Key result
Novel RT-qPCR assay detects DERSV in ~47% of clinical duck samples.
Why the study?
Duck egg-reducing syndrome virus is a novel Avihepatovirus causing laying rate declines, making a rapid detection method crucial for identification and control.
Does a novel TaqMan-based RT-qPCR assay accurately detect DERSV in clinical duck samples?
Does a novel TaqMan-based RT-qPCR assay accurately detect DERSV in clinical duck samples?
This novel RT-qPCR assay provides a rapid, sensitive, and specific method for detecting the emerging duck egg-reducing syndrome virus.
Duck egg-reducing syndrome virus (DERSV) is a novel Avihepatovirus and is responsible for a gradual decline in the laying rate of ducks, decreasing from a peak of 90% to 50%. The development of a rapid detection method for DERSV is crucial for the identification and control of virus infections. In this study, we developed a quantitative reverse transcription PCR (RT-qPCR) assay for detecting DERSV. Specific primers and a probe were designed to target a conserved region of the 3D gene. The assay demonstrated high specificity, with no cross-reactivity to other non-target duck viruses. It had a detection limit of 102 copies and a linear range from 102 to 109 copies per reaction. The assay’s efficiency was 92.59%, with a regression coefficient (R2) of 0.999. The coefficient of variation for both intra-and inter-assays was less than 2.00%. Among the 153 clinical samples collected from 2016 to 2023, the RT-qPCR detected a DERSV positive ratio of 47.06% (72/153). In conclusion, the utilization of the real-time RT-qPCR assay holds potential for the detection of DERSV in epidemiological and pathogenesis studies.
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Zhang et al. (2025) studied Duck egg-reducing syndrome (n=153). RT-qPCR assay targeting the 3D gene of DERSV was evaluated on Detection of DERSV RNA (positivity rate). The developed real-time RT-qPCR assay successfully detected DERSV in 47.06% of the evaluated clinical duck samples with a detection limit of 10^2 copies.
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