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1.
Diagnostics (Basel) ; 13(13)2023 Jul 07.
Article in English | MEDLINE | ID: mdl-37443699

ABSTRACT

Chikungunya (CHIK) is a debilitating mosquito-borne disease with an epidemiology and early clinical symptoms similar to those of other arboviruses-triggered diseases such as dengue or Zika. Accurate and rapid diagnosis of CHIK virus (CHIKV) infection is therefore challenging. This international study evaluated the performance of the automated VIDAS® anti-CHIKV IgM and IgG assays compared to that of manual competitor IgM and IgG ELISA for the detection of anti-CHIKV IgM and IgG antibodies in 660 patients with suspected CHIKV infection. Positive and negative agreements of the VIDAS® CHIKV assays with ELISA ranged from 97.5% to 100.0%. The sensitivity of the VIDAS® CHIKV assays evaluated in patients with a proven CHIKV infection confirmed reported kinetics of anti-CHIKV IgM and IgG response, with a positive detection of 88.2-100.0% for IgM ≥ 5 days post symptom onset and of 100.0% for IgG ≥ 11 days post symptom onset. Our study also demonstrated the superiority of ELISA and VIDAS® assays over rapid diagnostic IgM/IgG tests. The analytical performance of VIDAS® anti-CHIKV IgM and IgG assays was excellent, with a high precision (coefficients of variation ≤ 7.4%) and high specificity (cross-reactivity rate ≤ 2.9%). This study demonstrates the suitability of the automated VIDAS® anti-CHIKV IgM and IgG assays to diagnose CHIKV infections and supports its applicability for epidemiological surveillance and differential diagnosis in regions endemic for CHIKV.

2.
Viruses ; 14(7)2022 07 14.
Article in English | MEDLINE | ID: mdl-35891521

ABSTRACT

During these past years, several studies have provided serological evidence regarding the circulation of West Nile virus (WNV) in Brazil. Despite some reports, much is still unknown regarding the genomic diversity and transmission dynamics of this virus in the country. Recently, genomic monitoring activities in horses revealed the circulation of WNV in several Brazilian regions. These findings on the paucity of genomic data reinforce the need for prompt investigation of WNV infection in horses, which may precede human cases of encephalitis in Brazil. Thus, in this study, we retrospectively screened 54 suspicious WNV samples collected between 2017 and 2020 from the spinal cord and brain of horses with encephalitis and generated three new WNV genomes from the Ceará and Bahia states, located in the northeastern region of Brazil. The Bayesian reconstruction revealed that at least two independent introduction events occurred in Brazil. The first introduction event appears to be likely related to the North American outbreak, and was estimated to have occurred in March 2013.The second introduction event appears to have occurred in September 2017 and appears to be likely related to the South American outbreak. Together, our results reinforce the importance of increasing the priority of WNV genomic monitoring in equines with encephalitis in order to track the dispersion of this emerging pathogen through the country.


Subject(s)
Horse Diseases , West Nile Fever , West Nile virus , Animals , Antibodies, Viral , Bayes Theorem , Brazil/epidemiology , Horse Diseases/epidemiology , Horses , Humans , Retrospective Studies , West Nile Fever/epidemiology , West Nile Fever/veterinary , West Nile virus/genetics
3.
Vaccine ; 40(5): 798-810, 2022 01 31.
Article in English | MEDLINE | ID: mdl-34969545

ABSTRACT

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.


