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1.
Mem Inst Oswaldo Cruz ; 113(11): e180320, 2018 Oct 18.
Artigo em Inglês | MEDLINE | ID: mdl-30365646

RESUMO

BACKGROUND The first dengue cases in Brazil with laboratory confirmation occurred in the northern region of the country, with the isolation of two serotypes, dengue virus 1 (DENV-1) and DENV-4. In Ceará, the introduction of DENV-4 was reported during a DENV-1 epidemic in 2011, with only two isolations. OBJECTIVES The aim of this study was to characterise the first DENV-4 epidemic in the state of Ceará, Brazil. METHODS The study population was composed of patients with suspected dengue that were reported to health care units from January to December 2012. The laboratory confirmation of infection was made by viral isolation, reverse transcription polymerase chain reaction (RT-PCR), AgNS1, immunohistochemistry and IgM enzyme-linked immunosorbent assay (ELISA). MAIN CONCLUSIONS In the study year, 72,211 suspected dengue cases were reported and 51,865 of these cases (71.8%) were confirmed to be positive. Co-circulation of three serotypes, DENV-1, DENV-3 and DENV-4, was detected with a predominance of DENV-4 (95.3%). Most cases were not severe, but there were 44 fatal outcomes. DENV-4 Genotype II was identified for the first time in Ceará.


Assuntos
Vírus da Dengue/isolamento & purificação , Dengue/epidemiologia , Adolescente , Adulto , Distribuição por Idade , Idoso , Idoso de 80 Anos ou mais , Brasil/epidemiologia , Causas de Morte , Criança , Pré-Escolar , Ensaio de Imunoadsorção Enzimática , Epidemias , Feminino , Humanos , Imuno-Histoquímica , Lactente , Masculino , Pessoa de Meia-Idade , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Fatores de Risco , Sorogrupo , Distribuição por Sexo , Adulto Jovem
2.
Mem Inst Oswaldo Cruz ; 107(7): 940-5, 2012 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-23147153

RESUMO

In Niterói, state of Rio de Janeiro, dengue virus type 4 (DENV-4) was isolated for the first time in March 2011. We analysed the laboratory findings of the first cases and evaluated the use of molecular techniques for the detection of DENV-4 in Aedes aegypti that were field-caught. Conventional reverse transcriptase-polymerase chain reaction (RT-PCR) and Simplexa™ Dengue real-time RT-PCR confirmed DENV-4 infection in all cases. Additionally, DENV-4 was confirmed in a female Ae. aegypti with 1.08 x 10(3) copies/mL of virus, as determined by quantitative real-time RT-PCR. This is the first time the Simplexa™ Dengue real-time assay has been used for the classification of cases of infection and for entomological investigations. The use of these molecular techniques was shown to be important for the surveillance of dengue in humans and vectors.


Assuntos
Aedes/virologia , Vírus da Dengue/genética , Dengue/virologia , Insetos Vetores/virologia , Animais , Brasil , Vírus da Dengue/isolamento & purificação , Feminino , Humanos , Masculino , Reação em Cadeia da Polimerase Via Transcriptase Reversa
3.
Vaccine ; 40(5): 798-810, 2022 01 31.
Artigo em Inglês | MEDLINE | ID: mdl-34969545

