2009
DOI: 10.1016/j.vetmic.2009.04.034
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A review of RT-PCR technologies used in veterinary virology and disease control: Sensitive and specific diagnosis of five livestock diseases notifiable to the World Organisation for Animal Health

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Cited by 168 publications
(121 citation statements)
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“…The advantages of TaqMan real-time PCR method over the conventional PCR assay are generally approved as real-time PCR is a more sensitive and specific method with a much shorter detection time. Detection and analysis of real-time PCR product is performed simultaneously during the amplification process by the software, whereas in the case of traditional PCR, the analysis of the results requires an additional step of agarose gel electrophoresis using factors such as ethidium bromide and UV light, which can be hazardous for human health (11,17). In the current research, TaqMan real-time PCR technique allowed detecting JSRV proviral DNA in 18.75% (15 out of 80) of blood samples which showed a high infection rate in apparently healthy sheep.…”
Section: Discussionmentioning
confidence: 99%
“…The advantages of TaqMan real-time PCR method over the conventional PCR assay are generally approved as real-time PCR is a more sensitive and specific method with a much shorter detection time. Detection and analysis of real-time PCR product is performed simultaneously during the amplification process by the software, whereas in the case of traditional PCR, the analysis of the results requires an additional step of agarose gel electrophoresis using factors such as ethidium bromide and UV light, which can be hazardous for human health (11,17). In the current research, TaqMan real-time PCR technique allowed detecting JSRV proviral DNA in 18.75% (15 out of 80) of blood samples which showed a high infection rate in apparently healthy sheep.…”
Section: Discussionmentioning
confidence: 99%
“…This technique allows to assess gene expression analysis, determination of viral load and detection of genetically modified organisms 68 . The primers are designed in such a way that a fluorescent signal is generated only when the primers are incorporated into an amplification product.…”
Section: Real Time Pcrmentioning
confidence: 99%
“…CSFV has an unsegmented, plus-oriented, single-stranded RNA genome. Whereas the virus was traditionally detected by virus isolation on susceptible cell lines, RT-qPCR has become the method of choice for CSFV detection, based on its superior sensitivity and specificity (Hoffmann et al, 2009). Furthermore RT-qPCR still allows detecting CSFV-specific RNA in samples that do not contain any infectious virus anymore.…”
Section: Intmentioning
confidence: 99%