首页> 外文期刊>Science in China, Series C. Life science >Cloning,expression and protective immunity evaluation of the full-length cDNA encoding succinate dehydrogenase iron-sulfur protein of Schistosoma japonicum
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Cloning,expression and protective immunity evaluation of the full-length cDNA encoding succinate dehydrogenase iron-sulfur protein of Schistosoma japonicum

机译:日本血吸虫琥珀酸脱氢酶铁硫蛋白全长cDNA的克隆,表达及保护性免疫评价

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1071-bp fragment was obtained from the Schistosoma japonicum (Chinese strain) adult cDNA library after the 3' and 5' ends of the incomplete expression sequence tag (EST) of succinate dehydrogenase iron-sulfur protein of Schistosoma japonicum (SjSDISP) were amplified by the anchored PCR with 2 pairs of primers designed according to the EST of S/SDISP and the sequence of multiclone sites of the library vector.Sequence analysis indicated that the fragment was a full-length cDNA with a complete open reading frame (ORF),encoding 278 amino acid residues.The fragment was cloned into prokary-otic expression vector pQE30,and subsequently sequenced and expressed in Escherichia coli.SDS-PAGE and Western-blot analyses showed that the recombinant protein was about 32 kD and could be recognized by the polyclonal antisera from rabbits immunized with Schistosoma japonicum adult worm antigen.Compared with the FCA controls,mice vaccinated with rSjSDISP (test) or rSjGST (positive control) all revealed high levels of specific antibody and significant reduction in worm burden,liver eggs per gram (LEPG),fecal eggs per gram (FEPG) and intrauterine eggs.These results suggest that S/SDISP may be a novel and partially protective vaccine candidate against schistosomiasis.In contrast to the worm burden reduction rate,the higher degree of egg reduction rate in the test group also suggested that S/SDISP vaccine may primarily play a role in anti-embryonation or anti-fecundity immunity.
机译:扩增日本血吸虫琥珀酸脱氢酶铁硫蛋白(SjSDISP)不完全表达序列标签(EST)3'和5'端后,从日本血吸虫成人cDNA文库中获得1071 bp的片段。根据S / SDISP的EST和文库载体的多克隆位点序列设计的2对引物进行锚定PCR。序列分析表明该片段是具有完整开放阅读框(ORF)的全长cDNA,编码278个氨基酸残基。将该片段克隆到原核表达载体pQE30中,随后在大肠杆菌中进行测序和表达。SDS-PAGE和Western-blot分析表明该重组蛋白约为32 kD,可被大肠杆菌识别。用日本血吸虫成虫蠕虫抗原免疫的兔多克隆抗血清。与FCA对照相比,用rSjSDISP(测试)或rSjGST(阳性对照)接种的小鼠均显示出高gh特异性抗体水平高,蠕虫负担,每克肝卵数(LEPG),每克粪便卵数(FEPG)和子宫内卵显着减少。这些结果表明,S / SDISP可能是抗血吸虫病的新型且部分保护性疫苗。与降低蠕虫负担的速度相比,测试组中较高的降低鸡蛋率的速度也表明S / SDISP疫苗可能主要在抗胚胎或抗生殖力免疫中发挥作用。

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