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SDF-1 gene polymorphisms and syncytia induction in Brazilian HIV-1 infected individuals

机译:巴西HIV-1感染者的SDF-1基因多态性和合胞体诱导

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Stromal-derived factor (SDF-1) is the principal ligand for CXCR4, a co-receptor with CD4 for T lymphocyte cell line-tropic human immunodeficiency virus-type 1 (HIV-1). A common polymorphism, SDF1-3' A, was identified in an evolutionary conserved segment of the 3' untranslated region of the SDF-1 gene. Sequence analysis revealed a common variant at position 801, a G --> A transition referred to as SDF1-3' A. Because this variant eliminates the Msp I restriction site PCR-restriction fragment length polymorphism (RFLP) analysis was used for rapid detection of genotypes. We genotyped 62 HIV infected patients and 60 non-HIV blood donors by RFLP analysis. We also assessed syncytia formation through co-culture of MT-2 cells with peripheral blood mononuclear cells from HIV patients. Syncytium-inducing HIV-1 variants have been shown to be clinically significant in the pathogenesis of HIV-1 infection. In our study, we detected a low frequency of 3'A/3'A (5%) in the blood donors but this genotype was absent in all HIV patients. We found that 41 (68%) HIV patients including syncytia inducing (SI) and non-syncytia inducing (NSI) groups contained the wild type (wt/wt) genotype for SDF-1. Our data indicate that there is no correlation between SDF-1 alleles and syncytium inducing HIV.
机译:基质基质因子(SDF-1)是CXCR4的主要配体,CXCR4与T4细胞系嗜性人类免疫缺陷病毒1型(HIV-1)的CD4共同受体。在SDF-1基因的3'非翻译区的进化保守段中确定了常见的多态性,SDF1-3'A。序列分析显示在位置801处有一个常见变体,称为G-> A过渡,称为SDF1-3'A。因为该变体消除了Msp I限制性酶切位点,所以PCR限制性片段长度多态性(RFLP)分析用于快速检测基因型。通过RFLP分析,我们对62位HIV感染患者和60位非HIV献血者进行了基因分型。我们还通过将MT-2细胞与HI​​V患者的外周血单个核细胞共培养来评估合胞体的形成。合胞体诱导HIV-1变体已被证明在HIV-1感染的发病机理上具有重要的临床意义。在我们的研究中,我们在献血者中检测到3'A / 3'A的频率很低(5%),但是在所有HIV患者中都没有这种基因型。我们发现41名(68%)HIV患者,包括合胞体诱导(SI)和非合胞体诱导(NSI)组,包含SDF-1的野生型(wt / wt)基因型。我们的数据表明SDF-1等位基因与合胞体诱导HIV之间没有相关性。

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