Dobrava, but not Saaremaa, hantavirus is lethal and induces nitric oxide production in suckling mice

Autor: Jonas Hardestam, Åke Lundkvist, Jonas Klingström
Rok vydání: 2006
Předmět:
Orthohantavirus
DOBV
Dobrava virus

viruses
Nitric Oxide Synthase Type II
Antibodies
Viral

Virus Replication
Mice
chemistry.chemical_compound
PUUV
Puumala virus

TULV
Tula virus

HFRS
hemorrhagic fever with renal syndrome

SAAV
Saaremaa virus

FFU
focus-forming units

SEOV
Seoul virus

Mice
Knockout

HCPS
hantavirus cardiopulmonary syndrome

SNV
Sin Nombre virus

biology
FRNT
focus reduction neutralizing test

Brain
virus diseases
N
nucleocapsid protein

Animals
Suckling

HTNV
Hantaan virus

Infectious Diseases
OD405
optical density at 405 nm

iNOS
inducible nitric oxide synthase

Bunyaviridae
Hantavirus
Hantavirus Infections
Immunology
Viremia
Nitric Oxide
Microbiology
Article
Gene Expression Regulation
Enzymologic

Virus
Nitric oxide
Saaremaa virus
Species Specificity
medicine
Animals
Nitrites
Hantaan virus
NO
nitric oxide

Nitrates
RT-PCR
reverse transcriptase PCR

biology.organism_classification
medicine.disease
Virology
chemistry
Viral replication
ANDV
Andes virus

TOPV
Topografov virus
Zdroj: Microbes and Infection
ISSN: 1286-4579
DOI: 10.1016/j.micinf.2005.09.010
Popis: Hantaviruses are the causative agents of HFRS and HCPS (hemorrhagic fever with renal syndrome and hantavirus cardiopulmonary syndrome), two severe, and often fatal human diseases. Mortality from HFRS varies between hantaviruses; Hantaan and Dobrava show the highest, Seoul intermediate, and Puumala low mortality. Saaremaa, genetically closely related to Dobrava, is also known to induce HFRS, with low or no mortality. In this study, mice were inoculated with Dobrava and Saaremaa viruses to test for infectibility, lethality, viremia, nitric oxide production and antibody responses. Out of suckling mice intracerebrally inoculated with 50, 500 and 5,000 focus-forming units of Dobrava virus, respectively, 1/8, 2/8 and 7/8 died within 18-26 days. In all but one of the lethally infected mice high levels of replicating virus were detected, and most were positive for neutralizing antibodies and showed elevated levels of nitric oxide production. All suckling mice intracerebrally inoculated with 50, 500, or 5,000 focus-forming units of Saaremaa virus survived and all seroconverted. Clearly lower viral titers were observed for the Saaremaa virus-inoculated mice, also when sacrificed at day 18 after infection, compared to those in mice that died following Dobrava virus infection. Dobrava, Saaremaa, Puumala and Hantaan virus infections of adult mice were asymptomatic, and the anti-nucleocapsid protein IgG2a/IgG1-titer ratio was higher in mice inoculated with Dobrava virus than in those inoculated with Saaremaa virus. Elevated nitric oxide production was not detected in asymptomatically infected mice, and iNOS-/- mice, like normal mice, cleared viremia. In conclusion, we show that Dobrava virus and Saaremaa virus induce distinct differences in terms of survival, viremia, nitric oxide production and antibody responses in mice.
Databáze: OpenAIRE