Abstract

BackgroundCanine distemper virus (CDV) has been associated with outbreaks of canine infectious respiratory disease in shelters and boarding kennel environments. POCKITTM Nucleic Acid Analyzer is a field-deployable device capable of generating automatically interpreted insulated isothermal polymerase chain reaction (iiPCR) results from extracted nucleic acid within one hour. In this study, reverse transcription iiPCR (RT-iiPCR) was developed to facilitate point-of-need diagnosis of CDV infection.ResultsAnalytical sensitivity (limit of detection 95%) of the established CDV RT-iiPCR was about 11 copies of in vitro transcribed RNA per reaction. CDV RT-iiPCR generated positive signals from CDV, but not Bordetella bronchiseptica, canine parvovirus, canine herpesvirus, canine adenovirus 2, canine influenza virus (subtype H3N8), canine parainfluenza virus, and canine respiratory coronavirus. To evaluate accuracy of the established reaction in canine distemper clinical diagnosis, 110 specimens from dogs, raccoons, and foxes suspected with CDV infection were tested simultaneously by CDV RT-iiPCR and real-time RT-PCR. CDV RT-iiPCR demonstrated excellent sensitivity (100%) and specificity (100%), compared to real-time RT-PCR.ConclusionsThe results indicated an excellent correlation between RT-iiPCR and a reference real time RT-PCR method. Working in a lyophilized format, the established method has great potential to be used for point-of-care diagnosis of canine distemper in animals, especially in resource-limited facilities.

Highlights

  • Canine distemper virus (CDV) has been associated with outbreaks of canine infectious respiratory disease in shelters and boarding kennel environments

  • Validation of canine distemper virus (CDV) reverse transcription (RT)-insulated isothermal polymerase chain reaction (iiPCR) using clinical samples A clinical evaluation was further performed to determine whether the CDV RT-iiPCR was suitable for detection of CDV viruses from clinical samples

  • 110 clinical samples submitted to the University of Tennessee, College of Veterinary Medicine (UTCVM), Clinical Virology Lab from 2010 to 2014 were tested by RT-iiPCR and real-time reverse transcription polymerase chain reaction (RT-PCR)

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Summary

Introduction

Canine distemper virus (CDV) has been associated with outbreaks of canine infectious respiratory disease in shelters and boarding kennel environments. Canine distemper (CD), caused by canine distemper virus (CDV), is a highly contagious and lethal systemic disease in young dogs [1]. This virus infects and produces clinical disease in members of the order Carnivora, including members of the families Canidae (fox, coyote, wolf), Mustelidae (ferret, skunk, badger, mink, weasel, otter, fisher), Procyonidae (raccoon), Felidae (lions, tigers), Ailuridae (red panda), Hyaenidae (hyenas), Ursidae (bear), and Viverridae (palm civet, genets) [2]. CDV is a viral disease of global importance in common and endangered carnivores [3]. The source for the epizootic strain is still unknown but thought to be a terrestrial carnivore [10]

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