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Inoculation of cyprinid herpesvirus 3 (CyHV-3) on common carp brain cells-influence of process parameters on virus
A Mletzko1, A Amtmann1, S Bergmann2
1Department of Chemical and Biological Engineering, Institute of Bioprocess Engineering, Faculty of Engineering, Friedrich-Alexander University Erlangen-Nürnberg (FAU), Paul-Gordan-Str. 3, 91052, Erlangen, Germany.
Abstract:
Research of cyprinid herpesvirus 3 (CyHV-3) is focused on the infection mechanism and disease development in animals using genetic and immunological approaches to improve treatments and diagnostics. In contrast, only few tried to investigate the CyHV-3 replication behaviour in available cell cultures. Whereas, obtaining high virus yields by in vitro replication enables achieving of the mentioned above goals easier and more reliable. The following work presents an attempt to illuminate the KHV replication in common carp brain (CCB) cell cultures from the engineering point of view. The isolate KHV-TP30 was used testing the influence on process parameters, such as multiplicity of infection (MOI), time of infection (TOI) and time of harvest (TOH). Virus concentrations and infectivity at different time points of infection were examined using hydrolyzed probe qPCR (Gilad et al. 2004) and 50% tissue culture infectivity dose (TCID50). The data obtained show that while the amount of the virus DNA remains constant after reaching its maximum, the infectivity of the virus decreases. Thus, especially, TOH can be crucial for generating a high-quality virus stock. Applying optimized parameters improved the infectivity of the harvested virus and reached a robust titre as high as 1.9 × 108 TCID50/mL. To our knowledge, so far, there is no information in the peer-reviewed literature showing comparably high virus titres. Such virus yields not only facilitate conduction of further studies, including stability tests of the virus stock under various supplementation or disinfection trails, but also provide enough virus material to perform more detailed examinations of the infection mechanism.
Insights
Optimizing cyprinid herpesvirus 3 (CyHV-3) replication in common carp brain cells yields high-titer virus stocks. Careful control of harvest time is crucial for maximizing virus infectivity, essential for further research.
Area of Science:
- Virology
- Cell Biology
- Aquaculture Health
Background:
- Cyprinid herpesvirus 3 (CyHV-3) research primarily focuses on infection mechanisms and disease in animals.
- Investigating CyHV-3 replication in cell cultures is less explored but crucial for obtaining high virus yields.
- Efficient in vitro virus replication facilitates improved diagnostics and treatment development.
Purpose of the Study:
- To optimize CyHV-3 replication in common carp brain (CCB) cell cultures from an engineering perspective.
- To determine the impact of process parameters like multiplicity of infection (MOI), time of infection (TOI), and time of harvest (TOH) on virus yield and infectivity.
- To achieve high-titer virus stocks for further research.
Main Methods:
- Utilized the KHV-TP30 isolate for replication studies in CCB cell cultures.
- Varied MOI, TOI, and TOH to identify optimal replication conditions.
- Quantified virus concentrations using hydrolyzed probe qPCR and infectivity via 50% tissue culture infectivity dose (TCID50).
Main Results:
- Virus DNA levels plateaued while infectivity decreased over time, highlighting the importance of TOH.
- Optimized parameters significantly enhanced virus infectivity.
- Achieved a robust virus titre of 1.9 × 10^8 TCID50/mL, a novel high yield in peer-reviewed literature.
Conclusions:
- Optimized in vitro replication parameters, particularly TOH, are critical for generating high-quality CyHV-3 stocks.
- The achieved high virus titres facilitate further studies on virus stability, disinfection, and infection mechanisms.
- This research provides a foundation for enhanced CyHV-3 diagnostics and therapeutic development.
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