( 3,7%) em 1:640, 3 (11,1%) em 1:1.280, 2 (7,4%) em 1:2.560, 4 (14,8%) em 1:5.120 e 2 (7,4%) em 1:10.240. A partir da mistura de amostras de tecidos (cérebro e coração) das galinhas analisadas, 16 (40%) apresentaram bandas eletroforéticas compatíveis com T. gondii por PCR (gene B1). Na comparação das técnicas, revelou-se 59,26% de positividade na PCR entre os animais soropositivos no MAT (ponto de corte 1:5). Dos 141 camundongos inoculados, seis (4,44%) morreram de toxoplasmose aguda entre 15 e 23 dias após a inoculação. Os camundongos que sobreviveram foram sacrificados 74 dias após a inoculação, sendo encontrados 28 cistos nos cérebros de 10 grupos distintos. Das galinhas soropositivas, foram realizados 27 bioensaios e obtidos 11 (40,7%) isolados. Um maior número de isolamentos ocorreu em camundongos que foram inoculados com tecidos de galinhas que tinham altos títulos de anticorpos anti-T. gondii. Infecção crônica em camundongos foi observada em nove grupos (33,3%) de cinco propriedades diferentes. Entre os camundongos que sobreviveram, 25,6% foram positivos para T. gondii no MAT (1:25). Dos camundongos positivos na PCR, 87,5% também foram positivos no MAT. Já entre os camundongos PCR negativos 5,2% foram positivos para T. gondii no MAT. Concluiu-se através deste estudo que a ocorrência de infecção pelo T. gondii nas propriedades rurais estudadas foi alta, que a PCR direcionada ao gene B1, não confirma a viabilidade do parasita, porém pode ser utilizada como método de triagem para a seleção de galinhas infectadas por T. gondii, que os animais com título maior que 10 devem ser priorizados para a seleção de animais para bioensaio, pois para eles, as chances de isolamento do parasita são maiores e que a soroconversão em camundongos infectados experimentalmente não é um bom indicador de isolamento do agente.


#13 - Development of Polyclonal IgY antibodies in chickens and IgG in rabbits immunized against proteins of Pythium insidiosum isolated from horses in the state of Rio de Janeiro, 30(1):87-93

Abstract in English:

ABSTRACT.- Nunes Rangel M.F., Lemos L.S., Almeida C.M.C., Sales L.G. & Vieira-da-Motta O. 2010. Development of Polyclonal IgY antibodies in chickens and IgG in rabbits immunized against proteins of Pythium insidiosum isolated from horses in the state of Rio de Janeiro. Pesquisa Veterinária Brasileira 30(1):87-93. Micologia Veterinária do Setor de Doenças Infectocontagiosas, Laboratório de Sanidade Animal do Centro de Ciências e Tecnologias Agropecuárias, Universidade Estadual do Norte Fluminense Darcy Ribeiro, Av. Alberto Lamego 2000, Horto, Campos dos Goytacazes, RJ 28013-602, Brazil. E-mail: olney@uenf.br Pythiosis is caused by Pythium insidiosum and the occurrence of disease in horses was described in the North and Northwest State of Rio de Janeiro, Brazil. The disease was described in cattle, sheep, humans, and horses in different states and regions across the country. This paper describes the development of IgY and IgG polyclonal antibodies, in chicken and rabbits, respectively against proteins extracted from kunkers and hyphae of P. insidiosum from affected horses. The proteins were recognized by chicken, rabbit and horse antibodies by immunodiffusion and Western blot against majority bands of 27 and 43 KDa, and titrated by ELISA. The antibodies IgY developed by the first time against Brazilian strains of P. insidiosum may represent a valuable tool in the detection of antigens of the pathogen and contribute to further studies aimed at immunotherapy and knowledge about this disease in endemic areas in Rio de Janeiro and in Brazil.

