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1.
An Acad Bras Cienc ; 94(suppl 1): e20210600, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-35508018

RESUMO

The ionospheric investigations have improved our understanding of the space weather role in the upper atmosphere conditions, particularly at higher latitudes where the geospace phenomena print their signatures. The simultaneous observations using multi-instruments have improved our knowledge of the coupling processes inside the ionosphere, and their connection with the magnetosphere and neutral atmosphere processes under the space weather phenomena. The ionosphere probing at EACF started on 1986 using an analogical very low frequency (VLF) system, and after the year 2004 using digital VLF system, global navigation satellite system (GNSS), riometers and Canadian digital ionosonde (CADI). This paper presents the different radio techniques that have been used at Brazilian Antarctic Station Comandante Ferraz (EACF) to characterize the ionospheric conditions, and the highlights of the studies using multi-instrument observations performed in the last few decades.


Assuntos
Tempo (Meteorologia) , Regiões Antárticas , Brasil , Canadá
2.
Vet Microbiol ; 124(1-2): 25-34, 2007 Sep 20.
Artigo em Inglês | MEDLINE | ID: mdl-17521832

RESUMO

After 44 years of epidemiological silence, bluetongue virus (BTV) was reintroduced in Portugal in the autumn of 2004. The first clinical cases of bluetongue disease (BT) were notified in sheep farms located in the South of Portugal, close to the Spanish border. A total of six BTV, five of serotype 4 and one of serotype 2 were isolated from sheep and cattle during the 2004-2006 epizootics. The nucleotide sequence of gene segments L2, S7 and S10 of BTV-4 prototype strain (BTV4/22045/PT04) obtained from the initial outbreak and of BTV-2 (BTV2/26629/PT05) was fully determined and compared with those from other parts of the world. The phylogenetic analysis revealed that BTV4/22045/PT04 is related to other BTV-4 strains that circulate in the Mediterranean basin since 1998, showing the highest identity (99%) with BTV-4 isolates of 2003 from Sardinia and Corsica, whereas BTV2/26629/PT05 is almost indistinguishable from the Onderstepoort BTV-2 live-attenuated vaccine strain and its related field strain isolated in Italy. Since live-attenuated BTV-2 vaccine was never used in Portugal, the isolation of this strain may represent a natural circulation of the vaccine virus used in other countries in Mediterranean Europe.


Assuntos
Vírus Bluetongue/classificação , Vírus Bluetongue/genética , Bluetongue/epidemiologia , Bluetongue/virologia , Doenças dos Bovinos/epidemiologia , Animais , Sequência de Bases , Vírus Bluetongue/isolamento & purificação , Bovinos , Doenças dos Bovinos/virologia , Linhagem Celular , Embrião de Galinha , Surtos de Doenças/veterinária , Epidemiologia Molecular , Dados de Sequência Molecular , Filogenia , Portugal/epidemiologia , RNA Viral/química , Alinhamento de Sequência , Sorotipagem/veterinária , Ovinos , Organismos Livres de Patógenos Específicos
3.
Vet Microbiol ; 137(3-4): 252-9, 2009 Jun 12.
Artigo em Inglês | MEDLINE | ID: mdl-19233575

RESUMO

Vaccination programs for the control of bluetongue (BT) in ruminants have limitations due to difficulties in differentiating infected from vaccinated animals (DIVA). To overcome this problem a DIVA test that looks at a differential immune response to bluetongue virus (BTV) non-structural protein 3 (NS3) was developed. The NS3 encoding gene of strain BTV4/22045/PT04 was inserted into expression vector pET-28a and expressed in Escherichia coli strain JM109. Recombinant NS3 protein was used as an antigen in an indirect ELISA (NS3-ELISA) to measure the serologic response to NS3 protein in cattle and sheep. Following a cattle vaccination/challenge experiment with a bivalent inactivated BTV 2-4 vaccine, NS3 antibodies were detected at approximately 15 days post-infection in control unvaccinated animal, while vaccinated animals did not develop detectable NS3 antibodies and, with exception of one, remained negative even after virus challenge. The inactivated vaccine induced antibodies against the major core structural protein (VP7) of BTV as well as neutralizing antibodies in all animals. To evaluate the applicability of NS3-ELISA in field scenario, a total of 562 serum samples collected from uninfected, BTV-infected and vaccinated animals were tested for NS3 antibodies. Taken together, the results confirm that NS3 antibodies were induced to the greatest levels in animals infected with BTV in comparison to the levels induced in animals immunized with inactivated BTV vaccines, implying that antibody response to NS3 allows the differentiation between infected and vaccinated animals.


Assuntos
Anticorpos Antivirais/sangue , Doenças dos Bovinos/virologia , Proteínas não Estruturais Virais/genética , Proteínas não Estruturais Virais/imunologia , Vacinas Virais/imunologia , Animais , Bluetongue/prevenção & controle , Vírus Bluetongue/imunologia , Bovinos , Doenças dos Bovinos/prevenção & controle , Ensaio de Imunoadsorção Enzimática , Escherichia coli/metabolismo , Proteínas Recombinantes , Vacinação/veterinária
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