Characterizing replication kinetics and plaque production of type I feline infectious peritonitis virus in three feline cell lines.

Virology

Department of Microbiology and Immunology, Loyola University of Chicago, Stritch School of Medicine, Maywood, IL, United States. Electronic address:

Published: December 2018

AI Article Synopsis

  • Investigating type I feline coronaviruses (FCoVs) in tissue culture is essential for understanding their virology and how they interact with hosts, but these strains have difficulty adapting to cell cultures.
  • The study characterizes the replication and plaque formation of type I strain FIPV Black in a specialized cell line (Fcwf-4 CU), finding that high virus levels can be obtained by 20 hours post-infection.
  • It concludes that Fcwf-4 CU cells can be effectively used for standardized plaque assays and are morphologically and functionally different from other cell types, showing reduced sensitivity to interferon.

Article Abstract

Investigating type I feline coronaviruses (FCoVs) in tissue culture is critical for understanding the basic virology, pathogenesis, and virus-host interactome of these important veterinary pathogens. This has been a perennial challenge as type I FCoV strains do not easily adapt to cell culture. Here we characterize replication kinetics and plaque formation of a model type I strain FIPV Black in Fcwf-4 cells established at Cornell University (Fcwf-4 CU). We determined that maximum virus titers (>10 pfu/mL) were recoverable from infected Fcwf-4 CU cell-free supernatant at 20 h post-infection. Type I FIPV Black and both biotypes of type II FCoV formed uniform and enumerable plaques on Fcwf-4 CU cells. Therefore, these cells were employable in a standardized plaque assay. Finally, we determined that the Fcwf-4 CU cells were morphologically distinct from feline bone marrow-derived macrophages and were less sensitive to exogenous type I interferon than were Fcwf-4 cells purchased from ATCC.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6483087PMC
http://dx.doi.org/10.1016/j.virol.2018.08.022DOI Listing

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