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Registros recuperados : 371 | |
321. | | FALCÃO, M. V. D.; LAROUCAU, K.; VORIMORE, F.; DESHAYES, T.; SANTANA, V. L. A.; SILVA, K. P. C.; NASCIMENTO, S. A. DO; CASTRO, R. S. DE; ARAUJO, F. R.; MOTA, R. A. Molecular characterization of Burkholderia mallei strains isolated from horses in Brazil (2014-2017). Infection, Genetics and Evolution, v. 99, 2022. Biblioteca(s): Embrapa Gado de Corte. |
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322. | | CARNEIRO, P. A. M.; PASQUATTI, T. N.; TAKANI, H.; ZUMÁRRAGA, M. J.; MARFIL, M. J.; BARNARD, C.; FITZGERALD, S. D.; ABRAMOVITCH, R. B.; ARAUJO, F. R.; KANEENE, J. B. Molecular characterization of Mycobacterium bovis infection in cattle and buffalo in Amazon Region, Brazil. Veterinary Medicine and Science, v. 6, p. 133?141, 2020. Biblioteca(s): Embrapa Gado de Corte. |
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323. | | CARNEIRO, P. A. M.; PASQUATTI, T. N.; TAKATANI, H.; ZUMÁRRAGA, M. J.; MARFIL, M. J.; BARNARD, C.; FITZGERALD, S. D.; ABRAMOVITCH, R. B.; ARAUJO, F. R.; KANEEENE, J. B. Molecular characterization of Mycobacterium bovis infection in cattle and buffalo in Amazon Region, Brazil. Veterinary Medicine and Science, v. 6, n. 1, p. 1-9, December, 2019. Biblioteca(s): Embrapa Gado de Corte. |
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324. | | LIMA, M. L. F.; SOARES, P. T.; RAMOS, C. A. N.; ARAUJO, F. R.; RAMOS, R. A. N.; SOUZA, I. I. F.; FAUSTINO, M. A. G.; ALVES, L. C. A. Molecular detection of Anaplasma platys in a naturally-infected cat in Brazil. Brazilian Journal of Microbiology, v. 41, n. 2, p. 381-385, Apr./June 2010. Biblioteca(s): Embrapa Gado de Corte. |
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325. | | CARNEIRO, P. A. M.; PASQUATTI, T. N.; LIMA, D. A. R.; RODRIGUES, R. A.; TAKANI, H.; SILVA, C. B. D. G.; JARDIM, R.; ABRAMOVITCH, R. B.; WILKINS, M. J.; DAVILA, A. M. R.; ARAUJO, F. R.; KANEENE, J. B. Milk contamination by Mycobacterium tuberculosis complex, implications for public health in Amazonas, Brazil. Journal of Food Protection, 2022. Biblioteca(s): Embrapa Gado de Corte. |
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326. | | RAMOS, C. A. N.; ARAUJO, F. R.; SOUZA, I. I. F.; BACANELLI, G.; LUIZ, H. L.; RUSSI, L. S.; OLIVEIRA, R. H. M. de; SOARES, C. O.; ROSINHA, G. M. S.; ALVES, L. C. Real-time polymerase chain reaction based on msa2c gene for detection of Babesia bovis. Veterinary Parasitology, v.176, p.79-83, Feb. 2011. Issue 1. Biblioteca(s): Embrapa Gado de Corte. |
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327. | | RODRIGUES, R. A.; MENESES, I. I. F. S.; JORGE, K. S. G.; LEGUIZAMON, G. O. de C.; SILVA, M. R.; RAMOS C. A. N.; SANTOS, L. R. dos; LILENBAUM. W.; ETGES, R. N.; ARAUJO, F. R. Reações falso-negativas ao teste cervical comparativo para tuberculose bovina. Brasília, DF: Embrapa, 2017. 30 p. (Embrapa Gado de Corte. Boletim de pesquisa e desenvolvimento, 38). Biblioteca(s): Embrapa Gado de Corte. |
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328. | | SILVA, M. R.; ROCHA, A. da S.; ARAUJO, F. R.; FONSECA-JÚNIOR, A. A.; ALENCAR, A. P. de; SUFFYS, P. N.; COSTA, R. R. da; MOREIRA, M. A. S.; GUIMARÃES, M. D. C. Risk factors for human Mycobacterium bovis infections in an urban area of Brazil. Memórias do Instituto Oswaldo Cruz, v. 113, n. 8, p. e170445, 2018. 6 p. Biblioteca(s): Embrapa Gado de Corte; Embrapa Gado de Leite. |
