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. 2011 Nov 1;204(Suppl 3):S1066–S1074. doi: 10.1093/infdis/jir348

Table 1.

Recombinant Vesicular Stomatitis Virus Ebola Virus Glycoprotein Cross-Protective Efficacy in Rodent Models

Mice MA-ZEBOV Guinea Pigs GPA-ZEBOV
Vaccine survival (n survival/n total) Time to death (d) Survival (n survival/n total) Time to death (d)
Control 4/21 6.5 ± 1.5 0/6 7.3 ± 0.5
rVSVwt 5/21 5.6 ± 1.6 0/6 7.0 ± 0
rVSV-B-GP n.d. n.a. 1/6 9.4 ± 3.1
rVSV-CI-GP 22/22 n.a. 1/6 9.4 ± 2.3
rVSV-R-GP 20/20 n.a. 1/6 9.2 ± 2.5
rVSV-S Boniface-GP 15/20 6.8 ± 0.4 0/6 7.7 ± 0.5
rVSV-S Gulu-GP n.d. n.a. 0/6 7.8 ± 0.4
rVSV-Z Mayinga-GP 20/20 n.a. 6/6 n.d.
rVSV-Z Kikwit-GP n.a. n.a. 4/4 n.a.

NOTE. B = Bundibugyo ebolavirus (BEBOV); CI = Côte d'Ivoire ebolavirus (CIEBOV); GP = glycoprotein; GPA = guinea pig–adapted; MA - mouse-adapted; rVSV = recombinant vesicular stomatitis virus; R = Reston ebolavirus (REBOV); S = Sudan ebolavirus (SEBOV); wt = wild-type; Z = Zaire ebolavirus (ZEBOV); n.a., not applicable; n.d., not done.