Subject(s)
Yellow Fever Vaccine , Yellow Fever , Zika Virus Infection , Zika Virus , Adult , Antibodies, Neutralizing , Antibodies, Viral , Child , Humans , Immunity, Cellular , Vaccination , Yellow Fever/prevention & control , Yellow fever virus
4.
Slavov, Svetoslav Nanev; Fonseca, Vagner; Wilkinson, Eduan; Tegally, Houriiyah; Patané, José Salvatore Leister; Viala, Vincent Louis; San, Emmanuel James; Rodrigues, Evandra Strazza; Santos, Elaine Vieira; Aburjaile, Flavia; Xavier, Joilson; Fritsch, Hegger; Adelino, Talita Emile Ribeiro; Pereira, Felicidade; Leal, Arabela; Iani, Felipe Campos de Melo; Pereira, Glauco de Carvalho; Vazquez, Cynthia; Sanabria, Gladys Mercedes Estigarribia; Oliveira, Elaine Cristina de; Demarchi, Luiz; Croda, Julio; Bezerra, Rafael dos Santos; Lima, Loyze Paola Oliveira de; Barros, Claudia Renata dos Santos; Marqueze, Elaine Cristina; Bernardino, Jardelina de Souza Todão; Moretti, Debora Botequio; Brassaloti, Ricardo Augusto; Cassano, Raquel de Lello Rocha Campos; Mariani, Pilar Drummond Sampaio Corrêa; Kitajima, João Paulo; Santos, Bibiana; Proto-Siqueira, Rodrigo; Cantarelli, Vlademir Vicente; Tosta, Stephane; Nardy, Vanessa Brandão; Silva, Luciana Reboredo de Oliveira da; Gómez, Marcela Kelly Astete; Lima, Jaqueline Gomes; Ribeiro, Adriana Aparecida; Guimarães, Natália Rocha; Watanabe, Luiz Takao; Silva, Luana Barbosa Da; Ferreira, Raquel da Silva; Penha, Mara Patricia F. da; Ortega, María José; Fuente, Andrea Gómez de la; Villalba, Shirley; Torales, Juan; Gamarra, María Liz; Aquino, Carolina; Figueredo, Gloria Patricia Martínez; Fava, Wellington Santos; Motta-Castro, Ana Rita C.; Venturini, James; Oliveira, Sandra Maria do Vale Leone de; Gonçalves, Crhistinne Cavalheiro Maymone; Rossa, Maria do Carmo Debur; Becker, Guilherme Nardi; Giacomini, Mayra Presibella; Marques, Nelson Quallio; Riediger, Irina Nastassja; Raboni, Sonia; Mattoso, Gabriela; Cataneo, Allan D.; Zanluca, Camila; Santos, Claudia N. Duarte dos; Assato, Patricia Akemi; Costa, Felipe Allan da Silva da; Poleti, Mirele Daiana; Lesbon, Jessika Cristina Chagas; Mattos, Elisangela Chicaroni; Banho, Cecilia Artico; Sacchetto, Lívia; Moraes, Marília Mazzi; Grotto, Rejane Maria Tommasini; Souza-Neto, Jayme A.; Nogueira, Maurício Lacerda; Fukumasu, Heidge; Coutinho, Luiz Lehmann; Calado, Rodrigo Tocantins; Machado Neto, Raul; Filippis, Ana Maria Bispo de; Cunha, Rivaldo Venancio da; Freitas, Carla; Peterka, Cassio Roberto Leonel; Fernandes, Cássia de Fátima Rangel; Navegantes, Wildo; Said, Rodrigo Fabiano do Carmo; Melo, Carlos F. Campelo de A e; Almiron, Maria; Lourenço, José; Oliveira, Tulio de; Holmes, Edward C.; Haddad, Ricardo; Sampaio, Sandra Coccuzzo; Elias, Maria Carolina; Kashima, Simone; Alcantara, Luiz Carlos Junior de; Covas, Dimas Tadeu.
Nat Microbiol, in press, ago. 2022
Article in English | Sec. Est. Saúde SP, SESSP-IBPROD, Sec. Est. Saúde SP | ID: bud-4488

