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| Registros recuperados : 41 | |
| 6. |  | TEIXEIRA, M. F. da S.; LAMBERT, V.; MSELLI-LAKAHL, L.; CHETTAB, A.; CHEBLOUNE, Y.; MORNEX, J. F. Immortalization of caprine fibroblasts permissive for replication of small ruminant lentiviruses. American Journal of Veterinary Research, v.58, n.6, p.579-584, 1997.| Biblioteca(s): Embrapa Caprinos e Ovinos. |
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| 7. | | SILVA, D. F.; PEIXOTO, R. M.; ARAÚJO, J. F.; DAMASCENO, E. M.; TEIXEIRA, M. F. da S.; ANDRIOLI, A. Avaliação comparativa de diluidores na manutenção dos parâmetros seminais de caprinos. In: ENCONTRO DE INICIAÇÃO CIENTÍFICA DA EMBRAPA CAPRINOS E OVINOS, 5., 2016, Sobral. Anais... Sobral: Embrapa Caprinos e Ovinos, 2016. p. 29-30. [ALICE ANDRIOLI PINHEIRO].| Biblioteca(s): Embrapa Caprinos e Ovinos. |
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| 8. | | FERREIRA, R. C. S.; TEIXEIRA, M. F. da S.; ROCHA, M. F. G.; LIMA, S. M. C.; FROTA, M. N. L. da; MELO, A. C. M. Redução da população microbiana presente no leite de cabra submetido à temperatura de 56oC por 60 minutos. Ciência Animal, Fortaleza, v. 11, n. 1, p. 39-44, 2001.| Biblioteca(s): Embrapa Caprinos e Ovinos. |
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| 9. | | AZEVEDO, D. A. A. de; SANTOS, V. W. S. dos; SOUSA, A. L. M. de; PEIXOTO, R. M.; PINHEIRO, R. R.; ANDRIOLI, A.; TEIXEIRA, M. F. da S. Small ruminant lentiviruses: economic and productive losses, consequences of the disease. Arquivos do Instituto Biológico, v. 84, p. 1-10, e0552016, 2017.| Biblioteca(s): Embrapa Caprinos e Ovinos. |
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| 10. | | RICARTE, A. R. F.; TEIXEIRA, M. F. da S.; ANDRIOLI, A.; PINHEIRO, R. R.; BÁO, S. N.; SILVA, J. B. A. da. Análise molecular e ultraestrutural de espermatozóides caprinos oriundos de animais infectados naturalmente e experimentalmente com o CAEV. In: CONGRESSO NORDESTINO DE PRODUÇÃO ANIMAL, 6.; SIMPÓSIO NORDESTINO DE ALIMENTAÇÃO DE RUMINANTES, 7.; FÓRUM DE COORDENADORES DE PÓS GRADUAÇÃO EM PRODUÇÃO ANIMAL DO NORDESTE, 1.; FÓRUM DE AGROECOLOGIA RO RIO GRANDE DO NORTE, 1., 2010, Mossoró. Anais... Mossoró: Sociedade Nordestina de Producao Animal; UFERSA, 2010. 4 f. 1 CD-ROM.| Biblioteca(s): Embrapa Caprinos e Ovinos. |
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| 11. | | RODRIGUES, A. P. R.; PINTO, M. T.; TEIXEIRA, M. F. da S.; MELO, A. C. M.; FREITAS, V. J. de F. Análise macro e microscópica das lesões em caprinos soropositivos para o vírus da artrite-encefalite caprina sem a presença de sinais clínicos. Ciência Animal, Fortaleza, v. 11, n. 2, p. 113-118, 2001.| Biblioteca(s): Embrapa Caprinos e Ovinos. |
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| 12. | | GÓES, C. D. M. de M. B.; TEIXEIRA, M. F. da S.; ALVES, F. S. F.; BATISTA, L. M.; BEVILAQUA, C. M. L. Avaliação da transferência passiva de anticorpos em cabritos alimentados com três diferentes tipos de colostro. Ciência Animal, Fortaleza, v. 8, n. 2, p. 57-61, 1998.| Biblioteca(s): Embrapa Caprinos e Ovinos. |
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| 13. | | SOUZA, K. C. de; ANDRIOLI, A.; SIDER, L. H.; PINHEIRO, R. R.; BEZERRA JUNIOR, R. Q.; PEIXOTO, R. M.; TEIXEIRA, M. F. da S. Detecção de sequências do DNA proviral do vírus da Artrite Encefalite Caprina em saliva. Acta Scientiae Veterinariae, v. 43, n. 1266, p. 1-6, 2015.| Biblioteca(s): Embrapa Caprinos e Ovinos. |
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| 14. | | PEIXOTO, R. M.; TEIXEIRA, M. F. da S.; ANDRIOLI, A.; PINHEIRO, R. R.; SILVA, A. A. de S.; AGUIAR, T. D. de F.; SOUSA, A. L. M. de. Perspectivas do uso de fitoterápicos no tratamento do sêmen caprino infectado pelo vírus da Artrite Encefalite Caprina. Medicina Veterinária (UFRPE), v. 12, n. 3, p. 193-201, jul/set. 2018.| Biblioteca(s): Embrapa Caprinos e Ovinos. |
