Sensitive, Reproducible, and Economic Real-Time Reverse Transcription PCR Detecting Avian Metapneumovirus Subtypes A and B

• Published in: Avian diseases Vol. 58; no. 2; pp. 216 - 222
• Main Authors: Franzo, G, Drigo, M, Lupini, C, Catelli, E, Laconi, A, Listorti, V, Bonci, M, Naylor, C J, Martini, M, Cecchinato, M
• Format: Journal Article
• Language: English
• Published: United States American Association of Avian Pathologists 01.06.2014
• Subjects: Animals; Fluorescent Dyes - metabolism; Metapneumovirus - genetics; Metapneumovirus - isolation & purification; Metapneumovirus - metabolism; Organic Chemicals - metabolism; Paramyxoviridae Infections - diagnosis; Paramyxoviridae Infections - veterinary; Paramyxoviridae Infections - virology; Poultry Diseases - diagnosis; Poultry Diseases - virology; Reproducibility of Results; Reverse Transcriptase Polymerase Chain Reaction - methods; Reverse Transcriptase Polymerase Chain Reaction - veterinary; RNA, Viral - genetics; RNA, Viral - metabolism; Sensitivity and Specificity
• ISSN: 1938-4351; 0005-2086; 1938-4351
• DOI: 10.1637/10676-092413-Reg.1

Use of real-time PCR is increasing in the diagnosis of infectious disease due to its sensitivity, specificity, and speed of detection. These characteristics make it particularly suited for the diagnosis of viral infections, like avian metapneumovirus (AMPV), for which effective control benefits from continuously updated knowledge of the epidemiological situation. Other real-time reverse transcription (RT)-PCRs have been published based on highly specific fluorescent dye–labeled probes, but they have high initial cost, complex validation, and a marked susceptibility to the genetic variability of their target sequence. With this in mind, we developed and validated a SYBR Green I–based quantitative RT-PCR for the detection of the two most prevalent AMPV subtypes (i.e., subtypes A and B). The assay demonstrated an analytical sensitivity comparable with that of a previously published real-time RT-PCR and the ability to detect RNA equivalent to approximately 0.5 infectious doses for both A and B subtypes. The high efficiency and linearity between viral titer and crossing point displayed for both subtypes make it suited for viral quantification. Optimization of reaction conditions and the implementation of melting curve analysis guaranteed the high specificity of the assay. The stable melting temperature difference between the two subtypes indicated the possibility of subtyping through melting temperature analysis. These characteristics make our assay a sensitive, specific, and rapid tool, enabling contemporaneous detection, quantification, and discrimination of AMPV subtype A and B.