ABSTRACT

The high numbers of COVID-19 cases and deaths in Brazil have made Latin America an epicentre of the pandemic. SARS-CoV-2 established sustained transmission in Brazil early in the pandemic, but important gaps remain in our understanding of virus transmission dynamics at a national scale. We use 17,135 near-complete genomes sampled from 27 Brazilian states and bordering country Paraguay. From March to November 2020, we detected co-circulation of multiple viral lineages that were linked to multiple importations (predominantly from Europe). After November 2020, we detected large, local transmission clusters within the country. In the absence of effective restriction measures, the epidemic progressed, and in January 2021 there was emergence and onward spread, both within and abroad, of variants of concern and variants under monitoring, including Gamma (P.1) and Zeta (P.2). We also characterized a genomic overview of the epidemic in Paraguay and detected evidence of importation of SARS-CoV-2 ancestor lineages and variants of concern from Brazil. Our findings show that genomic surveillance in Brazil enabled assessment of the real-time spread of emerging SARS-CoV-2 variants.

5.
Pathogens ; 9(12)2020 Nov 26.
Article in English | MEDLINE | ID: mdl-33255865

ABSTRACT

The Chikungunya virus infection in Brazil has raised several concerns due to the rapid dissemination of the virus and its association with several clinical complications. Nevertheless, there is limited information about the genomic epidemiology of CHIKV circulating in Brazil from surveillance studies. Thus, to better understand its dispersion dynamics in Rio de Janeiro (RJ), one of the most affected states during the 2016-2019 epidemic waves, we generated 23 near-complete genomes of CHIKV isolates from two main cities located in the metropolitan mesoregion, obtained directly from clinical samples. Our phylogenetic reconstructions suggest the 2019-CHIKV-ECSA epidemic in RJ state was characterized by the co-circulation of multiple clade (clade A and B), highlighting that two independent introduction events of CHIKV-ECSA into RJ state have occurred between 2016-2019, both mediated from the northeastern region. Interestingly, we identified that the two-clade displaying eighteen characteristic amino acids changes among structural and non-structural proteins. Our findings reinforce that genomic data can provide information about virus genetic diversity and transmission dynamics, which might assist in the arbovirus epidemics establishing of an effective surveillance framework.

6.
PLoS Negl Trop Dis ; 13(5): e0007231, 2019 05.
Article in English | MEDLINE | ID: mdl-31067235

ABSTRACT

In recent years, an increasing number of outbreaks of Dengue, Chikungunya and Zika viruses have been reported in Asia and the Americas. Monitoring virus genotype diversity is crucial to understand the emergence and spread of outbreaks, both aspects that are vital to develop effective prevention and treatment strategies. Hence, we developed an efficient method to classify virus sequences with respect to their species and sub-species (i.e. serotype and/or genotype). This tool provides an easy-to-use software implementation of this new method and was validated on a large dataset assessing the classification performance with respect to whole-genome sequences and partial-genome sequences. Available online: http://krisp.org.za/tools.php.


Subject(s)
Chikungunya virus/isolation & purification , Computational Biology/methods , Dengue Virus/isolation & purification , Zika Virus/isolation & purification , Chikungunya Fever/virology , Chikungunya virus/classification , Chikungunya virus/genetics , Dengue/virology , Dengue Virus/classification , Dengue Virus/genetics , Genome, Viral , Genotype , Phylogeny , Zika Virus/classification , Zika Virus/genetics , Zika Virus Infection/virology
7.
Sci Rep ; 9(1): 2760, 2019 02 26.
Article in English | MEDLINE | ID: mdl-30809003

ABSTRACT

Brazil, which is hyperendemic for dengue virus (DENV), has had recent Zika (ZIKV) and (CHIKV) Chikungunya virus outbreaks. Since March 2016, CHIKV is the arbovirus infection most frequently diagnosed in Rio de Janeiro. In the analysis of 1835 syndromic patients, screened by real time RT-PCR, 56.4% of the cases were attributed to CHIKV, 29.6% to ZIKV, and 14.1% to DENV-4. Sequence analyses of CHIKV from sixteen samples revealed that the East-Central-South-African (ECSA) genotype of CHIKV has been circulating in Brazil since 2013 [95% bayesian credible interval (BCI): 03/2012-10/2013], almost a year before it was detected by arbovirus surveillance program. Brazilian cases are related to Central African Republic sequences from 1980's. To the best of our knowledge, given the available sequence published here and elsewhere, the ECSA genotype was likely introduced to Rio de Janeiro early on 2014 (02/2014; BCI: 07/2013-08/2014) through a single event, after primary circulation in the Bahia state at the Northestern Brazil in the previous year. The observation that the ECSA genotype of CHIKV was circulating undetected underscores the need for improvements in molecular methods for viral surveillance.


