Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 8 de 8
Filtrar
Mais filtros










Intervalo de ano de publicação
1.
Mem Inst Oswaldo Cruz ; 110(6): 786-92, 2015 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-26517658

RESUMO

Group A human rotaviruses (HuRVA) are causative agents of acute gastroenteritis. Six viral structural proteins (VPs) and six nonstructural proteins (NSPs) are produced in RV-infected cells. NSP4 is a diarrhoea-inducing viral enterotoxin and NSP4 gene analysis revealed at least 15 (E1-E15) genotypes. This study analysed the NSP4 genetic diversity of HuRVA G2P[4] strains collected in the state of São Paulo (SP) from 1994 and 2006-2010 using reverse transcription-polymerase chain reaction, sequencing and phylogenetic analysis. Forty (97.6%) G2P[4] strains displayed genotype E2; one strain (2.4%) displayed genotype E1. These results are consistent with the proposed linkage between VP4/VP7 (G2P[4]) and the NSP4 (E2) genotype of HuRVA. NSP4 phylogenetic analysis showed distinct clusters, with grouping of most strains by their genotype and collection year, and most strains from SP were clustered together with strains from other Brazilian states. A deduced amino acid sequence alignment for E2 showed many variations in the C-terminal region, including the VP4-binding domain. Considering the ability of NSP4 to generate host immunity, monitoring NSP4 variations, along with those in the VP4 or VP7 protein, is important for evaluating the circulation and pathogenesis of RV. Finally, the presence of one G2P[4]E1 strain reinforces the idea that new genotype combinations emerge through reassortment and independent segregation.


Assuntos
Antígenos Virais/isolamento & purificação , Glicoproteínas/genética , RNA Viral/genética , Rotavirus/genética , Toxinas Biológicas/genética , Proteínas não Estruturais Virais/genética , Adulto , Sequência de Aminoácidos , Sequência de Bases , Brasil , Criança , Fezes/virologia , Ligação Genética/genética , Variação Genética , Genótipo , Humanos , Técnicas Imunoenzimáticas , Dados de Sequência Molecular , Filogenia , RNA Viral/isolamento & purificação , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Rotavirus/classificação , Rotavirus/imunologia , Alinhamento de Sequência
2.
Mem. Inst. Oswaldo Cruz ; 110(6): 786-792, Sept. 2015. tab, graf
Artigo em Inglês | LILACS | ID: lil-763094

RESUMO

Group A human rotaviruses (HuRVA) are causative agents of acute gastroenteritis. Six viral structural proteins (VPs) and six nonstructural proteins (NSPs) are produced in RV-infected cells. NSP4 is a diarrhoea-inducing viral enterotoxin and NSP4 gene analysis revealed at least 15 (E1-E15) genotypes. This study analysed the NSP4 genetic diversity of HuRVA G2P[4] strains collected in the state of São Paulo (SP) from 1994 and 2006-2010 using reverse transcription-polymerase chain reaction, sequencing and phylogenetic analysis. Forty (97.6%) G2P[4] strains displayed genotype E2; one strain (2.4%) displayed genotype E1. These results are consistent with the proposed linkage between VP4/VP7 (G2P[4]) and the NSP4 (E2) genotype of HuRVA. NSP4 phylogenetic analysis showed distinct clusters, with grouping of most strains by their genotype and collection year, and most strains from SP were clustered together with strains from other Brazilian states. A deduced amino acid sequence alignment for E2 showed many variations in the C-terminal region, including the VP4-binding domain. Considering the ability of NSP4 to generate host immunity, monitoring NSP4 variations, along with those in the VP4 or VP7 protein, is important for evaluating the circulation and pathogenesis of RV. Finally, the presence of one G2P[4]E1 strain reinforces the idea that new genotype combinations emerge through reassortment and independent segregation.


