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| Acesso ao texto completo restrito à biblioteca da Embrapa Clima Temperado. Para informações adicionais entre em contato com cpact.biblioteca@embrapa.br. |
Registro Completo |
Biblioteca(s): |
Embrapa Clima Temperado. |
Data corrente: |
17/11/2015 |
Data da última atualização: |
31/05/2019 |
Tipo da produção científica: |
Resumo em Anais de Congresso |
Autoria: |
EICHOLZ, M. D.; PERES, M. M.; CAMPOS, A. D. S. de; EICHOLZ, E. D.; SILVA, S. D. dos A. e. |
Afiliação: |
Marcel Diedrich Eicholz, UFPEL; Milena Moreira Peres, UFPEL; Alexssandra Dayane Soares de Campos, UFPEL; EBERSON DIEDRICH EICHOLZ, CPACT; SERGIO DELMAR DOS ANJOS E SILVA, CPACT. |
Título: |
Caracterização morfoagronômica de genótipos de Tungue. |
Ano de publicação: |
2015 |
Fonte/Imprenta: |
In: SIMPÓSIO DE RECURSOS GENÉTICOS PARA A AMÉRICA LATINA E CARIBE, 10., 2015, Bento Gonçalves. Recursos genéticos no século 21: de Vavilov a Svalbard. Anais... [s.l.]: Sociedade Brasileira de Recursos Genéticos, 2015. |
Idioma: |
Português |
Palavras-Chave: |
Aleurites fordii Helms. |
Categoria do assunto: |
-- |
Marc: |
LEADER 00664nam a2200157 a 4500 001 2028732 005 2019-05-31 008 2015 bl uuuu u00u1 u #d 100 1 $aEICHOLZ, M. D. 245 $aCaracterização morfoagronômica de genótipos de Tungue.$h[electronic resource] 260 $aIn: SIMPÓSIO DE RECURSOS GENÉTICOS PARA A AMÉRICA LATINA E CARIBE, 10., 2015, Bento Gonçalves. Recursos genéticos no século 21: de Vavilov a Svalbard. Anais... [s.l.]: Sociedade Brasileira de Recursos Genéticos$c2015 653 $aAleurites fordii Helms 700 1 $aPERES, M. M. 700 1 $aCAMPOS, A. D. S. de 700 1 $aEICHOLZ, E. D. 700 1 $aSILVA, S. D. dos A. e
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Embrapa Clima Temperado (CPACT) |
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Registro Completo
Biblioteca(s): |
Embrapa Suínos e Aves. |
Data corrente: |
15/06/2016 |
Data da última atualização: |
15/06/2016 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Circulação/Nível: |
B - 1 |
Autoria: |
MORAES, D. M. C.; DUARTE, S. C.; BASTOS, T. S. A.; REZENDE, C. L. G.; LEANDRO, N. S. M.; CAFÉ, M. B.; STRINGHINI, J. H.; ANDRADE, M. A. |
Afiliação: |
DUNYA MARA CARDOSO MORAES, UFG/Escola de Veterinária e Zootecnia; SABRINA CASTILHO DUARTE, CNPSA; UFG/Escola de Veterinária e Zootecnia; UFG/Escola de Veterinária e Zootecnia; UFG/Escola de Veterinária e Zootecnia; UFG/Escola de Veterinária e Zootecnia; JOSÉ HENRIQUE STRINGHINI, UFG/Escola de Veterinária e Zootecnia; MARIA AUXILIADORA ANDRADE, UFG/Escola de Veterinária e Zootecnia. |
Título: |
Detection of Salmonella spp. by Conventional Bacteriology and by Quantitative Polymerase-Chain Reaction in Commercial Egg Structures. |
Ano de publicação: |
2016 |
Fonte/Imprenta: |
Brazilian Journal of Poultry Science, v. 18, n.1, p. 117-124, 2016. |
DOI: |
http://dx.doi.org/10.1590/18069061-2015-006 |
Idioma: |
Inglês |
Conteúdo: |
Abstract: Conventional bacteriology techniques and quantitative polymerasechain reaction (qPCR) were applied to the eggshell, albumen, and yolk of washed and unwashed commercial white and brown eggs, to detect Salmonella spp. Pooled samples of eggshells, albumen, and yolk of white and brown eggs were collected at the poultry house and at the egg-storage room. Salmonella spp. was detected by conventional bacteriology in 5.4% (21/387) of analyzed samples and in 16% (68/387) by qPCR. In the 114 unwashed white eggs samples of eggshell, albumen and yolk, the bacterium was identified in 2.6% of the eggs (3/114) by conventional bacteriology and in 13.2% (15/114) by qPCR. In the 90 samples of washed eggs, 6.7% (6/90) were contaminated as detected by conventional bacteriology and 10.0% (9/90) by qPCR. In the 81 samples of unwashed brown eggs, Salmonella spp. was detected in 6.1% of the eggs (5/81) by conventional bacteriology and 27.2% (22/81) by qPCR. In the 102 samples of brown washed eggs, 6.9% (7/102) where positive by conventional bacteriology and 35.3% (16/102) by qPCR. All samples detected as positive by conventional bacteriology were also positive by qPCR. Salmonella Agona represented 18.2% (4/22) of identified serovars, Salmonella enterica subs. enterica O: 4.5 18.2% (4/22), Salmonella Schwarzengrund 18.2% (4/22), Salmonella Cerro 13.6% (3/22), Salmonella Anatum 13.6% (3/22), Salmonella Enteritidis 9.1% (2/22), Salmonella Johannesburg 4.5% (1/22), and Salmonella Corvallis 4.5% (1/22). The qPCR method provided better