Abstract in Portuguese:

RESUMO.- Nunes Rangel M.F., Lemos L.S., Almeida C.M.C., Sales L.G. & Vieira-da-Motta O. 2010. Development of Polyclonal IgY antibodies in chickens and IgG in rabbits immunized against proteins of Pythium insidiosum isolated from horses in the state of Rio de Janeiro. [Desenvolvimento de Anticorpos IgY em galinhas e IgG em coelhos imunizados contra proteínas de Pythium insidiosum isolado de equinos no Estado do Rio de Janeiro, Brasil.] Pesquisa Veterinária Brasileira 30(1):87-93. Micologia Veterinária do Setor de Doenças Infectocontagiosas, Laboratório de Sanidade Animal do Centro de Ciências e Tecnologias Agropecuárias, Universidade Estadual do Norte Fluminense Darcy Ribeiro, Av. Alberto Lamego 2000, Horto, Campos dos Goytacazes, RJ 28013-602, Brazil. E-mail: olney@uenf.br Pitiose é causada por Pythium insidiosum e a doença foi descrita em equinos no Norte e Noroeste do Estado do Rio de Janeiro, Brasil. A doença foi descrita em bovinos, ovelhas, humanos e cavalos em diferentes estados e regiões do país. Este trabalho descreve o desenvolvimento de anticorpos policlonais, IgY e IgG, em galinha e coelho, respectivamente, contra proteínas extraídas de kunkers e hifas de P. insidiosum de cavalos doentes. As proteínas foram reconhecidas por anticorpos de galinha, coelho e cavalos contra as bandas majoritárias de 27 e 34 KDa em imunodifusão e Western blot tituladas por ELISA. Os anticorpos IgY desenvolvidos pela primeira vez contra cepas brasileiras de P. insidiosum podem representar um valioso instrumento na detecção de antígenos de patógenos e contribuem para novos estudos baseados na imunoterapia e no entendimento sobre esta doença em áreas endêmicas no Rio de Janeiro e em todo o país.


#14 - Uso de fixador esquelético externo Tipo II para osteossíntese de tibiotarso em galinhas da raça Plymouth Rock Branca: modelo experimental para uso em aves selvagens, 199-204

Abstract in English:

ABSTRACT.- De Conti J.B., Schossler J.E.W., Alievi M.M., Bonfada A.T., Novosad D., Silva D. & Pachaly J.R. 2007. [Use of Type II external skeletal fixator for tibiotarsus osteosynthesis in White Plymouth Rock chickens: An experimental model for using in wild birds.] Uso de fixador esquelético externo Tipo II para osteossíntese de tibiotarso em galinhas da raça Plymouth Rock Branca: modelo experimental para uso em aves selvagens. Pesquisa Veterinária Brasi-leira 27(5):199-204. Curso de Medicina Veterinária, Universidade Estadual de Maringá, Estrada da Paca s/n, Zona Rural, Umuarama, PR 87502-000, Brazil. E-mail: julianodeconti@yahoo.com.br The efficiency of the Type II external skeletal fixator for the treatment of tibiotarsus fracture in eight adult White Plymouth Rock chickens was evaluated. The individuals were pre-medicated with morphine sulfate and anesthetized with halothane, and submitted to a diaphysary osteotomy in the left tibiotarsus, performed with an oscillatory saw. Four Kirschner wires were inserted through the bone cortices, being two proximally and two distally to the fracture. After the fracture reduction the ends of both proximal and distal wires were twisted in distal or proximal direction, respectively, being the wires connected by two bars of autopolymerizing acrylic resin, in the external lateral and medial faces of the limb. The return to full capability to use the member was observed in 20.00±7.09 days, and the bone healing occurred in 35.12±8.72 days. The results of this study showed that open reduction and use of Type II external skeletal fixator is an effective method for the treatment of tibiotarsus fractures in White Plymouth Rock chickens.

