Biomedical Research Centre, Norwich Medical School, University of East Anglia, Norwich Research Park, Norwich, UK.
Department of Genetics and Bioinformatics, Division of Health Data and Digitalisation, Norwegian Institute of Public Health, Oslo, Norway.
Nat Microbiol. 2019 May;4(5):826-836. doi: 10.1038/s41564-019-0377-x. Epub 2019 Mar 4.
Human cryptosporidiosis is the leading protozoan cause of diarrhoeal mortality worldwide, and a preponderance of infections is caused by Cryptosporidium hominis and C. parvum. Both species consist of several subtypes with distinct geographical distributions and host preferences (that is, generalist zoonotic and specialist anthroponotic subtypes). The evolutionary processes that drive the adaptation to the human host and the population structures of Cryptosporidium remain unknown. In this study, we analyse 21 whole-genome sequences to elucidate the evolution of anthroponosis. We show that Cryptosporidium parvum splits into two subclades and that the specialist anthroponotic subtype IIc-a shares a subset of loci with C. hominis that is undergoing rapid convergent evolution driven by positive selection. C. parvum subtype IIc-a also has an elevated level of insertion and deletion mutations in the peri-telomeric genes, which is also a characteristic of other specialist subtypes. Genetic exchange between Cryptosporidium subtypes plays a prominent role throughout the evolution of the genus. Interestingly, recombinant regions are enriched for positively selected genes and potential virulence factors, which indicates adaptive introgression. Analysis of 467 gp60 sequences collected from locations across the world shows that the population genetic structure differs markedly between the main zoonotic subtype (isolation-by-distance) and the anthroponotic subtype (admixed population structure). We also show that introgression between the four anthroponotic Cryptosporidium subtypes and species included in this study has occurred recently, probably within the past millennium.
人类隐孢子虫病是全球导致腹泻死亡的主要原生动物病因,而大多数感染是由人隐孢子虫和小隐孢子虫引起的。这两个物种都由几个具有不同地理分布和宿主偏好的亚型组成(即通用的人畜共患和专门的人源人畜共患病亚型)。驱动适应人类宿主和隐孢子虫种群结构的进化过程仍然未知。在这项研究中,我们分析了 21 个全基因组序列,以阐明人源感染的进化过程。我们发现小隐孢子虫分为两个亚群,专门的人源人畜共患病亚型 IIc-a 与正在经历正选择驱动的快速趋同进化的人隐孢子虫共享一部分基因座。小隐孢子虫 IIc-a 亚型在端粒周围基因中也有较高水平的插入和缺失突变,这也是其他专门亚型的特征。隐孢子虫亚型之间的基因交换在该属的进化过程中起着重要作用。有趣的是,重组区域富含正选择基因和潜在的毒力因子,这表明适应性基因渗入。对从世界各地收集的 467 个 gp60 序列的分析表明,主要的人畜共患病亚型(隔离距离)和人源人畜共患病亚型之间的种群遗传结构明显不同(混合种群结构)。我们还表明,包括在本研究中的四个人源人畜共患病隐孢子虫亚型和物种之间的基因渗入是最近发生的,可能是在过去的一千年内。