TY - JOUR
T1 - Venezuelan equine encephalitis virus transmission and effect on pathogenesis
AU - Smith, Darci R.
AU - Aguilar, Patricia V.
AU - Coffey, Lark L.
AU - Gromowski, Gregory D.
AU - Wang, Eryu
AU - Weaver, Scott C.
PY - 2006
Y1 - 2006
N2 - Quantifying the dose of an arbovirus transmitted by mosquitoes is essential for designing pathogenesis studies simulating natural infection of vertebrates. Titration of saliva collected in vitro from infected mosquitoes may not accurately estimate titers transmitted during blood feeding, and infection by needle injection may affect vertebrate pathogenesis. We compared the amount of Venezuelan equine encephalitis virus collected from the saliva of Aedes taeniorhynchus to the amount injected into a mouse during blood feeding. Less virus was transmitted by mosquitoes in vivo (geometric mean 11 PFU) than was found for comparable times of salivation in vitro (mean saliva titer 74 PFU). We also observed slightly lower early and late viremia titers in mice that were needle injected with 8 PFU, which represents the low end of the in vivo transmission range. No differences in survival were detected, regardless of the dose or infection route.
AB - Quantifying the dose of an arbovirus transmitted by mosquitoes is essential for designing pathogenesis studies simulating natural infection of vertebrates. Titration of saliva collected in vitro from infected mosquitoes may not accurately estimate titers transmitted during blood feeding, and infection by needle injection may affect vertebrate pathogenesis. We compared the amount of Venezuelan equine encephalitis virus collected from the saliva of Aedes taeniorhynchus to the amount injected into a mouse during blood feeding. Less virus was transmitted by mosquitoes in vivo (geometric mean 11 PFU) than was found for comparable times of salivation in vitro (mean saliva titer 74 PFU). We also observed slightly lower early and late viremia titers in mice that were needle injected with 8 PFU, which represents the low end of the in vivo transmission range. No differences in survival were detected, regardless of the dose or infection route.
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U2 - 10.3201/eid1708.050841
DO - 10.3201/eid1708.050841
M3 - Article
C2 - 16965696
AN - SCOPUS:33750587276
SN - 1080-6040
VL - 12
SP - 1190
EP - 1196
JO - Emerging infectious diseases
JF - Emerging infectious diseases
IS - 8
ER -