2016
DOI: 10.1016/j.cimid.2016.09.005
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Occurrence of Pseudocowpox virus associated to Bovine viral diarrhea virus-1, Brazilian Amazon

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Cited by 12 publications
(10 citation statements)
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“…A BVDV-2b isolate was also detected in lung samples of a wild boar collected in a commercial slaughterhouse in RS in 2012 (Weber et al, 2016a(Weber et al, , 2016b. Alves et al (2016) detected a BVDV-1a genome in the sera of cattle during an outbreak of vesicular disease by pseudocowpox virus in Pará (PA), northern Brazil. Nucleotide sequencing and phylogeny based on the 5 ′ UTR demonstrated a high similarity with Oregon C24V BVDV strain.…”
Section: Animal Health Research Reviewsmentioning
confidence: 96%
“…A BVDV-2b isolate was also detected in lung samples of a wild boar collected in a commercial slaughterhouse in RS in 2012 (Weber et al, 2016a(Weber et al, , 2016b. Alves et al (2016) detected a BVDV-1a genome in the sera of cattle during an outbreak of vesicular disease by pseudocowpox virus in Pará (PA), northern Brazil. Nucleotide sequencing and phylogeny based on the 5 ′ UTR demonstrated a high similarity with Oregon C24V BVDV strain.…”
Section: Animal Health Research Reviewsmentioning
confidence: 96%
“…Nas últimas décadas, episódios envolvendo coinfecções em bovinos e em humanos também foram registrados em território nacional. A origem e o significado de coinfecções na patogenia das doenças não são totalmente elucidados e, na atualidade, a frequência das coinfecções no Brasil, é também desconhecida, mas encontra-se sob vigilância (Abrahão et al, 2010;Canal et al, 2012;Campos et al, 2011;Alves et al, 2016;Nascimento et al, 2016;Sant'ana et al, 2013; (Untergasser et al, 2007).…”
Section: Methodsunclassified
“…Reactions with amplification of duplicate samples were considered valid, with melting temperature (Tm) values in accordance with the previously established standard curve. The SYBR Green® PCR Master Mix (Applied Biosystems, USA) was used together with the VGF forward and VGF reverse primers, which were designed to amplify a 82‐bp fragment of the vgf gene (Alves et al., ) at concentrations of 400 μM of each primer in a reaction with a final volume of 10 μl. The thermocycling conditions used were as follows: 95°C—10 min; denaturation: 95°C—15 s; pairing and extension: 60°C—60 s (40 cycles); and dissociation curves: 60–95°C, according to the standard protocol from Applied Biosystems (USA).…”
Section: Methodsmentioning
confidence: 99%