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329. | | SOUZA, I. I. F.; MELO, E. S. P.; RAMOS, C. A. M.; FARIAS, T. A.; OSORIO, A. L. A. L.; JORGE, K. S. G.; VIDAL, C. E. S.; SILVA, A. A.; SILVA, M. R.; PELLEGRIN, A. O.; ARAUJO, F. R. Screening of recombinant proteins as antigens in indirect ELISA for diagnosis of bovine tuberculosis. SpringerPlus, v. 1, n. 77, p.1-6, dec. 2012. Biblioteca(s): Embrapa Pantanal. |
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330. | | SOUZA, I. I. F.; MELO, E. S. P.; RAMOS, C. A. M.; FARIAS, T. A.; OSORIO, A. L. A. R.; JORGE, K. S. G.; VIDAL, C. E. S.; SILVA, A. S.; SILVA, M. R.; PELLEGRIN, A. O.; ARAUJO, F. R. Screening of recombinant proteins as antigens in indirect elisa for diagnosis of bovine tuberculosis. SpringerPlus, v. 1, n. 1, article 77, 2012. Disponível em: http://www.springerplus.com/content/1/1/77 Biblioteca(s): Embrapa Gado de Corte; Embrapa Gado de Leite. |
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331. | | SOUZA, I. I.; MELO, E. S. P.; RAMOS, C. A. N.; FARIAS, T. A.; OZORIO, A. L. A. R.; JORGE, K. S. G.; VIDAL, C. E. S.; SILVA, A. S.; SILVA, M. R.; PELLEGRIN, A. O.; ARAUJO, F. R. Screening of recombinant proteins as antigens in indirect elisa for diagnosis of bovine tuberculosis. In: Simpósio Embrapa LabEx EUA de Sanidade Animal, 2., 2012, Brasília. Proceedings... Brasília: Embrapa Estudos e Capacitação, 2012 p. 40 Biblioteca(s): Embrapa Gado de Leite. |
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332. | | SOUZA, I. I.; MELO, E. S. P.; RAMOS, C. A. N.; FARIAS, T. A.; OZORIO, A. L. A. R.; JORGE, K. S. G.; VIDAL, C. E. S.; SILVA, A. S.; SILVA, M. R.; PELLEGRIN, A. O.; ARAUJO, F. R. Screening of recombinant proteins as antigens in indirect elisa for diagnosis of bovine tuberculosis. In: SIMPÓSIO EMBRAPA LABEX EUA DE SANIDADE ANIMAL, 2., Brasília, 2012. Proceedings... Brasília: Embrapa Estudos e Capacitação, 2012. p. 40 Biblioteca(s): Embrapa Gado de Corte. |
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333. | | CARVALHO, C. E. G.; ROSINHA, G. M. S.; SANCHES, C. C.; ELISEI, C.; GONÇALVES, A. N. D.; SANCHES, S. C.; ARAUJO, F. R.; FEIJO, G. L. D.; SOARES, C. O. Polimorfismos no gene da proteína príon em quatro raças bovinas criadas no Brasil. In: JORNADA CIENTÍFICA DA EMBRAPA GADO DE CORTE, 6., 2010, Campo Grande, MS. Ética na pesquisa científica: [Anais da ...]. Campo Grande, MS: Embrapa Gado de Corte, 2010. 1 CD-ROM. Coordenadora: Vanessa Felipe de Souza 1 Biblioteca(s): Embrapa Gado de Corte. |
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334. | | BIER, D.; SILVA, M. R.; RAMOS, C. A. do N.; MORININGO, G. D'A.; SILVA, T. A. dos S.; LIMA, A. C. de; CHULLI, J. V. M.; ARAUJO, F. R. Survey of verotoxin-producing Escherichia coli and faecal coliforms in beef carcasses destined for export at slaughterhouses in Brazil. Food Science and Technology, v. 38, n. 1, p. 60-66, 2018. Biblioteca(s): Embrapa Gado de Leite. |
