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Registro Completo |
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Biblioteca(s): |
Embrapa Semiárido. |
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Data corrente: |
26/12/2011 |
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Data da última atualização: |
27/04/2023 |
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Tipo da produção científica: |
Artigo em Anais de Congresso |
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Autoria: |
RIOS, E. S.; SILVA, R. de C. B. da; LOPES. A. P.; REIS, R. C. R.; ANGELOTTI, F.; DANTAS, B. F. |
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Afiliação: |
ÉLICA SANTOS RIOS; RITA DE CÁSSIA BARBOSA DA SILVA; ARMANDO PEREIRA LOPES; RENATA CONDURU RIBEIRO REIS; FRANCISLENE ANGELOTTI, CPATSA; BARBARA FRANCA DANTAS, CPATSA. |
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Título: |
Efeito do aumento da concentração do CO2 na emergência e no desenvolvimento de plântulas de alface. |
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Ano de publicação: |
2011 |
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Fonte/Imprenta: |
In: SIMPÓSIO DE MUDANÇAS CLIMÁTICAS E DESERTIFICAÇÃO NO SEMIÁRIDO BRASILEIRO, 3., 2011, Juazeiro. Experiências para mitigação e adaptação. Petrolina: Embrapa Semiárido, 2011. |
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Série: |
(Embrapa Semiárido. Documentos, 239). |
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Idioma: |
Português |
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Conteúdo: |
O objetivo do trabalho foi avaliar o efeito do aumento do CO2 na emergência e no desenvolvimento inicial de plântulas de alface. |
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Palavras-Chave: |
Aquecimento global. |
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Thesagro: |
Alface; Germinação; Mudança Climática; Semente. |
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Thesaurus Nal: |
Climate change. |
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Categoria do assunto: |
P Recursos Naturais, Ciências Ambientais e da Terra |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/51201/1/Fran6.pdf
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Marc: |
LEADER 01033nam a2200253 a 4500
001 1910822
005 2023-04-27
008 2011 bl uuuu u00u1 u #d
100 1 $aRIOS, E. S.
245 $aEfeito do aumento da concentração do CO2 na emergência e no desenvolvimento de plântulas de alface.$h[electronic resource]
260 $aIn: SIMPÓSIO DE MUDANÇAS CLIMÁTICAS E DESERTIFICAÇÃO NO SEMIÁRIDO BRASILEIRO, 3., 2011, Juazeiro. Experiências para mitigação e adaptação. Petrolina: Embrapa Semiárido$c2011
490 $a(Embrapa Semiárido. Documentos, 239).
520 $aO objetivo do trabalho foi avaliar o efeito do aumento do CO2 na emergência e no desenvolvimento inicial de plântulas de alface.
650 $aClimate change
650 $aAlface
650 $aGerminação
650 $aMudança Climática
650 $aSemente
653 $aAquecimento global
700 1 $aSILVA, R. de C. B. da
700 1 $aLOPES. A. P.
700 1 $aREIS, R. C. R.
700 1 $aANGELOTTI, F.
700 1 $aDANTAS, B. F.
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Registro original: |
Embrapa Semiárido (CPATSA) |
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Registro Completo
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Biblioteca(s): |
Embrapa Gado de Corte. |
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Data corrente: |
01/07/2003 |
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Data da última atualização: |
04/07/2023 |
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Autoria: |
MADRUGA, C. R.; LEAL, C. R. B.; FERREIRA, A. M. T.; ARAUJO, F. R.; BONATO, A. L. V.; KESSLER, R. H.; SCHENK, M. A. M.; SOARES, C. O. |
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Afiliação: |
CLAUDIO ROBERTO MADRUGA, CNPGC; CÁSSIA R. B. LEAL, UNIVERSIDADE CATÓLICA DOM BOSCO; ALDA M. T. FERREIRA, UNIVERSIDADE CATÓLICA DOM BOSCO; FLABIO RIBEIRO DE ARAUJO, CNPGC; ANA LIDIA VARIANI BONATO, CNPGC; RAUL HENRIQUE KESSLER, CNPGC; MARIA APARECIDA MOREIRA SCHENK, CNPGC; CLEBER OLIVEIRA SOARES, CNPGC. |
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Título: |
Genetic and antigenic analysis of Babesia bigemina isolates from five geographical regions of Brazil. |
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Ano de publicação: |
2002 |
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Fonte/Imprenta: |
Pesquisa Veterinária Brasileira, v. 22, n. 4, p. 153-160, out./dez. 2002. |
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DOI: |
https://doi.org/10.1590/S0100-736X2002000400005 |
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Idioma: |
Inglês |
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Conteúdo: |
A molecular epidemiological study was performed with Babesia bigemina isolates from five geographical regions of Brazil. The genetic analysis was done with random amplification of polymorphic DNA (RAPD), repetitive extragenic palindromic elements-polymerase chain reaction (REP-PCR) and enterobacterial repetitive intergenic consensus sequences-polymerase chain reaction (ERIC-PCR) that showed genetic polymorphism between these isolates and generated fingerprinting. In RAPD, ILO872 and ILO876 primers were able to detect at least one fingerprinting for each B. bigemina isolate. The amplification of B. bigemina DNA fragments by REP-PCR and ERIC-PCR gave evidence for the presence in this haemoprotozoan of the sequences described previously in microorganisms of the bacterial kingdom. For the first time it was demonstrated that both techniques can be used for genetic analysis of a protozoan parasite, although the ERIC-PCR was more discriminatory than REP-PCR. The dendogram with similarity coefficient among isolates showed two clusters and one subcluster. The Northeastern and Mid-Western isolates showed the greatest genetic diversity, while