Assuntos
Adulto , Criança , Humanos , Antígenos Virais/isolamento & purificação , Glicoproteínas/genética , RNA Viral/genética , Rotavirus/genética , Toxinas Biológicas/genética , Proteínas não Estruturais Virais/genética , Sequência de Aminoácidos , Sequência de Bases , Brasil , Fezes/virologia , Variação Genética , Genótipo , Ligação Genética/genética , Técnicas Imunoenzimáticas , Dados de Sequência Molecular , Filogenia , Reação em Cadeia da Polimerase Via Transcriptase Reversa , RNA Viral/isolamento & purificação , Rotavirus/classificação , Rotavirus/imunologia , Alinhamento de Sequência
3.
Mem. Inst. Oswaldo Cruz ; 105(8): 1040-1043, Dec. 2010. tab
Artigo em Inglês | LILACS | ID: lil-570676

RESUMO

In this study, 331 samples from calves less than one month old from a dairy herd in the district of Piracanjuba, state of Goiás, Brazil were tested for rotavirus. Thirty-three samples (9.9 percent) tested positive for rotavirus. Out of those, 31 were submitted to G and P characterization by reverse transcription followed by semi-nested polymerase chain reaction. Two samples were characterized as G6P[1], three as G10P[11] and five as G6P[11]. The majority of the samples (51.6 percent) displayed multiple P genotypes (P-genotype mixtures), including typical human genotypes P[4] and P[6M], suggesting the occurrence of co-infections and genetic reassortment. Also, the detection of human genotypes in bovine samples may be considered evidence of the zoonotic potential of rotaviruses. To our knowledge, this is the first report of such a high frequency of P genotype mixtures in bovine rotavirus samples. It also increases data on G and P rotavirus genotypes circulating in dairy herds in Brazil and can help in the development of more efficient immunization approaches, thereby controlling infection and reducing economical losses.


Assuntos
Animais , Bovinos , Humanos , Doenças dos Bovinos , Fezes , RNA Viral , Infecções por Rotavirus/veterinária , Rotavirus , Brasil , Doenças dos Bovinos , Eletroforese em Gel de Poliacrilamida , Genótipo , Reação em Cadeia da Polimerase , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Infecções por Rotavirus , Infecções por Rotavirus , Rotavirus , Rotavirus
4.
Mem Inst Oswaldo Cruz ; 105(8): 1040-3, 2010 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-21225202

RESUMO

In this study, 331 samples from calves less than one month old from a dairy herd in the district of Piracanjuba, state of Goiás, Brazil were tested for rotavirus. Thirty-three samples (9.9%) tested positive for rotavirus. Out of those, 31 were submitted to G and P characterization by reverse transcription followed by semi-nested polymerase chain reaction. Two samples were characterized as G6P[1], three as G10P[11] and five as G6P[11]. The majority of the samples (51.6%) displayed multiple P genotypes (P-genotype mixtures), including typical human genotypes P[4] and P[6M], suggesting the occurrence of co-infections and genetic reassortment. Also, the detection of human genotypes in bovine samples may be considered evidence of the zoonotic potential of rotaviruses. To our knowledge, this is the first report of such a high frequency of P genotype mixtures in bovine rotavirus samples. It also increases data on G and P rotavirus genotypes circulating in dairy herds in Brazil and can help in the development of more efficient immunization approaches, thereby controlling infection and reducing economical losses.


Assuntos
Doenças dos Bovinos/virologia , Fezes/virologia , RNA Viral/genética , Infecções por Rotavirus/veterinária , Rotavirus/genética , Animais , Brasil/epidemiologia , Bovinos , Doenças dos Bovinos/epidemiologia , Eletroforese em Gel de Poliacrilamida , Genótipo , Humanos , Reação em Cadeia da Polimerase , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Rotavirus/classificação , Rotavirus/isolamento & purificação , Infecções por Rotavirus/epidemiologia , Infecções por Rotavirus/virologia
5.
Mem. Inst. Oswaldo Cruz ; 102(8): 969-974, Dec. 2007. graf, tab
Artigo em Inglês | LILACS | ID: lil-471864

RESUMO

The purpose of this study was to characterize astrovirus in faecal samples collected from children with and without diarrhea in São Paulo, Brazil, grouped into two sets: EPM and HU. Detection and genotyping were carried out using reverse transcription nested polymerase chain reaction (RT-PCR) with specific primers directed towards the genome open reading frame 2 (ORF2). Results for EPM set showed that 66/234 (28.2 percent) were positive: 28/94 (29.7 percent) from children with acute diarrhea, 14/45 (31.1 percent) with persistent diarrhea, and 9/55 (16.3 percent) from control individuals. No data was available for 15/40 (37.5 percent) of samples. Mixed infections with other viruses were found in 33 samples. In the HU, 18/187 (9.6 percent) were positive: 12/158 (7.6 percent) from individuals with acute diarrhea and 6/29 (20.7 percent) from control children. Four samples were mixed with other viruses. Out of 66 astrovirus positive EPM samples, 18 (27.2 percent) were characterized as human astrovirus type-1 (HAstV-1), two (3.0 percent) as HAstV-2, two (3.0 percent) as HAstV-3, and three (4.5 percent) as HAstV-8. Among 18 astrovirus positive HU samples, one (5.5 percent) was characterized as HAstV-1, six (33.3 percent) as HAstV-2, and one (5.5 percent) as HAstV-8. Two HAstV-8 genotyped samples were further confirmed by nucleotide sequencing. Our results shows that astroviruses are circulating in a constant manner in the population, with multiple serotypes, in higher frequency than it was described for other Brazilian regions. For the first time in Sao Paulo, Brazil, it was shown that astroviruses play an important role in children gastroenteritis, as described for most locations where they were detected.


