UK Health Security Agency, Science Group, Porton Down, Salisbury, United Kingdom; Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom.
UK Health Security Agency, Science Group, Porton Down, Salisbury, United Kingdom.
J Virol Methods. 2024 Jan;323:114833. doi: 10.1016/j.jviromet.2023.114833. Epub 2023 Oct 23.
Crimean-Congo haemorrhagic fever (CCHF) is the most prevalent human tick-borne viral disease, endemic to the Balkans, Africa, Middle East and Asia. There are currently no licensed vaccines or effective antivirals against CCHF. CCHF virus (CCHFV) has a negative sense segmented tripartite RNA genome consisting of the small (S), medium (M) and large (L) segments. Depending on the segment utilised for genetic affiliation, there are up to 7 circulating lineages of CCHFV. The current lack of geographical representation of CCHFV sequences in various repositories highlights a requirement for increased CCHFV sequencing capabilities in endemic regions. We have optimised and established a multiplex PCR tiling methodology for the targeted enrichment of complete genomes of Europe 1 CCHFV lineage directly from clinical samples and compared its performance to a non-targeted enrichment approach on both short-read and long-read sequencing platforms. We have found a statistically significant increase in mapped viral sequencing reads produced with our targeted enrichment approach. This has allowed us to recover near complete S segment sequences and above 90% of the M and L segment sequences for samples with Ct values as high as 31.3. This study demonstrates the superiority of a targeted enrichment approach for recovery of CCHFV genomic sequences from samples with low virus titre. CCHFV is an important vector-borne human pathogen with wide geographical distribution. The validated methodology reported here adds value to front-line public health laboratories employing genomic sequencing for CCHFV Europe 1 lineage surveillance, particularly in the Balkan and Middle Eastern territories currently monitoring the spread of the pathogen. Tracking the genomic evolution of the virus across regions improves risk assessment and directly informs the development of diagnostics, therapeutics, and vaccines.
克里米亚-刚果出血热(CCHF)是最常见的人类蜱传病毒性疾病,流行于巴尔干、非洲、中东和亚洲。目前尚无针对 CCHF 的许可疫苗或有效抗病毒药物。CCHF 病毒(CCHFV)具有负义分段三部分 RNA 基因组,由小(S)、中(M)和大(L)片段组成。根据用于遗传关联的片段,CCHFV 有多达 7 种循环谱系。目前,不同存储库中 CCHFV 序列的地理代表性不足,突出了在流行地区增加 CCHFV 测序能力的必要性。我们已经优化并建立了一种多重 PCR 平铺方法,用于直接从临床样本中靶向富集欧洲 1 谱系的 CCHFV 完整基因组,并将其性能与短读长和长读长测序平台上的非靶向富集方法进行了比较。我们发现,使用我们的靶向富集方法产生的映射病毒测序读数有统计学意义的增加。这使我们能够恢复 Ct 值高达 31.3 的样本的近乎完整的 S 片段序列和超过 90%的 M 和 L 片段序列。这项研究表明,靶向富集方法在从低病毒载量样本中恢复 CCHFV 基因组序列方面具有优越性。CCHFV 是一种具有广泛地理分布的重要虫媒人类病原体。这里报道的经过验证的方法为使用基因组测序进行 CCHF 欧洲 1 谱系监测的一线公共卫生实验室增加了价值,特别是在目前正在监测病原体传播的巴尔干和中东地区。跟踪病毒在不同地区的基因组进化可以提高风险评估,并直接为诊断、治疗和疫苗的开发提供信息。