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| 15. | | PEIXOTO, R. M.; TEIXEIRA, M. F. da S.; ANDRIOLI, A.; PINHEIRO, R. R.; ALVES, F. S. F.; SANTOS, V. W. S. dos; SOUSA, M. M. de; AMARAL, G. R. Prevalência sorológica de Mycoplasma agalactiae em rebanhos de caprinos leiteiros na mesorregião metropolitana de Fortaleza - CE. In: CONGRESSO NORDESTINO DE PRODUÇÃO ANIMAL, 12., 2017, Juazeiro, BA. Construindo pontes entre o ensino, a pesquisa e a extensão: anais. Petrolina: Univasf: Embrapa Semiárido: Instituto Federal de Educação, Ciência e Tecnologia, Sertão de Pernambuco, 2017. 1 CD-ROM. p. 1284-1286.| Biblioteca(s): Embrapa Caprinos e Ovinos. |
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| 16. | | SOUSA, A. L. M. de; PINHEIRO, R. R.; ARAÚJO, J. F.; AZEVEDO, D. A. A. de; PEIXOTO, R. M.; ANDRIOLI, A.; BEZERRA, S. T. da C. S.; TEIXEIRA, M. F. da S. Sodium dodecyl sulfate as a viral inactivator and future perspectives in the control of small ruminant lentiviruses. Arquivos do Instituto Biológico, v. 86, p. 1-9, e0752018, 2019.| Biblioteca(s): Embrapa Caprinos e Ovinos. |
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| 17. | | FERRAZ, R. E. de O.; TEIXEIRA, M. F. da S.; ANDRIOLI, A.; PINHEIRO, R. R.; MELO, V. S. P. de; DANTAS, T. V. M.; CAMINHA, C. M. M.; BARROSO, I. C. Lavagem do sêmen de reprodutores caprinos com solução Krebs-Ringer-Fosfato no controle da Artrite Encefalite Caprina (CAE). In: SIMPÓSIO INTERNACIONAL SOBRE CAPRINOS E OVINOS DE CORTE, 4.; FEIRA NACIONAL DO AGRONEGÓCIO DA CAPRINO-OVINOCULTURA DE CORTE, 3., 2009, João Pessoa. Anais... João Pessoa: EMEPA-PB, 2009. 3 f. 1 CD-ROM.| Biblioteca(s): Embrapa Caprinos e Ovinos. |
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| 18. | | 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. Profile of the Caprine arthritis-encephalitis virus (CAEV) in blood, semen from bucks naturally and experimentally infected in the Semi-arid region of Brazil. Small Ruminant Research, v. 85, n. 1, p. 27-33, Jul. 2009.| Biblioteca(s): Embrapa Caprinos e Ovinos. |
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| 19. | | DANTAS, T. V. M.; ARAÚJO, S. A. C. de; RICARTE, A. R. F.; COSTA, E. C.; SILVA, J. B. A. da; MELO, V. S. P. de; FEITOS, A. L. V. de L.; TEIXEIRA, M. F. da S. Vacinas contra lentivírus animais. Ciência Animal, Fortaleza, v. 19, n. 1, p. 37-52, 2009.| Biblioteca(s): Embrapa Caprinos e Ovinos. |
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| 20. | | AZEVEDO, D. A. A. de; PINHEIRO, R. R.; SANTOS, V. W. S. dos; DAMASCENO, E. M.; SOUSA, A. L. M. de; ARAÚJO, J. F.; ANDRIOLI, A.; SIDER, L. H.; PEIXOTO, R. M.; TEIXEIRA, M. F. da S. Comparação de testes sorológicos e molecular para diagnóstico da Artrite Encefalite Caprina e avaliação clínica da glândula mamária de caprinos leiteiros infectados. Acta Scientiae Veterinariae, v. 47, Pub. 1668, 2019.| Biblioteca(s): Embrapa Caprinos e Ovinos. |
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| Registros recuperados : 41 | |
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Registro Completo
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Biblioteca(s): |
Embrapa Caprinos e Ovinos. |
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Data corrente: |
29/11/2020 |
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Data da última atualização: |
29/11/2020 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Circulação/Nível: |
A - 1 |
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Autoria: |
ARAÚJO, J. F.; ANDRIOLI, A.; PINHEIRO, R. R.; SIDER, L. H.; SOUSA, A. L. M. de; AZEVEDO, D. A. A. de; PEIXOTO, R. M.; LIMA, A. M. C.; DAMASCENO, E. M.; SOUZA, S. C. R.; TEIXEIRA, M. F. da S. |
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Afiliação: |
