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ABSTRACT: Background
Canine parvovirus 2, a linear single-stranded DNA virus belonging to the genus Parvovirus within the family Parvoviridae, is a highly contagious pathogen of domestic dogs and several wild canidae species. Early detection of canine parvovirus (CPV-2) is crucial to initiating appropriate outbreak control strategies. Recombinase polymerase amplification (RPA), a novel isothermal gene amplification technique, has been developed for the molecular detection of diverse pathogens. In this study, a real-time RPA assay was developed for the detection of CPV-2 using primers and an exo probe targeting the CPV-2 nucleocapsid protein gene.Results
The real-time RPA assay was performed successfully at 38 °C, and the results were obtained within 4-12 min for 105-10
SUBMITTER: Geng Y
PROVIDER: S-EPMC5674863 | biostudies-literature | 2017 Nov
REPOSITORIES: biostudies-literature