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2.
J Gen Virol ; 90(Pt 1): 223-33, 2009 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-19088293

RESUMEN

Melao virus (MELV) strains BE AR8033 and BE AR633512 were isolated from pools of Ochlerotatus scapularis mosquitoes in Belém, Pará State (1955), and Alta Floresta, Rondônia State (2000), Brazil, respectively. The aim of the present study was to molecularly characterize these strains and to describe the histopathological, biochemical and immunological changes in golden hamsters (Mesocricetus auratus) following intraperitoneal injection of MELV strains. Hamsters were susceptible to both of the MELV strains studied. Viraemia was observed 3-6 days post-infection (p.i.) for BE AR633512 and only on the second day p.i. for BE AR8033. Neutralizing antibodies against both strains were detected in blood samples obtained at 5 days p.i. and persisted up to 30 days p.i. Aspartate aminotransferase, alanine aminotransferase and blood urea nitrogen were significantly altered in animals infected with the two MELV strains, while creatinine was only altered in animals inoculated with BE AR633512. Histopathological changes were observed in the central nervous system, liver, kidney and spleen of hamsters, and infection was confirmed by detection of specific MELV antigens by immunohistochemistry. Strain BE AR633512 caused more severe tissue damage than strain BE AR8033, showing increased neurovirulence and pathogenicity. Genetic analysis based on the full-length sequences of the glycoprotein (Gn and Gc) and nucleocapsid protein (N) genes revealed high levels of homology between the MELV strains. Interestingly, the greatest genetic divergence was found for the Gn gene of strain BE AR633512, in which several synonymous and non-synonymous mutations causing changes in RNA secondary structure were observed. Further studies will be necessary to investigate the role of Gn and Gc mutations in the MELV pathogenicity.


Asunto(s)
Infecciones por Bunyaviridae/patología , Infecciones por Bunyaviridae/fisiopatología , Mesocricetus/virología , Orthobunyavirus/genética , Orthobunyavirus/patogenicidad , Alanina Transaminasa/sangre , Animales , Anticuerpos Antivirales/sangre , Aspartato Aminotransferasas/sangre , Brasil , Infecciones por Bunyaviridae/inmunología , Infecciones por Bunyaviridae/virología , Sistema Nervioso Central/patología , Creatinina/sangre , Cricetinae , Riñón/patología , Hígado/patología , Modelos Moleculares , Pruebas de Neutralización , Conformación de Ácido Nucleico , Orthobunyavirus/inmunología , ARN Viral/genética , Análisis de Secuencia de ADN , Homología de Secuencia de Aminoácido , Bazo/patología , Urea/sangre , Viremia
3.
Am J Trop Med Hyg ; 73(6): 1050-8, 2005 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-16354811

RESUMEN

This paper reports the results of serologic, structural, biochemical, and genetic studies indicating that Araguari virus, a previously unassigned viral agent, is a member of the family Orthomyxoviridae and genus Thogotovirus. Araguari virus has six RNA fragments; biologically, it shares several properties with other viruses in the family Orthomyxoviridae. Nucleotide sequencing of the RNA segments 4 (glycoprotein) and 5 (nucleoprotein) of Araguari virus aligned with the orthomyxoviruses, showing the closest relationship with Thogoto virus (sequence similarity = 61.9% and 69.1%, respectively, for glycoprotein and nucleoprotein), but also sharing a more distant similarity with Dhori and Influenza C viruses, especially for the glycoprotein gene. Based on these results, we propose that Araguari virus should be assigned as a new member of the family Orthomyxoviridae and genus Thogotovirus.


Asunto(s)
Orthomyxoviridae/clasificación , Animales , Secuencia de Bases , Chlorocebus aethiops , Pruebas de Fijación del Complemento , ADN Complementario/análisis , Pruebas de Inhibición de Hemaglutinación , Marsupiales/virología , Microscopía Electrónica de Rastreo , Microscopía Electrónica de Transmisión , Microscopía Inmunoelectrónica , Datos de Secuencia Molecular , Orthomyxoviridae/genética , Orthomyxoviridae/ultraestructura , ARN Viral/análisis , Alineación de Secuencia , Células Vero
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