Résumé
Abstract Human Bocavirus (HBoV) has been identified from feces and respiratory samples from cases of both acute gastroenteritis and respiratory illness as well as in asymptomatic individuals. The aim of this study was to detect and characterize HBoV from fecal samples collected from hospitalized children aged less than five years old with no symptoms of respiratory tract infection (RTI) or acute gastroenteritis (AGE). The study involved 119 children and one fecal sample was collected from each participant between 2014 and 2015. HBoV was detected using Nested-PCR, and the viral type identified by genomic sequencing. HBoV-4 was identified from one sample obtained from a hospitalized child with soft tissue tumor of the submandibular region. This is the first report of HBoV-4 identification in Brazil, but we consider that this type may be circulating in the country similar to the other types and new investigations are necessary.
Sujets)
Humains , Mâle , Femelle , Nourrisson , Enfant d'âge préscolaire , Enfant , Infections de l'appareil respiratoire/virologie , Infections à Parvoviridae/virologie , Bocavirus humain/isolement et purification , Gastroentérite/virologie , Infections de l'appareil respiratoire/complications , Infections de l'appareil respiratoire/épidémiologie , Tumeurs des tissus mous/complications , Brésil/épidémiologie , Tumeurs de la mandibule/complications , Maladie aigüe , Infections à Parvoviridae/complications , Infections à Parvoviridae/épidémiologie , Bocavirus humain/classification , Gastroentérite/complications , Gastroentérite/épidémiologieRésumé
The purpose of this study was to perform a comparative analysis of Rotavirus A (RVA) G and P genotypes circulating in the Brazilian Mid-West in the period 1986-2015. Seven studies conducted from 1986 to 2009 were included, as well as fecal samples obtained in the period 2014-2015. RVA was screened by ELISA and/or PAGE; genotyping by conventional RT-PCR and/or genomic sequencing. A temporal variation in the predominance of G genotypes mainly G1 and G2 with G9 and G12 emergence was observed. Even with vaccination, RVA continues to circulate in the population, requiring continuous virus monitoring
Sujets)
Infections à rotavirus , Vaccination , GénotypeRésumé
Norovirus is the leading cause of non-bacterial acute gastroenteritis outbreaks worldwide. Recently, third generation Enzyme Immunoassay (EIA) commercial kits have been developed, and controversial results have been obtained by different studies regarding the sensitivity and specificity of these assays. Therefore, the aim of this study was to test 60 fecal samples, previously tested as positive by RT-PCR for caliciviruses (40 norovirus-positive and 20 sapovirus-positive samples), for qualitative determination of genogroup I and II noroviruses by a commercial EIA kit (RIDASCREEN® Norovirus (C1401) 3rd Generation, R-Biopharm, Darmstadt, Germany). The samples were obtained from 30 children aged less than five years, mostly asymptomatic, who attend a day-care center in Goiânia, Goiás, Brazil. The results conferred a positivity rate for NoV of 35 percentand a specificity rate of 100 percent for the EIA, when compared to the RT-PCR. The test also failed to detect samples that were positive for GI.1 and GI.4 norovirus. The presumably lower viral load of asymptomatic children might be related to the poor sensitivity. Our results reinforce the notion that screening of samples by molecular assays, especially of samples that might have a low number of viral particles such as those obtained from asymptomatic patients, should not be replaced by the use of EIA kits...
Triagem de amostras fecais de crianças assintomáticas utilizando-se um kit comercial de Elisa 3a geração determinação qualitativa de norovírus dos genogrupos I e II por meio de kit comercial de EIE (RIDASCREEN® Norovirus (C1401) 3rd Generation, R-Biopharm, Darmstadt, Germany). Previamente testadas, elas se mostraram positivas para calicivírus por RT-PCR (40 positivas para norovirus e 20 positivas para sapovirus). As amostras foram obtidas de 30 crianças menores de 5 anos de idade, predominantemente assintomáticas, que frequentavam uma creche em Goiânia, Goiás, Brasil. Os resultados revelaram índices de 35 porcento de positividade para os norovírus e de 100 porcento de especificidade para o EIE quando comparado a RT-PCR. O teste também falhou em detectar amostras que eram positivas para norovírus GI.1 e GI.4. A carga viral, presumidamente mais baixa, das crianças assintomáticas pode estar relacionada com a baixa sensibilidade. Os resultados reforçam o entendimento de que a triagem de amostras por ensaios moleculares não deve ser substituída pelo uso de kits de EIE, especialmente quando se tratar de amostras que, presumidamente, apresentem um baixo número de partículas virais como as obtidas de pacientes assintomáticos...
