Project number: 2020-104
Project Status:
Completed
Budget expenditure: $149,650.00
Principal Investigator: Peter D. Kirkland
Organisation: NSW Department of Primary Industries
Project start/end date: 14 Apr 2021 - 14 Jan 2022
Contact:
FRDC

Need

Epidemiologic modelling to predict the disease outcomes for carp populations in Australia are important to predict the efficacy of KHV for biocontrol (Durr et al 2019). Key aspects of KHV delivery into a target carp population will be the time of year that infected fish are released and understanding the most significant ways in which the virus is spread between fish. One mechanism for virus delivery proposed is the introduction of “trojan” carp into the target population. Depending on the temperature at which they are held, carp may be subclinically infected and later go on to shed KHV and develop disease when the water temperature is increased (Sunarto et al., 2019). A release pathway that uses trojan carp that are infected with KHV by intraperitoneal (IP) injection requires knowledge of the survival time and detailed excretion dynamics (including at and after death) under different conditions for virus dose, water temperature and age/health/life history of the fish.
Modelling highlights the important influence of transmission dynamics on disease outcomes. A key for KHV models is to determine if direct transmission (i.e. requiring direct fish-to-fish contact) is more important than indirect transmission (whereby naïve carp can be infected by KHV shed into the water). This will determine the relative efficacy of KHV biocontrol during carp aggregation (Durr et al., 2019).
The present study will use a laboratory infection model to evaluate KHV replication and shedding in injected carp. Further, the relative importance of direct and indirect transmission of KHV will be compared. This will inform epidemiologic models to improve predictions and management of a controlled KHV release.
References
Sunarto A., Moody, N.J.G. and Durr, P.A. Essential studies on cyprinid herpesvirus 3 (CyHV-3) prior to release of the virus in Australian waters: Seasonality studies. FRDC. Canberra.

Objectives

1. Define dose-response parameters for KHV infection after challenge of wild Australian carp by immersion or injection challenge, including mortality, median survival time and 50% lethal dose estimates.
2. Measure the transmission efficiency of KHV in carp when derived from cell culture compared to excreted from an infected fish, with qPCR quantification of KHV DNA for normalisation.
3. Graph the excretion of infectious KHV from carp infected by IP injection when the infection is subclinical and during clinical disease up-to near death and for 24 hours after death.
4. Measure the transmission parameter β for horizontal transmission of KHV through direct and indirect contact. This parameter will be assessed under two levels of force of infection depending on the time before indirect exposure to KHV and the proportion of infected individuals for direct transmission.

Final report

ISBN: 978-1- 76058-610-2
Author: Peter Kirkland and Paul HIck
Final Report • 2022-09-30 • 2.00 MB
2020-104-DLD.pdf

Summary

Epidemiological modelling has been undertaken to evaluate the impact of CyHV-3 as part of an assessment of the feasibility of this virus as a potential biocontrol for carp in Australia. The present project provides information to support key components of the mechanisms of virus transmission which underpin the epidemiological model.

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