Cao Chun-Bao, Ma Xiu-Min, Ding Jian-Bing, Jia Hai-Ying, Mamuty Wulamu, Ma Hai-Mei, Wen Hao
Xinjiang Key Laboratory of Echinococcosis, The First Teaching Hospital of Xinjiang Medical University, Urumqi 830054, China.
Zhongguo Ji Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi. 2009 Apr;27(2):177-9.
A pair of primers (egG1Y162) were designed according to the nucleotide sequence of Echinococcus multilocularis emY162 antigen gene. Using genomic DNA and cDNA from protoscoleces and adult worms of E. granulosus as templates, PCR was performed with the primers to obtain fragments of egG1Y162 gene. PUCm-T/egG1Y162 recombinant plasmids and PUCm-T/egY162 cDNA recombinant plasmids were constructed and identified by PCR, digestion with restriction enzyme and sequencing. The egG1Y162 antigen gene was amplified in protoscoleces and adult worms of E. granulosus. The size of the egG1Y162 gene was 1 648 bp and cDNA was 459 bp, and GenBank accession numbers were AB458258 and AB458259, respectively.
根据多房棘球绦虫emY162抗原基因的核苷酸序列设计了一对引物(egG1Y162)。以细粒棘球绦虫原头节和成虫的基因组DNA及cDNA为模板,用该引物进行PCR,获得egG1Y162基因片段。构建了PUCm-T/egG1Y162重组质粒和PUCm-T/egY162 cDNA重组质粒,并通过PCR、限制性内切酶消化和测序进行鉴定。egG1Y162抗原基因在细粒棘球绦虫原头节和成虫中得到扩增。egG1Y162基因大小为1648 bp,cDNA为459 bp,GenBank登录号分别为AB458258和AB458259。