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1.
Genes (Basel) ; 12(6)2021 05 25.
Artigo em Inglês | MEDLINE | ID: mdl-34070451

RESUMO

Susceptibility to diseases is inherited and can be transmitted between populations. Single-nucleotide polymorphism (SNPs) in genes related to immune response is associated with diseases in cattle. This study investigated SNPs in the genomic region of cytokines in 702 samples of Curraleiro Pé-Duro cattle and associated them with the occurrence of antibodies in brucellosis, leptospirosis, neosporosis, leukosis, infectious bovine rhinotracheitis (IBR), and bovine viral diarrhea (BVD) tests. DNA samples were evaluated by the kompetitive allele-specific polymerase chain reaction (KASP) method to identify polymorphisms. The gametic phase and SNP haplotypes were determined with the help of PHASE 2.1.1 software. Haplotypes were associated with serological results against Brucella abortus, Leptospira sp., Neospora caninum, leukosis, infectious rhinotracheitis, and BVD using univariate analysis followed by logistic regression. Haplotype 2 of TLR2 was present in 70% of the animals that tested positive for N. caninum infection. Haplotypes of TLR10 and TLR6 and IL10RA were more common in seronegative animals. Haplotypes related to the gene IL10RA were associated with animals negative to all infections. Curraleiro Pé-Duro cattle presented polymorphisms related to resistance to bacterial, viral, and N. caninum infections.


Assuntos
Infecções Bacterianas/genética , Doenças dos Bovinos/genética , Coccidiose/genética , Polimorfismo de Nucleotídeo Único , Animais , Infecções Bacterianas/veterinária , Bovinos/genética , Coccidiose/veterinária , Citocinas/genética , Subunidade beta de Receptor de Interleucina-10/genética , Receptor 2 Toll-Like/genética
2.
Braz. j. infect. dis ; 21(4): 472-476, July-Aug. 2017. graf
Artigo em Inglês | LILACS | ID: biblio-1039195

RESUMO

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.


Assuntos
Humanos , Masculino , Feminino , Lactente , Pré-Escolar , Criança , Infecções Respiratórias/virologia , Infecções por Parvoviridae/virologia , Bocavirus Humano/isolamento & purificação , Gastroenterite/virologia , Infecções Respiratórias/complicações , Infecções Respiratórias/epidemiologia , Neoplasias de Tecidos Moles/complicações , Brasil/epidemiologia , Neoplasias Mandibulares/complicações , Doença Aguda , Infecções por Parvoviridae/complicações , Infecções por Parvoviridae/epidemiologia , Bocavirus Humano/classificação , Gastroenterite/complicações , Gastroenterite/epidemiologia
3.
Acta Trop ; 173: 153-159, 2017 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-28606817

RESUMO

Reduction in morbimortality rates for acute gastroenteritis (AGE) by Rotavirus A (RVA) has been observed after the introduction of vaccines, however the agent continues to circulate. The present study described the genomic characterization of the 11 dsRNA segments of two RVA samples G1P[8] obtained in the pre- and post-vaccination periods and one of G12P[8] sample (post-vaccine), compared to Rotarix™ vaccine. Analysis by molecular sequencing of the samples showed that the three samples belonged to genogroup I. In addition, the analysis of VP7 gene revealed that the samples G1 (pre-vaccine), G1 (post-vaccine) and G12 were characterized as lineages II, I and III, respectively. Regarding to VP4 and NSP4 gene it was observed that all samples belonged to lineage III, whereas for VP6 gene, the sample of the pre- and post-vaccine belonged to the lineage IV and I, respectively. Considering the VP7 gene, it was observed high nucleotide and amino acid identity for the two G1 samples when compared to Rotarix™ vaccine and lesser identity for the G12 sample. In relation to antigenic epitope of VP7 greater modifications were observed for the G12 sample in the 7-2 epitope that was confirmed by molecular modeling. On the other hand, for VP4, some changes in the 8-1 and 8-3 antigenic epitopes was observed for the three samples. This data could be interpreted as a low selective pressure exerted by vaccination in relation to G1P[8] samples and lesser protection in relation to G12P[8]. Thus, the continuous monitoring of RVA circulating samples remains important.


Assuntos
Antígenos Virais/genética , Proteínas do Capsídeo/genética , Infecções por Rotavirus/virologia , Vacinas contra Rotavirus/imunologia , Rotavirus/genética , Epitopos/genética , Gastroenterite/prevenção & controle , Gastroenterite/virologia , Regulação Viral da Expressão Gênica , Genômica , Genótipo , Humanos , Modelos Moleculares , Filogenia , Rotavirus/classificação , Vacinação
4.
Braz J Infect Dis ; 21(4): 472-476, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28500864

RESUMO

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.


Assuntos
Gastroenterite/virologia , Bocavirus Humano/isolamento & purificação , Infecções por Parvoviridae/virologia , Infecções Respiratórias/virologia , Doença Aguda , Brasil/epidemiologia , Criança , Pré-Escolar , Feminino , Gastroenterite/complicações , Gastroenterite/epidemiologia , Bocavirus Humano/classificação , Humanos , Lactente , Masculino , Neoplasias Mandibulares/complicações , Infecções por Parvoviridae/complicações , Infecções por Parvoviridae/epidemiologia , Infecções Respiratórias/complicações , Infecções Respiratórias/epidemiologia , Neoplasias de Tecidos Moles/complicações
5.
Rev. patol. trop ; 46(1): 105-112, abr. 2017. tab
Artigo em Inglês | LILACS | ID: biblio-913448

RESUMO

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


Assuntos
Infecções por Rotavirus , Vacinação , Genótipo
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