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一种全自动高通量多重检测分析方法用于检测和区分 SARS-CoV-2 B.1.1.529(奥密克戎)和 B.1.617.2(德尔塔)谱系变异的临床评估。

Clinical Evaluation of a Fully-Automated High-Throughput Multiplex Screening-Assay to Detect and Differentiate the SARS-CoV-2 B.1.1.529 (Omicron) and B.1.617.2 (Delta) Lineage Variants.

机构信息

Institute of Medical Microbiology, Virology and Hygiene, University Medical Center Hamburg-Eppendorf (UKE), 20246 Hamburg, Germany.

Leibniz Institute for Experimental Virology (HPI), Virus Genomics, 20251 Hamburg, Germany.

出版信息

Viruses. 2022 Mar 15;14(3):608. doi: 10.3390/v14030608.

Abstract

BACKGROUND

The recently emerged SARS-CoV-2 B.1.1.529 lineage and its sublineages (Omicron variant) pose a new challenge to healthcare systems worldwide due to its ability to efficiently spread in immunized populations and its resistance to currently available monoclonal antibody therapies. RT-PCR-based variant tests can be used to screen large sample-sets rapidly and accurately for relevant variants of concern (VOC). The aim of this study was to establish and validate a multiplex assay on the cobas 6800/8800 systems to allow discrimination between the two currently circulating VOCs, Omicron and Delta, in clinical samples.

METHODS

Primers and probes were evaluated for multiplex compatibility. Analytic performance was assessed using cell culture supernatant of an Omicron variant isolate and a clinical Delta variant sample, normalized to WHO-Standard. Clinical performance of the multiplex assay was benchmarked against NGS results.

RESULTS

In silico testing of all oligos showed no interactions with a high risk of primer-dimer formation or amplification of human DNA/RNA. Over 99.9% of all currently available Omicron variant sequences are a perfect match for at least one of the three Omicron targets included in the multiplex. Analytic sensitivity was determined as 19.0 IU/mL (CI95%: 12.9-132.2 IU/mL) for the A67V + del-HV69-70 target, 193.9 IU/mL (CI95%: 144.7-334.7 IU/mL) for the E484A target, 35.5 IU/mL (CI95%: 23.3-158.0 IU/mL) for the N679K + P681H target and 105.0 IU/mL (CI95%: 80.7-129.3 IU/mL) for the P681R target. All sequence variances were correctly detected in the clinical sample set (225/225 Targets).

CONCLUSION

RT-PCR-based variant screening compared to whole genome sequencing is both rapid and reliable in detecting relevant sequence variations in SARS-CoV-2 positive samples to exclude or verify relevant VOCs. This allows short-term decision-making, e.g., for patient treatment or public health measures.

摘要

背景

最近出现的 SARS-CoV-2 B.1.1.529 谱系及其亚谱系(Omicron 变体)由于其在免疫人群中高效传播的能力以及对目前可用的单克隆抗体治疗的耐药性,对全球的医疗系统构成了新的挑战。基于 RT-PCR 的变体测试可用于快速、准确地筛选大量样本,以筛查相关的关注变体(VOC)。本研究旨在建立和验证 cobas 6800/8800 系统上的多重检测方法,以区分临床样本中的两种当前流行的 VOC,Omicron 和 Delta。

方法

评估引物和探针的多重兼容性。使用 Omicron 变体分离株的细胞培养上清液和临床 Delta 变体样本进行分析性能评估,标准化至世卫组织标准。该多重检测方法的临床性能与 NGS 结果进行了基准测试。

结果

所有寡核苷酸的计算机测试均未显示出相互作用的风险,也没有高风险的引物二聚体形成或人类 DNA/RNA 的扩增。超过 99.9%的所有当前可用的 Omicron 变体序列与多重检测中包含的三个 Omicron 靶标中的至少一个完全匹配。对于 A67V + del-HV69-70 靶标,分析灵敏度为 19.0 IU/mL(95%CI:12.9-132.2 IU/mL),对于 E484A 靶标为 193.9 IU/mL(95%CI:144.7-334.7 IU/mL),对于 N679K + P681H 靶标为 35.5 IU/mL(95%CI:23.3-158.0 IU/mL),对于 P681R 靶标为 105.0 IU/mL(95%CI:80.7-129.3 IU/mL)。在临床样本集中正确检测到所有序列变异(225/225 个靶标)。

结论

与全基因组测序相比,基于 RT-PCR 的变体筛查在检测 SARS-CoV-2 阳性样本中的相关序列变异方面既快速又可靠,可排除或验证相关的 VOC。这允许进行短期决策,例如患者治疗或公共卫生措施。

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