Zhang Guang-jun, Qiu Chi-ping, Qiu Dong-chuan, Xia Ming-yi
Institute for Parasitic Disease Control and Prevention, Chinese Center for Disease Control and Prenention, Shanghai 200025.
Zhongguo Ji Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi. 2002;20(1):10-3.
To determine the phylogenetic position of Schistosoma sinensium in the genus Schistosoma using mitochondrial cytochrome C oxidase 1 (CO1) and NADH dehydrogenase 1(ND1) as molecular markers.
The genomic DNA of adult worms were extracted by the GNT-K method. The target regions were amplified by PCR using specific primers. The PCR products were purified before ligation into the plasmid Zero-Blunt. Recombinant plasmids were amplified in E. coli, extracted and purified using routine methods and then sequenced using M13 primers (F/R) on a Licor long-read auto-sequencer. Sequences of related schistosomes were retrieved from GenBank and aligned with our data in the sequence editor ESEE. Gene trees were constructed in PHYLIP and MEGA using both maximum parsimony and neighbor-joining methods. For parsimony analysis, all characters were treated as unordered and with equal weights. At least 3,000 cycles of bootstrapping were carried out. For analysis in MEGA, all gap columns were deleted. The third position of codon was included.
The nucleotide and amino acid sequences of CO1 and ND1 of S. sinensium were obtained.
The phylogenetic trees from these molecular data suggested that S. sinensium belongs to the Asian schistosome group, and the results coincided with the previous rDNA (ITS2 & LSU) analysis results.
以线粒体细胞色素C氧化酶1(CO1)和烟酰胺腺嘌呤二核苷酸脱氢酶1(ND1)作为分子标记,确定中华血吸虫在血吸虫属中的系统发育位置。
采用GNT-K法提取成虫基因组DNA。使用特异性引物通过PCR扩增目标区域。PCR产物在连接到Zero-Blunt质粒之前进行纯化。重组质粒在大肠杆菌中扩增,采用常规方法提取和纯化,然后在Licor长读长自动测序仪上使用M13引物(F/R)进行测序。从GenBank中检索相关血吸虫的序列,并在序列编辑器ESEE中与我们的数据进行比对。使用最大简约法和邻接法在PHYLIP和MEGA中构建基因树。对于简约分析,所有特征均视为无序且权重相等。至少进行3000次自展循环。对于在MEGA中的分析,删除所有间隙列。包含密码子的第三位。
获得了中华血吸虫CO1和ND1的核苷酸和氨基酸序列。
这些分子数据构建得到的系统发育树表明,中华血吸虫属于亚洲血吸虫组,结果与之前的rDNA(ITS2和LSU)分析结果一致。