Luo Dong-jiao, Hu Ye, Dennin R H, Yan Jie
Department of Medical Microbiology and Parasitology, College od Medicine, Zhejiang University, Hangzhou 310058, China.
Zhejiang Da Xue Xue Bao Yi Xue Ban. 2007 Sep;36(5):458-64. doi: 10.3785/j.issn.1008-9292.2007.05.009.
To reconstruct the nucleotide sequence of Leptospira interrogans lipL21 gene for increasing the output of prokaryotic expression and to understand the changes on immunogenicity of the expression products before and after reconstruction, and to determine the position of envelope lipoprotein LipL21 on the surface of leptospiral body.
According to the preferred codons of E.coli, the nucleotide sequence of lipL21 gene was designed and synthesized, and then its prokaryotic expression system was constructed. By using SDS-PAGE plus BioRad agarose image analysor, the expression level changes of lipL21 genes before and after reconstruction were measured. A Western blot assay using rabbit anti-TR/Patoc I serum as the first antibody was performed to identify the immunoreactivity of the two target recombinant proteins rLipL21s before and after reconstruction. The changes of cross agglutination titers of antisera against two rLipL21s before and after reconstruction to the different leptospiral serogroups were demonstrated using microscope agglutination test (MAT). Immuno-electronmicroscopy was applied to confirm the location of LipL21s.
The expression outputs of original and reconstructed lipL21 genes were 8.5 % and 46.5 % of the total bacterial proteins, respectively. Both the two rLipL21s could take place immune conjugation reaction with TR/Patoc I antiserum. After immunization with each of the two rLipL21s in rabbits, the animals could produce specific antibody. Similar MAT titers with 1:80 - 1:320 of the two antisera against rLipL21s were present. LipL21 was confirmed to locate on the surface of leptospiral envelope.
LipL21 is a superficial antigen of Leptospira interrogans. The expression output of the reconstructed lipL21 gene is remarkably increased. The expression rLipL21 maintains fine antigenicity and immunoreactivity and its antibody still shows an extensive cross immunoagglutination activity. The high expression of the reconstructed lipL21 gene will offer a favorable condition to use its product for further developing a novel universal vaccine as well as detection kit of leptospirosis.
对问号钩端螺旋体lipL21基因的核苷酸序列进行改造,以提高原核表达产量,了解改造前后表达产物免疫原性的变化,并确定外膜脂蛋白LipL21在钩端螺旋体菌体表面的定位。
根据大肠杆菌的偏爱密码子设计并合成lipL21基因的核苷酸序列,构建其原核表达系统。采用SDS-PAGE加BioRad琼脂糖图像分析仪,检测改造前后lipL21基因的表达水平变化。以兔抗TR/Patoc I血清为一抗进行Western blot分析,鉴定改造前后两种目的重组蛋白rLipL21s的免疫反应性。采用显微镜凝集试验(MAT)检测改造前后两种rLipL21s抗血清对不同钩端螺旋体血清群的交叉凝集效价变化。应用免疫电镜确定LipL21s的定位。
原始和改造后的lipL21基因表达量分别占细菌总蛋白的8.5%和46.5%。两种rLipL21s均能与TR/Patoc I抗血清发生免疫结合反应。用两种rLipL21s分别免疫家兔后,动物均可产生特异性抗体。两种rLipL21s抗血清的MAT效价相似,均为1:80 - 1:320。证实LipL21位于钩端螺旋体外膜表面。
LipL21是问号钩端螺旋体的表面抗原。改造后的lipL21基因表达量显著提高。表达的rLipL21保持良好的抗原性和免疫反应性,其抗体仍具有广泛的交叉免疫凝集活性。改造后的lipL21基因的高表达将为利用其产物进一步开发新型通用疫苗以及钩端螺旋体病检测试剂盒提供有利条件。