White Tiffany, Hagen Moira, Gudza Ivy, White Irene E, Ndemera Buxton, Gwanzura Lovemore, Borok Margaret, Campbell Thomas B
Division of Infectious Diseases, Department of Medicine, University of Colorado at Denver and Health Sciences Center, Denver, CO 80262, USA.
J Clin Virol. 2008 Jun;42(2):165-71. doi: 10.1016/j.jcv.2008.02.006. Epub 2008 Apr 3.
Kaposi's sarcoma-associated herpesvirus (KSHV) encodes genetically diverse K1 alleles which have unique geographic distributions. Little is known about K1 genetic diversity in Zimbabwe where acquired immunodeficiency syndrome-associated KS (AIDS-KS) is epidemic.
Evaluate K1 diversity in Zimbabwe and compare Zimbabwean K1 diversity to other areas in Africa.
K1 nucleotide sequence was determined for AIDS-KS cases in Zimbabwe. K1 references sequences were obtained from Genbank.
Among 65 Zimbabwean AIDS-KS cases, 26 (40%) were K1 subtype A and 39 (60%) were subtype B. Zimbabwean subtype A sequences grouped only with African intratype A5 variants. Zimbabwean subtype B sequences grouped with multiple intratype African variants: 26 B1 (26%), four B3 (6%) and nine highly divergent B4 (14%). Zimbabwean subtype B had a lower synonymous to nonsynonymous mutation ratio (median 0.59 versus 0.66; P=0.008) and greater distance to the most recent common ancestor (median 0.03 versus 0.009; P<0.001) compared to subtype A. Within the B subgroup, the distribution of intratype B variants differed in Zimbabwe and Uganda (P=0.004).
Greater positive selection and genetic diversity in K1 subtype B compared to subtype A5 exist in Zimbabwe. However, there were no significant associations between K1 subtype and the clinical or demographic characteristics of AIDS-KS cases.
卡波西肉瘤相关疱疹病毒(KSHV)编码具有遗传多样性的K1等位基因,这些等位基因具有独特的地理分布。在获得性免疫缺陷综合征相关卡波西肉瘤(AIDS-KS)流行的津巴布韦,人们对K1基因多样性知之甚少。
评估津巴布韦的K1多样性,并将津巴布韦的K1多样性与非洲其他地区进行比较。
测定了津巴布韦AIDS-KS病例的K1核苷酸序列。从Genbank获得K1参考序列。
在65例津巴布韦AIDS-KS病例中,26例(40%)为K1 A亚型,39例(60%)为B亚型。津巴布韦的A亚型序列仅与非洲A5型内变体聚类。津巴布韦的B亚型序列与多个非洲型内变体聚类:26例B1(26%)、4例B3(6%)和9例高度分化的B4(14%)。与A亚型相比,津巴布韦B亚型的同义突变与非同义突变比率较低(中位数分别为0.59和0.66;P=0.008),与最近共同祖先的距离更大(中位数分别为0.03和0.009;P<0.001)。在B亚组中,津巴布韦和乌干达的型内B变体分布不同(P=0.004)。
在津巴布韦,K1 B亚型比A5亚型存在更大的正选择和遗传多样性。然而,K1亚型与AIDS-KS病例的临床或人口统计学特征之间没有显著关联。