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