TY - JOUR
T1 - Venezuelan equine encephalitis virus infection of spiny rats
AU - Carrara, Anne Sophie
AU - Gonzales, Marta
AU - Ferro, Cristina
AU - Tamayo, Margarita
AU - Aronson, Judith
AU - Paessler, Slobodan
AU - Anishchenko, Michael
AU - Boshell, Jorge
AU - Weaver, Scott C.
PY - 2005/5
Y1 - 2005/5
N2 - Enzootic strains of Venezuelan equine encephalitis virus (VEEV) circulate in forested habitats of Mexico, Central, and South America, and spiny rats (Proechimys spp.) are believed to be the principal reservoir hosts in several foci. To better understand the host-pathogen interactions and resistance to disease characteristic of many reservoir hosts, we performed experimental infections of F1 progeny from Proechimys chrysaeolus collected at a Colombian enzootic VEEV focus using sympatric and allopatric virus strains. All animals became viremic with a mean peak titer of 3.3 log10 PFU/mL, and all seroconverted with antibody titers from 1:20 to 1:640, which persisted up to 15 months. No signs of disease were observed, including after intracerebral injections. The lack of detectable disease and limited histopathologic lesions in these animals contrast dramatically with the severe disease and histopathologic findings observed in other laboratory rodents and humans, and support their role as reservoir hosts with a long-term coevolutionary relationship to VEEV.
AB - Enzootic strains of Venezuelan equine encephalitis virus (VEEV) circulate in forested habitats of Mexico, Central, and South America, and spiny rats (Proechimys spp.) are believed to be the principal reservoir hosts in several foci. To better understand the host-pathogen interactions and resistance to disease characteristic of many reservoir hosts, we performed experimental infections of F1 progeny from Proechimys chrysaeolus collected at a Colombian enzootic VEEV focus using sympatric and allopatric virus strains. All animals became viremic with a mean peak titer of 3.3 log10 PFU/mL, and all seroconverted with antibody titers from 1:20 to 1:640, which persisted up to 15 months. No signs of disease were observed, including after intracerebral injections. The lack of detectable disease and limited histopathologic lesions in these animals contrast dramatically with the severe disease and histopathologic findings observed in other laboratory rodents and humans, and support their role as reservoir hosts with a long-term coevolutionary relationship to VEEV.
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U2 - 10.3201/eid1105.041251
DO - 10.3201/eid1105.041251
M3 - Article
C2 - 15890116
AN - SCOPUS:17844407188
SN - 1080-6040
VL - 11
SP - 663
EP - 669
JO - Emerging infectious diseases
JF - Emerging infectious diseases
IS - 5
ER -