Arnedo-Muñoz Maria, Prats-Méndez Ignasi, Gónzalez-Sánchez Alejandra, Martín Maria Carmen, Rando-Segura Ariadna, Arcos Ibai Los, Nadal-Barón Patricia, Saubi Narcís, Mendoza-Palomar Natalia, Bernat-Sole Marta, Albasanz-Puig Adaia, Piñana Maria, Andrés Cristina, Melendo-Pérez Susana, Larrosa Nieves, Antón Andrés, Esperalba Juliana
Microbiology Department, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Universitat Autònoma de Barcelona, Barcelona, Spain.
Department of Genetics and Microbiology, Universitat Autònoma de Barcelona (UAB), Barcelona, Spain.
J Med Virol. 2025 Aug;97(8):e70523. doi: 10.1002/jmv.70523.
This study introduces a new procedure for antiviral resistance analysis and genetic classification of human cytomegalovirus (HCMV) using next-generation sequencing (NGS) adapted to existing methodologies, aiming for more targets due to the recent use of new antivirals. It expands the classical investigation of mutations in UL54 and UL97 genes, associated with resistance to (val)ganciclovir, foscarnet and cidofovir, to include UL27, UL56 and UL89 genes, which target newer antivirals like maribavir and letermovir. Additionally, it includes the genetic analysis of UL55 (glycoprotein B) for genotype classification. This new methodology involves multiplex-PCR for DNA enrichment, followed by NGS using Illumina MiSeq platform and data analysis through an in-house pipeline. Several validations were performed by firstly using genome sequence from wild-type sensitive reference strain (AD-169), secondly comparing to previously characterized samples by Sanger, and lastly the use of external quality controls. A new NGS technique based on amplicons approach has been developed. Validation using wild-type control material showed 100% identity with the reference genome across all replicates. Only one minority variant was detected in one replicate. Compared to Sanger sequencing, NGS revealed additional low-frequency mutations not detected by Sanger, without impacting resistance interpretation. The method also performed reliably in external quality assessment controls. Moreover, the detection limit of the technique was established at 17 894.60 IU/mL. Finally, this approach enabled the identification of HCMV genotypes. This approach improves the monitoring of antiviral resistance and viral diversity, enhancing early clinical decision-making in immunocompromised patients.
本研究引入了一种新的程序,用于使用适用于现有方法的下一代测序(NGS)对人巨细胞病毒(HCMV)进行抗病毒耐药性分析和基因分型,由于最近新型抗病毒药物的使用,旨在检测更多靶点。它将与对(缬)更昔洛韦、膦甲酸钠和西多福韦耐药相关的UL54和UL97基因突变的经典研究扩展到包括UL27、UL56和UL89基因,这些基因针对如马立巴韦和来特莫韦等新型抗病毒药物。此外,它还包括用于基因型分类的UL55(糖蛋白B)基因分析。这种新方法包括用于DNA富集的多重PCR,随后使用Illumina MiSeq平台进行NGS,并通过内部流程进行数据分析。通过首先使用野生型敏感参考菌株(AD-169)的基因组序列、其次与之前通过桑格测序表征的样本进行比较以及最后使用外部质量控制进行了多项验证。开发了一种基于扩增子方法的新NGS技术。使用野生型对照材料进行的验证显示,所有重复样本与参考基因组的一致性均为100%。在一个重复样本中仅检测到一个少数变异。与桑格测序相比,NGS揭示了桑格测序未检测到的额外低频突变,且不影响耐药性解读。该方法在外部质量评估对照中也表现可靠。此外,该技术的检测限确定为17 894.60 IU/mL。最后,这种方法能够鉴定HCMV基因型。这种方法改善了对抗病毒耐药性和病毒多样性的监测,增强了免疫受损患者的早期临床决策。