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. Author manuscript; available in PMC: 2012 Jan 1.
Published in final edited form as: Virus Res. 2010 Sep 21;155(1):112–122. doi: 10.1016/j.virusres.2010.09.007

Table 1.

In vitro host range and replicative capacity of DURV and other selected rhabdoviruses.

DURV FARV FLAV KLAV VSINV
Vero 6.68 (3)a 9.15 (2) 5.73 (2) 7.63 (4) 9.20 (2)
CPAE 5.67 (2) 7.60 (3) nd 6.67 (6) 8.06 (2)
Tb 1 Lu 5.24 (3) 7.62 (3) nd 4.26 (4) 7.27 (5)
PDE ndb 7.63 (2) nd 4.20 (3) 6.42 (5)c
QNR/K2 6.72 (4) 8.33 (3) nd nd 7.55 (2)
C6/36 nd nd 3.30 (4) nd nd
FHM nd 6.94 (3) nd nd nd
TH-1 nd 6.89 (3) nd nd 8.63 (3)
VH-2 nd nd nd nd 7.58 (5)
a

Maximum titers (log10 PFU/mL) reached over the 8-day growth period are given, followed by the day at which the maximum titer was reached in parentheses.

b

nd, not detected above input level; i.e., maximum titer recovered never exceeded the initial inoculum/mL.

c

PDE cells were essentially non-permissive to VSINV infection, as previously reported by Levinson et al. (1978); titer given at day 5 represents the single well of eight in which a titer above the initial inoculum was recorded. Nucleotide sequencing of the G protein from the initial inoculum versus virus harvested on day 5 did not disclose any nucleotide substitutions, suggesting adaptation of VSINV to PDE cells was not at the level of receptor binding.