RESUMO

The present investigation comprised two independent observational arms to evaluate the influence of pre-existing flavivirus humoral immunity and the age-impact on 17DD-YF vaccination immunity. Flavivirus (YFV; DENV; ZIKV) serology and YF-specific cellular immunity was evaluated in 288 children/9Mths-4Yrs and 288 adults/18-49Yrs residents of areas without YFV circulation. Data demonstrated that flavivirus seropositivity at baseline was higher in Adults as compared to Children (26%;87%;67% vs 6%;13%;15%, respectively). The heterologous flavivirus seropositivity (DENV; ZIKV) did not impact the YF-specific cellular immune response at baseline. However, higher levels of NCD4, EMCD8, IFN-MCD8, NCD19 and nCMCD19 were observed in subjects with pre-existing YFV seropositivity. Primary vaccination of YFV-seronegative volunteers led to higher levels of YF-neutralizing antibodies in Adults as compared to Younger Children (9Mths-2Yrs). Although similar seropositivity rates observed amongst Children and Adults at D30-45, lower rates were observed in Younger Children (9Mths-2Yrs) at D365 (94%;95%;100% vs 87%;96%;99%, respectively). A progressive decline in antibody levels were reported at D365, being more expressive in Children as compared to Adults. All age-subgroups exhibited at D30-45 increased levels of eEfCD4, EMCD4, IFN-MCD8 and nCMCD19 together with a decrease of eEfCD8 and CMCD8. While an increase of EMCD8 were observed in all subgroups at D30-45, a declined duration at D365 was reported only in Younger Children (9Mths-2Yrs). Biomarker signatures further support that only Younger Children (9Mths-2Yrs) presented a progressive decline of EMCD8 at D365. Together, these findings demonstrated that regardless the similarities observed in YF-neutralizing antibodies, the age impacts the duration of cellular immune response to primary 17DD-YF vaccination.


Assuntos
Vacina contra Febre Amarela , Febre Amarela , Infecção por Zika virus , Zika virus , Adulto , Anticorpos Neutralizantes , Anticorpos Antivirais , Criança , Humanos , Imunidade Celular , Vacinação , Febre Amarela/prevenção & controle , Vírus da Febre Amarela
4.
PLoS Negl Trop Dis ; 7(3): e2095, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-23516646

RESUMO

In Brazil, dengue has been a major public health problem since its introduction in the 1980s. Phylogenetic studies constitute a valuable tool to monitor the introduction and spread of viruses as well as to predict the potential epidemiological consequences of such events. Aiming to perform the molecular characterization and phylogenetic analysis of DENV-2 during twenty years of viral activity in the country, viral strains isolated from patients presenting different disease manifestations (n = 34), representing six states of the country, from 1990 to 2010, were sequenced. Partial genome sequencing (genes C/prM/M/E) was performed in 25 DENV-2 strains and full-length genome sequencing (coding region) was performed in 9 strains. The percentage of similarity among the DENV-2 strains in this study and reference strains available in Genbank identified two groups epidemiologically distinct: one represented by strains isolated from 1990 to 2003 and one from strains isolated from 2007 to 2010. No consistent differences were observed on the E gene from strains isolated from cases with different clinical manifestations analyzed, suggesting that if the disease severity has a genetic origin, it is not only due to the differences observed on the E gene. The results obtained by the DENV-2 full-length genome sequencing did not point out consistent differences related to a more severe disease either. The analysis based on the partial and/or complete genome sequencing has characterized the Brazilian DENV-2 strains as belonging to the Southeast Asian genotype, however a distinction of two Lineages within this genotype has been identified. It was established that strains circulating prior DENV-2 emergence (1990-2003) belong to Southeast Asian genotype, Lineage I and strains isolated after DENV-2 emergence in 2007 belong to Southeast Asian genotype, Lineage II. Furthermore, all DENV-2 strains analyzed presented an asparagine (N) in E390, previously identified as a probable genetic marker of virulence observed in DHF strains from Asian origin. The percentage of identity of the latter with the Dominican Republic strain isolated in 2001 combined to the percentage of divergence with the strains first introduced in the country in the 1990s suggests that those viruses did not evolve locally but were due to a new viral Lineage introduction in the country from the Caribbean.


