Author: Ambagala, A.; Fisher, M.; Goolia, M.; Nfon, C.; Furukawaâ€Stoffer, T.; Ortega Polo, R.; Lung, O.
Title: Fieldâ€Deployable Reverse Transcriptionâ€Insulated Isothermal PCR (RTâ€iiPCR) Assay for Rapid and Sensitive Detection of Footâ€andâ€Mouth Disease Virus Cord-id: hp1iw7np Document date: 2016_9_3
ID: hp1iw7np
Snippet: Footâ€andâ€mouth disease (FMD) is a highly contagious viral disease of clovenâ€hoofed animals, which can decimate the livestock industry and economy of countries previously free of this disease. Rapid detection of footâ€andâ€mouth disease virus (FMDV) is critical to containing an FMD outbreak. Availability of a rapid, highly sensitive and specific, yet simple and fieldâ€deployable assay would support local decisionâ€making during an FMDV outbreak. Here we report validation of a novel reve
Document: Footâ€andâ€mouth disease (FMD) is a highly contagious viral disease of clovenâ€hoofed animals, which can decimate the livestock industry and economy of countries previously free of this disease. Rapid detection of footâ€andâ€mouth disease virus (FMDV) is critical to containing an FMD outbreak. Availability of a rapid, highly sensitive and specific, yet simple and fieldâ€deployable assay would support local decisionâ€making during an FMDV outbreak. Here we report validation of a novel reverse transcriptionâ€insulated isothermal PCR (RTâ€iiPCR) assay that can be performed on a commercially available, compact and portable POCKIT (â„¢) analyser that automatically analyses data and displays ‘+’ or ‘−’ results. The FMDV RTâ€iiPCR assay targets the 3D region of the FMDV genome and was capable of detecting 9 copies of in vitroâ€transcribed RNA standard with 95% confidence. It accurately identified 63 FMDV strains belonging to all seven serotypes and showed no crossâ€reactivity with viruses causing similar clinical diseases in clovenâ€hoofed animals. The assay was able to identify FMDV RNA in multiple sample types including oral, nasal and lesion swabs, epithelial tissue suspensions, vesicular and oral fluid samples, even before the appearance of clinical signs. Clinical sensitivity of the assay was comparable or slightly higher than the laboratoryâ€based realâ€time RTâ€PCR assay in use. The assay was able to detect FMDV RNA in vesicular fluid samples without nucleic acid extraction. For RNA extraction from more complex sample types, a commercially available taco(â„¢) mini transportable magnetic beadâ€based, automated extraction system was used. This assay provides a potentially useful fieldâ€deployable diagnostic tool for rapid detection of FMDV in an outbreak in FMDâ€free countries or for routine diagnostics in endemic countries with less structured laboratory systems.
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