The following cell types are recommended for isolation of FMD virus
from clarified suspensions of field material.
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When grown as monolayers in tube cultures and rolled
after inoculation, BTY cells have been shown to be the most sensitive
for detecting field strains of all seven serotypes of FMD virus
(Snowdon, 1966;
Donaldson et
al., 1970; Ferris
and Donaldson, 1984).
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House
and House, (1989) compared the sensitivity of cattle, mice,
primary cell cultures, cryopreserved cell cultures and established
cell lines for demonstrating FMD virus and found that infectivity
titres obtained in freshly prepared BTY cells and by cattle intradermolingual
inoculation were highest and statistically indistinguishable.
Titres obtained by neonatal mouse inoculation were significantly
lower than the titres obtained in thyroid cultures for serotypes
A, C, Asia 1 and SAT 3. The cell cultures from cryopreserved newborn
ovine kidney and embryonic ovine kidney were significantly less
susceptible to serotype Asia1 than BTY cells but not significantly
different when compared with the cattle assay for all serotypes.
In terms of practicability and overall susceptibility cryopreserved
ovine kidney cells are a good alternative when BTY cells are unavailable.
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These systems are also sensitive for detecting FMD
virus strains, although less so (log10 0.5 - 1.0) than BTY cells.
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When maintained in a cell suspension plaque system,
BHK-21-CT cells have been found to be more sensitive than BHK
cells in other assay systems or neonatal mice, and can be used
to detect the presence of FMD virus under certain circumstances.
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Mice are an alternative to cell cultures. For maximum
sensitivity the mice must be 2-7 days of age and of selected breed
strains. Some field strains of virus may require several passages
before they become adapted to mice.
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