Replication of infectious bursal disease virus in continuous cell lines
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Abstract:
Three mammalian continuous cell lines--MA-104, Vero, and BGM-70--were tested for their ability to support replication of infectious bursal disease virus (IBDV). Selected tissue-culture-adapted vaccine strains and tissue-culture-adapted field isolates of IBDV replicated in the MA-104, Vero, and BGM-70 cells; cytopathic effects were most pronounced in the BGM-70 cells. The cytopathic effects of the viruses in BGM-70 cells and chicken embryo fibroblast (CEF) cultures were similar. Virus-neutralization titers of selected serum samples determined in BGM-70 cultures compared well with those obtained from CEF cultures.
Insights
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.