2013
DOI: 10.1590/s0102-09352013000300028
|View full text |Cite
|
Sign up to set email alerts
|

PCR em tempo real para detecção do vírus da doença de Aujeszky

Abstract: RESUMOO objetivo deste trabalho foi desenvolver uma PCR em tempo real (qPCR) para o diagnóstico rápido e sensível da doença de Aujeszky. Os iniciadores amplificaram um fragmento de 123 pares de base do gene codificante da glicoproteína D. A qPCR foi testada em 25 amostras de cérebro de suíno positivas e 85 amostras negativas para DA no isolamento viral e na soroneutralização. A sensibilidade analítica foi calculada com acréscimo de um isolado brasileiro do SuHV-1 titulado em amostras de cérebro de suíno negati… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2

Citation Types

0
2
0

Year Published

2014
2014
2020
2020

Publication Types

Select...
5

Relationship

0
5

Authors

Journals

citations
Cited by 7 publications
(2 citation statements)
references
References 11 publications
0
2
0
Order By: Relevance
“…Diagnostic specificity was tested using seventy samples (swine brain) collected from three FONSECA JR et al (2013). Testing repeatability occurred on three consecutive days, using seven different samples in triplicate (a sample in LD concentration, three samples a log above LD and three samples ½ log above LD in the respective concentrations from, 10 -1.5 TCID50 mL -1 , 10 -1.0 TCID50 mL -1 and 10 -0.5 TCID50 mL -1 ).…”
Section: Methodsmentioning
confidence: 99%
“…Diagnostic specificity was tested using seventy samples (swine brain) collected from three FONSECA JR et al (2013). Testing repeatability occurred on three consecutive days, using seven different samples in triplicate (a sample in LD concentration, three samples a log above LD and three samples ½ log above LD in the respective concentrations from, 10 -1.5 TCID50 mL -1 , 10 -1.0 TCID50 mL -1 and 10 -0.5 TCID50 mL -1 ).…”
Section: Methodsmentioning
confidence: 99%
“…At 3, 6, and 24 h after inoculation, cells were harvested and subjected to DNA extraction using a Maxwell® 16 Tissue DNA Purification Kit (Promega, USA). Virus DNA and reference genes were quantified by real-time PCR as described previously [32]. Virus concentration was measured using virus growth in PK15 as a reference.…”
Section: Methodsmentioning
confidence: 99%