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335. | | PANDOLFI, J. R. C.; SILVA, V. S.; KRAMER, B.; ARAUJO, F. R.; PEIXOTO, J. de O.; COLDEBELLA, A.; LOPES, L. dos S.; IBELLI, A. M. G.; TESSMANN, A. L.; BRENTANO, L.; MAGARELLI, G. Validation and improvement of mycobacterial diagnostic methods. In: SIMPÓSIO EMBRAPA LabEx EUA DE SANIDADE ANIMAL, 2., 2012, Brasília. Anais... Brasília: Embrapa Estudos e Capacitação, 2012. p. 46-47. Projeto/Plano de Ação: 05.11.11.002. Biblioteca(s): Embrapa Suínos e Aves. |
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336. | | SILVA, H. G. C. da; FARIAS, T. A.; ARAÚJO, F. R.; RAMOS, C. A. N.; SOARES, C. O.; OSÓRIO, A. L. A. R.; JORGE, K. S. G.; ROSINHA, G. M. S. Utilização de peptídeos sintéticos derivados das proteínas MPB70 e ESAT-6 no diagnóstico da tuberculose bovina. In: JORNADA CIENTÍFICA DA EMBRAPA GADO DE CORTE, 3., 2007, Campo Grande, MS. Anais [da]... Campo Grande, MS: Embrapa Gado de Corte, 2007. p. 38 1 CD-ROM. Biblioteca(s): Embrapa Gado de Corte. |
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337. | | GALLENTI, R.; HUSSEIN, H. E.; ALZAN, H. F.; SUAREZ, C. E.; UETI, M.; ASURMENDI, S.; BENITEZ, D.; ARAUJO, F. R.; ROLLS, P.; SIBEKO-MATJILA, K.; SCHNITTGER, L.; FLORIN-CHRISTENSEN, M. Unraveling the complexity of the Rhomboid Serine Protease 4 Family of Babesia bovis using bioinformatics and experimental studies. Pathogens, v. 11, n. 344, 2022. Biblioteca(s): Embrapa Gado de Corte. |
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338. | | GASPAR, E. B.; SANTOS, L. R. dos; EGITO, A. A. do; SANTOS, M. G. dos; MANTOVANI, C.; RIEGER, J. DA S. G.; ABRANTES, G. A. DE S.; SUNIGA, P. A. P.; FAVACHO, J. DE M.; PINTO, I. B.; NASSAR, A. F. DE C.; SANTOS, F. L. DOS; ARAUJO, F. R. Assessment of the virulence of the Burkholderia mallei Strain BAC 86/19 in BALB/c Mice. Microorganisms, v. 11, issue 10, e2597, 2023. Biblioteca(s): Embrapa Gado de Corte; Embrapa Pecuária Sul. |
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339. | | BIGI, M.; VAZQUEZ, C. L.; CASTELÃO, A. B. C.; GARCÍA, E. A.; CATALDI, A. A.; JACKSON, M.; MAcNEIL, M.; SORIA, M.; ZUMÁRRAGA, M. J.; MATIAS, C.; GAGO, G.; BLANCO, F. C.; NISHIBEF, C.; ALMEIDA, N. F.; ARAUJO, F. R.; BIGI, F. Analysing nonsynonymous mutations between two Mycobacterium bovis strains with contrasting pathogenic profiles. Veterinary Microbiology, v. 239, 2019. Biblioteca(s): Embrapa Gado de Corte. |
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340. | | ARAÚJO, C. P. de; ARAÚJO, C. P.; OSÓRIO, A. L. A. R.; JORGE, K. S. G.; RAMOS, C. A. N.; SOUZA FILHO, A. F.; VIDAL, C. E. S.; ROXO, E.; DIB, C. C.; ROCHA, A; FONSECA JÚNIOR, A. A.; SILVA, M. R.; ARAUJO, F. R. Diagnóstico de tuberculose por PCR Tempo Real em tecidos de bovinos. In: JORNADA CIENTÍFICA EMBRAPA GADO DE CORTE, 7., 2011, CAMPO GRANDE, MS. [Anais da]... Campo Grande, MS: Embrapa Gado de Corte, 2011. Biblioteca(s): Embrapa Gado de Corte. |
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Registros recuperados : 371 | |
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Registro Completo
Biblioteca(s): |
Embrapa Gado de Corte; Embrapa Gado de Leite. |
Data corrente: |
17/03/2014 |
Data da última atualização: |
05/02/2024 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Circulação/Nível: |
A - 1 |
Autoria: |
ARAUJO, C. P.; OSÓRIO, A. L. A. R.; JORGE, K. S. G.; RAMOS, C. A. N.; S. FILHO, A. F.; VIDAL, C. E. S.; ROXO, E.; NISHIBE, c.; ALMEIDA, N. F.; F. JUNIOR, A. A.; SILVA, M. R.; B. NETO, J. D.; CERQUEIRA, V. D.; ZUMÁRRAGA, M.; ARAUJO, F. R. |
