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1.
PLoS Pathog ; 16(9): e1008903, 2020 09.
Artículo en Inglés | MEDLINE | ID: mdl-32946524

RESUMEN

Vaccines are urgently needed to combat the global coronavirus disease 2019 (COVID-19) pandemic, and testing of candidate vaccines in an appropriate non-human primate (NHP) model is a critical step in the process. Infection of African green monkeys (AGM) with a low passage human isolate of SARS-CoV-2 by aerosol or mucosal exposure resulted in mild clinical infection with a transient decrease in lung tidal volume. Imaging with human clinical-grade 18F-fluoro-2-deoxy-D-glucose positron emission tomography (18F-FDG PET) co-registered with computed tomography (CT) revealed pulmonary lesions at 4 days post-infection (dpi) that resolved over time. Infectious virus was shed from both respiratory and gastrointestinal (GI) tracts in all animals in a biphasic manner, first between 2-7 dpi followed by a recrudescence at 14-21 dpi. Viral RNA (vRNA) was found throughout both respiratory and gastrointestinal systems at necropsy with higher levels of vRNA found within the GI tract tissues. All animals seroconverted simultaneously for IgM and IgG, which has also been documented in human COVID-19 cases. Young AGM represent an species to study mild/subclinical COVID-19 disease and with possible insights into live virus shedding. Future vaccine evaluation can be performed in AGM with correlates of efficacy being lung lesions by PET/CT, virus shedding, and tissue viral load.


Asunto(s)
Betacoronavirus , Infecciones por Coronavirus/diagnóstico por imagen , Tracto Gastrointestinal/virología , Neumonía Viral/diagnóstico por imagen , Esparcimiento de Virus/fisiología , Animales , COVID-19 , Chlorocebus aethiops , Infecciones por Coronavirus/virología , Pulmón/patología , Pulmón/virología , Pandemias , Neumonía Viral/virología , Tomografía Computarizada por Tomografía de Emisión de Positrones/métodos , SARS-CoV-2
2.
Pathog Dis ; 71(2): 219-26, 2014 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-24453160

RESUMEN

The use of common marmosets as an alternative non-human primate model for infectious disease research using BSL-3 viruses such as Rift Valley fever virus (RVFV) presents unique challenges with respect to housing, handling, and safety. Subject matter experts from veterinary care, animal husbandry, biosafety, engineering, and research were consulted to design a pilot experiment using marmosets infected with RVFV. This paper reviews the caging, handling, and safety-related adaptations and modifications that were required to humanely utilize marmosets as a model for high-hazard BSL-3 viral diseases.


Asunto(s)
Experimentación Animal , Animales de Laboratorio , Callithrix/fisiología , Control de Enfermedades Transmisibles/métodos , Contención de Riesgos Biológicos , Fiebre del Valle del Rift/diagnóstico , Fiebre del Valle del Rift/terapia , Animales , Investigación Biomédica/métodos , Modelos Animales de Enfermedad , Vivienda para Animales , Humanos , Masculino , Salud Laboral
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