Development and validation of a TaqMan-MGB real-time RT-PCR assay for simultaneous detection and characterization of infectious bursal disease virus

• DOI: 10.1016/j.jviromet.2012.06.012
• Publication Date: 2012-06-21T15:25:02Z
• Authors: Gonzalo Tomás; Martín Hernández; Ana Marandino; Yanina Panzera; Leticia Maya; Diego Hernández; Ariel Pereda; Alejandro Banda; Pedro Villegas; Sebastián Aguirre; Ruben Pérez
• Keywords: IBDV; 0301 basic medicine; Reverse Transcriptase Polymerase Chain Reaction; INFECTIOUS BURSAL DISEASE (GUMBORO); STRAIN CHARACTERIZATION; Reproducibility of Results; DIAGNOSIS; Birnaviridae Infections; Real-Time Polymerase Chain Reaction; Infectious bursal disease virus; Sensitivity and Specificity; 3. Good health; 03 medical and health sciences; https://purl.org/becyt/ford/4.3; Virology; Animals; https://purl.org/becyt/ford/4; REAL-TIME PCR; DNA Primers

Rapid and reliable detection and classification of infectious bursal disease viruses (IBDVs) is of crucial importance for disease surveillance and control. This study presents the development and validation of a real-time RT-PCR assay to detect and discriminate very virulent (vv) from non-vv (classic and variant) IBDV strains. The assay uses two fluorogenic, minor groove-binding (MGB) TaqMan probes targeted to a single nucleotide polymorphism (SNP) embedded in a highly conserved genomic region. The analytical sensitivity of the assay was determined using serial dilutions of in vitro-transcribed RNA. The assay demonstrated a wide dynamic range between 10(2) and 10(8) standard RNA copies per reaction. Good reproducibility was also detected, with intra- and inter-assay coefficients of variation ranging from 0.13% to 2.23% and 0.26% to 1.92%, respectively. The assay detected successfully all the assessed vv, classical, and variant field and vaccine strains and correctly discriminated all vvIBDV strains from non-vvIBDV strains. Other common avian RNA viruses tested negative, indicating high specificity of the assay. The high sensitivity, rapidity, reproducibility, and specificity of the real-time RT-PCR assay make this method suitable for general and genotype-specific detection and quantitation.