The genotypes of hepatitis B (HBV) and delta (HDV) viruses circulating among fulminant hepatitis cases from the western Amazon Basin of Brazil were characterized in this study. HBV and HDV isolates were obtained from liver samples from 14 patients who developed fulminant hepatitis and died during [1978][1979][1980][1981][1982][1983][1984][1985][1986][1987][1988][1989]. HBV DNA and HDV RNA were detected in all samples. Phylogenetic analyses of HDV sequences showed that they all clustered with previously characterized sequences of HDV genotype 3 (HDV-3). HBV genotypes F, A and D were found in 50.0, 28.6 and 21.4 % of cases, respectively. These results confirm the predominance of HDV-3 in South America and its association with the severe form of hepatitis, and the finding of the co-infection of HDV-3 with different genotypes of HBV suggests that the association between HDV-3 and HBV-F is not necessarily causally related to a more severe clinical course of infection.The Brazilian western Amazon Basin is considered a highly endemic area for hepatitis B (HBV) and delta (HDV) viruses (Bensabath & Dias, 1983; Bensabath et al., 1987;Braga et al., 2001;Fonseca et al., 1988;Viana et al., 2005). Severe hepatitis cases with peculiar clinical and histopathological features have been reported in this region. Cases of fulminant hepatitis with similar features have been described in other countries in northern South America (Colombia, Venezuela, Peru and Ecuador) and in the Central African Republic. This severe form of liver disease has been identified as HBV and HDV super-or coinfection (Bensabath et al., 1987; Buitrago et al., 1986;Casey, 1996;Casey et al., 1996; Hadler et al., 1984;Lesbordes et al., 1987;Ljunggren et al., 1985;Manock et al., 2000;Popper et al., 1983;Sjogren & Colichon, 1991;Torres & Mondolfi, 1991).The disease associated with HDV infection is typically more severe than that due to HBV infection alone, but its clinical spectrum ranges from asymptomatic carriage of the virus to very severe disease. A factor that may influence the course of disease is the genetical heterogeneity of HDV prevalent in different geographical areas (Casey, 1996;Rizzetto & Durazzo, 1991;Smedile et al., 1982). Only HDV genotype 3 (HDV-3) was identified in cases of fulminant hepatitis from different countries of South America and has been associated with the co-infecting HBV genotype F (HBV-F), which is also indigenous to South America, suggesting that HDV-3 alone or in combination with HBV-F could be an important determinant of the particularly severe form of HDV-related disease in this region (Casey, 1996;Nakano et al., 2001a, b). Bensabath et al. (1987) carried out a 5 year protocol during 1979-1984 in the Brazilian western Amazon Basin to study the epidemiology of HDV infection and its role in the aetiology of fulminant hepatitis. In that study, the authors observed a high endemicity of HBV and HDV infection and confirmed the presence of HDV as a major factor forThe GenBank/EMBL/DDBJ accession numbers for the sequences reported in ...

Oropouche fever has reemerged in Parauapebas and Porto de Moz municipalities, Pará State, Brazil. Serologic analysis (immunoglobulin M–ELISA) and virus isolation confirmed Oropouche virus (OROV) in both municipalities. Nucleotide sequencing of 2 OROV isolates from each location indicated genotypes I (Parauapebas) and II (Porto de Moz) in Brazil.

We describe 2 bat-transmitted outbreaks in remote, rural areas of Portel and Viseu Municipalities, Pará State, northern Brazil. Central nervous system specimens were taken after patients' deaths and underwent immunofluorescent assay and histopathologic examination for rabies antigens; also, specimens were injected intracerebrally into suckling mice in an attempt to isolate the virus. Strains obtained were antigenically and genetically characterized. Twenty-one persons died due to paralytic rabies in the 2 municipalities. Ten rabies virus strains were isolated from human specimens; 2 other cases were diagnosed by histopathologic examination. Isolates were antigenically characterized as Desmodus rotundus variant 3 (AgV3). DNA sequencing of 6 strains showed that they were genetically close to D. rotundus–related strains isolated in Brazil. The genetic results were similar to those obtained by using monoclonal antibodies and support the conclusion that the isolates studied belong to the same rabies cycle, the virus variants found in the vampire bat D. rotundus.

No abstract

We describe 2 bat-transmitted outbreaks in remote, rural areas of Portel and Viseu Municipalities, Pará State, northern Brazil. Central nervous system specimens were taken after patients' deaths and underwent immunofluorescent assay and histopathologic examination for rabies antigens; also, specimens were injected intracerebrally into suckling mice in an attempt to isolate the virus. Strains obtained were antigenically and genetically characterized. Twenty-one persons died due to paralytic rabies in the 2 municipalities. Ten rabies virus strains were isolated from human specimens; 2 other cases were diagnosed by histopathologic examination. Isolates were antigenically characterized as Desmodus rotundus variant 3 (AgV3). DNA sequencing of 6 strains showed that they were genetically close to D. rotundus–related strains isolated in Brazil. The genetic results were similar to those obtained by using monoclonal antibodies and support the conclusion that the isolates studied belong to the same rabies cycle, the virus variants found in the vampire bat D. rotundus.