Sujets)
Enfant , Fèces/parasitologie , Gastroentérite/épidémiologie , Norovirus , SapovirusRésumé
To determine the positivity rate of human bocavirus (HBoV) 1 and 3 among children who presented with acute gastroenteritis symptoms during the period of 1994-2004 in the Central-West Region of Brazil, 762 faecal samples were tested using polymerase chain reaction (PCR) for the detection of HBoV DNA. Primers for a segment of the non-structural viral protein 1 (NS1) gene of HBoV-1 and HBoV-3 were used. Twelve HBoV-positive samples were further characterised via genomic sequencing and phylogenetic analysis. Of the samples tested, 5.8% (n = 44) were positive for HBoV-1 or HBoV-3 and co-infection was observed in 14 (31.8%) of the 44 HBoV-positive samples. Nine of the 14 samples were also positive for Rotavirus A and five were positive for Aichi virus. The genomic sequencing of the NS1 partial sequence of 12 HBoV-samples showed that 11 samples were characterised as HBoV-1 and that one was characterised as HBoV-3. The phylogenetic analysis showed that the HBoV-1 samples had a high sequence homology to others previously identified in China, Sweden and Brazil. This is the first study conducted in the Central-West Region of Brazil to detect HBoV-1 and HBoV-3 in faecal samples from children with acute gastroenteritis. Further studies are required to define the role of HBoVs as aetiological agents of gastroenteritis.
Sujets)
Enfant d'âge préscolaire , Femelle , Humains , Mâle , Gastroentérite/virologie , Bocavirus humain/génétique , Infections à Parvoviridae/virologie , Maladie aigüe , Brésil/épidémiologie , ADN viral/analyse , Fèces/virologie , Gastroentérite/épidémiologie , Bocavirus humain/classification , Bocavirus humain/isolement et purification , Phylogenèse , Réaction de polymérisation en chaîne , Infections à Parvoviridae/épidémiologie , SaisonsRésumé
The epidemiological features of rotavirus A (RVA) infection differ between children from developing and developed countries which could result in differences in vaccine efficacy around the world. To evaluate the impact of RotarixTM on RVA prevalence, we monitored RVA genotypes circulating in Goiânia by monitoring virus in faecal samples from children that had or had not been previously vaccinated. From February-November of 2008, 220 faecal samples were collected from children in seven day-care centres. RVA detection was performed by two methodologies and the results were confirmed by polyacrylamide gel electrophoresis. From the 220 samples, eight were RVA-positive (3.6 percent) and five were from children that had received either one or two doses of the vaccine. All positive samples were collected from children with diarrhoea during August and September. Genotyping of the RVA characterised five of the viral samples as genotype G2P[4] and one as G8P[4], suggesting that G2P[4] was the predominant circulating genotype in Goiânia during the study. The fact that vaccinated children were also infected by RVA suggests that the vaccine does not fully protect against infection by the G2[P4] RVA genotype.