Afiliação: |
MARCIO ROBERTO SILVA, CNPGL. |
Título: |
Detection of Mycobacterium bovis in Bovine and Bubaline Tissues Using Nested-PCR for TbD1. |
Ano de publicação: |
2014 |
Fonte/Imprenta: |
Plos One, v. 9, n. 3, p. 1-6, 2014 |
Idioma: |
Inglês Português |
Conteúdo: |
In the present study, a nested-PCR system, targeting the TbD1 region, involving the performance of conventional PCR followed by real-time PCR, was developed to detect Mycobacterium bovis in bovine/bubaline tissue homogenates. The sensitivity and specificity of the reactions were assessed with DNA samples extracted from tuberculous and non-tuberculous mycobacteria, as well as other actinomycetales species and DNA samples extracted directly from bovine and bubaline tissue homogenates. In terms of analytical sensitivity, the DNA of M. bovis AN5 was detected up to 1.56 ng with conventional PCR, 97.6 pg with real-time PCR, and 1.53 pg with nested-PCR in the reaction mixture. The nested-PCR exhibited 100% analytical specificity for M. bovis when tested with the DNA of reference strains of environmental mycobacteria and closely-related Actinomycetales. A clinical sensitivity value of 76.0% was detected with tissue samples from animals that exhibited positive results in the comparative intradermal tuberculin test (CITT), as well as from those with lesions compatible with tuberculosis (LCT) that rendered positive cultures. A clinical specificity value of 100% was detected with tissue samples from animals with CITT- results, with no visible lesions (NVL) and negative cultures. No significant differences were found between the nested-PCR and culture in terms of detecting CITT+ animals with LCT or with NVL. No significant differences were recorded in the detection of CITT- animals with NVL. However, nested-PCR detected a significantly higher number of positive animals than the culture in the group of animals exhibiting LCT with no previous records of CITT. The use of the nested-PCR assay to detect M. bovis in tissue homogenates provided a rapid diagnosis of bovine and bubaline tuberculosis. MenosIn the present study, a nested-PCR system, targeting the TbD1 region, involving the performance of conventional PCR followed by real-time PCR, was developed to detect Mycobacterium bovis in bovine/bubaline tissue homogenates. The sensitivity and specificity of the reactions were assessed with DNA samples extracted from tuberculous and non-tuberculous mycobacteria, as well as other actinomycetales species and DNA samples extracted directly from bovine and bubaline tissue homogenates. In terms of analytical sensitivity, the DNA of M. bovis AN5 was detected up to 1.56 ng with conventional PCR, 97.6 pg with real-time PCR, and 1.53 pg with nested-PCR in the reaction mixture. The nested-PCR exhibited 100% analytical specificity for M. bovis when tested with the DNA of reference strains of environmental mycobacteria and closely-related Actinomycetales. A clinical sensitivity value of 76.0% was detected with tissue samples from animals that exhibited positive results in the comparative intradermal tuberculin test (CITT), as well as from those with lesions compatible with tuberculosis (LCT) that rendered positive cultures. A clinical specificity value of 100% was detected with tissue samples from animals with CITT- results, with no visible lesions (NVL) and negative cultures. No significant differences were found between the nested-PCR and culture in terms of detecting CITT+ animals with LCT or with NVL. No significant differences were recorded in the detection of CITT- animals with ... Mostrar Tudo |
