Widmer G
Tufts Cummings School of Veterinary Medicine, Division of Infectious Diseases, North Grafton, MA, USA.
Epidemiol Infect. 2009 Dec;137(12):1800-8. doi: 10.1017/S0950268809990215. Epub 2009 Jun 16.
Due to its extensive polymorphism, a partial sequence of the Cryptosporidium surface glycoprotein gene gp60 has been frequently used as a genetic marker. I explored the global diversity of this protein, and compared its sequence diversity in Cryptosporidium parvum and Cryptosporidium hominis. In marked contrast to the geographical partition of C. parvum and C. hominis multi-locus genotypes, gp60 allelic groups showed no evidence of segregating in space, or of differing with respect to geographical diversity. Globally, genetic diversity of C. hominis gp60 exceeded that of C. parvum. Within C. parvum, gp60 alleles originating from human isolates were more diverse than those infecting ruminants. Phylogenetic analysis grouped gp60 sequences into a small number of relatively homogenous allelic groups, with only a small number of alleles having evolved independently. With the notable exception of a group of alleles restricted to humans, C. parvum alleles are found in ruminants and humans.
由于其广泛的多态性,隐孢子虫表面糖蛋白基因gp60的部分序列常被用作遗传标记。我探究了该蛋白的全球多样性,并比较了其在微小隐孢子虫和人隐孢子虫中的序列多样性。与微小隐孢子虫和人隐孢子虫多位点基因型的地理划分形成显著对比的是,gp60等位基因群没有表现出在空间上隔离或在地理多样性方面存在差异的证据。在全球范围内,人隐孢子虫gp60的遗传多样性超过了微小隐孢子虫。在微小隐孢子虫中,源自人类分离株的gp60等位基因比感染反刍动物的等位基因更加多样。系统发育分析将gp60序列分为少数几个相对同质的等位基因群,只有少数等位基因是独立进化的。除了一组仅限于人类的等位基因外,微小隐孢子虫的等位基因在反刍动物和人类中均有发现。