Abstract in Portuguese:

ABSTRACT.- De Conti J.B., Schossler J.E.W., Alievi M.M., Bonfada A.T., Novosad D., Silva D. & Pachaly J.R. 2007. [Use of Type II external skeletal fixator for tibiotarsus osteosynthesis in White Plymouth Rock chickens: An experimental model for using in wild birds.] Uso de fixador esquelético externo Tipo II para osteossíntese de tibiotarso em galinhas da raça Plymouth Rock Branca: modelo experimental para uso em aves selvagens. Pesquisa Veterinária Brasi-leira 27(5):199-204. Curso de Medicina Veterinária, Universidade Estadual de Maringá, Estrada da Paca s/n, Zona Rural, Umuarama, PR 87502-000, Brazil. E-mail: julianodeconti@yahoo.com.br The efficiency of the Type II external skeletal fixator for the treatment of tibiotarsus fracture in eight adult White Plymouth Rock chickens was evaluated. The individuals were pre-medicated with morphine sulfate and anesthetized with halothane, and submitted to a diaphysary osteotomy in the left tibiotarsus, performed with an oscillatory saw. Four Kirschner wires were inserted through the bone cortices, being two proximally and two distally to the fracture. After the fracture reduction the ends of both proximal and distal wires were twisted in distal or proximal direction, respectively, being the wires connected by two bars of autopolymerizing acrylic resin, in the external lateral and medial faces of the limb. The return to full capability to use the member was observed in 20.00±7.09 days, and the bone healing occurred in 35.12±8.72 days. The results of this study showed that open reduction and use of Type II external skeletal fixator is an effective method for the treatment of tibiotarsus fractures in White Plymouth Rock chickens.


#15 - Um protocolo de “nested-PCR” para detecção do virus da anemia das galinhas, p.106-110

Abstract in English:

Simionatto S., Lima-Rosa C.A.V., Rubin L.L. & Canal C.W. 2005. [A nested-PCR protocol for detection of the chicken anemia virus.] Um protocolo de “nested-PCR” para detecção do virus da anemia das galinhas. Pesquisa Veterinária Brasileira 25(2):106-110. Laboratório de Virologia, Faculdade de Veterinária, Universidade Federal do Rio Grande do Sul, Av. Bento Gonçalves 9090, Porto Alegre, RS 91540-000, Brazil. E-mail: claudio.canal@ufrgs.br This paper reports a nested polymerase chain reaction (nested-PCR) protocol for detection of chicken anemia virus (CAV), the causal agent of infectious chicken anemia. For DNA extraction from clinical samples, a method based on guanidine thiocyanate was found more sensitive and practical than other extraction protocols tested. The pair of primers used in the initial PCR targeted a 664 bp fragment on the VP1 gene. The primers for the internal PCR targeted a fragment of 520 bp. The specificity of the primers was evaluated on samples of CAV controlled flocks. Thirty different viruses and bacteria isolated from chickens did not give rise to any amplification product in the assay. The sensitivity of the nested-PCR was determined on serial dilutions of a CAV vaccine. The nested-PCR was more sensitive than a one step PCR and was able to detect at least 0.16 TCID50 of the vaccine strain. In addition, the protocol employed here detected viral DNA from tissues, sera and litter from flocks with or without clinical signs of disease. It is concluded that the nested-PCR protocol described here is more sensitive, faster and less cumbersome than virus isolation in cell culture as a diagnostic technique for detection of CAV.

Abstract in Portuguese:

Simionatto S., Lima-Rosa C.A.V., Rubin L.L. & Canal C.W. 2005. [A nested-PCR protocol for detection of the chicken anemia virus.] Um protocolo de “nested-PCR” para detecção do virus da anemia das galinhas. Pesquisa Veterinária Brasileira 25(2):106-110. Laboratório de Virologia, Faculdade de Veterinária, Universidade Federal do Rio Grande do Sul, Av. Bento Gonçalves 9090, Porto Alegre, RS 91540-000, Brazil. E-mail: claudio.canal@ufrgs.br This paper reports a nested polymerase chain reaction (nested-PCR) protocol for detection of chicken anemia virus (CAV), the causal agent of infectious chicken anemia. For DNA extraction from clinical samples, a method based on guanidine thiocyanate was found more sensitive and practical than other extraction protocols tested. The pair of primers used in the initial PCR targeted a 664 bp fragment on the VP1 gene. The primers for the internal PCR targeted a fragment of 520 bp. The specificity of the primers was evaluated on samples of CAV controlled flocks. Thirty different viruses and bacteria isolated from chickens did not give rise to any amplification product in the assay. The sensitivity of the nested-PCR was determined on serial dilutions of a CAV vaccine. The nested-PCR was more sensitive than a one step PCR and was able to detect at least 0.16 TCID50 of the vaccine strain. In addition, the protocol employed here detected viral DNA from tissues, sera and litter from flocks with or without clinical signs of disease. It is concluded that the nested-PCR protocol described here is more sensitive, faster and less cumbersome than virus isolation in cell culture as a diagnostic technique for detection of CAV.