Assuntos
Vírus da Dengue/classificação , Vírus da Dengue/isolamento & purificação , Dengue/epidemiologia , Dengue/virologia , Filogenia , Brasil/epidemiologia , Análise por Conglomerados , Vírus da Dengue/genética , Genótipo , Humanos , Epidemiologia Molecular , Dados de Sequência Molecular , RNA Viral/genética , Análise de Sequência de DNA
5.
Mem. Inst. Oswaldo Cruz ; 113(11): e180320, 2018. tab, graf
Artigo em Inglês | LILACS | ID: biblio-976230

RESUMO

BACKGROUND The first dengue cases in Brazil with laboratory confirmation occurred in the northern region of the country, with the isolation of two serotypes, dengue virus 1 (DENV-1) and DENV-4. In Ceará, the introduction of DENV-4 was reported during a DENV-1 epidemic in 2011, with only two isolations. OBJECTIVES The aim of this study was to characterise the first DENV-4 epidemic in the state of Ceará, Brazil. METHODS The study population was composed of patients with suspected dengue that were reported to health care units from January to December 2012. The laboratory confirmation of infection was made by viral isolation, reverse transcription polymerase chain reaction (RT-PCR), AgNS1, immunohistochemistry and IgM enzyme-linked immunosorbent assay (ELISA). MAIN CONCLUSIONS In the study year, 72,211 suspected dengue cases were reported and 51,865 of these cases (71.8%) were confirmed to be positive. Co-circulation of three serotypes, DENV-1, DENV-3 and DENV-4, was detected with a predominance of DENV-4 (95.3%). Most cases were not severe, but there were 44 fatal outcomes. DENV-4 Genotype II was identified for the first time in Ceará.


Assuntos
Causas de Morte/tendências , Dengue/transmissão , Dengue/epidemiologia , Brasil/epidemiologia
11.
Artigo em Inglês | Arca: Repositório institucional da Fiocruz | ID: arc-47306
17.
Tese em Português | Arca: Repositório institucional da Fiocruz | ID: arc-30264

RESUMO

Este trabalho apresenta a análise filogenética, filogeográfica e caracterização molecular de amostras do vírus dengue tipo 1 (DENV-1) no Brasil no período de 30 anos (1986 - 2016). O estudo foi conduzido, inicialmente, com a análise filogenética, caracterização molecular e análise de recombinação do gene E de 48 amostras e da região codificante completa de 6 amostras do período de 1986 a 2011. Foi demonstrado que todos os vírus analisados pertenciam ao genótipo V, porém agrupando-se em diferentes linhagens no Brasil. Posteriormente, foi realizada a reconstrução da história evolutiva do genótipo V nas Américas com mais de 3 mil sequências disponíveis no Genbank, incluindo as brasileiras e observou-se que a diversidade do genótipo V do DENV-1 no continente resultou da evolução local a partir de duas cepas introduzidas da Índia por volta do início dos anos 70 e 80, independentemente. A primeira cepa sendo responsável pela maioria das infecções pelo genótipo V nas Américas, enquanto a segunda parecendo estar restrita principalmente ao Brasil As Pequenas Antilhas foram a principal origem das linhagens de DENV-1 disseminadas nas Américas até meados da década de 1980; e Venezuela e Nicarágua se tornaram posteriormente os países mais importantes de manutenção e disseminação viral no continente. Embora várias linhagens de DENV-1 tenham estabelecido surtos de sucesso em diferentes países da América durante os anos 1980, elas foram posteriormente disseminadas e extintas com dinâmicas distintas. Com o intuito de demonstrar a circulação continuada do DENV-1 no Brasil até 2016, conduzimos o estudo sobre a caracterização molecular e o padrão de dispersão dos DENV-1 brasileiros entre os anos de 2012 a 2016, período após a reemergência deste sorotipo no país. Nossos achados demonstraram que as diferentes linhagens do genótipo V continuaram cocirculando no Brasil até o ano de 2016. No entanto, duas novas substituições de aminoácidos localizadas nos domínios II e III do gene E foram identificadas nas amostras do Brasil e Argentina. Foram também demonstrado um evento de dispersão do Brasil para China, provavelmente relacionado a um caso pontual de viagem e um caso de coinfecção por DENV-1/DENV-4 em um paciente do estado do Rio de Janeiro no ano de 2012, nunca identificado até então. Os dados desta tese ressaltam a importância da vigilância molecular constante dos sorotipos, genótipos e linhagens no território brasileiro.


Assuntos
Vírus da Dengue , Evolução Molecular
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