University of Washington, Department of Microbiology, Seattle, Washington, United States of America.
University of Washington, Department of Medicine Seattle, Washington, United States of America.
PLoS Pathog. 2021 Jan 19;17(1):e1008594. doi: 10.1371/journal.ppat.1008594. eCollection 2021 Jan.
Intra-host tumor virus variants may influence the pathogenesis and treatment responses of some virally-associated cancers. However, the intra-host variability of Kaposi sarcoma-associated herpesvirus (KSHV), the etiologic agent of Kaposi sarcoma (KS), has to date been explored with sequencing technologies that possibly introduce more errors than that which occurs in the viral population, and these studies have only studied variable regions. Here, full-length KSHV genomes in tumors and/or oral swabs from 9 Ugandan adults with HIV-associated KS were characterized. Furthermore, we used deep, short-read sequencing using duplex unique molecular identifiers (dUMI)-random double-stranded oligonucleotides that barcode individual DNA molecules before library amplification. This allowed suppression of PCR and sequencing errors to ~10-9/base as well as afforded accurate determination of KSHV genome numbers sequenced in each sample. KSHV genomes were assembled de novo, and rearrangements observed were confirmed by PCR and Sanger sequencing. 131-kb KSHV genome sequences, excluding major repeat regions, were successfully obtained from 23 clinical specimens, averaging 2.3x104 reads/base. Strikingly, KSHV genomes were virtually identical within individuals at the point mutational level. The intra-host heterogeneity that was observed was confined to tumor-associated KSHV mutations and genome rearrangements, all impacting protein-coding sequences. Although it is unclear whether these changes were important to tumorigenesis or occurred as a result of genomic instability in tumors, similar changes were observed across individuals. These included inactivation of the K8.1 gene in tumors of 3 individuals and retention of a region around the first major internal repeat (IR1) in all instances of genomic deletions and rearrangements. Notably, the same breakpoint junctions were found in distinct tumors within single individuals, suggesting metastatic spread of rearranged KSHV genomes. These findings define KSHV intra-host heterogeneity in vivo with greater precision than has been possible in the past and suggest the possibility that aberrant KSHV genomes may contribute to aspects of KS tumorigenesis. Furthermore, study of KSHV with use of dUMI provides a proof of concept for utilizing this technique for detailed study of other virus populations in vivo.
宿主内肿瘤病毒变异可能影响某些病毒相关性癌症的发病机制和治疗反应。然而,迄今为止,卡波西肉瘤相关疱疹病毒(KSHV),即卡波西肉瘤(KS)的病原体,在宿主内的变异性仅通过可能比病毒群体中发生的错误更多的测序技术进行了探索,而且这些研究仅研究了可变区。在这里,我们对 9 名乌干达患有 HIV 相关 KS 的成年人的肿瘤和/或口腔拭子中的全长 KSHV 基因组进行了特征描述。此外,我们使用深度、短读测序技术,使用双链独特分子标识符(dUMI)-随机双链寡核苷酸,在文库扩增前对单个 DNA 分子进行条码标记。这使得 PCR 和测序错误的抑制率达到约 10-9/碱基,并且能够准确确定每个样本中测序的 KSHV 基因组数量。从头组装 KSHV 基因组,并通过 PCR 和 Sanger 测序确认观察到的重排。从 23 个临床标本中成功获得了排除主要重复区的 131kb KSHV 基因组序列,平均每个碱基 2.3x104 个读数。引人注目的是,在个体内 KSHV 基因组在点突变水平上几乎完全相同。观察到的个体内异质性仅限于肿瘤相关的 KSHV 突变和基因组重排,所有这些都影响蛋白质编码序列。虽然尚不清楚这些变化是否对肿瘤发生很重要,或者是否是肿瘤中基因组不稳定性的结果,但在个体之间观察到了类似的变化。这些变化包括在 3 名个体的肿瘤中 K8.1 基因失活,以及在所有基因组缺失和重排的情况下保留第一个主要内部重复(IR1)周围的区域。值得注意的是,在单个个体的不同肿瘤中发现了相同的断裂点连接,这表明重排的 KSHV 基因组发生了转移。这些发现比以往更精确地定义了体内 KSHV 的个体内异质性,并表明异常的 KSHV 基因组可能有助于 KS 肿瘤发生的某些方面。此外,使用 dUMI 研究 KSHV 为利用该技术对体内其他病毒群体进行详细研究提供了概念验证。