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Registro Completo |
Biblioteca(s): |
Embrapa Caprinos e Ovinos. |
Data corrente: |
28/07/2009 |
Data da última atualização: |
10/07/2023 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Autoria: |
PAULA, N. R. de O.; ANDRIOLI, A.; CARDOSO, J. de F. S.; PINHEIRO, R. R.; SOUSA, F. M. L.; SOUZA, K. C. de; ALVES, F. S. F.; CAMPELLO, C. C.; RICARTE, A. R. F.; TEIXEIRA, M. F. da S. |
Afiliação: |
Ney Rômulo Oliveira de Paula, Universidade Estadual do Ceará (UECe); ALICE ANDRIOLI, CNPC; Janaína de Fátima Saraiva Cardoso; RAYMUNDO RIZALDO PINHEIRO, CNPC; Fabiane Maria Lima Sousa, Universidade Estadual Vale do Acaraú (UVA); Kelma Costa de Souza, Universidade Estadual Vale do Acaraú (UVA); FRANCISCO SELMO FERNANDES ALVES, CNPC; Claudio Cabral Campello, Universidade Estadual do Ceará (UECe); Aracely Rafaelle Fernandes Ricarte, Universidade Estadual do Ceará (UECe); Maria Fátima da Silva Teixeira, Universidade Estadual do Ceará (UECe). |
Título: |
Profile of the Caprine arthritis-encephalitis virus (CAEV) in blood, semen from bucks naturally and experimentally infected in the Semi-arid region of Brazil. |
Ano de publicação: |
2009 |
Fonte/Imprenta: |
Small Ruminant Research, v. 85, n. 1, p. 27-33, Jul. 2009. |
Idioma: |
Inglês |
Conteúdo: |
Abstract: The aim of this study was to report the chronology of Caprine arthritis-encephalitis virus elimination and compare the blood and semen viral profiles of animals naturally and experimentally infected by SRLV raised in the semi-arid region of Brazil. The experiment was carried out at the Brazilian Center for Goat Research (Embrapa). Nine bucks were selected, four naturally infected by CAEV and five animals proven negative thatwere inoculated with the goat lentivirus (CAEV-Cork strain). Every week the animals were submitted to semen collection using an artificial vagina. The blood was collected by puncturing the jugular vein with tubes containing EDTA, 7 days after inoculation (experimentally infected group) or at the start of the experiment (naturally infectedgroup) and then at every 30days. The genomic viral DNA was extracted from semen and blood and then Nested-PCR was applied. An agar gel microimmunodiffusionwas performed to detect anti-CAEV antibodies. The resultswere described in percentage and analyzed by the Chi square test (P < 0.05). The presence of anti-CAEV antibodies was detected in the 16th week after inoculation that characterized the seroconversion from four of the five naturally infected goat bucks (80%). The fifth reproducer presented late seroconversion, totaling 32 weeks post-inoculation. A quantity was observed in the total of samples collected of 12.50 and 17.14% positive results in the blood and 10.98 and 11.25% positive results in the semen of the naturally and experimentally infected animals, respectively, and there was no statistical difference. No statistically significant differences were observed regarding the presence of proviral DNA in the blood and semen of the naturally and experimentally infected animals. A viral elimination pattern was not identified during the assessment period, but the presence of proviral DNA was shown at shorter intervals after the 18th week and the 22nd week, for the experimentally and naturally infected bucks, respectively. Therefore, recently infected goats in the period prior to seroconversion eliminated small ruminant lentivirus proviralDNA in the semen and are important sources of infection that should be considered in a control program of this lentivirus, and the Nested-PCR technique is a relevant tool to select virus-free ejaculates. MenosAbstract: The aim of this study was to report the chronology of Caprine arthritis-encephalitis virus elimination and compare the blood and semen viral profiles of animals naturally and experimentally infected by SRLV raised in the semi-arid region of Brazil. The experiment was carried out at the Brazilian Center for Goat Research (Embrapa). Nine bucks were selected, four naturally infected by CAEV and five animals proven negative thatwere inoculated with the goat lentivirus (CAEV-Cork strain). Every week the animals were submitted to semen collection using an artificial vagina. The blood was collected by puncturing the jugular vein with tubes containing EDTA, 7 days after inoculation (experimentally infected group) or at the start of the experiment (naturally infectedgroup) and then at every 30days. The genomic viral DNA was extracted from semen and blood and then Nested-PCR was applied. An agar gel microimmunodiffusionwas performed to detect anti-CAEV antibodies. The resultswere described in percentage and analyzed by the Chi square test (P < 0.05). The presence of anti-CAEV antibodies was detected in the 16th week after inoculation that characterized the seroconversion from four of the five naturally infected goat bucks (80%). The fifth reproducer presented late seroconversion, totaling 32 weeks post-inoculation. A quantity was observed in the total of samples collected of 12.50 and 17.14% positive results in the blood and 10.98 and 11.25% positive results in the semen of ... Mostrar Tudo |
Palavras-Chave: |
Artrite encefalite caprina; Brasil; CAEV; Semi-árido. |
Thesagro: |
Caprino; Doença Animal; Sêmen. |
Thesaurus Nal: |
