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J Virol Methods. 2003 Feb;107(2):163-7.

A feline kidney cell line-based plaque assay for feline calicivirus, a surrogate for Norwalk virus.

Author information

1
Health Canada, Food Directorate, Bureau of Microbial Hazards, PL#2204A2, Tunney's Pasture, Sir F.R.G. Banting Building, Rose Ave., Ont., K1A 0L2, Ottawa, Canada. sabah_bidawid@hc-sc.gc.ca

Abstract

Feline calicivirus (FCV) has been used by researchers as a surrogate for Norwalk virus (NV), since they share a similar genomic organization, physicochemical characteristics, and are grouped in the same family, Caliciviridae. Unlike NV, however, FCV can grow in established cell lines and produce a syncytial form of cytopathic effect. In this report, we describe the development and standardization of a plaque assay for FCV using monolayers of an established line of feline kidney (CrFK) cells in 12-well cell culture plates. The assay method has demonstrated reproducibility, ease of performance and resulted in clear plaque zones, readable in 24 h after virus inoculation. The infectivity titre of the virus by this plaque assay agreed well with tissue culture infectious dose(50) (TCID(50)) determinations. The described plaque assay would be a valuable tool in conducting various quantitative investigations using FCV as a model for NV and Norwalk-like viruses (NLV).

PMID:
12505630
DOI:
10.1016/s0166-0934(02)00214-8
[Indexed for MEDLINE]

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