Department of Pathology, Immunology and Laboratory Medicine, USA.
AIDS. 2011 Jan 14;25(2):143-52. doi: 10.1097/QAD.0b013e328340fdaf.
the origin and evolution of HIV-1 in breast milk is unclear, despite the continuing significance of this tissue as a transmitting compartment. To elucidate the evolutionary trajectory of viral populations in a transient mucosal compartment, longitudinal sequences of the envelope glycoprotein (gp120) region from plasma and breast milk spanning the first year after delivery were analyzed in six women infected by HIV-1 subtype C.
multiple phylogenetic algorithms were used to elucidate the evolutionary history and spatial structure of virus populations between tissues.
overall persistent mixing of viral sequences between plasma and breast milk indicated that breast milk is not a distinct genetic viral compartment. Unexpectedly, longitudinal phylogenies showed multiple lineages defined by long branches that included virus from both the breast milk and the plasma. Plasma was unlikely the anatomical origin of the most recent common ancestor (MRCA) in at least three of the patients, although in other women, the temporal origin of the MRCA of the viral populations following delivery occurred well before the onset of breast milk production.
these findings suggest that during pregnancy/lactation, a viral variant distinct from the plasma virus initially seeds the breast milk, followed by subsequent gene flow between the plasma and breast milk tissues. This study indicates the potential for reactivation or reintroduction of distinct lineages during major immunological disruptions during the course of natural infection.
尽管母乳仍然是传播的一个重要部位,但 HIV-1 在母乳中的起源和进化仍不清楚。为了阐明短暂的黏膜部位病毒群体的进化轨迹,对 6 名感染 HIV-1 亚型 C 的妇女在分娩后第一年的血浆和母乳中包膜糖蛋白(gp120)区域的纵向序列进行了分析。
使用多种系统发育算法阐明了组织间病毒群体的进化历史和空间结构。
总体上,血浆和母乳之间的病毒序列持续混合,表明母乳不是一个独特的遗传病毒部位。出乎意料的是,纵向系统发育树显示了多个由长分支定义的谱系,其中包括来自母乳和血浆的病毒。在至少 3 名患者中,血浆不太可能是最近共同祖先(MRCA)的解剖学起源,尽管在其他女性中,分娩后母乳中病毒群体的 MRCA 的时间起源发生在母乳产生之前。
这些发现表明,在妊娠/哺乳期,与血浆病毒不同的病毒变体最初在母乳中定植,随后在血浆和母乳组织之间发生基因流。这项研究表明,在自然感染过程中发生重大免疫破坏时,可能会重新激活或重新引入不同的谱系。