Department of Biological Sciences, Macquarie University, Sydney, NSW 2109, Australia.
Infect Genet Evol. 2011 Aug;11(6):1388-95. doi: 10.1016/j.meegid.2011.05.008. Epub 2011 May 13.
Ninety percent of human cryptosporidiosis infections are attributed to two species; the anthroponotic Cryptosporidium hominis and the zoonotic Cryptosporidium parvum. Sequence analysis of the hypervariable gp60 gene, which is used to classify Cryptosporidium to the subtype level, has highlighted extensive intra-species diversity within both C. hominis and C. parvum. The gp60 has also facilitated contamination source tracking and increased understanding of the epidemiology of cryptosporidiosis. Two surface glycoproteins, the gp40 and gp15 are encoded in the gp60 gene; both are exposed to the hosts' immune system and play a pivotal role in the disease initiation process. The extent of genetic diversity observed within the gp60 would support the hypotheses of significant selection pressure placed on the gp40 and gp15. This study used a dual fluorescent terminal-restriction fragment length polymorphism (T-RFLP) analysis to investigate the genetic diversity of Cryptosporidium subtype populations in a single host infection. Terminal-RFLP showed subtype variation within one human Cryptosporidium sample and mouse samples from seven consecutive passages with C. parvum. Furthermore, this was the first study to show that differences in the ratio of subtype populations occur between infections. T-RFLP has provided a novel platform to study infection populations and to begin to investigate the impact of the hosts' immune system on the gp60 gene.
90%的人类隐孢子虫病感染归因于两种物种; 人际传播的隐孢子虫人和动物传播的隐孢子虫微小隐孢子虫。对高度可变的 gp60 基因进行序列分析,该基因用于将隐孢子虫分类为亚类水平,突出了 C. 人和 C. 微小隐孢子虫内种内的广泛多样性。gp60 还促进了污染来源的追踪,并增加了对隐孢子虫病流行病学的了解。两种表面糖蛋白,gp40 和 gp15,编码在 gp60 基因中;两者都暴露于宿主的免疫系统中,在疾病起始过程中发挥关键作用。在 gp60 中观察到的遗传多样性程度支持对 gp40 和 gp15 施加了重大选择压力的假设。本研究使用双重荧光末端限制性片段长度多态性 (T-RFLP) 分析来研究单一宿主感染中隐孢子虫亚型群体的遗传多样性。末端-RFLP 显示了一个人类隐孢子虫样本和七个连续传代的 C. 微小隐孢子虫鼠样本中的亚型变异。此外,这是第一项表明感染之间存在亚群比例差异的研究。T-RFLP 为研究感染群体提供了一个新的平台,并开始研究宿主免疫系统对 gp60 基因的影响。