Palavras-Chave: |
Bovine and bubaline tuberculosis; Nested-PCR system. |
Thesaurus NAL: |
Mycobacterium abscessus. |
Categoria do assunto: |
-- L Ciência Animal e Produtos de Origem Animal |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/119848/1/ARAUJO-C.-P..pdf
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/99300/1/pone.0091023-1..6-2014-Nested-PCR.pdf
|
Marc: |
LEADER 02739naa a2200325 a 4500 001 2010358 005 2024-02-05 008 2014 bl uuuu u00u1 u #d 100 1 $aARAUJO, C. P. 245 $aDetection of Mycobacterium bovis in Bovine and Bubaline Tissues Using Nested-PCR for TbD1.$h[electronic resource] 260 $c2014 520 $aIn the present study, a nested-PCR system, targeting the TbD1 region, involving the performance of conventional PCR followed by real-time PCR, was developed to detect Mycobacterium bovis in bovine/bubaline tissue homogenates. The sensitivity and specificity of the reactions were assessed with DNA samples extracted from tuberculous and non-tuberculous mycobacteria, as well as other actinomycetales species and DNA samples extracted directly from bovine and bubaline tissue homogenates. In terms of analytical sensitivity, the DNA of M. bovis AN5 was detected up to 1.56 ng with conventional PCR, 97.6 pg with real-time PCR, and 1.53 pg with nested-PCR in the reaction mixture. The nested-PCR exhibited 100% analytical specificity for M. bovis when tested with the DNA of reference strains of environmental mycobacteria and closely-related Actinomycetales. A clinical sensitivity value of 76.0% was detected with tissue samples from animals that exhibited positive results in the comparative intradermal tuberculin test (CITT), as well as from those with lesions compatible with tuberculosis (LCT) that rendered positive cultures. A clinical specificity value of 100% was detected with tissue samples from animals with CITT- results, with no visible lesions (NVL) and negative cultures. No significant differences were found between the nested-PCR and culture in terms of detecting CITT+ animals with LCT or with NVL. No significant differences were recorded in the detection of CITT- animals with NVL. However, nested-PCR detected a significantly higher number of positive animals than the culture in the group of animals exhibiting LCT with no previous records of CITT. The use of the nested-PCR assay to detect M. bovis in tissue homogenates provided a rapid diagnosis of bovine and bubaline tuberculosis. 650 $aMycobacterium abscessus 653 $aBovine and bubaline tuberculosis 653 $aNested-PCR system 700 1 $aOSÓRIO, A. L. A. R. 700 1 $aJORGE, K. S. G. 700 1 $aRAMOS, C. A. N. 700 1 $aS. FILHO, A. F. 700 1 $aVIDAL, C. E. S. 700 1 $aROXO, E. 700 1 $aNISHIBE, c. 700 1 $aALMEIDA, N. F. 700 1 $aF. JUNIOR, A. A. 700 1 $aSILVA, M. R. 700 1 $aB. NETO, J. D. 700 1 $aCERQUEIRA, V. D. 700 1 $aZUMÁRRAGA, M. 700 1 $aARAUJO, F. R. 773 $tPlos One$gv. 9, n. 3, p. 1-6, 2014
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