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本文引用的文献

1
The Third International Consensus Guidelines on the Management of Cytomegalovirus in Solid-organ Transplantation.《实体器官移植中巨细胞病毒管理的第三次国际共识指南》。
Transplantation. 2018 Jun;102(6):900-931. doi: 10.1097/TP.0000000000002191.
2
Risk Factors and Outcomes of Ganciclovir-Resistant Cytomegalovirus Infection in Solid Organ Transplant Recipients.实体器官移植受者中更昔洛韦耐药巨细胞病毒感染的危险因素和结局。
Clin Infect Dis. 2017 Jul 1;65(1):57-63. doi: 10.1093/cid/cix259.
3
Characterization of Human Cytomegalovirus Genome Diversity in Immunocompromised Hosts by Whole-Genome Sequencing Directly From Clinical Specimens.通过直接从临床标本进行全基因组测序,对免疫功能低下宿主的人类巨细胞病毒基因组多样性进行表征。
J Infect Dis. 2017 Jun 1;215(11):1673-1683. doi: 10.1093/infdis/jix157.
4
Detection of cytomegalovirus drug resistance mutations in solid organ transplant recipients with suspected resistance.对疑似耐药的实体器官移植受者进行巨细胞病毒耐药突变检测。
J Clin Virol. 2017 May;90:57-63. doi: 10.1016/j.jcv.2017.03.014. Epub 2017 Mar 21.
5
Detection of Low Frequency Multi-Drug Resistance and Novel Putative Maribavir Resistance in Immunocompromised Pediatric Patients with Cytomegalovirus.免疫功能低下的小儿巨细胞病毒感染患者低频多药耐药性及新型假定的马里巴韦耐药性的检测
Front Microbiol. 2016 Sep 9;7:1317. doi: 10.3389/fmicb.2016.01317. eCollection 2016.
6
Contribution of next generation sequencing to early detection of cytomegalovirus UL97 emerging mutants and viral subpopulations analysis in kidney transplant recipients.下一代测序技术在肾移植受者巨细胞病毒UL97新出现突变体的早期检测及病毒亚群分析中的贡献
J Clin Virol. 2016 Jul;80:74-81. doi: 10.1016/j.jcv.2016.04.017. Epub 2016 Apr 27.
7
Management of cytomegalovirus infection in solid organ transplant recipients: SET/GESITRA-SEIMC/REIPI recommendations.实体器官移植受者巨细胞病毒感染的管理:SET/GESITRA-SEIMC/REIPI建议
Transplant Rev (Orlando). 2016 Jul;30(3):119-43. doi: 10.1016/j.trre.2016.04.001. Epub 2016 Apr 29.
8
Approach to drug-resistant cytomegalovirus in transplant recipients.移植受者中耐药巨细胞病毒的处理方法。
Curr Opin Infect Dis. 2015 Aug;28(4):293-9. doi: 10.1097/QCO.0000000000000170.
9
Sambamba: fast processing of NGS alignment formats.Sambamba:快速处理 NGS 比对格式。
Bioinformatics. 2015 Jun 15;31(12):2032-4. doi: 10.1093/bioinformatics/btv098. Epub 2015 Feb 19.
10
Orchestrating high-throughput genomic analysis with Bioconductor.使用Bioconductor编排高通量基因组分析。
Nat Methods. 2015 Feb;12(2):115-21. doi: 10.1038/nmeth.3252.

使用下一代测序提高疑似耐药的实体器官移植受者中巨细胞病毒耐药突变的检测。

Improvement in detecting cytomegalovirus drug resistance mutations in solid organ transplant recipients with suspected resistance using next generation sequencing.

机构信息

Department of Clinical Microbiology, Hospital Clinic, Universidad de Barcelona, Institute for Global Health, (ISGlobal), Barcelona, Spain.

Unit of Infectious Diseases, Instituto de Investigación Hospital 12 Octubre (i + 12) University Hospital 12 de Octubre, Universidad Complutense, Madrid, Spain.

出版信息

PLoS One. 2019 Jul 18;14(7):e0219701. doi: 10.1371/journal.pone.0219701. eCollection 2019.

DOI:10.1371/journal.pone.0219701
PMID:31318908
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6638921/
Abstract

OBJETIVES

The aim of this study was to identify CMV drug resistance mutations (DRM) in solid organ transplant (SOT) recipients with suspected resistance comparing next-generation sequencing (NGS) with Sanger sequencing and assessing risk factors and the clinical impact of resistance.

METHODS

Using Sanger sequencing as the reference method, we prospectively assessed the ability of NGS to detect CMV DRM in the UL97 and UL54 genes in a nationwide observational study from September 2013 to August 2016.

RESULTS

Among 44 patients recruited, 14 DRM were detected by Sanger in 12 patients (27%) and 20 DRM were detected by NGS, in 16 (36%). NGS confirmed all the DRM detected by Sanger. The additional six mutations detected by NGS were present in <20% of the sequenced population, being located in the UL97 gene and conferring high-level resistance to ganciclovir. The presence of DRM by NGS was associated with lung transplantation (p = 0.050), the administration of prophylaxis (p = 0.039), a higher mean time between transplantation and suspicion of resistance (p = 0.038) and longer antiviral treatment duration before suspicion (p = 0.024). However, the latter was the only factor independently associated with the presence of DRM by NGS in the multivariate analysis (OR 2.24, 95% CI 1.03 to 4.87).

CONCLUSIONS

NGS showed a higher yield than Sanger sequencing for detecting CMV resistance mutations in SOT recipients. The presence of DRM detected by NGS was independently associated with longer antiviral treatment.

摘要

目的

本研究旨在比较下一代测序(NGS)与 Sanger 测序,在疑似耐药的实体器官移植(SOT)受者中识别巨细胞病毒(CMV)药物耐药突变(DRM),评估耐药的危险因素和临床影响。

方法

我们使用 Sanger 测序作为参考方法,前瞻性评估 NGS 在 2013 年 9 月至 2016 年 8 月进行的一项全国性观察性研究中检测 UL97 和 UL54 基因中 CMV DRM 的能力。

结果

在招募的 44 名患者中,12 名患者(27%)通过 Sanger 检测到 14 种 DRM,16 名患者(36%)通过 NGS 检测到 20 种 DRM。NGS 证实了 Sanger 检测到的所有 DRM。NGS 检测到的另外 6 种突变存在于<20%的测序人群中,位于 UL97 基因中,对更昔洛韦具有高水平耐药性。NGS 检测到的 DRM 与肺移植(p = 0.050)、预防治疗(p = 0.039)、移植后与疑似耐药的平均时间间隔较长(p = 0.038)和疑似耐药前抗病毒治疗时间较长有关(p = 0.024)。然而,在后多变量分析中,这是唯一与 NGS 检测到 DRM 相关的因素(OR 2.24,95%CI 1.03 至 4.87)。

结论

与 Sanger 测序相比,NGS 检测 SOT 受者 CMV 耐药突变的检出率更高。NGS 检测到的 DRM 与更长的抗病毒治疗时间独立相关。