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Registro Completo |
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Biblioteca(s): |
Embrapa Amapá. |
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Data corrente: |
24/02/2016 |
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Data da última atualização: |
01/03/2016 |
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Tipo da produção científica: |
Resumo em Anais de Congresso |
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Autoria: |
SANTOS, J. C. R. dos; GOMES, M. A.; JESUS-BARROS, C. R. de; BARIANI, A.; ADAIME, R. |
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Afiliação: |
Jonh Carlo Reis dos Santos; Merian Araújo Gomes, FAMA, Macapá, AP; CRISTIANE RAMOS DE JESUS-BARROS, CPAF-AP; ADRIANA BARIANI, CPAF-AP; RICARDO ADAIME DA SILVA, CPAF-AP. |
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Título: |
Ação de Metarhizium anisopliae sobre imaturos de Bactrocera carambolae em laboratório. |
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Ano de publicação: |
2015 |
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Fonte/Imprenta: |
In: JORNADA CIENTÍFICA DA EMBRAPA AMAPÁ, 1., 2015, Macapá. Resumos... Macapá: Embrapa Amapá, 2015. |
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Idioma: |
Português |
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Notas: |
1 CD ROM. |
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Palavras-Chave: |
Entomopatógeno. |
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Thesagro: |
Controle biológico; Praga quarentenária. |
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Categoria do assunto: |
O Insetos e Entomologia |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/139972/1/CPAF-AP-2015-Jornada-Acao-de-Metarhizium.pdf
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Marc: |
LEADER 00661nam a2200193 a 4500
001 2038371
005 2016-03-01
008 2015 bl uuuu u00u1 u #d
100 1 $aSANTOS, J. C. R. dos
245 $aAção de Metarhizium anisopliae sobre imaturos de Bactrocera carambolae em laboratório.$h[electronic resource]
260 $aIn: JORNADA CIENTÍFICA DA EMBRAPA AMAPÁ, 1., 2015, Macapá. Resumos... Macapá: Embrapa Amapá$c2015
500 $a1 CD ROM.
650 $aControle biológico
650 $aPraga quarentenária
653 $aEntomopatógeno
700 1 $aGOMES, M. A.
700 1 $aJESUS-BARROS, C. R. de
700 1 $aBARIANI, A.
700 1 $aADAIME, R.
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Embrapa Amapá (CPAF-AP) |
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 | Acesso ao texto completo restrito à biblioteca da Embrapa Caprinos e Ovinos. Para informações adicionais entre em contato com cnpc.biblioteca@embrapa.br. |
Registro Completo
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Biblioteca(s): |
Embrapa Caprinos e Ovinos. |
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Data corrente: |
28/07/2009 |
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Data da última atualização: |
10/07/2023 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Circulação/Nível: |
A - 2 |
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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. |
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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). |
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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. |
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Ano de publicação: |
2009 |
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Fonte/Imprenta: |
Small Ruminant Research, v. 85, n. 1, p. 27-33, Jul. 2009. |
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Idioma: |
Inglês |
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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 |
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Palavras-Chave: |
Artrite encefalite caprina; Brasil; CAEV; Semi-árido. |
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Thesagro: |
Caprino; Doença Animal; Sêmen. |
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Thesaurus NAL: |
Brazil; Caprine arthritis encephalitis virus; Caprine arthritis-encephalitis; Goat diseases; Goats; Semiarid zones. |
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Categoria do assunto: |
H Saúde e Patologia |
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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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