Brazil; Caprine arthritis encephalitis virus; Caprine arthritis-encephalitis; Goat diseases; Goats; Semiarid zones. |
Categoria do assunto: |
H Saúde e Patologia |
Marc: |
LEADER 03488naa a2200385 a 4500 001 1532293 005 2023-07-10 008 2009 bl uuuu u00u1 u #d 100 1 $aPAULA, N. R. de O. 245 $aProfile of the Caprine arthritis-encephalitis virus (CAEV) in blood, semen from bucks naturally and experimentally infected in the Semi-arid region of Brazil. 260 $c2009 520 $aAbstract: The aim of this study was to report the chronology of Caprine arthritis-encephalitis virus elimination and compare the blood and semen viral profiles of animals naturally and experimentally infected by SRLV raised in the semi-arid region of Brazil. The experiment was carried out at the Brazilian Center for Goat Research (Embrapa). Nine bucks were selected, four naturally infected by CAEV and five animals proven negative thatwere inoculated with the goat lentivirus (CAEV-Cork strain). Every week the animals were submitted to semen collection using an artificial vagina. The blood was collected by puncturing the jugular vein with tubes containing EDTA, 7 days after inoculation (experimentally infected group) or at the start of the experiment (naturally infectedgroup) and then at every 30days. The genomic viral DNA was extracted from semen and blood and then Nested-PCR was applied. An agar gel microimmunodiffusionwas performed to detect anti-CAEV antibodies. The resultswere described in percentage and analyzed by the Chi square test (P < 0.05). The presence of anti-CAEV antibodies was detected in the 16th week after inoculation that characterized the seroconversion from four of the five naturally infected goat bucks (80%). The fifth reproducer presented late seroconversion, totaling 32 weeks post-inoculation. A quantity was observed in the total of samples collected of 12.50 and 17.14% positive results in the blood and 10.98 and 11.25% positive results in the semen of the naturally and experimentally infected animals, respectively, and there was no statistical difference. No statistically significant differences were observed regarding the presence of proviral DNA in the blood and semen of the naturally and experimentally infected animals. A viral elimination pattern was not identified during the assessment period, but the presence of proviral DNA was shown at shorter intervals after the 18th week and the 22nd week, for the experimentally and naturally infected bucks, respectively. Therefore, recently infected goats in the period prior to seroconversion eliminated small ruminant lentivirus proviralDNA in the semen and are important sources of infection that should be considered in a control program of this lentivirus, and the Nested-PCR technique is a relevant tool to select virus-free ejaculates. 650 $aBrazil 650 $aCaprine arthritis encephalitis virus 650 $aCaprine arthritis-encephalitis 650 $aGoat diseases 650 $aGoats 650 $aSemiarid zones 650 $aCaprino 650 $aDoença Animal 650 $aSêmen 653 $aArtrite encefalite caprina 653 $aBrasil 653 $aCAEV 653 $aSemi-árido 700 1 $aANDRIOLI, A. 700 1 $aCARDOSO, J. de F. S. 700 1 $aPINHEIRO, R. R. 700 1 $aSOUSA, F. M. L. 700 1 $aSOUZA, K. C. de 700 1 $aALVES, F. S. F. 700 1 $aCAMPELLO, C. C. 700 1 $aRICARTE, A. R. F. 700 1 $aTEIXEIRA, M. F. da S. 773 $tSmall Ruminant Research$gv. 85, n. 1, p. 27-33, Jul. 2009.
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2. |  | CAMARAO, A. P.; MARQUES, J. R. F.; MENDONÇA, C. L. G.; RODRIGUES FILHO, J. A.; CARVALHO, N. N. de. Composição botânica da forragem disponível e dieta de bubalinos do tipo Baio em pastagens nativas de várzeas. In: REUNIÃO ANUAL DA SOCIEDADE BRASILEIRA DE ZOOTECNIA, 34., 1997, Juiz de Fora, MG. Anais. Juiz de Fora: SBZ, 1997. v. 2, p. 287-289.Biblioteca(s): Embrapa Amazônia Oriental. |
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3. |  | MARQUES, J. R. F.; CARDOSO, L. dos S.; COSTA, N. A. da; LOURENCO JUNIOR, J. de B.; CARVALHO, N. N. de. Efeitos de meio sobre características reprodutivas de búfalos (Bubalus bubalis L.). In: REUNIÃO ANUAL DA SOCIEDADE BRASILEIRA DE ZOOTECNIA, 34., 1997, Juiz de Fora, MG. Anais. Juiz de Fora: SBZ, 1997. 3 p. 344-346.Biblioteca(s): Embrapa Amazônia Oriental. |
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4. |  | CAMARÃO, A. P.; MARQUES, J. R. F.; MARTINEZ, G. B.; LOPES, C. A. C.; COSTA, N. A. da; LOURENÇO JÚNIOR, J. B.; CARVALHO, N. N. de; PIMENTEL, E. S.; CRUZ FILHO, R. N. da. Recursos forrageiros nas várzeas. In: MARQUES, J. R. F.; LOPES, C. A. C.; MARTINEZ, G. B. (Ed.). Produção animal nas várzeas do Rio Amazonas. Belém, PA: Embrapa Amazônia Oriental, 2003. p. 255-301.Tipo: Capítulo em Livro Técnico-Científico |
Biblioteca(s): Embrapa Amazônia Oriental. |
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5. |  | MARQUES, J. R. F.; LOPES, C. A. C.; COSTA, N. A. da; LÁU, H. D.; CARVALHO, L. O. D. de M.; LOURENÇO JÚNIOR, J. de B.; CAMARÃO, A. P.; CARVALHO, N. N.; PIMENTEL, E. S.; MARQUES, L. C.; CRUZ FILHO, R. N. da. Criação de bovinos. In: MARQUES, J. R. F.; LOPES, C. A. C.; MARTINEZ, G. B. (Ed.). Produção animal nas várzeas do Rio Amazonas. Belém, PA: Embrapa Amazônia Oriental, 2003. p. 115-131.Tipo: Capítulo em Livro Técnico-Científico |
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