Institute of Clinical Molecular Biology, Kiel University, Kiel, Germany.
Department of Archaeology, Hanseatic City of Lübeck Historic Monuments Protection Authority, Lübeck, Germany.
Front Immunol. 2021 Jul 15;12:691475. doi: 10.3389/fimmu.2021.691475. eCollection 2021.
Outbreaks of infectious diseases repeatedly affected medieval Europe, leaving behind a large number of dead often inhumed in mass graves. Human remains interred in two burial pits from 14 century CE Germany exhibited molecular evidence of Paratyphi C ( Paratyphi C) infection. The pathogen is responsible for paratyphoid fever, which was likely the cause of death for the buried individuals. This finding presented the unique opportunity to conduct a paratyphoid fever association study in a European population. We focused on HLA-DRB103:01 that is a known risk allele for enteric fever in present-day South Asians. We generated HLA profiles for 29 medieval Paratyphi C cases and 24 contemporaneous controls and compared these to a modern German population. The frequency of the risk allele was higher in the medieval cases (29.6%) compared to the contemporaneous controls (13%; ), albeit not significantly so, possibly because of small sample sizes. Indeed, in comparison with the modern controls (; 10.2%; ) the frequency difference became statistically significant. This comparison also suggested a slight decrease in the allele's prevalence between the medieval and modern controls. Up to now, this is the first study on the genetic predisposition to infection in Europeans and the only association analysis on paratyphoid fever C. Functional investigation using computational binding prediction between HLA variants and Paratyphi and Typhi peptides supported a reduced recognition capacity of bacterial proteins by DRB103:01 relative to other common DRB1 variants. This pattern could potentially explain the disease association. Our results suggest a slightly reduced predisposition to paratyphoid fever in modern Europeans. The causative allele, however, is still common today, which can be explained by a trade-off, as DRB1*03:01 is protective against infectious respiratory diseases such as severe respiratory syndrome (SARS). It is thus possible that the allele also provided resistance to corona-like viruses in the past.
传染病的爆发反复袭击中世纪的欧洲,留下了大量的死者,他们经常被埋在万人坑里。从 14 世纪的德国两个墓穴中挖掘出的人类遗骸显示出 C 型副伤寒(Paratyphi C)感染的分子证据。该病原体是引起副伤寒的原因,很可能是这些被埋葬的人的死因。这一发现为在欧洲人群中进行副伤寒关联研究提供了独特的机会。我们专注于 HLA-DRB103:01,这是当今南亚肠热病的已知风险等位基因。我们为 29 名中世纪 C 型副伤寒病例和 24 名同期对照生成了 HLA 图谱,并将这些与现代德国人群进行了比较。风险等位基因在中世纪病例中的频率(29.6%)高于同期对照(13%),尽管差异不显著,这可能是由于样本量小。实际上,与现代对照相比(10.2%),这种频率差异具有统计学意义。这一比较还表明,该等位基因在中世纪和现代对照之间的流行率略有下降。到目前为止,这是第一项关于欧洲人感染遗传易感性的研究,也是唯一一项关于 C 型副伤寒的关联分析。使用 HLA 变异体与副伤寒和伤寒肽之间的计算结合预测进行功能研究,支持 DRB103:01 相对于其他常见 DRB1 变异体对细菌蛋白的识别能力降低。这种模式可能可以解释疾病的关联。我们的研究结果表明,现代欧洲人对副伤寒的易感性略有降低。然而,致病等位基因今天仍然很常见,这可以通过权衡来解释,因为 DRB1*03:01 对呼吸道传染病如严重呼吸道综合征(SARS)具有保护作用。因此,在过去,该等位基因也可能对类似冠状病毒的病毒提供了抵抗力。