国际医学寄生虫病杂志
國際醫學寄生蟲病雜誌
국제의학기생충병잡지
INTERNATIONAL JOURNAL OF MEDICAL PARASITIC DISEASES
2012年
2期
72-79
,共8页
徐长志%吕志跃%郑焕钦%吴忠道
徐長誌%呂誌躍%鄭煥欽%吳忠道
서장지%려지약%정환흠%오충도
广州管圆线虫%Ⅳ期幼虫%cDNA文库%未知基因%表达序列标签
廣州管圓線蟲%Ⅳ期幼蟲%cDNA文庫%未知基因%錶達序列標籤
엄주관원선충%Ⅳ기유충%cDNA문고%미지기인%표체서렬표첨
Angiostrongylus cantonensis%4th stage larvae%cDNA Library%Unknown genes%Expressed sequence tags
目的 筛选和鉴定广州管圆线虫未知基因序列,丰富该虫的基因序列数据,为寻找诊断或药物靶点分子提供实验依据.方法 构建广州管圆线虫Ⅳ期幼虫cDNA噬菌体文库,随机挑选单个噬菌斑,提取噬菌体DNA进行PCR,扩增其插入的cDNA片段并对PCR产物进行序列测定;采用生物信息学方法对表达序列标签(expressed sequence tags,EST)序列进行分析.结果 获得了51条广州管圆线虫基因的EST序列,并提交至GenBank,这些基因包括半乳糖凝集素10,半乳糖凝集素140,表皮蛋白,CRE-RPS-24蛋白等.序列分析结果提示,表皮蛋白和CRE-RPS-24蛋白可能为具有诊断价值的抗原分子,值得进一步研究.结论 获得51条广州管圆线虫基因序列,为进一步研究广州管圆线虫致病机制及候选抗原分子提供了新的序列信息.
目的 篩選和鑒定廣州管圓線蟲未知基因序列,豐富該蟲的基因序列數據,為尋找診斷或藥物靶點分子提供實驗依據.方法 構建廣州管圓線蟲Ⅳ期幼蟲cDNA噬菌體文庫,隨機挑選單箇噬菌斑,提取噬菌體DNA進行PCR,擴增其插入的cDNA片段併對PCR產物進行序列測定;採用生物信息學方法對錶達序列標籤(expressed sequence tags,EST)序列進行分析.結果 穫得瞭51條廣州管圓線蟲基因的EST序列,併提交至GenBank,這些基因包括半乳糖凝集素10,半乳糖凝集素140,錶皮蛋白,CRE-RPS-24蛋白等.序列分析結果提示,錶皮蛋白和CRE-RPS-24蛋白可能為具有診斷價值的抗原分子,值得進一步研究.結論 穫得51條廣州管圓線蟲基因序列,為進一步研究廣州管圓線蟲緻病機製及候選抗原分子提供瞭新的序列信息.
목적 사선화감정엄주관원선충미지기인서렬,봉부해충적기인서렬수거,위심조진단혹약물파점분자제공실험의거.방법 구건엄주관원선충Ⅳ기유충cDNA서균체문고,수궤도선단개서균반,제취서균체DNA진행PCR,확증기삽입적cDNA편단병대PCR산물진행서렬측정;채용생물신식학방법대표체서렬표첨(expressed sequence tags,EST)서렬진행분석.결과 획득료51조엄주관원선충기인적EST서렬,병제교지GenBank,저사기인포괄반유당응집소10,반유당응집소140,표피단백,CRE-RPS-24단백등.서렬분석결과제시,표피단백화CRE-RPS-24단백가능위구유진단개치적항원분자,치득진일보연구.결론 획득51조엄주관원선충기인서렬,위진일보연구엄주관원선충치병궤제급후선항원분자제공료신적서렬신식.
Objective To screen and identify unknown gene sequences of Angiostrongylus cantonensis for enriching the genetic database of the parasite and providing experimental evidences of drug targets or diagnostic molecules.Methods A 4th stage larvae cDNA library of A.cantonensis was constructed,then phage clones were randomly selected,fostered and sequenced.Meanwhile,all the expressed sequence tags (EST) sequences we got were analyzed by bioinformatics tools.Results 51 EST sequences ofA.cantonensis were obtained and submitted to the GenBank,including galectin 10,galectin 140,cuticle protein,CRE-RPS-24 protein.Sequence analysis showed that cuticle protein and CRE-RPS-24 protein may be antigens with potential diagnostic value.Conclusion 51 EST sequences obtained will be useful for further study on pathogenesis mechanisms and molecular basis for candidate antigens of A.cantonensis.