detection of Salmonella spp. in commercial eggs than conventional bacteriology. The conventional egg washing and disinfection procedures are not efficient to eliminate Salmonella. MenosAbstract: Conventional bacteriology techniques and quantitative polymerasechain reaction (qPCR) were applied to the eggshell, albumen, and yolk of washed and unwashed commercial white and brown eggs, to detect Salmonella spp. Pooled samples of eggshells, albumen, and yolk of white and brown eggs were collected at the poultry house and at the egg-storage room. Salmonella spp. was detected by conventional bacteriology in 5.4% (21/387) of analyzed samples and in 16% (68/387) by qPCR. In the 114 unwashed white eggs samples of eggshell, albumen and yolk, the bacterium was identified in 2.6% of the eggs (3/114) by conventional bacteriology and in 13.2% (15/114) by qPCR. In the 90 samples of washed eggs, 6.7% (6/90) were contaminated as detected by conventional bacteriology and 10.0% (9/90) by qPCR. In the 81 samples of unwashed brown eggs, Salmonella spp. was detected in 6.1% of the eggs (5/81) by conventional bacteriology and 27.2% (22/81) by qPCR. In the 102 samples of brown washed eggs, 6.9% (7/102) where positive by conventional bacteriology and 35.3% (16/102) by qPCR. All samples detected as positive by conventional bacteriology were also positive by qPCR. Salmonella Agona represented 18.2% (4/22) of identified serovars, Salmonella enterica subs. enterica O: 4.5 18.2% (4/22), Salmonella Schwarzengrund 18.2% (4/22), Salmonella Cerro 13.6% (3/22), Salmonella Anatum 13.6% (3/22), Salmonella Enteritidis 9.1% (2/22), Salmonella Johannesburg 4.5% (1/22), and Salmonella Corvallis 4.... Mostrar Tudo |
Palavras-Chave: |
QPCR. |
Thesagro: |
Bacteriologia; Casca de ovo; Gema de ovo; Salmonella. |
Thesaurus NAL: |
Egg albumen; Egg shell; Egg yolk; Quantitative polymerase chain reaction. |
Categoria do assunto: |
-- |
Marc: |
LEADER 02730naa a2200325 a 4500 001 2047116 005 2016-06-15 008 2016 bl uuuu u00u1 u #d 024 7 $ahttp://dx.doi.org/10.1590/18069061-2015-006$2DOI 100 1 $aMORAES, D. M. C. 245 $aDetection of Salmonella spp. by Conventional Bacteriology and by Quantitative Polymerase-Chain Reaction in Commercial Egg Structures.$h[electronic resource] 260 $c2016 520 $aAbstract: Conventional bacteriology techniques and quantitative polymerasechain reaction (qPCR) were applied to the eggshell, albumen, and yolk of washed and unwashed commercial white and brown eggs, to detect Salmonella spp. Pooled samples of eggshells, albumen, and yolk of white and brown eggs were collected at the poultry house and at the egg-storage room. Salmonella spp. was detected by conventional bacteriology in 5.4% (21/387) of analyzed samples and in 16% (68/387) by qPCR. In the 114 unwashed white eggs samples of eggshell, albumen and yolk, the bacterium was identified in 2.6% of the eggs (3/114) by conventional bacteriology and in 13.2% (15/114) by qPCR. In the 90 samples of washed eggs, 6.7% (6/90) were contaminated as detected by conventional bacteriology and 10.0% (9/90) by qPCR. In the 81 samples of unwashed brown eggs, Salmonella spp. was detected in 6.1% of the eggs (5/81) by conventional bacteriology and 27.2% (22/81) by qPCR. In the 102 samples of brown washed eggs, 6.9% (7/102) where positive by conventional bacteriology and 35.3% (16/102) by qPCR. All samples detected as positive by conventional bacteriology were also positive by qPCR. Salmonella Agona represented 18.2% (4/22) of identified serovars, Salmonella enterica subs. enterica O: 4.5 18.2% (4/22), Salmonella Schwarzengrund 18.2% (4/22), Salmonella Cerro 13.6% (3/22), Salmonella Anatum 13.6% (3/22), Salmonella Enteritidis 9.1% (2/22), Salmonella Johannesburg 4.5% (1/22), and Salmonella Corvallis 4.5% (1/22). The qPCR method provided better detection of Salmonella spp. in commercial eggs than conventional bacteriology. The conventional egg washing and disinfection procedures are not efficient to eliminate Salmonella. 650 $aEgg albumen 650 $aEgg shell 650 $aEgg yolk 650 $aQuantitative polymerase chain reaction 650 $aBacteriologia 650 $aCasca de ovo 650 $aGema de ovo 650 $aSalmonella 653 $aQPCR 700 1 $aDUARTE, S. C. 700 1 $aBASTOS, T. S. A. 700 1 $aREZENDE, C. L. G. 700 1 $aLEANDRO, N. S. M. 700 1 $aCAFÉ, M. B. 700 1 $aSTRINGHINI, J. H. 700 1 $aANDRADE, M. A. 773 $tBrazilian Journal of Poultry Science$gv. 18, n.1, p. 117-124, 2016.
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