Smith Davey, Delport Wayne, Butler David, Little Susan, Richman Douglas, Pond Sergei Kosakovsky
University of California, San Diego, La Jolla, CA 92093, USA.
Sci Transl Med. 2010 Sep;2(50):501r1. doi: 10.1126/scitranslmed.3001473.
In this investigation, we evaluated explanations for the unusual degree of genetic diversity in HIV populations within the sampled seminal cell and plasma compartments observed in our previous study. These analyses included clonal sequencing of HIV DNA in peripheral blood mononuclear cells, ultradeep sequencing of HIV RNA in blood plasma, human leukocyte antigen (HLA) haplotyping of previously used samples, and a BLAST screen against both a local and public repository of HIV-1 sequences, and the investigations to determine whether these observations were secondary to contamination or artifact were unsuccessful. As there are very few HIV sequences from seminal cell tissues and transmission pairs described in the literature, future studies that evaluate more transmission pairs with sampling from multiple anatomic compartments and at multiple time points will most likely be required to resolve this controversy.
在本研究中,我们评估了对我们之前研究中观察到的精液细胞和血浆区室中HIV群体异常程度的遗传多样性的解释。这些分析包括外周血单核细胞中HIV DNA的克隆测序、血浆中HIV RNA的超深度测序、先前使用样本的人类白细胞抗原(HLA)单倍型分析,以及针对本地和公共HIV-1序列库的BLAST筛选,并且确定这些观察结果是否继发于污染或假象的研究未成功。由于文献中描述的来自精液细胞组织和传播配对的HIV序列非常少,未来可能需要进行更多研究,从多个解剖区室和多个时间点进行采样,以评估更多的传播配对,从而解决这一争议。