RESUMO
Rodent-borne hantaviruses cause hemorrhagic fever with renal syndrome (HFRS) in the old world and hantavirus cardio-pulmonary syndrome (HCPS) in the new. Most cases of HCPS in North America are caused by Sin Nombre Virus (SNV). Current viral detection technologies depend upon the identification of anti-viral antibodies in patient serum. Detection of viral antigen may facilitate earlier detection of the pathogen. We describe here the characterization of two single-chain Fv antibodies (scFvs), selected from a large naïve phage antibody library, which are capable of identifying the Sin Nombre Virus nucleocapsid protein (SNV-N), with no cross reactivity with the nucleocapsid protein from other hantaviruses. The utility of such selected scFvs was increased by the creation of an scFv-alkaline phosphatase fusion protein which was able to directly detect virally produced material without the need for additional reagents.
Assuntos
Anticorpos Antivirais/imunologia , Síndrome Pulmonar por Hantavirus/imunologia , Região Variável de Imunoglobulina/imunologia , Proteínas do Nucleocapsídeo/imunologia , Vírus Sin Nombre/imunologia , Fosfatase Alcalina/genética , Fosfatase Alcalina/imunologia , Animais , Anticorpos Antivirais/genética , Afinidade de Anticorpos , Especificidade de Anticorpos , Chlorocebus aethiops , Clonagem Molecular , Reações Cruzadas , Ensaio de Imunoadsorção Enzimática , Síndrome Pulmonar por Hantavirus/diagnóstico , Região Variável de Imunoglobulina/genética , Proteínas do Nucleocapsídeo/análise , Proteínas do Nucleocapsídeo/genética , Biblioteca de Peptídeos , Proteínas Recombinantes de Fusão/imunologia , Proteínas Recombinantes/imunologia , Vírus Sin Nombre/genética , Células VeroRESUMO
The mechanism(s) by which Sin Nombre (SN) hantavirus is maintained in deer mouse populations is unclear. Field studies indicate that transmission occurs primarily if not exclusively via a horizontal mechanism. Using an experimental deer mouse infection model in an outdoor laboratory, we tested whether infected rodents shed SN virus in urine, feces, and saliva, whether infected mice transmit infection to naïve cage mates, and whether infected dams are able to vertically transmit virus or antibody to offspring. Using pooled samples of urine, feces, and saliva collected from mice infected 8 to 120 days postinoculation (p.i.), we found that a subset of saliva samples, collected between 15 and 90 days p.i., contained viral RNA. Parallel studies conducted on wild-caught, naturally infected deer mice showed a similar pattern of intermittent positivity, also only in saliva samples. Attempts to isolate virus through inoculation of cells or naïve deer mice with the secreta or excreta of infected mice were uniformly negative. Of 54 attempts to transmit infection by cohousing infected deer mice with seronegative cage mates, we observed only a single case of transmission, which occurred between 29 and 42 days p.i. Dams passively transferred antibodies to neonatal pups via milk, and those antibodies persisted for at least 2 months after weaning, but none transmitted infection to their pups. Compared to other hantavirus models, SN virus is shed less efficiently and transmits inefficiently among cage mates. Transmission of SN virus among reservoir rodents may require factors that are not required for other hantaviruses.