#16 - Detecção do vírus da laringotraqueíte das galinhas no Brasil

Abstract in English:

Beltrão N., Furian T.Q., Leão J.A., Pereira R.A., Moraes L.B. & Canal C.W. 2004. [Detection of infectious laryngotracheitis virus in chickens in Brazil.] Detecção do vírus da laringotraqueíte das galinhas no Brasil. Pesquisa Veterinária Brasileira 24(2):85-88. Centro de Diagnóstico e Pesquisa em Patologia Aviária (CDPA), Faculdade de Veterinária, UFRGS, Porto Alegre, RS 91540-000, Brazil. E-mail: nilzaneb@hotmail.com A study was carried out in search for evidences of infectious laryngotracheitis virus (ILTV) infections in some Brazilian chicken flocks. Tracheal tissues and swabs were collected from 10 different flocks of layers and broilers displaying respiratory signs of disease. Samples were processes for virus isolation in embryonated eggs and the membranes examined by histopathology. In addition, specimens were examined by polymerase chain reaction (PCR). Three flocks had ILTV positive chickens by virus isolation and PCR. These results confirm the occurrence of ILTV in chickens in Brazil.

Abstract in Portuguese:

Beltrão N., Furian T.Q., Leão J.A., Pereira R.A., Moraes L.B. & Canal C.W. 2004. [Detection of infectious laryngotracheitis virus in chickens in Brazil.] Detecção do vírus da laringotraqueíte das galinhas no Brasil. Pesquisa Veterinária Brasileira 24(2):85-88. Centro de Diagnóstico e Pesquisa em Patologia Aviária (CDPA), Faculdade de Veterinária, UFRGS, Porto Alegre, RS 91540-000, Brazil. E-mail: nilzaneb@hotmail.com A study was carried out in search for evidences of infectious laryngotracheitis virus (ILTV) infections in some Brazilian chicken flocks. Tracheal tissues and swabs were collected from 10 different flocks of layers and broilers displaying respiratory signs of disease. Samples were processes for virus isolation in embryonated eggs and the membranes examined by histopathology. In addition, specimens were examined by polymerase chain reaction (PCR). Three flocks had ILTV positive chickens by virus isolation and PCR. These results confirm the occurrence of ILTV in chickens in Brazil.


#17 - Production of bacteriocins by Salmonella isolated from chickens and turkeys

Abstract in English:

Production of bacteriocins was investigated in 24 strains of Salmonella isolated from two flocks of birds: one of breeder turkeys and another of breeder chickens, both apparently healthy. Eleven strains of S. typhimurium, two of S. saintpaul, two of S. eimsbuettel and nine of S. arizonae were used in this experiment. All strains but S. arizonae produced bacteriocins. As far as bacteriocinogenicity was concerned, the strains tested apparently belonged to two groups.

Abstract in Portuguese:

Investigou-se a produção de bacteriocinas de 24 amostras de salmonela isoladas de dois lotes de aves: um de perus e outro de galinhas reprodutoras, aparentemente normais. Foram testadas onze amostras de Salmonella typhimurium, duas de S. saintpaul, duas amostras de S. eimsbuettel e nove S. arizonae. Todas as amostras, com exceção de S. arizonae, produziram bacteriocinas. Neste estudo, houve formação de dois grupos do ponto de vista de bacteriocinogenicidade.