JUSCILÂNIA FURTADO ARAÚJO; ALICE ANDRIOLI, CNPC; RAYMUNDO RIZALDO PINHEIRO, CNPC; LUCIA HELENA SIDER, CNPC; ANA LÍDIA MADEIRA DE SOUSA; DALVA ALANA ARAGÃO DE AZEVEDO; RENATO MESQUITA PEIXOTO; ANA MILENA CESAR LIMA; EDGAR MARQUES DAMASCENO; SAMARA CRISTINA ROCHA SOUZA; MARIA FÁTIMA DA SILVA TEIXEIRA. |
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Título: |
Vertical transmissibility of small ruminant lentivirus. |
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Ano de publicação: |
2020 |
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Fonte/Imprenta: |
PLoSONE, v. 15, n. 11, e0239916, Nov. 2020. |
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DOI: |
https://doi.org/10.1371/journal.pone.0239916 |
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Idioma: |
Inglês |
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Conteúdo: |
Abstract: This study aimed to evaluate by means of Nested Polymerase Chain Reaction (nPCR), co-cultivation and sequencing, with genetic comparison between strains (mother/newborn), the occurrence of vertical transmission of Small Ruminant Lentiviruses (SRLV) from naturally occurring nannies infected for their offspring. For the detection of SRLV seropositive progenitors, blood was collected from 42 nannies in the final third of gestation in tubes with and without anticoagulant. The diagnostic tests used were Western Blot (WB) and nPCR. During the period of birth, the same blood collection procedure was performed on 73 newborns at zero hours of birth, with the same diagnostic tests. Seventeen blood samples from seven-day-old kids, proven positive for SRLV by nPCR, chosen at random, were subjected to coculture in goat synovial membrane (GSM) cells for 105 days. The pro-viral DNA extracted from the cell supernatant from the coculture was subjected to nPCR. For DNA sequencing from the nPCR products, nine positive samples were chosen at random, four nannies with their respective offspring, also positive. Each sample was performed in triplicate, thus generating 27 nPCR products of which only 19 were suitable for analysis. Among the 42 pregnant goats, in 50% (21/42) pro-viral DNA was detected by nPCR, while in the WB, only 7.14% (3/42) presented antibodies against SRLV. Regarding neonates, of the 73 kids, 34 (46.57%) were positive for the virus, using the nPCR technique, while in the serological test (WB), three positive animals (4.10%) were observed. The coculture of the 17 samples with a positive result in the nPCR was confirmed in viral isolation by amplification of the SRLV pro-viral DNA. When aligned, the pro-viral DNA sequences (nannies and their respective offspring) presented homology in relation to the standard strain CAEV Co. It was concluded that the transmission of SRLV through intrauterine route was potentially the source of infection in the newborn goats. MenosAbstract: This study aimed to evaluate by means of Nested Polymerase Chain Reaction (nPCR), co-cultivation and sequencing, with genetic comparison between strains (mother/newborn), the occurrence of vertical transmission of Small Ruminant Lentiviruses (SRLV) from naturally occurring nannies infected for their offspring. For the detection of SRLV seropositive progenitors, blood was collected from 42 nannies in the final third of gestation in tubes with and without anticoagulant. The diagnostic tests used were Western Blot (WB) and nPCR. During the period of birth, the same blood collection procedure was performed on 73 newborns at zero hours of birth, with the same diagnostic tests. Seventeen blood samples from seven-day-old kids, proven positive for SRLV by nPCR, chosen at random, were subjected to coculture in goat synovial membrane (GSM) cells for 105 days. The pro-viral DNA extracted from the cell supernatant from the coculture was subjected to nPCR. For DNA sequencing from the nPCR products, nine positive samples were chosen at random, four nannies with their respective offspring, also positive. Each sample was performed in triplicate, thus generating 27 nPCR products of which only 19 were suitable for analysis. Among the 42 pregnant goats, in 50% (21/42) pro-viral DNA was detected by nPCR, while in the WB, only 7.14% (3/42) presented antibodies against SRLV. Regarding neonates, of the 73 kids, 34 (46.57%) were positive for the virus, using the nPCR technique, while in t... Mostrar Tudo |
