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1.
J Interferon Cytokine Res ; 33(12): 783-9, 2013 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-23742258

RESUMO

The genetic association of CCR5 with human immunodeficiency virus-1 (HIV-1) pathogenesis is well known. The HIV-1 entry into target cells is initiated by the binding of the viral envelope glycoproteins (gp120-gp41) with the cell surface receptor (CD4) and the coreceptor (CCR5), followed by fusion of the viral and cell membranes. Genetic variants of the gene-encoding HIV-1 coreceptor are implicated in the susceptibility to HIV-1 infection. The prevalence of these mutations may vary according to population ethnicity. In the current study, characterization and frequency distribution of the HIV-related gene variants in 135 samples of the Saudi populations were conducted. Polymerase chain reaction (PCR) of 276 bp amplicons was used to rapidly detect Δ32 deletion in the initial sample of DNA. The direct sequence of 2 overlapping PCR amplicons flanking 1,059 bp was used to detect single-nucleotide polymorphisms. A single hetrozygous Δ32 deletion allele and 6 single-nucleotide polymorphisms were detected. Only one of the identified haplotypes, Taif-1, which was found in the majority of the tested sample, is identical to CCR5 wild-type alleles. Furthermore, the results of this study raised a concern about the prospective role of the mutations detected among Saudi nationals in the HIV pathogenesis and the clinical use of CCR5 antagonists, which are currently being developed as therapeutics for HIV-1 and inflammatory diseases.


Assuntos
Infecções por HIV/genética , HIV-1/genética , Mutação , Receptores CCR5/genética , Receptores de HIV/genética , Alelos , Sequência de Aminoácidos , Feminino , Genótipo , Humanos , Masculino , Modelos Moleculares , Dados de Sequência Molecular , Polimorfismo Genético , Vigilância da População , Conformação Proteica , Receptores CCR5/química , Receptores de HIV/química , Arábia Saudita , Alinhamento de Sequência
2.
PLoS One ; 8(1): e55500, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-23383205

RESUMO

Human bocavirus (HBoV) was recently discovered in children with respiratory distress and/or diarrhea. To our knowledge, no previous study has reported the existence of bocavirus in Saudi Arabia. Swabs samples from 80 children with respiratory tract infections were examined for the presence of HBoV. Real-time polymerase chain reaction was used as a sensitive method to detect the HBoV. Direct gene sequencing was used to determine the genotype of the detected virus isolates. HBoV was detected in 22.5% of the examined patients. The NP1 partial gene sequence from all patients showed that the circulated strains were related to HBoV-1 genotype. Most of HBoV infected patients showed evidence of mixed coinfection with other viral pathogens. The current study clearly demonstrated that genetically conserved HBoV1 circulates in Saudi Arabia. Interestingly, most of the HBoV1 infected cases were associated with high rates of co-infections with other viruses.


Assuntos
Bocavirus Humano/genética , Infecções por Parvoviridae/epidemiologia , Infecções Respiratórias/epidemiologia , Criança , Pré-Escolar , Feminino , Bocavirus Humano/classificação , Humanos , Lactente , Recém-Nascido , Masculino , Dados de Sequência Molecular , Filogenia , Prevalência , Arábia Saudita/epidemiologia , Proteínas Virais/genética
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