Assuntos
Criança , Humanos , Infecções por Astroviridae/virologia , Gastroenterite/virologia , Mamastrovirus/genética , Doença Aguda , Infecções por Astroviridae/diagnóstico , Infecções por Astroviridae/epidemiologia , Brasil/epidemiologia , Estudos de Casos e Controles , Fezes/virologia , Genótipo , Gastroenterite/diagnóstico , Gastroenterite/epidemiologia , Mamastrovirus/isolamento & purificação , Fases de Leitura Aberta , Reação em Cadeia da Polimerase Via Transcriptase Reversa , RNA Viral/genética
6.
Braz. j. microbiol ; 38(3): 459-466, July-Sept. 2007. ilus, graf, tab
Artigo em Inglês | LILACS | ID: lil-464771

RESUMO

From a total of 187 fecal samples from children with ages between 0 and 5 years, collected in the Hospital Universitário -USP, Brazil, from 1994 to 1996, 54 (28.9 percent) were positive for rotavirus. Positive samples were characterized by electropherotyping, subgrouping, G serotype and genotype and P genotype. Rotavirus electropherotypes were characterized in four different long genome patterns (38.9 percent), one short genome pattern (34.0 percent) and 18.0 percent were characterized as an unusual pattern. Subgroup I was found in 38.9 percent strains, subgroup II in 50.0 percent and 7.7 percent was subgroup nonI-nonII. For G serotypes, G2 was found in 59.3 percent, G1 was identified in 33.3 percent of strains, two samples showed mixtures of G1+G2 and one sample was G1+G3. Ten samples characterized as serotype G2 showed a long eletropherotype. Genotype G2 was the most frequently and was found in 37 (44.0 percent) samples (23 samples as a single genotype and 14 as mixtures of genotypes). G1 was found in 15 samples. G3 and G4 was detected mainly in mixtures of genotypes and G5, G6 and G9 were identified only in mixtures. A total of 20 (38.5 percent) samples were characterized as G genotype mixtures and P mixtures were found in 16 (29.6 percent) samples. P[4] was found in 55.6 percent of samples, P[8] in 51.9 percent and P[6-M37 like] in 22.3 percent of cases. P[6-Gottfried like] and P[11] were detected only in mixtures. One sample with G6 specificity, mixed with a G2 rotavirus and a P[11] strain, mixed with P[4] and P[8]strain was described for the first time in Latin America.


De um total de 187 amostras fecais de crianças com idades entre 0 e 5 anos, coletadas no Hospital Universitário -USP, Brasil, de 1994 a 1996, 54 (28.9 por cento) foram positivas para rotavírus. As amostras positivas foram caracterizadas quanto ao eletroferótipo, subgrupo, sorotipo G e genotipo G e P. Foram identificados quatro diferentes eletroferótipo longos em 38.9 por cento das amostras, um eletroferótipo curto (34,0 por cento) e 18,0 por cento foram caracterizadas como um eletroferótipo não usual. O subgrupo I foi encontrado em 38,9 por cento amostras, o subgrupo II em 50,0 por cento e nãoI-nãoII em 7,7 por cento. O sorotipo G2 foi encontrado em 59,3 por cento e G1 em 33,3 por cento. Duas amostras apresentaram misturas de G1+G2 e outra amostra G1+G3. Dez amostras caracterizadas como sorotipo G2 mostraram perfil eletroferótico longo. O genotipo G2 foi o mais freqüente, encontrado em 37 amostras (23 como único genotipo e 14 associados a outro genotipo). G1 foi encontrado em 15 amostras; G3 e G4 foram detectados principalmente em misturas e G5, G6 e G9, identificados somente em misturas. Um total de 20 (38,5 por cento) amostras foram identificadas como misturas de genotipo G e foram encontradas 16 (29,6 por cento) amostras com misturas de genotipo P. P[4] foi encontrado em 55,6 por cento das amostras, P[8] em 51,9 por cento e P[6-M37 like], em 5,5 por cento das amostras. P[6-Gottfried like] e P[11] foram detectados somente em misturas. Uma amostra com especificidade G6, associada ao genotipo G2 e outra P[11] misturada com P[4] e de P[8] foram identificadas pela primeira vez na América Latina.