Sujets)
Enfant , Femelle , Humains , Mâle , Diarrhée , Infections à rotavirus , Vaccins anti-rotavirus , Rotavirus , Brésil , Électrophorèse sur gel de polyacrylamide , Fèces , Génotype , Prévalence , Infections à rotavirus , Rotavirus , Vaccins atténuésRésumé
INTRODUCTION: This was a prospective study that included women seen in the obstetrics and gynecology sector of Hospital das Clínicas, Federal University of Goiás, in Goiânia, State of Goiás, with the aim of detecting rotaviruses, adenoviruses, caliciviruses and astroviruses. Eighty-four women participated in the study and from these, 314 fecal samples were collected. Out of all of the women, 29 were seropositive for HIV and 55 were seronegative, and 45 and 39 were pregnant and non-pregnant, respectively. METHODS: Fecal samples were collected from each woman once every two months over the period from July 2006 to June 2007, and they were screened for rotaviruses by means of polyacrylamide gel electrophoresis and immunoenzymatic assays, for caliciviruses and astroviruses by means of RT-PCR and for adenovirus by means of immunoenzymatic assays. The astroviruses were genotyped using nested PCR. RESULTS: Among the 84 patients, 19 (22.6 percent) were positive for either calicivirus (14/19) or astrovirus (6/19), while one women was positive for both viruses in fecal samples collected on different occasions. Most of the positive samples were collected during the months of July and August (astrovirus) and September and October (calicivirus). None of the samples analyzed was positive for rotavirus or adenovirus. Gastroenteric viruses were detected in 13/19 (68.4 percent) of the pregnant women, whether HIV-seropositive or not. CONCLUSIONS: The results from the present study showed that neither pregnancy nor HIV-seropositive status among the women increased the risk of infection by any of the gastroenteric viruses studied. This study presents data on gastroenteric virus detection among pregnant and/or HIV-positive women.
INTRODUÇÃO: Este foi um estudo prospectivo que incluiu mulheres atendidas no setor de obstetrícia e ginecologia do Hospital das Clínicas da Universidade Federal de Goiás, em Goiânia, Estado de Goiás com o objetivo de detectar rotavírus, adenovírus, calicivírus e astrovírus. Oitenta e quatro mulheres participaram no estudo e destas, 314 amostras fecais foram coletadas. Do total de mulheres, 29 eram soropositivas para HIV, 55 soronegativas, 45 e 39 estavam grávidas e não-grávidas, respectivamente. MÉTODOS: Amostras fecais foram coletadas de cada mulher uma vez a cada dois meses pelo período de Julho-2006 a Junho-2007, foram triadas para rotavírus pela metodologia de eletroforese em gel de poliacrilamida (EGPA) e através de ensaio imunoenzimático (EIE), para calicivírus e astrovírus por RT-PCR e por EIE para adenovírus. Os astrovírus foram genotipados por Nested-PCR. RESULTADOS: De 84 pacientes, 19 (22,6 por cento) foram positivas para calicivírus (14/19) ou astrovírus (6/19), sendo que uma mulher foi positiva para ambos os vírus em amostras fecais coletadas em diferentes ocasiões. A maioria das amostras positivas foi coletada no período de Julho a Agosto (astrovírus) e de Setembro a Outubro (calicivírus). Nenhuma das amostras analisadas foi positiva para rotavírus ou adenovírus. Os vírus gastroentéricos foram detectados em 13/19 (68,4 por cento) mulheres grávidas, as quais eram HIV-soropositivas ou não. CONCLUSÕES: Os resultados do presente estudo mostram que nem o estado gravídico das mulheres nem a soropositividade para HIV aumentaram o risco para a infecção por nenhum dos vírus gastroentéricos estudados. Este estudo apresenta dados sobre a detecção de vírus gastroentéricos entre mulheres grávidas e/ou HIV-positivas.
