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首页> 外文期刊>Revista do Instituto de Medicina Tropical de So Paulo >TESTING A SUBTYPE-SPECIFIC GP41 AMPLIFICATION METHOD FOR GENOTYPING INDIVIDUALS INFECTED BY HUMAN IMMUNODEFICIENCY VIRUS TYPE-1 IN THE BRAZILIAN POPULATION OF ITAJAí, SOUTH BRAZIL
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TESTING A SUBTYPE-SPECIFIC GP41 AMPLIFICATION METHOD FOR GENOTYPING INDIVIDUALS INFECTED BY HUMAN IMMUNODEFICIENCY VIRUS TYPE-1 IN THE BRAZILIAN POPULATION OF ITAJAí, SOUTH BRAZIL

机译:在巴西伊塔雅伊的巴西人口中,针对亚型人免疫缺陷病毒1型感染的个体进行基因分型的亚型GP41扩增方法的测试

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The method used by YAGYU et al. for the subtype-specific polymerase chain reaction (PCR) amplification of the gp41 transmembrane region of the human immunodeficiency virus type-1 (HIV-1) env gene, was tested. HIV-1 proviral DNA from 100 infected individuals in Itajaí, South Brazil was used to analyze this method. Seventy individuals were determined according to this method as having PCR products at the expected size for subtypes B, C, D and F. Of these individuals, 26 (37.1%) were observed as having the expected amplification for subtype C, and 42 (60%) were observed as having the expected products for subtypes B and D. Of the subtype B and D amplicons, 16 (22.9%) were classified as subtype D, and 26 (37.1%) were classified as subtype B. Two individuals (2.9%) had amplicons that were observed after subtype F-specific amplification was performed. Sequencing and comparing the patient sequences to reference sequences confirmed the classification of sequences of subtypes C and B. However, sequences that were falsely determined as being D and F in the PCR assay were determined as being subtypes C and B, respectively, by sequence analysis. For those individuals from whom no amplified products were obtained, a low viral load that was indicated in their patient history may explain the difficulty in subtyping by PCR methods. This issue was demonstrated by the results of ANOVA when testing the effect of viral load on the success of PCR amplification. The alignment of the obtained sequences with HIV-1 reference sequences demonstrated that there is high intra-subtype diversity. This indicates that the subtype-specific primer binding sites were not conserved or representative of the subtypes that are observed in the Brazilian populations, and that they did not allow the correct classification of HIV-1 subtypes. Therefore, the proposed method by YAGYU et al. is not applicable for the classification of Brazilian HIV-1 subtypes.
机译:YAGYU等人使用的方法。为了检测亚型特异性聚合酶链反应(PCR),对人类免疫缺陷病毒1型(HIV-1)env基因的gp41跨膜区域进行了扩增。来自巴西南部伊塔亚伊的100个受感染个体的HIV-1前病毒DNA被用于分析该方法。根据该方法,确定了70个个体具有B,C,D和F亚型的预期大小的PCR产物。在这些个体中,观察到26个(37.1%)具有C型的预期扩增,而42个(60)观察到具有B型和D型亚型的预期产物。在B型和D型亚型扩增子中,有16种(22.9%)被归为D型,而26种(37.1%)被归为B型。两个个体(2.9 %)具有在进行亚型F特异性扩增后观察到的扩增子。将患者序列与参考序列进行测序并进行比较,确认了C和B型亚型的分类。但是,通过序列分析,在PCR分析中被错误确定为D和F的序列分别被确定为C型和B型。 。对于那些未获得扩增产物的个体,其患者病史中显示的低病毒载量可能解释了通过PCR方法进行亚型分型的困难。测试病毒载量对PCR扩增成功的影响时,ANOVA的结果证明了这一问题。获得的序列与HIV-1参考序列的比对证明存在高的亚型内多样性。这表明亚型特异性引物结合位点不保守或不代表在巴西人群中观察到的亚型,并且它们不允许对HIV-1亚型进行正确分类。因此,YAGYU等人提出的方法。不适用于巴西HIV-1亚型的分类。

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