#18 - Drug resistance in Salmonella isolated from chicken and turkey breeder flocks

Abstract in English:

Studies were conducted to determine drug resistance in Salmonella isolated using the plate dilution method. The following drugs were used: ampicillin, sulphodiazine, oxytetracycline, kanamycin, chloramphenicol, gentamicin, polymixin B, nalidixic acid, dehydrostreptomycin and nitrofurazone. Twentyfour Salmonella strains isolated from apparently healthy chicken and turkey breeder flocks were examined. The following strains were tested: Eleven S. typhimurium, two S. saintpaul, two S. eimsbuettel and nine S. arizonae 18:z4,z32:- (Ar. -7:1, 7, 7:-). All these strains presented a resistance level below 2 μg of the base per ml of the culture medium when following drugs were used: gentamicin, ampicillin, kanamycin, polymycin. A resistance level of 2 or 5 μg/ml was found with the following: streptomycin, chloramphenicol, nalidixic acid and oxytetracycline. The strain isolated from turkeys showed a resistance level of 5 μg/ml with nitrofurazone while those isolated from chickens showed a resistance of 10 μg/ml. The only exception was S. typhimurium strain 185 which showed resistance to 20 μg/ml of the same drug. All these strains tested were resistant to sulphadiazine.

Abstract in Portuguese:

Utilizando-se o método de diluição em placa, foram determinados os níveis de resistência de amostras de Salmonella isoladas de galinhas e perus às seguintes drogas: ampicilina, sulfadiazina, oxitetraciclina, sulfato de canamicina, cloranfenicol, sulfato de gentamicina, poliximina B, ácido nalidíxico, sulfato de diidroestreptomicina e nitrofurazona. Foram analisadas 24 amostras de samonelas isoladas de espécimens colhidas de um lote de perus e de outro de galinhas reprodutoras aparentemente normais. Foram usadas as seguintes amostras: onze S. thyphimurium, duas S. saintpaul, duas S. eimsbuettel e nove S. arizonae 18: z4,z32:- (Ar. 7-1,7,8:-). Todas as amostras apresentaram níveis de resistência inferiores a 2 μg/ml frente às seguintes drogas: gentamicina, ampicilina, canamicina, polimixina; e níveis de 2 ou 5 μg/ml, frente às seguintes: estreptomicina, cloranfenicol, ácido nalidíxico, e oxitetraciclina. As amostras isoladas de perus apresentaram níveis de 5 μg/ml à nitrofurazona, enquanto que naquelas oriundas de galinhas, os níveis alcançaram até 10 μg/ml. A única exceção foi apresentada por S. typhimurium 185 que se mostrou resistente a 20 μg/ml da mesma droga. Todas as amostras estudadas foram resistentes à sulfadiazina.


#19 - Vaccination of chickens against chronic respiratory disease with an oil-emulsion Mycoplasma gallisepticum bacterin

Abstract in English:

Subcutimeous inoculation of 30-day old SPF chickens with a·commercial oilaemulsfon Mycoplasma gallisepticum bacterin (MG-Bac, lot 23009, Salsbury Lab., Inc., Charles City,·Iowa 50616, USA) protected them against chronic respiratory disease. The·birds were challenged 30 days after vaccination with the R strain of M. gallisepticum injected into the left thoracic air·sac. The vaccinated birds presented, before and after the challenge, geometric mean titers higher than the nonvaccinated ones. Air sacculitis lesions bccurred with lower frequency and intensity among the vaccinated birds than among the nonvaccinated, showing a positive relationship between the protection and the serological response.

Abstract in Portuguese:

A inoculação subcutânea de galinhas "SPF" de 30 dias de idade com uma vacina oleosa comercial de Mycoplasma gallisepticum (MG-Bac, partida 23009, Salsbury Lab., Inc., Charles City, Iowa 50616, EUA) protegeu-as contra a doença respiratória crônica. As aves foram desafiadas 30 dias após a vacinação pela injeção no saco aéreo torácico esquerdo com a amostra R de M gallisepticum. As aves vacinadas apresentaram, antes e após o desafio, médias geométricas dos títulos de inibição da hemaglutinação maiores do que as aves não vacinadas. As lesões de aerossaculite ocorreram com frequência e intensidade menores entre as aves vacinadas, relacionando-se positivamente proteção obtida com a resposta sorológica observada.


Colégio Brasileiro de Patologia Animal SciELO Brasil CAPES CNPQ UNB UFRRJ CFMV