Subject(s)
Chikungunya Fever/diagnosis , Chikungunya virus/genetics , Bayes Theorem , Brazil/epidemiology , Chikungunya Fever/epidemiology , Chikungunya Fever/virology , Chikungunya virus/classification , Chikungunya virus/isolation & purification , Genotype , High-Throughput Nucleotide Sequencing , Humans , Phylogeny , RNA, Viral/chemistry , RNA, Viral/metabolism , Sequence Analysis, RNA
8.
Mem Inst Oswaldo Cruz ; 113(8): e180036, 2018 Jun 25.
Article in English | MEDLINE | ID: mdl-29947712

ABSTRACT

The dengue virus (DENV), of the genus Flavivirus (Flaviviridae), has four antigenically distinct serotypes, of which DENV-3 is classified into five genotypes. Here, we describe the detection of DENV-3 genotype I in sera of a Brazilian patient travelling from Singapore to Rio de Janeiro, Brazil, by using multiplex real-time RT-PCR, DNA sequencing of the whole envelope protein gene, and phylogenetic analysis. The virus shares ancestry with those identified in Bali, Indonesia, in 2015. It is possible that arboviruses such as Chikungunya ECSA genotype, DENV-4 genotype I, and Zika were introduced in Brazil from other continents during the multiple international events hosted by the country over the last four years, including World Youth Day, the Soccer World Cup, and the Summer Olympics.


Subject(s)
Communicable Diseases, Imported/virology , Dengue Virus/genetics , Dengue/virology , Genotype , Zika Virus Infection/virology , Zika Virus/genetics , Brazil , Dengue Virus/isolation & purification , Genetic Variation , Humans , Phylogeny , Polymerase Chain Reaction , Sequence Analysis, DNA , Serogroup
9.
Mem Inst Oswaldo Cruz ; 111(8): 532-4, 2016 Aug.
Article in English | MEDLINE | ID: mdl-27581122

ABSTRACT

Zika virus (ZIKV) has infected thousands of Brazilian people and spread to other American countries since 2015. The introduction of ZIKV brought a strong impact to public health in Brazil. It is of utmost importance to identify a susceptible cell line that will enable the isolation and identification of the virus from patient samples, viral mass production, and testing of drug and vaccine candidates. Besides real-time reverse transcriptase polymerase chain reaction diagnosis for detecting the viral genome, virus isolation in cell lines was useful in order to study the structure of the viral particle and its behaviour inside cells. Analysis of ZIKV infected cell lines was achieved using transmission electron microscopy (TEM). Blood was obtained from a Brazilian patient during the first days after presenting with signs of the disease, and ZIKV from the patient's blood was isolated in the C6/36 mosquito cell line. Afterwards, Vero cells were inoculated with the viral suspension, fixed six days after inoculation, embedded in polymers, and ultra-thin cut. Like dengue viruses, this flavivirus showed numerous virus particles present inside cellular vesicles thereby confirming the susceptibility of the Vero cell line to ZIKV replication. TEM is a unique technique available to make the virus visible.


