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1.
BMC Med ; 13: 102, 2015 Apr 30.
Article in English | MEDLINE | ID: mdl-25976325

ABSTRACT

BACKGROUND: In December 2013, an outbreak of Chikungunya virus (CHIKV) caused by the Asian genotype was notified in the Caribbean. The outbreak has since spread to 38 regions in the Americas. By September 2014, the first autochthonous CHIKV infections were confirmed in Oiapoque, North Brazil, and in Feira de Santana, Northeast Brazil. METHODS: We compiled epidemiological and clinical data on suspected CHIKV cases in Brazil and polymerase-chain-reaction-based diagnostic was conducted on 68 serum samples from patients with symptom onset between April and September 2014. Two imported and four autochthonous cases were selected for virus propagation, RNA isolation, full-length genome sequencing, and phylogenetic analysis. We then followed CDC/PAHO guidelines to estimate the risk of establishment of CHIKV in Brazilian municipalities. RESULTS: We detected 41 CHIKV importations and 27 autochthonous cases in Brazil. Epidemiological and phylogenetic analyses indicated local transmission of the Asian CHIKV genotype in Oiapoque. Unexpectedly, we also discovered that the ECSA genotype is circulating in Feira de Santana. The presumed index case of the ECSA genotype was an individual who had recently returned from Angola and developed symptoms in Feira de Santana. We estimate that, if CHIKV becomes established in Brazil, transmission could occur in 94% of municipalities in the country and provide maps of the risk of importation of each strain of CHIKV in Brazil. CONCLUSIONS: The etiological strains associated with the early-phase CHIKV outbreaks in Brazil belong to the Asian and ECSA genotypes. Continued surveillance and vector mitigation strategies are needed to reduce the future public health impact of CHIKV in the Americas.


Subject(s)
Chikungunya Fever/epidemiology , Chikungunya Fever/transmission , Chikungunya Fever/virology , Chikungunya virus/genetics , Adolescent , Adult , Aged , Brazil/epidemiology , Child , Child, Preschool , Disease Outbreaks , Female , Genotype , Humans , Infant , Infant, Newborn , Male , Middle Aged , Phylogeny , Public Health , Risk , Young Adult
2.
Genome Announc ; 2(6)2014 Nov 13.
Article in English | MEDLINE | ID: mdl-25395636

ABSTRACT

We report here the first nearly complete genome sequence related to curionopolis virus (CURV), that of strain AR440009, isolated from a pool of Culicoides sp. midges in Serra Norte, Pará State, northern Brazil. All genes showed similarities to those belonging to members of the family Rhabdoviridae.

3.
Genome Announc ; 2(6)2014 Nov 20.
Article in English | MEDLINE | ID: mdl-25414513

ABSTRACT

We report the genome, in a single chromosome, of Lactococcus lactis strain AI06, isolated from the mesocarp of the açaí fruit (Euterpe oleracea) in eastern Amazonia, Brazil. This strain is an endophyte of the açaí palm and also a component of the microbiota of the edible food product.

4.
PLoS One ; 3(3): e1733, 2008 Mar 05.
Article in English | MEDLINE | ID: mdl-18320052

ABSTRACT

In previous reports we proposed a new genus for Rhabdoviridae and described neurotropic preference and gross neuropathology in newborn albino Swiss mice after Curionopolis and Itacaiunas infections. In the present report a time-course study of experimental encephalitis induced by Itacaiunas and Curionopolis virus was conducted both in vivo and in vitro to investigate cellular targets and the sequence of neuroinvasion. We also investigate, after intranasal inoculation, clinical signs, histopathology and apoptosis in correlation with viral immunolabeling at different time points. Curionopolis and Itacaiunas viral antigens were first detected in the parenchyma of olfactory pathways at 2 and 3 days post-inoculation (dpi) and the first clinical signs were observed at 4 and 8 dpi, respectively. After Curionopolis infection, the mortality rate was 100% between 5 and 6 dpi, and 35% between 8 and 15 dpi after Itacaiunas infection. We identified CNS mice cell types both in vivo and in vitro and the temporal sequence of neuroanatomical olfactory areas infected by Itacaiunas and Curionopolis virus. Distinct virulences were reflected in the neuropathological changes including TUNEL immunolabeling and cytopathic effects, more intense and precocious after intracerebral or in vitro inoculations of Curionopolis than after Itacaiunas virus. In vitro studies revealed neuronal but not astrocyte or microglial cytopathic effects at 2 dpi, with monolayer destruction occurring at 5 and 7 dpi with Curionopolis and Itacaiunas virus, respectively. Ultrastructural changes included virus budding associated with interstitial and perivascular edema, endothelial hypertrophy, a reduced and/or collapsed small vessel luminal area, thickening of the capillary basement membrane, and presence of phagocytosed apoptotic bodies. Glial cells with viral budding similar to oligodendrocytes were infected with Itacaiunas virus but not with Curionopolis virus. Thus, Curionopolis and Itacaiunas viruses share many pathological and clinical features present in other rhabdoviruses but distinct virulence and glial targets in newborn albino Swiss mice brain.


Subject(s)
Encephalitis, Viral/pathology , Rhabdoviridae Infections/pathology , Rhabdoviridae/classification , Rhabdoviridae/pathogenicity , Animals , Animals, Newborn , Apoptosis , Brain/embryology , Brain/pathology , Brain/virology , Cells, Cultured , Disease Models, Animal , Encephalitis, Viral/etiology , Female , Fluorescent Antibody Technique , Immunoenzyme Techniques , Mice , Neuroglia/cytology , Neuroglia/metabolism , Neuroglia/virology , Neurons/cytology , Neurons/metabolism , Neurons/virology , Pregnancy , Rhabdoviridae Infections/virology
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