Mulder-Kampinga G A, Simonon A, Kuiken C L, Dekker J, Scherpbier H J, van de Perre P, Boer K, Goudsmit J
Human Retrovirus Laboratory, Academic Medical Center, Amsterdam, The Netherlands.
J Virol. 1995 Apr;69(4):2285-96. doi: 10.1128/JVI.69.4.2285-2296.1995.
Variation in the env (V3 region) and gag (p17 region) genes of genomic RNA of human immunodeficiency virus type 1 was studied in three mother-child pairs. One infant was human immunodeficiency virus type 1 RNA positive at birth (pair 114), one became positive 6 weeks after birth (pair 127), and one became positive 30 months after birth (pair 564). The first two children were born to seropositive mothers, and the last child was infected by breast-feeding following seroconversion of the mother after delivery. In both V3 and p17gag, intrasample variability was much higher in the maternal samples, including the first seropositive sample of the seroconverted mother, than in the infants' samples. Variability was less in p17gag than in V3, except in the postnatally infected child. In all three cases, infection of the child was established by variants representing a minority of the cell-free virus population in the maternal samples. For the two infants born to seropositive mothers, V3 sequences were more similar to the sequence populations of maternal samples collected during pregnancy than to those of samples collected at delivery or thereafter. However, in pair 114 a V3 variant identical to the child's virus was also detected in the sample collected at delivery. In contrast to the V3 region, p17gag sequences of maternal samples of the first trimester of pregnancy and at delivery had comparable resemblance to the child's sequences in pair 114, while in pair 127, similarity to sequences of the sample collected at delivery was higher than that to sequences of the sample from early in pregnancy. In the last pair, V3 and p17gag sequences from a maternal sample collected 18 months prior to the first RNA-positive sample of the child resembled the infant's sequences as much as the sample collected close to the presumed time of infection. Taken together, the evolutionary characteristics for genomic RNA env and gag genes did not point to a particular time of mother-to-child transmission.
对三对母婴的人类免疫缺陷病毒1型基因组RNA的env(V3区)和gag(p17区)基因变异情况进行了研究。一名婴儿出生时人类免疫缺陷病毒1型RNA呈阳性(第114对),一名在出生6周后呈阳性(第127对),另一名在出生30个月后呈阳性(第564对)。前两个孩子的母亲血清学呈阳性,最后一个孩子是在母亲分娩后血清转化后通过母乳喂养感染的。在V3和p17gag中,包括血清转化母亲的首个血清阳性样本在内,母亲样本中的样本内变异性远高于婴儿样本。除了出生后感染的儿童外,p17gag中的变异性低于V3。在所有三例中,儿童感染是由代表母亲样本中无细胞病毒群体少数的变异株引起的。对于血清学呈阳性母亲所生的两名婴儿,V3序列与孕期采集的母亲样本的序列群体更相似,而与分娩时或之后采集的样本的序列群体不太相似。然而,在第114对中,在分娩时采集的样本中也检测到了与儿童病毒相同的V3变异株。与V3区不同,妊娠早期和分娩时母亲样本的p17gag序列与第114对中儿童的序列具有相当的相似性,而在第127对中,与分娩时采集的样本序列的相似性高于与妊娠早期样本序列的相似性。在最后一对中,在儿童首个RNA阳性样本之前18个月采集的母亲样本的V3和p17gag序列与婴儿序列的相似程度与接近推测感染时间采集的样本相似程度相同。综上所述,基因组RNA env和gag基因的进化特征并未指向母婴传播的特定时间。