Subject(s)
Virion/ultrastructure , Zika Virus/ultrastructure , Animals , Cell Culture Techniques , Chlorocebus aethiops , Genome, Viral , Humans , Microscopy, Electron, Transmission , Real-Time Polymerase Chain Reaction , Vero Cells , Virus Replication
10.
Mem. Inst. Oswaldo Cruz ; 111(8): 532-534, Aug. 2016. graf
Article in English | LILACS | ID: lil-788996

ABSTRACT

Zika virus (ZIKV) has infected thousands of Brazilian people and spread to other American countries since 2015. The introduction of ZIKV brought a strong impact to public health in Brazil. It is of utmost importance to identify a susceptible cell line that will enable the isolation and identification of the virus from patient samples, viral mass production, and testing of drug and vaccine candidates. Besides real-time reverse transcriptase polymerase chain reaction diagnosis for detecting the viral genome, virus isolation in cell lines was useful in order to study the structure of the viral particle and its behaviour inside cells. Analysis of ZIKV infected cell lines was achieved using transmission electron microscopy (TEM). Blood was obtained from a Brazilian patient during the first days after presenting with signs of the disease, and ZIKV from the patient’s blood was isolated in the C6/36 mosquito cell line. Afterwards, Vero cells were inoculated with the viral suspension, fixed six days after inoculation, embedded in polymers, and ultra-thin cut. Like dengue viruses, this flavivirus showed numerous virus particles present inside cellular vesicles thereby confirming the susceptibility of the Vero cell line to ZIKV replication. TEM is a unique technique available to make the virus visible.


Subject(s)
Humans , Animals , Virion/ultrastructure , Zika Virus/ultrastructure , Cell Culture Techniques , Chlorocebus aethiops , Genome, Viral , Microscopy, Electron, Transmission , Real-Time Polymerase Chain Reaction , Vero Cells , Virus Replication
11.
Mem. Inst. Oswaldo Cruz ; 111(5): 347-348, May 2016. graf
Article in English | LILACS | ID: lil-782053

ABSTRACT

Chikungunya virus (CHIKV) is a mosquito-borne pathogen that emerged in Brazil by late 2014. In the country, two CHIKV foci characterized by the East/Central/South Africa and Asian genotypes, were established in North and Northeast regions. We characterized, by phylogenetic analyses of full and partial genomes, CHIKV from Rio de Janeiro state (2014-2015). These CHIKV strains belong to the Asian genotype, which is the determinant of the current Northern Brazilian focus, even though the genome sequence presents particular single nucleotide variations. This study provides the first genetic characterisation of CHIKV in Rio de Janeiro and highlights the potential impact of human mobility in the spread of an arthropod-borne virus.


Subject(s)
Humans , Chikungunya virus/genetics , Brazil , Chikungunya Fever/transmission , Chikungunya virus/isolation & purification , Phylogeny
12.
Mem Inst Oswaldo Cruz ; 111(5): 347-8, 2016 May.
Article in English | MEDLINE | ID: mdl-27120007

ABSTRACT

Chikungunya virus (CHIKV) is a mosquito-borne pathogen that emerged in Brazil by late 2014. In the country, two CHIKV foci characterized by the East/Central/South Africa and Asian genotypes, were established in North and Northeast regions. We characterized, by phylogenetic analyses of full and partial genomes, CHIKV from Rio de Janeiro state (2014-2015). These CHIKV strains belong to the Asian genotype, which is the determinant of the current Northern Brazilian focus, even though the genome sequence presents particular single nucleotide variations. This study provides the first genetic characterisation of CHIKV in Rio de Janeiro and highlights the potential impact of human mobility in the spread of an arthropod-borne virus.


Subject(s)
Chikungunya virus/genetics , Brazil , Chikungunya Fever/transmission , Chikungunya virus/isolation & purification , Genotype , Humans , Phylogeny
13.
Mem Inst Oswaldo Cruz ; 110(6): 820-1, 2015 Sep.
Article in English | MEDLINE | ID: mdl-26517666

ABSTRACT

Parvovirus B19 (B19V) infects individuals worldwide and is associated with an ample range of pathologies and clinical manifestations. B19V is classified into three distinct genotypes, all identified in Brazil. Here, we report a complete sequence of a B19V genotype 1A that was obtained by high-throughput metagenomic sequencing. This genome provides information that will contribute to the studies on B19V epidemiology and evolution.