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Adulte , Femelle , Humains , Grossesse , Jeune adulte , Adenoviridae/isolement et purification , Fèces/virologie , Gastroentérite/virologie , Complications infectieuses de la grossesse/virologie , Virus à ARN/isolement et purification , Infections opportunistes liées au SIDA/virologie , Brésil , Caliciviridae/isolement et purification , Électrophorèse sur gel de polyacrylamide , Techniques immunoenzymatiques , Mamastrovirus/isolement et purification , Réaction de polymérisation en chaîne , Prévalence , Études prospectives , Virus à ARN/classification , Rotavirus/isolement et purification , Jeune adulteRésumé
Hepatitis A virus (HAV) infection is a public health problem worldwide and the virus has been classified into six genotypes. In Brazil, the only genotype that has been found is genotype I, predominately from subgenotype IA. Here, the HAV genotypes were analyzed of 18 isolates circulating between 1996-2001 in Goiânia, state of Goiás, Brazil. Viral RNA was extracted from 18 serum samples and amplified (RT-PCR/nested-PCR), followed by the genomic sequencing of the VP1/2A junction region of the HAV genome. Sequences of 168 nucleotides were compared and analyzed using the BLAST N, Clustal X and PAUP v. 4.10b programs. All samples were classified as genotype I, with 10 belonging to subgenotype IA and eight to subgenotype IB. The subgenotype IA isolates showed greater diversity than the subgenotype IB isolates at the nucleotide level. Elevated identity values were found between isolates obtained in this study and those from other regions of the world, including Brazil, highlighting the high conservation among different isolates of this virus. However, changes in the HAV subgenotype circulation could also be observed during the evaluated period.
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Adolescent , Adulte , Enfant , Enfant d'âge préscolaire , Femelle , Humains , Mâle , Jeune adulte , Virus de l'hépatite A/génétique , Hépatite A/virologie , ARN viral/génétique , Séquence nucléotidique , Brésil , Virus de l'hépatite A/isolement et purification , Données de séquences moléculaires , Phylogenèse , RT-PCR , Jeune adulteRésumé
We analyzed fecal samples from hospitalized children up to three years of age with acute gastroenteritis at Campo Grande, Mato Grosso do Sul, Brazil, from May 2000-January 2004. Astrovirus and calicivirus were detected by Reverse Transcription-Polymerase Chain Reaction and adenovirus was detected using the Rotavirus and Adenovirus combined immunoenzyme assay. Astrovirus, adenovirus and calicivirus were detected at rates of 3.1 percent, 3.6 percent and 7.6 percent, respectively. These results re-emphasize the need for the establishment of regional vigilance systems to evaluate the impact of enteric viruses on viral gastroenteritis.
Sujets)
Enfant d'âge préscolaire , Humains , Nourrisson , Nouveau-né , Infections humaines à adénovirus/épidémiologie , Infections à Astroviridae/épidémiologie , Infections à Caliciviridae/épidémiologie , Diarrhée/virologie , Gastroentérite/virologie , Maladie aigüe , Infections humaines à adénovirus/diagnostic , Adénovirus humains/isolement et purification , Infections à Astroviridae/diagnostic , Brésil/épidémiologie , Infections à Caliciviridae/diagnostic , Caliciviridae/isolement et purification , Fèces/virologie , Techniques immunoenzymatiques , Mamastrovirus/isolement et purification , RT-PCRRésumé
Nonstructural protein 4 (NSP4), encoded by group A rotavirus genome segment 10, is a multifunctional protein and the first recognized virus-encoded enterotoxin. The NSP4 gene has been sequenced, and five distinct genetic groups have been described: genotypes A-E. NSP4 genotypes A, B, and C have been detected in humans. In this study, the NSP4-encoding gene of human rotavirus strains of different G and P genotypes collected from children between 1987 and 2003 in three cities of West Central region of Brazil was characterized. NSP4 gene of 153 rotavirus-positive fecal samples was amplified by reverse transcriptase-polymerase chain reaction and then sequenced. For phylogenetic analysis, NSP4 nucleotide sequences of these samples were compared to nucleotide sequences of reference strains available in GenBank. Two distinct NSP4 genotypes could be identified: 141 (92.2 percent) sequences clustered with NSP4 genotype B, and 12 sequences (7.8 percent) clustered with NSP4 genotype A. These results reinforce that further investigations are needed to assess the validity of NSP4 as a suitable target for epidemiologic surveillance of rotavirus infections and vaccine development.
