间隙
纳米孔测序
纳米孔
医学
病毒
病毒学
基因型
计算生物学
DNA测序
生物
基因
遗传学
纳米技术
材料科学
泌尿科
作者
Xiulan Li,Xiaoke Wei,Xin Liu,Nan Wang,Fuqiang Xu,Xingyu Liu,Yanmei Li,Yuxiang Zhou,Huadong Tang,Meina Bian,Ying Hou,Lili Zhang,Weiwei Wang,Qing Liu
出处
期刊:BMC Cancer
[Springer Nature]
日期:2023-11-02
卷期号:23 (1)
被引量:3
标识
DOI:10.1186/s12885-023-11538-2
摘要
Abstract Objective To detect the HPV genotype and integration sites in patients with high-risk HPV infection at different stages of photodynamic therapy using nanopore technology and to evaluate the treatment effect. Methods Four patients with HPV infection were selected and subjected to photodynamic therapy, and cervical exfoliated cell was sampled at before treatment, after three courses of treatment and six courses of treatment, their viral abundance and insertion sites were analyzed by nanopore technology, and pathological examinations were performed before and after treatment. In this study, we developed a novel assay that combined viral sequence enrichment and Nanopore sequencing for identification of HPV genotype and integration sites at once. The assay has obvious advantages over qPCR or NGS-based methods, as it has better sensitivity after viral sequences enrichment and can generate long-reads (kb to Mb) for better detection rate of structure variations, moreover, fast turn-around time for real-time viral sequencing and analysis. Results The pathological grade was reduced in all four patients after photodynamic therapy. Virus has been cleared in two cases after treatment, the virus amount reduced after treatment but not completely cleared in one case, and two type viruses were cleared and one type virus persisted after treatment in the last patient with multiple infection. Viral abundance and the number of integration sites were positively correlated. Gene enrichment analysis showed complete viral clearance in 1 patient and 3 patients required follow-up. Conclusion Nanopore sequencing can effectively monitor the abundance of HPV viruses and integration sites to show the presence status of viruses, and combined with the results of gene enrichment analysis, the treatment effect can be dynamically assessed.
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