Subject(s)
Genome, Viral/genetics , Parvovirus B19, Human/genetics , Brazil , Child , Fatal Outcome , High-Throughput Nucleotide Sequencing , Humans , Male , Parvovirus B19, Human/classification , Sequence Analysis, DNA
14.
Mem. Inst. Oswaldo Cruz ; 110(6): 820-821, Sept. 2015. graf
Article in English | LILACS | ID: lil-763091

ABSTRACT

Parvovirus B19 (B19V) infects individuals worldwide and is associated with an ample range of pathologies and clinical manifestations. B19V is classified into three distinct genotypes, all identified in Brazil. Here, we report a complete sequence of a B19V genotype 1A that was obtained by high-throughput metagenomic sequencing. This genome provides information that will contribute to the studies on B19V epidemiology and evolution.


Subject(s)
Child , Humans , Male , Genome, Viral/genetics , /genetics , Brazil , Fatal Outcome , High-Throughput Nucleotide Sequencing , /classification , Sequence Analysis, DNA
15.
J Virol Methods ; 204: 105-8, 2014 Aug.
Article in English | MEDLINE | ID: mdl-24747585

ABSTRACT

The secreted form of the dengue virus (DENV) nonstructural-1 (NS1) glycoprotein has been shown to be useful for the diagnosis of DENV infections in patients' serum samples. In a number of studies, the sensitivity of the commercially available DENV NS1 glycoprotein detection assays was higher against some DENV serotypes (DENV-1>DENV-3>DENV-2=DENV-4) than others and were also lower using patients' serum samples with secondary versus primary DENV infections. In this study, 471 DENV-4 positive acute phase patients' serum samples were selected from a large panel collected in Brazil from March 2011 to October 2012 by RT-PCR and/or virus isolation followed by serotype determination. The sera from primary (n=228) and secondary (n=238) DENV-4 infections were identified using IgM and IgG capture ELISAs. The sensitivity of a commercial DENV NS1 glycoprotein detection ELISA was then assessed when these serum samples were not pre-treated or pre-treated by acid or heat dissociation prior to being tested. Acid and heat dissociation of patients' serum samples with primary and secondary DENV-4 infections increased significantly the sensitivity of the DENV NS1 glycoprotein detection ELISA from 54.4% to 77.2% (p<0.05) and 82% (p<0.05) and from 39.1% to 63.9% (p<0.05) and 73.1% (p<0.05), respectively. Treatment of DENV infected patients' serum samples using simple and rapid heat dissociation step (100°C for 5min) was, therefore, shown to be very useful for increasing the sensitivity of the DENV NS1 glycoprotein detection ELISA using serum samples from either primary or secondary DENV infected patients.


Subject(s)
Antigens, Viral/blood , Dengue Virus/isolation & purification , Dengue/diagnosis , Hot Temperature , Specimen Handling/methods , Acids , Brazil , Dengue Virus/immunology , Enzyme-Linked Immunosorbent Assay , Glycoproteins/blood , Humans , Sensitivity and Specificity , Viral Nonstructural Proteins/blood
16.
Mem Inst Oswaldo Cruz ; 107(7): 940-5, 2012 Nov.
Article in English | MEDLINE | ID: mdl-23147153

ABSTRACT

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.


Subject(s)
Aedes/virology , Dengue Virus/genetics , Dengue/virology , Insect Vectors/virology , Animals , Brazil , Dengue Virus/isolation & purification , Female , Humans , Male , Reverse Transcriptase Polymerase Chain Reaction
17.
Mem. Inst. Oswaldo Cruz ; 107(7): 940-945, Nov. 2012. ilus
Article in English | LILACS | ID: lil-656054

ABSTRACT

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 SimplexaTM 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 10³ copies/mL of virus, as determined by quantitative real-time RT-PCR. This is the first time the SimplexaTM 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.


