Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters










Database
Language
Publication year range
1.
J Med Virol ; 89(6): 1108-1111, 2017 06.
Article in English | MEDLINE | ID: mdl-27787907

ABSTRACT

Oropouche virus (OROV) is a frequent cause of arboviral febrile disease in the Amazon. The present report describes studies done in two patients, one of them; the first OROV human case acquired outside of the Amazon, which have revealed for the first time the presence of OROV in peripheral blood leukocytes. This novel finding raises important issues regarding pathogenesis of human infections and may offer a new tool, for the rapid diagnosis of this neglected infection. J. Med. Virol. 89:1108-1111, 2017. © 2017 Wiley Periodicals, Inc.


Subject(s)
Bunyaviridae Infections/virology , Leukocytes/virology , Orthobunyavirus/isolation & purification , Adolescent , Animals , Female , Humans , Male , Middle Aged
2.
Virus Res ; 155(1): 35-41, 2011 Jan.
Article in English | MEDLINE | ID: mdl-20727376

ABSTRACT

Oropouche virus (OROV), of the family Bunyaviridae, is the second most frequent arbovirus causing febrile disease in Brazil. In spite of this, little is known about pathogenesis of OROV infection. This report describes an experimental model of OROV in golden hamster (Mesocricetus auratus). Following subcutaneous inoculation of OROV, over 50% of the animals developed disease characterized by lethargy, ruffled fur, shivering, paralysis, and approximately one third died. Animals were sacrificed on days 1, 3, 5, 8 and 11 post-inoculation to collect tissue samples from brain, heart, liver, lung, spleen, muscle and blood for virus titration, histology and OROV immunohistochemistry. OROV was detected in high titers in blood, liver and brain, but not in the other organs. Histopathology revealed meningoencephalitis and hepatitis, with abundant OROV antigen detected in liver and brain. Diffuse galectin-3 immunostaining in brain and liver supports microglial and Kupfer cells activation. This is the first description of an experimental model for OROV infection and should be helpful to study pathogenesis and possibly to test antiviral interventions such as drugs and vaccine candidates.


Subject(s)
Bunyaviridae Infections/veterinary , Disease Models, Animal , Orthobunyavirus/pathogenicity , Rodent Diseases/pathology , Rodent Diseases/virology , Animal Structures/pathology , Animal Structures/virology , Animals , Brazil , Bunyaviridae Infections/pathology , Bunyaviridae Infections/virology , Cricetinae , Hepatitis, Viral, Animal/pathology , Hepatitis, Viral, Animal/virology , Histocytochemistry , Male , Meningoencephalitis/pathology , Meningoencephalitis/veterinary , Meningoencephalitis/virology , Mesocricetus/virology , Microscopy
3.
Virus Res ; 149(1): 56-63, 2010 Apr.
Article in English | MEDLINE | ID: mdl-20080135

ABSTRACT

Oropouche (OROV) is a single-stranded RNA arbovirus of the family Bunyaviridae, genus Orthobunyavirus, which has caused over half a million cases of febrile illness in Brazil in the past 30 years. OROV fever has been registered almost exclusively in the Amazon region, but global warming, deforestation and redistribution of vectors and animal reservoirs increases the risk of Oropouche virus emergence in other areas. OROV causes a cytolytical infection in cultured cells with characteristic cytopathic effect 48h post-infection. We have studied the mechanisms of apoptosis induced by OROV in HeLa cells and found that OROV causes DNA fragmentation detectable by gel electrophoresis and by flow cytometric analysis of the Sub-G1 population at 36h post-infection. Mitochondrial release of cytochrome C and activation of caspases 9 and 3 were also detected by western blot analysis. Lack of apoptosis induced by UV-inactivated OROV reveals that virus-receptor binding is not sufficient to induce cell death. Results obtained in cells treated with chloroquine and cycloheximide indicated that viral uncoating and replication are required for apoptosis induction by OROV. Furthermore, treatment of the cells with pan-caspase inhibitor prevented OROV-induced apoptosis without affecting virus progeny production. The results show that OROV infection in vitro causes apoptosis by an intracellular pathway involving mitochondria, and activated by a mechanism dependent on viral replication and protein synthesis.


Subject(s)
Apoptosis , Orthobunyavirus/pathogenicity , Viral Proteins/biosynthesis , Virulence Factors/biosynthesis , Caspase 3/metabolism , Caspase 9/metabolism , Cytochromes c/analysis , Cytoplasm/chemistry , DNA Fragmentation , HeLa Cells , Humans
SELECTION OF CITATIONS
SEARCH DETAIL
...