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本文引用的文献

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Optimized amplification of BK polyomavirus in urine.优化尿液 BK 多瘤病毒的扩增。
J Virol Methods. 2022 Jan;299:114319. doi: 10.1016/j.jviromet.2021.114319. Epub 2021 Oct 7.
2
Human APOBEC3 Variations and Viral Infection.人类 APOBEC3 变异与病毒感染。
Viruses. 2021 Jul 14;13(7):1366. doi: 10.3390/v13071366.
3
MEGA11: Molecular Evolutionary Genetics Analysis Version 11.MEGA11:分子进化遗传学分析版本 11。
Mol Biol Evol. 2021 Jun 25;38(7):3022-3027. doi: 10.1093/molbev/msab120.
4
Generation of BK and JC Polyomavirus Defective Viral Genomes in Human Urine Samples Associated with Higher Viral Loads.在与较高病毒载量相关的人类尿液样本中生成 BK 和 JC 多瘤病毒缺陷型病毒基因组。
J Virol. 2021 May 24;95(12). doi: 10.1128/JVI.00250-21.
5
BK polyomavirus diversity-Why viral variation matters.BK 多瘤病毒多样性——病毒变异为何重要。
Rev Med Virol. 2020 Jul;30(4):e2102. doi: 10.1002/rmv.2102. Epub 2020 Mar 3.
6
BK polyomavirus nephropathy with systemic viral spread: Whole genome sequencing data from a fatal case of BKPyV infection.伴有全身病毒播散的BK多瘤病毒肾病:一例BKPyV感染致死病例的全基因组测序数据
Transpl Infect Dis. 2020 Apr;22(2):e13269. doi: 10.1111/tid.13269. Epub 2020 Mar 14.
7
Presentation of BK polyomavirus-associated hemorrhagic cystitis after allogeneic hematopoietic cell transplantation.异基因造血细胞移植后 BK 多瘤病毒相关性出血性膀胱炎的表现。
Blood Adv. 2020 Feb 25;4(4):617-628. doi: 10.1182/bloodadvances.2019000802.
8
The Natural History of BK Polyomavirus and the Host Immune Response After Stem Cell Transplantation.BK 多瘤病毒的自然史与干细胞移植后宿主免疫反应。
Clin Infect Dis. 2020 Dec 15;71(12):3044-3054. doi: 10.1093/cid/ciz1194.
9
The detection of BKPyV genotypes II and IV after renal transplantation as a simple tool for risk assessment for PyVAN and transplant outcome already at early stages of BKPyV reactivation.肾移植后检测 BKPyV 基因型 II 和 IV 可作为一种简单的工具,用于在 BKPyV 再激活的早期阶段评估 PyVAN 风险和移植结果。
J Clin Virol. 2019 Apr;113:14-19. doi: 10.1016/j.jcv.2019.02.002. Epub 2019 Feb 10.
10
Bayesian phylogenetic and phylodynamic data integration using BEAST 1.10.使用BEAST 1.10进行贝叶斯系统发育和系统动力学数据整合。
Virus Evol. 2018 Jun 8;4(1):vey016. doi: 10.1093/ve/vey016. eCollection 2018 Jan.

BK 多瘤病毒在造血干细胞移植后的多样性。

BK Polyomavirus Diversity After Hematopoietic Stem Cell Transplantation.

机构信息

Division of Digestive Diseases, University of Cincinnati College of Medicine, Ohio.

Eurofins Viracor Laboratories, Lenexa, Kansas.

出版信息

J Infect Dis. 2023 Nov 2;228(9):1208-1218. doi: 10.1093/infdis/jiad117.

DOI:10.1093/infdis/jiad117
PMID:37165301
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10629712/
Abstract

BK polyomavirus (BKPyV) infection is common after hematopoietic stem cell transplantation (HSCT) and is associated with the development of hemorrhagic cystitis (HC). The role that BKPyV plays in the pathogenesis of HC is not well characterized. We investigated the impact of BKPyV diversity on the development of HC using a previously established cohort of pediatric HSCT patients. There were 147 urine samples with quantifiable BKPyV at month 1 after HSCT; 137 (93.2%) were amplified using our in-house polymerase chain reaction approach and sent for next-generation sequencing. Subtype Ia was most frequent (61.3%), followed by subtype Ib1 (31.4%). The median viral load of subtype Ia samples was higher than for subtype Ib1 at month 1. Across the protein coding regions, APOBEC-induced mutations and signature patterns associated with HC were identified. This is the largest sequencing study of a single cohort of HSCT patients, providing a vast resource of sequence data for future analyses.

摘要

BK 多瘤病毒 (BKPyV) 感染在造血干细胞移植 (HSCT) 后很常见,并且与出血性膀胱炎 (HC) 的发展有关。BKPyV 在 HC 发病机制中的作用尚未很好地描述。我们使用先前建立的儿科 HSCT 患者队列研究了 BKPyV 多样性对 HC 发展的影响。在 HSCT 后 1 个月有 147 份可定量 BKPyV 的尿液样本;137 份(93.2%)使用我们的内部聚合酶链反应方法进行了扩增,并进行了下一代测序。亚型 Ia 最为常见(61.3%),其次是 Ib1 亚型(31.4%)。在 1 个月时,Ia 型样本的病毒载量中位数高于 Ib1 型。在整个蛋白编码区中,鉴定了 APOBEC 诱导的突变和与 HC 相关的特征模式。这是对单个 HSCT 患者队列的最大测序研究,为未来的分析提供了大量的序列数据资源。