Development of a novel nonhuman primate model for Rift Valley fever.

Abstract:

:Rift Valley fever (RVF) virus (RVFV) can cause severe human disease characterized by either acute-onset hepatitis, delayed-onset encephalitis, retinitis and blindness, or a hemorrhagic syndrome. The existing nonhuman primate (NHP) model for RVF utilizes an intravenous (i.v.) exposure route in rhesus macaques (Macaca mulatta). Severe disease in these animals is infrequent, and large cohorts are needed to observe significant morbidity and mortality. To overcome these drawbacks, we evaluated the infectivity and pathogenicity of RVFV in the common marmoset (Callithrix jacchus) by i.v., subcutaneous (s.c.), and intranasal exposure routes to more closely mimic natural exposure. Marmosets were more susceptible to RVFV than rhesus macaques and experienced higher rates of morbidity, mortality, and viremia and marked aberrations in hematological and chemistry values. An overwhelming infection of hepatocytes was a major consequence of infection of marmosets by the i.v. and s.c. exposure routes. Additionally, these animals displayed signs of hemorrhagic manifestations and neurological impairment. Based on our results, the common marmoset model more closely resembles severe human RVF disease and is therefore an ideal model for the evaluation of potential vaccines and therapeutics.

journal_name

J Virol

journal_title

Journal of virology

authors

Smith DR,Bird BH,Lewis B,Johnston SC,McCarthy S,Keeney A,Botto M,Donnelly G,Shamblin J,Albariño CG,Nichol ST,Hensley LE

doi

10.1128/JVI.06190-11

subject

Has Abstract

pub_date

2012-02-01 00:00:00

pages

2109-20

issue

4

eissn

0022-538X

issn

1098-5514

pii

JVI.06190-11

journal_volume

86

pub_type

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