Sujets)
Enfant , Enfant d'âge préscolaire , Humains , Glycoprotéines/génétique , Infections à rotavirus/virologie , Rotavirus/génétique , Toxines biologiques/génétique , Protéines virales non structurales/génétique , Séquence nucléotidique , Brésil , Fèces/virologie , Génotype , Phylogenèse , RT-PCR , Rotavirus/classification , Analyse de séquence d'ARNRésumé
Através da eletroforese em gel de poliacrilamida e do ensaio imunenzimático combinado para rotavírus e adenovirus, foram analisadas 380 amostras fecais de crianças com até 3 anos, hospitalizadas com diarréia aguda, entre maio de 2000 e janeiro de 2004, em Campo Grande, MS. Do total de amostras, 88 (23,2 por cento) foram positivas para Rotavirus A. Dentre essas, 81 (92 por cento) tiveram padrão eletroferotípico definido, sendo 77 (87,5 por cento) de padrão longo e quatro (4,5 por cento) de padrão curto. A caracterização genotípica G e P foi feita por RT-Nested-PCR para 85 amostras, sendo 56 (65,9 por cento) genotipáveis para genótipo G. Dentre essas, 49 (87,5 por cento) foram G1, cinco (8,9 por cento) G4, uma (1,8 por cento) G3 e uma (1,8 por cento) G9. Considerando a genotipagem P, 37 (43,5 por cento) foram genotipáveis e todas eram P[8]. A associação G e P mais observada foi G1P[8], 33 (89,2 por cento) amostras; seguida de G4P[8], duas (5,4 por cento) amostras; G3P[8], uma (2,7 por cento) amostra; e G9P[8], uma (2,7 por cento) amostra.
Polyacrylamide gel electrophoresis and combined immunoenzyme assay for rotavirus and adenovirus were used to analyze 380 fecal samples from children up to three years of age who were hospitalized with acute diarrhea in Campo Grande, State of Mato Grosso do Sul, between May 2000 and January 2004. Among all the samples, 88 (23. 2 percent) were positive for Rotavirus A. Out of these, 81 (92 percent) had a defined electrophoretic pattern: 77 (87. 5 percent) with a long pattern and four (4. 5 percent) with a short pattern. Genotype G and P characterization was done by nested RT-PCR for 85 samples, of which 56 (65. 9 percent) were genotyped as type G. Among these, 49 (87. 5 percent) were G1, five (8. 9 percent) were G4, one (1. 8 percent) was G3 and one (1. 8 percent) was G9. The genotype was found to be type P in 37 samples (43. 5 percent) and all of these were P[8]. The G and P association most observed was G1P[8], with 33 samples (89. 2 percent), followed by G4P[8], two samples (5. 4 percent); G3P[8], one sample (2. 7 percent); and G9P[8], one sample (2. 7 percent).
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Enfant , Enfant d'âge préscolaire , Femelle , Humains , Nourrisson , Nouveau-né , Mâle , Diarrhée/virologie , Gastroentérite/épidémiologie , Infections à rotavirus/virologie , Rotavirus/classification , Maladie aigüe , Brésil/épidémiologie , Diarrhée/épidémiologie , Électrophorèse sur gel de polyacrylamide , Fèces/virologie , Génotype , Gastroentérite/virologie , Prévalence , RT-PCR , Infections à rotavirus/épidémiologie , Rotavirus/génétique , SaisonsRésumé
The objective of this study was to describe the circulation of caliciviruses in the West Central region of Brazil and its correlation with children's gender and age, as well as with the year and months of the sample collection. Reverse transcriptase-polymerase chain reaction was performed to detect the human calicivirus genome in 1006 fecal samples that were collected in Goiânia (n = 696) and Brasília (n = 310). Viral RNA was detected in 8.6 percent of the samples. No significant difference in viral prevalence was found regarding gender, age or year of the sample. However, it was observed that in Goiânia, there is a higher incidence of caliciviruses from September to March. The analysis employing three primer pairs demonstrated that the Ni/E3 or JV12/13 primer pairs, which detect norovirus (NoV), detected 41 positive samples while the 289/290 primer pair, which detects NoV or sapovirus, detected the remaining 46 samples. Calicivirus circulates in the West Central region of Brazil and for better detection of this virus it is important to use more than one primer pair. Also, we conclude that the seasonality presented by this virus is related to higher humidity in the period.
