Stenger Brianna L S, Clark Mark E, Kváč Martin, Khan Eakalak, Giddings Catherine W, Dyer Neil W, Schultz Jessie L, McEvoy John M
Department of Veterinary and Microbiological Sciences, North Dakota State University, Fargo, ND, USA; Department of Biological Sciences, North Dakota State University, Fargo, ND, USA; Environmental and Conservation Sciences Program, North Dakota State University, Fargo, ND, USA.
Department of Biological Sciences, North Dakota State University, Fargo, ND, USA; Environmental and Conservation Sciences Program, North Dakota State University, Fargo, ND, USA.
Infect Genet Evol. 2015 Jun;32:113-23. doi: 10.1016/j.meegid.2015.03.003. Epub 2015 Mar 12.
Cryptosporidium is an apicomplexan parasite that causes the disease cryptosporidiosis in humans, livestock, and other vertebrates. Much of the knowledge on Cryptosporidium diversity is derived from 18S rRNA gene (18S rDNA) phylogenies. Eukaryote genomes generally have multiple 18S rDNA copies that evolve in concert, which is necessary for the accurate inference of phylogenetic relationships. However, 18S rDNA copies in some genomes evolve by a birth-and-death process that can result in sequence divergence among copies. Most notably, divergent 18S rDNA paralogs in the apicomplexan Plasmodium share only 89-95% sequence similarity, encode structurally distinct rRNA molecules, and are expressed at different life cycle stages. In the present study, Cryptosporidium 18S rDNA was amplified from 28/72 (38.9%) eastern chipmunks (Tamias striatus). Phylogenetic analyses showed the co-occurrence of two 18S rDNA types, Type A and Type B, in 26 chipmunks, and Type B clustered with a sequence previously identified as Cryptosporidium chipmunk genotype II. Types A and B had a sister group relationship but shared less than 93% sequence similarity. In contrast, actin and heat shock protein 70 gene sequences were homogeneous in samples with both Types A and B present. It was therefore concluded that Types A and B are divergent 18S rDNA paralogs in Cryptosporidium chipmunk genotype II. Substitution patterns in Types A and B were consistent with functionally constrained evolution; however, Type B evolved more rapidly than Type A and had a higher G+C content (46.3% versus 41.0%). Oocysts of Cryptosporidium chipmunk genotype II measured 4.17 μm (3.73-5.04 μm) × 3.94 μm (3.50-4.98 μm) with a length-to-width ratio of 1.06 ± 0.06 μm, and infection occurred naturally in the jejunum, cecum, and colon of eastern chipmunks. The findings of this study have implications for the use of 18S rDNA sequences to infer phylogenetic relationships.
隐孢子虫是一种顶复门寄生虫,可在人类、家畜和其他脊椎动物中引发隐孢子虫病。关于隐孢子虫多样性的许多知识都来自于18S核糖体RNA基因(18S rDNA)系统发育研究。真核生物基因组通常有多个协同进化的18S rDNA拷贝,这对于准确推断系统发育关系是必要的。然而,一些基因组中的18S rDNA拷贝通过生死过程进化,这可能导致拷贝之间的序列差异。最值得注意的是,顶复门疟原虫中不同的18S rDNA旁系同源物仅具有89 - 95%的序列相似性,编码结构不同的rRNA分子,并在不同的生命周期阶段表达。在本研究中,从28只(占72只的38.9%)东部花栗鼠(Tamias striatus)中扩增出了隐孢子虫18S rDNA。系统发育分析表明,在26只花栗鼠中同时存在两种18S rDNA类型,即A型和B型,并且B型与先前鉴定为隐孢子虫花栗鼠基因型II的一个序列聚类。A型和B型具有姐妹群关系,但序列相似性低于93%。相比之下,在同时存在A型和B型的样本中,肌动蛋白和热休克蛋白70基因序列是一致的。因此得出结论,A型和B型是隐孢子虫花栗鼠基因型II中不同的18S rDNA旁系同源物。A型和B型的替换模式与功能受限的进化一致;然而,B型比A型进化得更快,并且具有更高的G + C含量(分别为46.3%和41.0%)。隐孢子虫花栗鼠基因型II的卵囊大小为4.17μm(3.73 - 5.04μm)×3.94μm(3.50 - 4.98μm),长宽比为1.06±0.06μm,并且在东部花栗鼠的空肠、盲肠和结肠中自然发生感染。本研究结果对使用18S rDNA序列推断系统发育关系具有启示意义。