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.

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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