2016
DOI: 10.1016/j.jviromet.2016.03.002
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Real-time PCR for differential quantification of CVI988 vaccine virus and virulent strains of Marek’s disease virus

Abstract: HighlightsDeveloped, optimised and validated q-PCR to distinguish CVI988 and virulent MDV.Based on differential detection of single nucleotide polymorphism in pp38 gene.Specific, sensitive, efficient, reproducible assay with no false-positive results.Accurate differential quantification over biological range of virus levels.Replication of CVI988 and virulent MDV examined in chicken feathers and blood.

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Cited by 50 publications
(56 citation statements)
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“…These results suggest that flocks of birds differ in their susceptibility to virus and in their shedding rate should they become infectious. High susceptibility and shedding rates might be rapidly assessed in the field by determining the virus concentration in dust samples or feather tips (Baigent et al, 2016). Our results also suggest that cleanout efficiency varies on this farm and that this variation has had detectable effects on virus dynamics.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…These results suggest that flocks of birds differ in their susceptibility to virus and in their shedding rate should they become infectious. High susceptibility and shedding rates might be rapidly assessed in the field by determining the virus concentration in dust samples or feather tips (Baigent et al, 2016). Our results also suggest that cleanout efficiency varies on this farm and that this variation has had detectable effects on virus dynamics.…”
Section: Discussionmentioning
confidence: 99%
“…Infectious MDV can be contained in this dust (Carrozza et al, 1973), being shed with the epithelial cells of infectious chickens and transmitted through the inhalation of virus-contaminated dust (Colwell and Schmittle, 1968). The concentration of MDV in dust can be measured through quantitative polymerase chain reaction (qPCR) (Baigent et al, 2005, 2016; Islam et al, 2006). Our model is constructed with this type of data in mind.…”
Section: Methodsmentioning
confidence: 99%
“…DIVA assays were developed to provide differential molecular detection assays for vaccine and field viruses of ILTV (Shil et al, 2015). Baigent et al (2016) described the pp38 MDV DIVA real-time PCR for differential identification of MDV-1 vaccine DNAs from MDV-1 virulent isolate DNAs. That assay was developed using cell-cultured prototype viruses, however, and its employment on feather tip extracts of commercial chickens that have been vaccinated commercially, did not provided the desired differential specificity between the wild-type and the vaccine viruses.…”
Section: Differentiation Between Wild-type and Vaccine Viruses -Divamentioning
confidence: 99%
“…Marek's disease virus have made it possible to detect and quantify virus collected from field settings (2,3,23). Four studies have used qPCR methods to study field samples to study virus dynamics in Australia (18,38,44) and Iraq (43).…”
Section: The Development Of Quantitative Polymerase Chain Reaction (Qmentioning
confidence: 99%
“…These strains are related but not identical to wild-type virus. Once vaccinated, a bird can shed these vaccine strains (3,24), and so we used the primer-probe combination of Baigent et al (2) that is capable of quantifying wild-type virus in the presence of each of the vaccine strains. This specificity is necessary because all chickens included in our study were vaccinated against Marek's disease.…”
Section: Introductionmentioning
confidence: 99%