the Southeastern and Southern isolates were the closest. The antigenic analysis was done through indirect fluorescent antibody technique and Western blotting using a panel of monoclonal antibodies directed against epitopes on the merozoite membrane surface, rhoptries and membrane of infected erythrocytes. As expected, the merozoite variable surface antigens, major surface antigen (MSA)-1 and MSA-2 showed antigenic diversity. However, B cell epitopes on rhoptries and infected erythrocytes were conserved among all isolates studied. In this study it was possible to identify variable and conserved antigens, which had already been described as potential immunogens. Considering that an attenuated Babesia clone used as immunogen selected populations capable of evading the immunity induced by this vaccine, it is necessary to evaluate more deeply the cross-protection conferred by genetically more distant Brazilian B. bigemina isolates and make an evaluation of the polymorphism degree of variable antigens such as MSA-1 and MSA-2. MenosA molecular epidemiological study was performed with Babesia bigemina isolates from five geographical regions of Brazil. The genetic analysis was done with random amplification of polymorphic DNA (RAPD), repetitive extragenic palindromic elements-polymerase chain reaction (REP-PCR) and enterobacterial repetitive intergenic consensus sequences-polymerase chain reaction (ERIC-PCR) that showed genetic polymorphism between these isolates and generated fingerprinting. In RAPD, ILO872 and ILO876 primers were able to detect at least one fingerprinting for each B. bigemina isolate. The amplification of B. bigemina DNA fragments by REP-PCR and ERIC-PCR gave evidence for the presence in this haemoprotozoan of the sequences described previously in microorganisms of the bacterial kingdom. For the first time it was demonstrated that both techniques can be used for genetic analysis of a protozoan parasite, although the ERIC-PCR was more discriminatory than REP-PCR. The dendogram with similarity coefficient among isolates showed two clusters and one subcluster. The Northeastern and Mid-Western isolates showed the greatest genetic diversity, while the Southeastern and Southern isolates were the closest. The antigenic analysis was done through indirect fluorescent antibody technique and Western blotting using a panel of monoclonal antibodies directed against epitopes on the merozoite membrane surface, rhoptries and membrane of infected erythrocytes. As expected, the merozoite variable surfac... Mostrar Tudo |
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Thesagro: |
Antígeno; Babesia Bigemina; Polimorfismo Genético. |
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Thesaurus NAL: |
Antigens; Genetic polymorphism. |
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Categoria do assunto: |
-- |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/253106/1/Genetic-antigenic-analysis-2002.pdf
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Marc: |
LEADER 03037naa a2200277 a 4500
001 1325288
005 2023-07-04
008 2002 bl uuuu u00u1 u #d
024 7 $ahttps://doi.org/10.1590/S0100-736X2002000400005$2DOI
100 1 $aMADRUGA, C. R.
245 $aGenetic and antigenic analysis of Babesia bigemina isolates from five geographical regions of Brazil.
260 $c2002
520 $aA molecular epidemiological study was performed with Babesia bigemina isolates from five geographical regions of Brazil. The genetic analysis was done with random amplification of polymorphic DNA (RAPD), repetitive extragenic palindromic elements-polymerase chain reaction (REP-PCR) and enterobacterial repetitive intergenic consensus sequences-polymerase chain reaction (ERIC-PCR) that showed genetic polymorphism between these isolates and generated fingerprinting. In RAPD, ILO872 and ILO876 primers were able to detect at least one fingerprinting for each B. bigemina isolate. The amplification of B. bigemina DNA fragments by REP-PCR and ERIC-PCR gave evidence for the presence in this haemoprotozoan of the sequences described previously in microorganisms of the bacterial kingdom. For the first time it was demonstrated that both techniques can be used for genetic analysis of a protozoan parasite, although the ERIC-PCR was more discriminatory than REP-PCR. The dendogram with similarity coefficient among isolates showed two clusters and one subcluster. The Northeastern and Mid-Western isolates showed the greatest genetic diversity, while the Southeastern and Southern isolates were the closest. The antigenic analysis was done through indirect fluorescent antibody technique and Western blotting using a panel of monoclonal antibodies directed against epitopes on the merozoite membrane surface, rhoptries and membrane of infected erythrocytes. As expected, the merozoite variable surface antigens, major surface antigen (MSA)-1 and MSA-2 showed antigenic diversity. However, B cell epitopes on rhoptries and infected erythrocytes were conserved among all isolates studied. In this study it was possible to identify variable and conserved antigens, which had already been described as potential immunogens. Considering that an attenuated Babesia clone used as immunogen selected populations capable of evading the immunity induced by this vaccine, it is necessary to evaluate more deeply the cross-protection conferred by genetically more distant Brazilian B. bigemina isolates and make an evaluation of the polymorphism degree of variable antigens such as MSA-1 and MSA-2.
650 $aAntigens
650 $aGenetic polymorphism
650 $aAntígeno
650 $aBabesia Bigemina
650 $aPolimorfismo Genético
700 1 $aLEAL, C. R. B.
700 1 $aFERREIRA, A. M. T.
700 1 $aARAUJO, F. R.
700 1 $aBONATO, A. L. V.
700 1 $aKESSLER, R. H.
700 1 $aSCHENK, M. A. M.
700 1 $aSOARES, C. O.
773 $tPesquisa Veterinária Brasileira$gv. 22, n. 4, p. 153-160, out./dez. 2002.
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