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Palavras-Chave: |
SRLV. |
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Thesaurus NAL: |
Genetic techniques and protocols; Goat diseases; Goats; Lentivirus; Sheep diseases. |
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Categoria do assunto: |
H Saúde e Patologia |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/218347/1/CNPC-2020-Art-40.pdf
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Marc: |
LEADER 02915naa a2200325 a 4500
001 2127175
005 2020-11-29
008 2020 bl uuuu u00u1 u #d
024 7 $ahttps://doi.org/10.1371/journal.pone.0239916$2DOI
100 1 $aARAÚJO, J. F.
245 $aVertical transmissibility of small ruminant lentivirus.$h[electronic resource]
260 $c2020
520 $aAbstract: This study aimed to evaluate by means of Nested Polymerase Chain Reaction (nPCR), co-cultivation and sequencing, with genetic comparison between strains (mother/newborn), the occurrence of vertical transmission of Small Ruminant Lentiviruses (SRLV) from naturally occurring nannies infected for their offspring. For the detection of SRLV seropositive progenitors, blood was collected from 42 nannies in the final third of gestation in tubes with and without anticoagulant. The diagnostic tests used were Western Blot (WB) and nPCR. During the period of birth, the same blood collection procedure was performed on 73 newborns at zero hours of birth, with the same diagnostic tests. Seventeen blood samples from seven-day-old kids, proven positive for SRLV by nPCR, chosen at random, were subjected to coculture in goat synovial membrane (GSM) cells for 105 days. The pro-viral DNA extracted from the cell supernatant from the coculture was subjected to nPCR. For DNA sequencing from the nPCR products, nine positive samples were chosen at random, four nannies with their respective offspring, also positive. Each sample was performed in triplicate, thus generating 27 nPCR products of which only 19 were suitable for analysis. Among the 42 pregnant goats, in 50% (21/42) pro-viral DNA was detected by nPCR, while in the WB, only 7.14% (3/42) presented antibodies against SRLV. Regarding neonates, of the 73 kids, 34 (46.57%) were positive for the virus, using the nPCR technique, while in the serological test (WB), three positive animals (4.10%) were observed. The coculture of the 17 samples with a positive result in the nPCR was confirmed in viral isolation by amplification of the SRLV pro-viral DNA. When aligned, the pro-viral DNA sequences (nannies and their respective offspring) presented homology in relation to the standard strain CAEV Co. It was concluded that the transmission of SRLV through intrauterine route was potentially the source of infection in the newborn goats.
650 $aGenetic techniques and protocols
650 $aGoat diseases
650 $aGoats
650 $aLentivirus
650 $aSheep diseases
653 $aSRLV
700 1 $aANDRIOLI, A.
700 1 $aPINHEIRO, R. R.
700 1 $aSIDER, L. H.
700 1 $aSOUSA, A. L. M. de
700 1 $aAZEVEDO, D. A. A. de
700 1 $aPEIXOTO, R. M.
700 1 $aLIMA, A. M. C.
700 1 $aDAMASCENO, E. M.
700 1 $aSOUZA, S. C. R.
700 1 $aTEIXEIRA, M. F. da S.
773 $tPLoSONE$gv. 15, n. 11, e0239916, Nov. 2020.
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Embrapa Caprinos e Ovinos (CNPC) |
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