Assuntos
Recém-Nascido , Criança , Humanos , Variação Genética , Técnicas In Vitro , Rotavirus , Infecções por Rotavirus , Técnicas e Procedimentos Diagnósticos , Fenótipo , Reação em Cadeia da Polimerase , Amostragem
7.
Mem Inst Oswaldo Cruz ; 102(8): 969-74, 2007 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-18209936

RESUMO

The purpose of this study was to characterize astrovirus in faecal samples collected from children with and without diarrhea in São Paulo, Brazil, grouped into two sets: EPM and HU. Detection and genotyping were carried out using reverse transcription nested polymerase chain reaction (RT-PCR) with specific primers directed towards the genome open reading frame 2 (ORF2). Results for EPM set showed that 66/234 (28.2%) were positive: 28/94 (29.7%) from children with acute diarrhea, 14/45 (31.1%) with persistent diarrhea, and 9/55 (16.3%) from control individuals. No data was available for 15/40 (37.5%) of samples. Mixed infections with other viruses were found in 33 samples. In the HU, 18/187 (9.6%) were positive: 12/158 (7.6%) from individuals with acute diarrhea and 6/29 (20.7%) from control children. Four samples were mixed with other viruses. Out of 66 astrovirus positive EPM samples, 18 (27.2%) were characterized as human astrovirus type-1 (HAstV-1), two (3.0%) as HAstV-2, two (3.0%) as HAstV-3, and three (4.5%) as HAstV-8. Among 18 astrovirus positive HU samples, one (5.5%) was characterized as HAstV-1, six (33.3%) as HAstV-2, and one (5.5%) as HAstV-8. Two HAstV-8 genotyped samples were further confirmed by nucleotide sequencing. Our results shows that astroviruses are circulating in a constant manner in the population, with multiple serotypes, in higher frequency than it was described for other Brazilian regions. For the first time in Sao Paulo, Brazil, it was shown that astroviruses play an important role in children gastroenteritis, as described for most locations where they were detected.


Assuntos
Infecções por Astroviridae/virologia , Gastroenterite/virologia , Mamastrovirus/genética , Doença Aguda , Infecções por Astroviridae/diagnóstico , Infecções por Astroviridae/epidemiologia , Brasil/epidemiologia , Estudos de Casos e Controles , Criança , Fezes/virologia , Gastroenterite/diagnóstico , Gastroenterite/epidemiologia , Genótipo , Humanos , Mamastrovirus/isolamento & purificação , Fases de Leitura Aberta , RNA Viral/genética , Reação em Cadeia da Polimerase Via Transcriptase Reversa
8.
Braz. j. microbiol ; 31(2): 140-5, Apr.-Jun. 2000. ilus, tab
Artigo em Inglês | LILACS | ID: lil-297653

RESUMO

Ten faecal samples of bovine rotavirus from calves less than 30 days old from an outbreak of diarrhea in Hidrolândia, Goiás, Brazil were submitted to serological and molecular characterization, using enzyme immonuassay for subgrouping and serotyping, PAGE for determination of electropherotypes and PCR for genome typing. Nine samples belonged to group A/subgroup I rotavirus one samples was group A / soubgroup non-I/non-II. Four samples were characterized as G10P[11] (B223-like), four samples showed a mixture of two rotavirus strains (G6G10 and P[5]P[11]), one sample was characterized as G6P[11] and one sample was characterized only by G serotyping/genotyping, and did not react with any primer used. Two electropherotypes were detected and both were present in the same animal. This study demonstrates that two different electropherotypes and/or serotypes of bovine rotavirus can circulate in the same outbreak.


Assuntos
Animais , Bovinos , Infecções por Rotavirus/diagnóstico , Rotavirus/genética , Rotavirus/isolamento & purificação , Vírus da Diarreia Viral Bovina/genética , Vírus da Diarreia Viral Bovina/isolamento & purificação , Bovinos , Sorotipagem
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...