Key result
A real-time RT-PCR and high resolution melting assay successfully detected DHAV-1 with a limit of 100 viral RNA copies and differentiated between vaccine and field strains.
A novel real-time RT-PCR and HRM assay can rapidly detect and differentiate between vaccine and field strains of DHAV-1, aiding in diagnosis and surveillance.
May aid DHAV-1 diagnosis and surveillance in ducks; leaves open prospective field validation before routine use.
Duck hepatitis A virus type 1 (DHAV-1) infection is a highly contagious and fatal disease of young ducklings. A live attenuated vaccine strain designated as 5886 has been used in Taiwan for the control of DHAV-1. Although several molecular biological methods are reported for diagnosis of DHAV-1 infection, none of them is able to discriminate between the vaccine strain and field viruses of DHAV-1. In the present study, a real-time reverse transcriptase polymerase chain reaction (RT-PCR) and high resolution melting (HRM) assay was developed for rapid detection and differentiation between the vaccine strain and field viruses of DHAV-1. This assay is highly specific for DHAV-1 and the detection limit is about 100 copies of the viral RNA. Experiments using fecal samples collected from ducklings experimentally infected with DHAV-1 showed that DHAV-1 could be detected in fecal samples as early as 6 h post-infection. In summary, a real-time RT-PCR and HRM assay is developed in this study and this assay could be valuable for diagnosis and surveillance of DHAV-1 infection in the field.
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Li et al. (2015) studied Duck hepatitis A virus type 1 (DHAV-1) infection. Real-time RT-PCR and high resolution melting (HRM) assay was evaluated on Detection and differentiation of DHAV-1 vaccine strain and field viruses. A real-time RT-PCR and high resolution melting assay successfully detected DHAV-1 with a limit of 100 viral RNA copies and differentiated between vaccine and field strains.
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