Sujets)
Humains , Nourrisson , Enfant d'âge préscolaire , Infections à Caliciviridae/virologie , Caliciviridae/isolement et purification , Fèces/virologie , Gastroentérite/virologie , Maladie aigüe , Répartition par âge , Brésil/épidémiologie , Infections à Caliciviridae/diagnostic , Infections à Caliciviridae/épidémiologie , Gastroentérite/diagnostic , Gastroentérite/épidémiologie , Prévalence , RT-PCR , SaisonsRésumé
In this study, a total of 865 serum samples were collected between 1995 and 2002 from individuals living in Goiânia, Central Brazil, and clinically suspected of hepatitis. After exclusion of 162 samples which were positive for hepatitis B virus or hepatitis C virus, 703 samples were tested for anti-hepatitis A virus (anti-HAV) IgM antibodies by enzyme immunoassay. In addition, 588 of these samples and 22 fecal samples were analyzed by reverse transcription-nested PCR for HAV RNA detection, with positivity indices of 13.1 percent (77/588) and 54.5 percent (12/22), respectively. A similar index of viral RNA detection in anti-HAV-IgM positive or negative samples was observed in serum samples. HAV infection is a public health problem worldwide and this study underscores the extent of HAV circulation in our region.
Sujets)
Adolescent , Adulte , Enfant , Enfant d'âge préscolaire , Humains , Nourrisson , Nouveau-né , Virus de l'hépatite A , Anticorps de l'hépatite A/sang , Hépatite A/épidémiologie , Immunoglobuline M/sang , Brésil/épidémiologie , Fèces/virologie , Virus de l'hépatite A/génétique , Virus de l'hépatite A/immunologie , Hépatite A/diagnostic , Techniques immunoenzymatiques , Prévalence , Réaction de polymérisation en chaîne/méthodes , ARN viral/génétique , ARN viral/isolement et purification , Études séroépidémiologiquesRésumé
Neste estudo, foram analisadas 648 amostras de soro, provenientes de profissionais de laboratório de Goiânia-Goiás, visando a detecção de três marcadores sorológicos do VHB: HBsAg, anti-HBsAg e anti-HBcAg. As amostras HBsAg e anti-HBcAg positivas foram também analisadas para os marcadores HBeAg, anti-HBeAg e anti-HBcAgIgM. Foi observado um percentual de soropositividade para infecção pelo VHB de 24,1% sendo que 0,7% destes foram positivos para o HBsAg. O DNA viral foi detectado por PCR nas duas amostras HBsAg positivas. Dos 648 profissionais, 74,5% relataram vacinação para o VHB e, destes, 89,9% apresentaram soroconversão. Trabalho direto com fluidos biológicos bem como trabalho em serviços gerais representaram risco significativo para aquisição da infecção pelo VHB. Os resultados do estudo mostram que embora tenha havido um aumento no índice de vacinação entre os trabalhadores de laboratório, o índice de infecção pelo VHB manteve-se inalterado em relação ao tempo na região.
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Humains , Mâle , Femelle , Adolescent , Adulte , Adulte d'âge moyen , Anticorps de l'hépatite B/sang , Antigènes de surface du virus de l'hépatite B/sang , Virus de l'hépatite B/immunologie , Hépatite B/épidémiologie , Personnel de laboratoire , Marqueurs biologiques/sang , Brésil/épidémiologie , ADN viral/analyse , Test ELISA , Vaccins anti-hépatite B , Hépatite B/diagnostic , Hépatite B/transmission , Réaction de polymérisation en chaîne , Prévalence , Facteurs de risque , Études séroépidémiologiquesRésumé
Objetivo: analisar as manifestações clínicas e aspectos epidemiológicos relacionados ao rotavirus A. Casusuistica e Métodos: foi realizado estudo prospectivo com crianças de Goiânia, GO, que apresentavam diarréia aguda. Amostras fecais foram avaliadas para rotavírus através de eletroforese em gel e ensaio imunoenzimático...