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首页> 外文期刊>Journal of Clinical Microbiology >Discrimination between human T-cell lymphotropic virus type I and II (HTLV-I and HTLV-II) infections by using synthetic peptides representing an immunodominant region of the core protein (p19) of HTLV-I and HTLV-II.
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Discrimination between human T-cell lymphotropic virus type I and II (HTLV-I and HTLV-II) infections by using synthetic peptides representing an immunodominant region of the core protein (p19) of HTLV-I and HTLV-II.

机译:通过使用代表HTLV-I和HTLV-II核心蛋白(p19)免疫主要区域的合成肽,区分人T细胞I型和II型T细胞(HTLV-I和HTLV-II)感染。

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摘要

We describe enzyme immunoassays that use synthetic oligopeptides to discriminate serologically between human T-cell lymphotropic virus type I and II (HTLV-I and HTLV-II) infections. The peptides represented 20-amino acid segments between residues 111 and 130 (MA1) and residues 116 and 135 (MA2) of the p19 gag proteins of HTLV-I and HTLV-II, respectively. The assays were sensitive since 69 of 74 HTLV-positive sera were reactive to at least one of the two matrix (MA) peptides (sensitivity, 93.2%). By using the ratio of the optical density of MA1 to the optical density of MA2, which represents for every serum sample the ratio between the absorbance value obtained in the MA1 assay and the absorbance value obtained in the MA2 assay, 59 of the 69 reactive serum samples were clearly and easily typed as positive for either antibody to HTLV-I or antibody to HTLV-II. Eight of the 10 remaining reactive serum samples were analyzed further by an inhibition procedure, and their type specificities were then clearly identifiable. Therefore, the results indicate that all MA-reactive sera were serologically distinguished by our peptide assays.
机译:我们描述了使用合成的寡肽来区分人类T细胞淋巴病毒I型和II型(HTLV-I和HTLV-II)感染的血清学的酶免疫法。所述肽分别代表HTLV-1和HTLV-II的p19gag蛋白的残基111和130(MA1)和残基116和135(MA2)之间的20个氨基酸区段。由于74种HTLV阳性血清中有69种对两种基质(MA)肽中的至少一种具有反应性(敏感性,93.2%),因此该测定法具有敏感性。通过使用MA1的光密度与MA2的光密度之比(代表每个血清样品),在69种反应性血清中,有59种在MA1分析中获得的吸光度值与MA2分析中获得的吸光度值之比可以轻松,轻松地将样品分类为HTLV-I抗体或HTLV-II抗体阳性。通过抑制程序进一步分析了剩余的10个反应性血清样品中的8个,然后可以明确鉴定其类型特异性。因此,结果表明,所有的MA反应血清均通过我们的肽检测在血清学上得以区分。

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