Institute of Microbiology and Immunology, Faculty of Medicine, University of Ljubljana, SI-1000 Ljubljana, Slovenia.
Department of Infectious Diseases, Ljubljana University Medical Center, SI-1000 Ljubljana, Slovenia.
Viruses. 2022 Jun 10;14(6):1267. doi: 10.3390/v14061267.
The clinical presentation of tick-borne encephalitis virus (TBEV) infection varies from asymptomatic to severe meningoencephalitis or meningoencephalomyelitis. The TBEV subtype has been suggested as one of the most important risk factors for disease severity, but TBEV genetic characterization is difficult. Infection is usually diagnosed in the post-viremic phase, and so relevant clinical samples of TBEV are extremely rare and, when present, are associated with low viral loads. To date, only two complete TBEV genomes sequenced directly from patient clinical samples are publicly available. The aim of this study was to develop novel protocols for the direct sequencing of the TBEV genome, enabling studies of viral genetic determinants that influence disease severity. We developed a novel oligonucleotide primer scheme for amplification of the complete TBEV genome. The primer set was tested on 21 clinical samples with various viral loads and collected over a 15-year period using the two most common sequencing platforms. The amplicon-based strategy was compared to direct shotgun sequencing. Using the novel primer set, we successfully obtained nearly complete TBEV genomes (>90% of genome) from all clinical samples, including those with extremely low viral loads. Comparison of consensus sequences of the TBEV genome generated using the novel amplicon-based strategy and shotgun sequencing showed no difference. We conclude that the novel primer set is a powerful tool for future studies on genetic determinants of TBEV that influence disease severity and will lead to a better understanding of TBE pathogenesis.
蜱传脑炎病毒(TBEV)感染的临床特征从无症状到严重的脑膜脑炎或脑膜脊髓炎不等。TBEV 亚型被认为是疾病严重程度的最重要危险因素之一,但 TBEV 的遗传特征分析具有一定难度。感染通常发生在病毒血症后阶段,因此相关的 TBEV 临床样本极其罕见,而且存在时病毒载量也很低。迄今为止,仅公开了从患者临床样本中直接测序的两个完整 TBEV 基因组。本研究旨在开发用于直接测序 TBEV 基因组的新方案,以研究影响疾病严重程度的病毒遗传决定因素。我们开发了一种新的寡核苷酸引物方案,用于扩增完整的 TBEV 基因组。使用两种最常见的测序平台,在 21 个具有不同病毒载量的临床样本中对该引物集进行了测试。该基于扩增子的策略与直接鸟枪法测序进行了比较。使用新的引物集,我们成功地从所有临床样本中获得了近乎完整的 TBEV 基因组(>基因组的 90%),包括那些病毒载量极低的样本。使用新的基于扩增子的策略生成的 TBEV 基因组共识序列与鸟枪法测序的比较结果无差异。我们得出结论,该新引物集是未来研究影响 TBE 严重程度的 TBEV 遗传决定因素的有力工具,将有助于更好地了解 TBE 的发病机制。