Multiplex RT‐PCR and Automated Microarray for Detection of Eight Bovine Viruses. Issue 6 (23rd November 2016)

• Record Type: Journal Article
• Authors: Lung, O.; Furukawa‐Stoffer, T.; Burton Hughes, K.; Pasick, J.; King, D. P.; Hodko, D.
• Is Part Of: Transboundary and emerging diseases. Volume 64:Issue 6(2017)
• Page Start: 1929
• Page End: 1934
• Publication Date: 2016-11-23
• Subjects: multiplex PCR -- microarray -- automation -- rinderpest -- bovine viral diarrhoea -- bovine herpesvirus -- malignant catarrhal fever -- bluetongue; Veterinary medicine -- Periodicals; 636.089
• DOI: 10.1111/tbed.12591
• Languages: English
• ISSNs: 1865-1674

Abstract

Summary: Microarrays can be a useful tool for pathogen detection as it allow for simultaneous interrogation of the presence of a large number of genetic sequences in a sample. However, conventional microarrays require extensive manual handling and multiple pieces of equipment for printing probes, hybridization, washing and signal detection. In this study, a reverse transcription (RT)–PCR with an accompanying novel automated microarray for simultaneous detection of eight viruses that affect cattle [vesicular stomatitis virus (VSV), bovine viral diarrhoea virus type 1 and type 2, bovine herpesvirus 1, bluetongue virus, malignant catarrhal fever virus, rinderpest virus (RPV) and parapox viruses] is described. The assay accurately identified a panel of 37 strains of the target viruses and identified a mixed infection. No non‐specific reactions were observed with a panel of 23 non‐target viruses associated with livestock. Vesicular stomatitis virus was detected as early as 2 days post‐inoculation in oral swabs from experimentally infected animals. The limit of detection of the microarray assay was as low as 1 TCID50 /ml for RPV. The novel microarray platform automates the entire post‐PCR steps of the assay and integrates electrophoretic‐driven capture probe printing in a single user‐friendly instrument that allows array layout and assay configuration to be user‐customized on‐site.