Replication of infectious bursal disease virus in continuous cell lines

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Infectious bursal disease virus (IBDV) replicates in mammalian cell lines MA-104, Vero, and BGM-70. BGM-70 cells showed the most significant cytopathic effects, proving effective for IBDV research.

Area of Science:

  • Veterinary Virology
  • Cell Biology
  • Animal Health

Background:

  • Infectious bursal disease virus (IBDV) is a significant pathogen in poultry.
  • Effective cell culture models are crucial for studying IBDV replication and developing vaccines.
  • Mammalian cell lines offer potential alternatives to traditional avian cell cultures for virological studies.

Purpose of the Study:

  • To evaluate the susceptibility of three mammalian continuous cell lines (MA-104, Vero, BGM-70) to IBDV replication.
  • To compare the cytopathic effects (CPE) of IBDV in these cell lines with chicken embryo fibroblast (CEF) cultures.
  • To assess the utility of BGM-70 cells for virus-neutralization assays.

Main Methods:

  • Inoculation of MA-104, Vero, and BGM-70 cell lines with tissue-culture-adapted IBDV strains (vaccine and field isolates).
  • Observation and documentation of cytopathic effects (CPE) in the tested cell lines.
  • Comparison of CPE in BGM-70 cells and CEF cultures.
  • Determination of virus-neutralization titers using BGM-70 and CEF cultures.

Main Results:

  • IBDV replicated successfully in all three tested mammalian cell lines: MA-104, Vero, and BGM-70.
  • BGM-70 cells exhibited the most pronounced cytopathic effects upon IBDV infection.
  • The CPE observed in BGM-70 cells closely resembled that seen in CEF cultures.
  • Virus-neutralization titers determined in BGM-70 cultures showed good correlation with those obtained from CEF cultures.

Conclusions:

  • Mammalian cell lines, particularly BGM-70, can effectively support IBDV replication.
  • BGM-70 cells demonstrate a high susceptibility to IBDV and can serve as a suitable model for studying viral cytopathology.
  • BGM-70 cell cultures are a reliable alternative to CEF cultures for virus-neutralization assays in IBDV research.

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