基于流产布鲁氏菌局部分离株外膜蛋白(OMP) 36kda决定抗原的布鲁氏菌疫苗的研制

A. Aulanni’am, W. Tyasningsih, D. Wuragil, F. Rantam
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引用次数: 1

摘要

布鲁氏菌病是一种可以通过接种疫苗来预防的疾病。然而,人们认为接种疫苗对抗这种疾病的效力很弱。幸运的是,改良布鲁氏菌病疫苗的尝试仍在继续。在过去的一段时间里,一些布鲁氏菌病疫苗已被发现并开发出来,如产弧菌疫苗19-BA和104M,它们是由在苏联和中国广泛使用的弱化微生物制成的。过去使用的其他布鲁氏菌病疫苗是法国制造的酚不溶性肽聚糖疫苗和俄罗斯使用的多糖蛋白疫苗。本研究试图寻找具有免疫原性的36 kDa流产布鲁氏菌局部分离抗原外膜蛋白(OM)的决定因素,以开发一种高级布鲁氏菌疫苗。本研究采用PCR技术对产布鲁氏菌本地分离株的Omp2基因进行检测。然后对PCR结果进行测序,分析T细胞或B细胞的决定抗原和免疫应答的结合预测。本研究结果表明,原株本地分离的流产布鲁氏菌OMP 36 kDa的Omp2基因编码原株JPF 5 ' GCG CTC AGG CTG CCG ACG CAA 3 '和JPR 5 ' CAT TGC GGT CGG TAC CGG AG 3 '靶向基因162 bp,并将其翻译成氨基酸,随后采用Kolaskar & Tongaonkar抗原性预测方法进行计算机测试。表位预测结果为MSRVCDAYGAGYFYI和TETCLRVHGYVRYD。MSRVCDAYGAGYFYI的表位预测结果显示,YGAGYFYI的8 ~ 15个氨基酸序列与MHC I有结合,而TETCLRVHGYVRYD的表位预测结果显示,与2 ~ 10个氨基酸序列的ETCLRVHGY有结合。与MHC II结合存在于MSRVCDAYGAGYFYI氨基酸系列中,与B细胞结合存在于BCSAYGA和CLRVHG氨基酸系列中。本研究成功预测了当地分离的OMP 36kda流产布鲁氏菌的表位,该菌株具有与MHC I、MHC II和B细胞结合的免疫原性特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of Brucellosis Vaccine Based on Determinant Antigenic of Outer Membrane Protein (OMP) 36 kDa From Brucella abortus Local Isolate
Brucellosis is a disease that can be prevented through vaccination. Yet, the effectiveness of the vaccination to fight this disease is considered weak. Fortunately, attempts to modify brucellosis vaccine is still keep going. Some brucellosis vaccines have been found and developed in the past time such as the vaccine B.abortus strain 19-BA and 104M which was made from weakened microbes which had been widely used in Uni Soviet and China. The other brucellosis vaccine that were used in the past were the phenolinsoluble peptidoglycan vaccine which was made in France and polysaccharideprotein vaccine which was used in Russia. This research attempted to see the determinant of antigenic Outer Membrane Protein (OM) 36 kDa Brucella abortus local isolation which has immunogenic character to be developed as an advanced brucellosis vaccine. The method used in this research was the Omp2 gene of Brucella abortus of local isolate employed the PCR technique. The result of the PCR was then sequenced to analyze the determinant antigenic and the bounding prediction of either the T cell or the B cell which were responsible for immune response. The result of this study showed that the gen Omp2 which encoded the OMP 36 kDa Brucella abortus of local isolation with primary JPF 5’ GCG CTC AGG CTG CCG ACG CAA 3’ and JPR 5’ CAT TGC GGT CGG TAC CGG AG 3’ targeted the gene 162 bp, was then translated into amino acids to be later undergo the in silico test using Kolaskar & Tongaonkar Antigenicity Prediction method. The epitope prediction resulted were MSRVCDAYGAGYFYI and TETCLRVHGYVRYD. The result of the epitope prediction of MSRVCDAYGAGYFYI showed that there was a bond with MHC I in YGAGYFYI of the 8 amino acid series to the 15 series, while the epitope prediction of TETCLRVHGYVRYD showed that there was a bond to the ETCLRVHGY of the series of amino acids number 2 to 10. Bond with MHC II existed in the amino acid series of MSRVCDAYGAGYFYI, while the bond with the B cells existed in BCSAYGA and CLRVHG amino acid series. This research has been successful in predicting the epitope of the OMP 36 kDa Brucella abortus of local isolate which had immunogenic characteristic for its ability to bond with the MHC I, MHC II and B cells.
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