Department of Poultry Diseases, Faculty of Veterinary Medicine, Assiut University, Assiut 71526, Egypt.
Int J Parasitol. 2013 Jul;43(8):679-85. doi: 10.1016/j.ijpara.2013.03.005. Epub 2013 Apr 30.
Multiple 18S rDNA sequences were obtained from two single-oocyst-derived lines of each of Eimeria meleagrimitis and Eimeria adenoeides. After analysing the 15 new 18S rDNA sequences from two lines of E. meleagrimitis and 17 new sequences from two lines of E. adenoeides, there were clear indications that divergent, paralogous 18S rDNA copies existed within the nuclear genome of E. meleagrimitis. In contrast, mitochondrial cytochrome c oxidase subunit I (COI) partial sequences from all lines of a particular Eimeria sp. were identical and, in phylogenetic analyses, COI sequences clustered unambiguously in monophyletic and highly-supported clades specific to individual Eimeria sp. Phylogenetic analysis of the new 18S rDNA sequences from E. meleagrimitis showed that they formed two distinct clades: Type A with four new sequences; and Type B with nine new sequences; both Types A and B sequences were obtained from each of the single-oocyst-derived lines of E. meleagrimitis. Together these rDNA types formed a well-supported E. meleagrimitis clade. Types A and B 18S rDNA sequences from E. meleagrimitis had a mean sequence identity of only 97.4% whereas mean sequence identity within types was 99.1-99.3%. The observed intraspecific sequence divergence among E. meleagrimitis 18S rDNA sequence types was even higher (approximately 2.6%) than the interspecific sequence divergence present between some well-recognized species such as Eimeria tenella and Eimeria necatrix (1.1%). Our observations suggest that, unlike COI sequences, 18S rDNA sequences are not reliable molecular markers to be used alone for species identification with coccidia, although 18S rDNA sequences have clear utility for phylogenetic reconstruction of apicomplexan parasites at the genus and higher taxonomic ranks.
从两个单卵囊衍生的柔嫩艾美耳球虫和鹌鹑艾美耳球虫的每条虫株中都获得了多个 18S rDNA 序列。分析了柔嫩艾美耳球虫的两条虫株的 15 个新的 18S rDNA 序列和鹌鹑艾美耳球虫的两条虫株的 17 个新序列后,有明确的迹象表明,在柔嫩艾美耳球虫的核基因组中存在着不同的、平行的 18S rDNA 拷贝。相比之下,来自特定艾美耳球虫所有虫株的线粒体细胞色素 c 氧化酶亚单位 I(COI)部分序列完全相同,在系统发育分析中,COI 序列明确地聚类在与各个艾美耳球虫特异的单系和高度支持的分支中。柔嫩艾美耳球虫新的 18S rDNA 序列的系统发育分析表明,它们形成了两个不同的分支:A 型有 4 个新序列;B 型有 9 个新序列;A 型和 B 型序列都来自柔嫩艾美耳球虫的每条单卵囊衍生的虫株。这两种 rDNA 类型共同形成了一个支持良好的柔嫩艾美耳球虫分支。柔嫩艾美耳球虫的 A 型和 B 型 18S rDNA 序列的平均序列同一性仅为 97.4%,而类型内的平均序列同一性为 99.1-99.3%。在柔嫩艾美耳球虫 18S rDNA 序列类型之间观察到的种内序列分歧甚至高于某些公认物种(如柔嫩艾美耳球虫和毒害艾美耳球虫)之间的种间序列分歧(1.1%)。我们的观察表明,与 COI 序列不同,18S rDNA 序列不是用于球虫种识别的可靠分子标记,尽管 18S rDNA 序列对于属和更高分类阶元的顶复门寄生虫的系统发育重建具有明显的实用性。