生物技术通讯
生物技術通訊
생물기술통신
LETTERS IN BIOTECHNOLOGY
2015年
2期
199-202
,共4页
潘婷%郭彦%邱洪杰%于虹%太万博%孙世惠%赵光宇%周育森
潘婷%郭彥%邱洪傑%于虹%太萬博%孫世惠%趙光宇%週育森
반정%곽언%구홍걸%우홍%태만박%손세혜%조광우%주육삼
中东呼吸综合征冠状病毒%S1蛋白%昆虫细胞%杆状病毒表达系统
中東呼吸綜閤徵冠狀病毒%S1蛋白%昆蟲細胞%桿狀病毒錶達繫統
중동호흡종합정관상병독%S1단백%곤충세포%간상병독표체계통
Middle East respiratory syndrome coronavirus%insect cells%baculovirus expression system
目的:利用昆虫杆状病毒表达系统重组表达中东呼吸综合征冠状病毒(MERS-CoV)S1蛋白,并对其免疫效果进行评价。方法:构建含有MERS-CoV S1基因的重组杆状病毒质粒,转染Sf9细胞包装杆状病毒;重组病毒传代3次获得种子病毒,感染Sf9细胞,收获感染上清,通过镍离子亲和层析纯化获得S1重组蛋白;用纯化的S1蛋白免疫BALB/c小鼠,采用ELISA检测免疫小鼠血清抗原特异性的抗体水平;采用假病毒中和试验检测血清中抗体的中和活性。结果:获得了表达MERS-CoV S1蛋白的重组病毒株,在昆虫细胞中表达并纯化了S1重组蛋白;利用重组表达的S1蛋白免疫小鼠3次,血清S1特异性IgG抗体滴度可达1∶102400,免疫小鼠血清稀释至1/5120后中和百分比仍达50%以上。结论:利用昆虫细胞重组表达的MERS-CoV S1蛋白具有良好的免疫原性,并能有效诱导产生高滴度中和抗体,为发展MERS-CoV重组蛋白疫苗奠定了基础。
目的:利用昆蟲桿狀病毒錶達繫統重組錶達中東呼吸綜閤徵冠狀病毒(MERS-CoV)S1蛋白,併對其免疫效果進行評價。方法:構建含有MERS-CoV S1基因的重組桿狀病毒質粒,轉染Sf9細胞包裝桿狀病毒;重組病毒傳代3次穫得種子病毒,感染Sf9細胞,收穫感染上清,通過鎳離子親和層析純化穫得S1重組蛋白;用純化的S1蛋白免疫BALB/c小鼠,採用ELISA檢測免疫小鼠血清抗原特異性的抗體水平;採用假病毒中和試驗檢測血清中抗體的中和活性。結果:穫得瞭錶達MERS-CoV S1蛋白的重組病毒株,在昆蟲細胞中錶達併純化瞭S1重組蛋白;利用重組錶達的S1蛋白免疫小鼠3次,血清S1特異性IgG抗體滴度可達1∶102400,免疫小鼠血清稀釋至1/5120後中和百分比仍達50%以上。結論:利用昆蟲細胞重組錶達的MERS-CoV S1蛋白具有良好的免疫原性,併能有效誘導產生高滴度中和抗體,為髮展MERS-CoV重組蛋白疫苗奠定瞭基礎。
목적:이용곤충간상병독표체계통중조표체중동호흡종합정관상병독(MERS-CoV)S1단백,병대기면역효과진행평개。방법:구건함유MERS-CoV S1기인적중조간상병독질립,전염Sf9세포포장간상병독;중조병독전대3차획득충자병독,감염Sf9세포,수획감염상청,통과얼리자친화층석순화획득S1중조단백;용순화적S1단백면역BALB/c소서,채용ELISA검측면역소서혈청항원특이성적항체수평;채용가병독중화시험검측혈청중항체적중화활성。결과:획득료표체MERS-CoV S1단백적중조병독주,재곤충세포중표체병순화료S1중조단백;이용중조표체적S1단백면역소서3차,혈청S1특이성IgG항체적도가체1∶102400,면역소서혈청희석지1/5120후중화백분비잉체50%이상。결론:이용곤충세포중조표체적MERS-CoV S1단백구유량호적면역원성,병능유효유도산생고적도중화항체,위발전MERS-CoV중조단백역묘전정료기출。
Objective: To prepare the recombinant S1 protein of Middle East respiratory syndrome coronavirus (MERS-CoV) in the baculovirus expression system and evaluate the immunogenicity of purified recombinant S1 pro?tein. Methods: Recombinant bacmid inserted S1 gene of MERS-CoV was constructed, which was followed by trans?fection into Sf9 cells to package recombinant baculovirus. The Sf9 cells were infected by recombinant baculovirus seed derived from the third passage. Cell cultures were collected and the recombinant S1 protein was purified by nickel column affinity chromatography. Following vaccination with purified recombinant S1 protein, the S1-specific IgG antibody responses in BALB/c mouse sera were measured by ELISA, and the neutralizing antibodies were detect?ed by pseudo-MERS-CoV neutralizing assay. Results: The recombinant baculovirus isolate expressing recombinant S1 protein was obtained and recombinant S1 protein was successfully expressed and purified in insect cells. Follow?ing three vaccinations with recombinant S1 protein, titer of S1-specific IgG antibody in mouse sera reaches 1∶102 400, and inhibition percentage against pseudo-MERS-CoV can be still over 50% at 1∶5120 dilutions. Conclusion:Recombinant MERS-CoV S1 protein expressed in insect cells has ability to induce good immunogenicity with high titers of neutralizing activity, which lays a foundation of development of recombinant vaccine against MERS-CoV.