Quantification of chicken anaemia virus by competitive polymerase chain reaction

A quantitative method for chicken anaemia virus (CAV) was developed using competitive polymerase chain reaction (PCR). Competitive template was constructed by deletion of 33 nucleotides from a wildtype DNA clone of CAV. Quantification of CAV DNA molecules by the competitive PCR was rapid and highly...

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Veröffentlicht in:Avian pathology 2000-08, Vol.29 (4), p.305-310
Hauptverfasser: Yamaguchi, S., Kaji, N., Munang'andu, H. M., Kojima, C., Mase, M., Tsukamoto, K.
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container_end_page 310
container_issue 4
container_start_page 305
container_title Avian pathology
container_volume 29
creator Yamaguchi, S.
Kaji, N.
Munang'andu, H. M.
Kojima, C.
Mase, M.
Tsukamoto, K.
description A quantitative method for chicken anaemia virus (CAV) was developed using competitive polymerase chain reaction (PCR). Competitive template was constructed by deletion of 33 nucleotides from a wildtype DNA clone of CAV. Quantification of CAV DNA molecules by the competitive PCR was rapid and highly reproducible when compared with conventional infectivity titration methods. The ratios of the viral DNA molecules and infectivity titres in MDCC-MSB1 cells varied between 1.3 and 3.55 log10 among several isolates, suggesting the existence of different infection efficiencies to MDCC-MSB1 cells by isolates. The competitive PCR will be useful for studying CAV infection in vivo and/or in vitro.
doi_str_mv 10.1080/03079450050118421
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source Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; IngentaConnect Free/Open Access Journals
subjects Biochemistry
Deoxyribonucleic acid
DNA
Poultry
Viruses
title Quantification of chicken anaemia virus by competitive polymerase chain reaction
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