Loading…

User-friendly Taqman probe coupled-insulated isothermal PCR (iiPCR) for rapid detection of emerging Ambystoma tigrinum virus (ATV) in western tiger salamanders (Ambystoma mavortium) on a compact, portable instrument

•Performance of portable device for detection of Ambystoma tigrinum virus (ATV) DNA is described.•The iiPCR assay was more sensitive than conventional PCR and had a LOD95% of 20 copies per reaction.•The instrument automatically analyzes and displays results within approximately 40min.•The field-depl...

Full description

Saved in:
Bibliographic Details
Published in:Journal of virological methods 2017-11, Vol.249, p.21-24
Main Authors: Lung, Oliver, Reimer, Stephanie A., Goater, Cameron P.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:•Performance of portable device for detection of Ambystoma tigrinum virus (ATV) DNA is described.•The iiPCR assay was more sensitive than conventional PCR and had a LOD95% of 20 copies per reaction.•The instrument automatically analyzes and displays results within approximately 40min.•The field-deployable technology would enhance detection of, and response to wildlife pathogens. Portable user-friendly diagnostic tests can benefit detection and surveillance of wildlife diseases. Here, the performance of a compact POCKIT™ Nucleic Acid Analyzer for detection of Ambystoma tigrinum virus (ATV), an emerging Iridovirus that is associated with high host mortality in the western tiger salamander (Ambystoma mavortium) in North America was assessed. Tissue samples from 188 larval tiger salamanders collected from sites in Alberta, Canada were tested by both iiPCR and by conventional PCR. Results of the two assays showed 96.3% agreement. All 176 samples that tested positive by conventional PCR were also positive by iiPCR, while 12 of the samples that were negative by conventional PCR were positive by iiPCR. Comparison of the limits of detection of the two assays shows that the iiPCR assay was more sensitive than conventional PCR and had a LOD95 of 20 copies per reaction. The instrument automatically analyzes and displays results within 40min following nucleic acid extraction. The novel technology could enhance detection of, and response to, wildlife pathogens, particularly those that occur sporadically, cause rapid outbreaks, and/or occur within isolated geographical regions.
ISSN:0166-0934
1879-0984
DOI:10.1016/j.jviromet.2017.08.008