Subject(s)
Animals , Female , Humans , Male , Aedes/virology , Dengue Virus/genetics , Dengue/virology , Insect Vectors/virology , Brazil , Dengue Virus/isolation & purification , Reverse Transcriptase Polymerase Chain Reaction
18.
Vaccine ; 22(9-10): 1073-8, 2004 Mar 12.
Article in English | MEDLINE | ID: mdl-15003633

ABSTRACT

A mass vaccination was carried out in the state of Minas Gerais, Southeast region of Brazil, to control an outbreak of sylvatic yellow fever in 2001. During the outbreak the surveillance system identified two fatal cases temporally associated with YF vaccination. Virus recovered from blood and postmortem samples of both cases was identified as yellow fever virus. Partial nucleotide sequence of parts of prM/E and the non-structural (NS) 5 genes and 3' non-coding region (3' NCR) was employed to characterize the origin of yellow fever virus (YFV) involved in both cases. Wild-type YFV was identified as the etiologic agent responsible for the disease.


Subject(s)
Disease Outbreaks , Mass Vaccination/adverse effects , Yellow Fever/transmission , Yellow Fever/virology , Yellow fever virus/immunology , Adult , Amino Acid Sequence , Base Sequence , Brazil , Enzyme-Linked Immunosorbent Assay , Humans , Immunoglobulin M/analysis , Immunoglobulin M/biosynthesis , Male , Molecular Sequence Data , Open Reading Frames/genetics , RNA, Viral/analysis , Reverse Transcriptase Polymerase Chain Reaction , Viral Envelope Proteins/genetics , Viral Envelope Proteins/immunology , Yellow Fever/diagnosis , Yellow fever virus/genetics
19.
Mem. Inst. Oswaldo Cruz ; 97(3): 437-439, Apr. 2002. tab
Article in English | LILACS | ID: lil-307985

ABSTRACT

The oral susceptibility to yellow fever virus was evaluated in 23 Aedes aegypti samples from Brazil. Six Ae. aegypti samples from Africa, America and Asia were also tested for comparison. Mosquito samples from Asia showed the highest infection rates. Infection rates for the Brazilian Ae. aegypti reached 48.6 percent, but were under 13 percent in 60 percent of sample tested. We concluded that although the low infection rates estimated for some Brazilian mosquito samples may not favor the establishment of urban cycle of yellow fever in some parts of the country, the founding of Ae. aegypti of noteworthy susceptibility to the virus in cities located in endemic and transition areas of sylvatic yellow fever, do pose a threat of the re-emergence of the urban transmission of the disease in Brazil


Subject(s)
Animals , Male , Female , Rabbits , Aedes , Insect Vectors , Yellow Fever , Yellow fever virus , Africa, Western , Asia, Southeastern , Brazil , Chickens , Mouth , North America , Risk Factors , South America
20.
Hist. ciênc. saúde-Manguinhos ; 9(1): 11-24, jan.-abr. 2002. graf
Article in Portuguese | LILACS | ID: lil-334577

ABSTRACT

A erradicaçäo dos vírus selvagens da poliomielite nas Américas constituiu um marco notável da saúde pública no continente americano. A Fundaçäo Oswaldo Cruz (Fiocruz) contribuiu de forma decisiva para este resultado de várias formas, como o apoio laboratorial do Centro Nacional de Enteroviroses, do Departamento de Virologia do Instituto Oswaldo Cruz, a formulaçäo e o fornecimento da vacina oral por Bio-Manguinhos, o apoio laboratorial e epidemiológico da Escola Nacional de Saúde Pública e o controle das vacinas pelo Instituto Nacional de Controle da Qualidade em Saúde. A Fiocruz também desenvolveu importantes projetos de pesquisa em enterovírus. Sendo a poliomielite ainda um problema para vários países do mundo, é oportuno relatar a importância do trabalho realizado pela Fiocruz para a erradicaçäo da doença no Brasil e nas Américas.


Subject(s)
Poliomyelitis , Public Health/history , Poliovirus Vaccine, Oral/history , Brazil , Poliomyelitis
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