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Perinatal Transmission of Major Minor and Multiple Maternal Human Immunodeficiency Virus Type 1 Variants In Utero and Intrapartum

机译:主要次要和多种母体免疫缺陷病毒1型变异在围产期和围产期的围产期传播

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摘要

Previous studies have provided conflicting data on the presence of selective pressures in the transmission of a homogeneous maternal viral subpopulation to the infant. Therefore, the purpose of this study was to definitively characterize the human immunodeficiency virus type 1 (HIV-1) quasispecies transmitted in utero and intrapartum. HIV-1 envelope gene diversity from peripheral blood mononuclear cells and plasma was measured during gestation and at delivery in mothers who did and did not transmit HIV perinatally by using a DNA heteroduplex mobility assay. Children were defined as infected in utero or intrapartum based on the timing of the first detection of HIV. Untreated transmitting mothers (n = 19) had significantly lower HIV-1 quasispecies diversity at delivery than untreated nontransmittting mothers (n = 18) (median Shannon entropy, 0.711 [0.642 to 0.816] versus 0.853 [0.762 to 0.925], P = 0.005). Eight mothers transmitted a single major env variant to their infants in utero, and one mother transmitted a single major env variant intrapartum. Four mothers transmitted multiple HIV-1 env variants to their infants in utero, and two mothers transmitted multiple env variants intrapartum. The remaining six intrapartum- and two in utero-infected infants had a homogeneous HIV-1 env quasispecies which did not comigrate with their mothers' bands at their first positive time point. In conclusion, in utero transmitters were more likely to transmit single or multiple major maternal viral variants. In contrast, intrapartum transmitters were more likely to transmit minor HIV-1 variants. These data indicate that different selective pressures, depending on the timing of transmission, may be involved in determining the pattern of maternal HIV-1 variant transmission.
机译:先前的研究提供了关于均质母体病毒亚群向婴儿传播中存在选择性压力的矛盾数据。因此,本研究的目的是明确鉴定在子宫内和产后传播的人类免疫缺陷病毒1型(HIV-1)准种的特征。通过使用DNA异源双链流动性测定,在围产期和未围产HIV传播的母亲中,在妊娠期间和分娩时测量了外周血单核细胞和血浆的HIV-1包膜基因多样性。根据首次检测到HIV的时间,将儿童定义为子宫内或分娩期感染。未经治疗的传播母亲(n = 19)分娩时的HIV-1准种多样性明显低于未经治疗的未传播母亲(n = 18)(中位数香农熵,分别为0.711 [0.642至0.816]和0.853 [0.762至0.925],P = 0.005) 。八名母亲向子宫内的婴儿传播了一个单一的主要环境变体,一名母亲在产时传播了一个单一的主要环境变体。四名母亲向子宫内的婴儿传播了多个HIV-1 env变异体,两名母亲在产时传播了多个env变异体。其余的六个分娩期和两个在子宫内感染的婴儿具有同质的HIV-1 env准种,在他们的第一个阳性时间点与母体的谱带不相称。总之,在子宫内的传播者更可能传播单个或多个主要的母体病毒变异。相反,产时传播者更可能传播较小的HIV-1变异体。这些数据表明,取决于传播的时机,不同的选择压力可能涉及确定孕妇HIV-1变异传播的方式。

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