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引起人类感染的 种的遗传多样性比较。

Comparative genetic diversity of species causing human infections.

机构信息

Molecular Epidemiology and Public Health Laboratory, Hopkirk Research Institute, School of Veterinary Science, Massey University, Private Bag 11 222, Palmerston North, 4442, New Zealand.

Statistics and Bioinformatics Group, School of Fundamental Sciences, Massey University, Private Bag 11 222, Palmerston North4442, New Zealand.

出版信息

Parasitology. 2020 Nov;147(13):1532-1537. doi: 10.1017/S0031182020001493. Epub 2020 Aug 10.

Abstract

Parasites sometimes expand their host range and cause new disease aetiologies. Genetic changes can then occur due to host-specific adaptive alterations, particularly when parasites cross between evolutionarily distant hosts. Characterizing genetic variation in Cryptosporidium from humans and other animals may have important implications for understanding disease dynamics and transmission. We analyse sequences from four loci (gp60, HSP-70, COWP and actin) representing multiple Cryptosporidium species reported in humans. We predicted low genetic diversity in species that present unusual human infections due to founder events and bottlenecks. High genetic diversity was observed in isolates from humans of Cryptosporidium meleagridis, Cryptosporidium cuniculus, Cryptosporidium hominis and Cryptosporidium parvum. A deviation of expected values of neutrality using Tajima's D was observed in C. cuniculus and C. meleagridis. The high genetic diversity in C. meleagridis and C. cuniculus did not match our expectations but deviations from neutrality indicate a recent decrease in genetic variability through a population bottleneck after an expansion event. Cryptosporidium hominis was also found with a significant Tajima's D positive value likely caused by recent population expansion of unusual genotypes in humans. These insights indicate that changes in genetic diversity can help us to understand host-parasite adaptation and evolution.

摘要

寄生虫有时会扩大宿主范围并导致新的疾病病因。由于宿主特异性的适应性改变,特别是当寄生虫在进化上相距较远的宿主之间传播时,就会发生遗传变化。分析来自人类和其他动物的四种基因座(gp60、HSP-70、COWP 和肌动蛋白)的序列,这些基因座代表了在人类中报道的多种隐孢子虫物种。我们预测由于创始事件和瓶颈,在因罕见人类感染而出现的物种中,遗传多样性较低。来自人类的隐孢子虫美利奴亚种、隐孢子虫兔形目亚种、隐孢子虫人亚种和隐孢子虫微小亚种的分离株观察到高遗传多样性。在隐孢子虫兔形目亚种和隐孢子虫美利奴亚种中观察到 Tajima 的 D 值偏离中性预期值。隐孢子虫美利奴亚种和隐孢子虫兔形目亚种的高遗传多样性与我们的预期不符,但偏离中性表明,在扩张事件后,由于种群瓶颈,遗传变异性最近有所下降。还发现隐孢子虫人亚种的 Tajima 的 D 值为正,这可能是由于人类中罕见基因型的种群最近扩张所致。这些发现表明遗传多样性的变化可以帮助我们理解宿主-寄生虫适应和进化。

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