Vázquez Pérez J A, Basualdo Sigales M C, Reyes-Terán G, Gudiño Rosales J C, Soler Claudín C
Unidad de Servicios Para Diagnóstico y Referencia en VIH, Instituto de Investigaciones Biomédicas UNAM/Secretaría de Salud del DF, México D.F.
Virol J. 2006 Jun 29;3:52. doi: 10.1186/1743-422X-3-52.
Some individuals repeatedly exposed to Human Immunodeficiency Virus do not seroconvert and are resistant to HIV infection. Here, in a pediatric cohort of HIV seronegative infants born of HIV-infected mothers, we have studied eight non-breastfed children in whom viral DNA was detected in their PBMC. Our objective was to assess whether silent infection in these children can be explained by the presence of integrated viral DNA.
The presence of viral DNA was corroborated by nested PCR with primers for gag and the nef/LTR regions of HIV-1. Integration of HIV DNA into the host genome was assessed by an Alu-LTR PCR. Amplicons were sequenced and phylogenetic analyzes were done.
HIV-1 DNA was detected in the earliest available PBMC sample from all eight infants, and two of them tested positive for HIV DNA at 2 years of age. Nested PCR resulted in the amplification of gag, nef/LTR and Alu-LTR fragments, which demostrated that HIV-1 DNA was integrated in the host cell genome. Each individual has a characteristic sequence pattern and is different from the LTR sequence of HXB2 prototype virus and other Mexican isolates.
HIV-1 DNA was observed in PBMC from HIV exposed seronegative children in this pediatric cohort.
一些反复接触人类免疫缺陷病毒的个体不会发生血清转化,并且对HIV感染具有抗性。在此,在一组由感染HIV的母亲所生的HIV血清阴性婴儿的儿科队列中,我们研究了8名非母乳喂养的儿童,在他们的外周血单核细胞中检测到了病毒DNA。我们的目的是评估这些儿童中的隐匿感染是否可以通过整合的病毒DNA的存在来解释。
通过使用针对HIV-1的gag和nef/LTR区域的引物进行巢式PCR来证实病毒DNA的存在。通过Alu-LTR PCR评估HIV DNA整合到宿主基因组中的情况。对扩增产物进行测序并进行系统发育分析。
在所有8名婴儿最早可获得的外周血单核细胞样本中均检测到HIV-1 DNA,其中2名在2岁时HIV DNA检测呈阳性。巢式PCR导致gag、nef/LTR和Alu-LTR片段的扩增,这表明HIV-1 DNA整合到了宿主细胞基因组中。每个个体都有独特的序列模式,并且不同于HXB2原型病毒和其他墨西哥分离株的LTR序列。
在该儿科队列中,在暴露于HIV的血清阴性儿童的外周血单核细胞中观察到了HIV-1 DNA。