Lednicky John A, Butel Janet S, Luetke Maya C, Loeb Julia C
Department of Environmental and Global Health, College of Public Health and Health Professions, University of Florida, Box 100188, Gainesville, FL, 32610-0188, USA,
Virus Genes. 2014 Dec;49(3):490-2. doi: 10.1007/s11262-014-1119-z. Epub 2014 Sep 27.
A complete Human polyomavirus 9 (HPyV9) genome, designated HPyV9 UF-1, was amplified by rolling circle DNA amplification from DNA extracted from the peripheral blood mononuclear cells (PBMC) of an AIDS patient. The noncoding control (enhancer/promoter) region (NCCR) of HPyV9 UF-1 has one less AML-1a binding site and three more potential Sp1/GC box binding sites than the NCCRs of two previously described HPyV9 genomes. Nucleotide polymorphisms within the coding regions result in two amino acid differences in the deduced VP2 and VP3 proteins of HPyV9 UF-1 relative to those of the two previously described HPyV9 genomes. Exhaustive attempts to detect HPyV9 in DNA samples extracted from the PBMC of 40 healthy humans and 9 other AIDS patients were unsuccessful, highlighting the need for improved search strategies and optimal specimens for the detection of HPyV9 in humans.
通过滚环DNA扩增技术,从一名艾滋病患者外周血单个核细胞(PBMC)提取的DNA中扩增出一个完整的人类多瘤病毒9型(HPyV9)基因组,命名为HPyV9 UF-1。与之前描述的两个HPyV9基因组的非编码控制(增强子/启动子)区域(NCCR)相比,HPyV9 UF-1的NCCR少一个AML-1a结合位点,多三个潜在的Sp1/GC盒结合位点。编码区域内的核苷酸多态性导致HPyV9 UF-1推导的VP2和VP3蛋白与之前描述的两个HPyV9基因组相比有两个氨基酸差异。在从40名健康人和其他9名艾滋病患者的PBMC提取的DNA样本中,进行了详尽的检测HPyV9的尝试,但均未成功,这凸显了改进检测策略和优化样本以检测人类HPyV9的必要性。