TY - JOUR
T1 - Absolute quantification using real-time polymerase chain reaction of Marek's disease virus serotype 2 in field dust samples, feather tips and spleens
AU - G., Renz Katrin
AU - Islam, Aminul
AU - Cheetham, Brian F.
AU - Walkden-Brown, Stephen W.
N1 - Imported on 12 Apr 2017 - DigiTool details were: month (773h) = August, 2006; Journal title (773t) = Journal of Virological Methods. ISSNs: 0166-0934;
PY - 2006/8
Y1 - 2006/8
N2 - Methods for Taqman quantitative real-time PCR (qPCR) assays to detect the three serotypes of Marek's disease virus (MDV) are available, and absolute quantification has been developed for MDV serotype 1 and serotype 3. The development of a method for absolute quantification of Marek's disease virus serotype 2 (MDV2) is described in this paper. Using plasmid DNA, the lower detection limit of the MDV2 assay was determined to be 10 copies. Three independent assay runs showed highly reproducible Ct values and calculated copy numbers, with mean intra- and inter-assay coefficients of variation of less than 3% for Ct and less than 21.5% for calculated copy number. Absolute quantification of MDV2 was performed successfully on dust samples collected from poultry farms across Australia, material from infectious spleens and feather tips from chickens vaccinated with an attenuated strain of MDV2. Thus, it is now possible to use qPCR assays for absolute quantification of all three serotypes of MDV in a sample.
AB - Methods for Taqman quantitative real-time PCR (qPCR) assays to detect the three serotypes of Marek's disease virus (MDV) are available, and absolute quantification has been developed for MDV serotype 1 and serotype 3. The development of a method for absolute quantification of Marek's disease virus serotype 2 (MDV2) is described in this paper. Using plasmid DNA, the lower detection limit of the MDV2 assay was determined to be 10 copies. Three independent assay runs showed highly reproducible Ct values and calculated copy numbers, with mean intra- and inter-assay coefficients of variation of less than 3% for Ct and less than 21.5% for calculated copy number. Absolute quantification of MDV2 was performed successfully on dust samples collected from poultry farms across Australia, material from infectious spleens and feather tips from chickens vaccinated with an attenuated strain of MDV2. Thus, it is now possible to use qPCR assays for absolute quantification of all three serotypes of MDV in a sample.
KW - Absolute quantification
KW - Marek's disease virus serotype 2
KW - QPCR
KW - Real-time PCR
U2 - 10.1016/j.jviromet.2006.03.017
DO - 10.1016/j.jviromet.2006.03.017
M3 - Article
SN - 0166-0934
VL - 135
SP - 186
EP - 191
JO - Journal of Virological Methods
JF - Journal of Virological Methods
IS - 2
ER -