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结核分枝杆菌特异性抗原基因的分离、特性鉴定及分子克隆:种特异性序列的鉴定

Isolation, characterization, and molecular cloning of a specific Mycobacterium tuberculosis antigen gene: identification of a species-specific sequence.

作者信息

Parra C A, Londoño L P, Del Portillo P, Patarroyo M E

机构信息

Instituto de Inmunología, Hospital San Juan de Dios, Universidad Nacional de Colombia, Bogotá.

出版信息

Infect Immun. 1991 Oct;59(10):3411-7. doi: 10.1128/iai.59.10.3411-3417.1991.

Abstract

A rabbit polyclonal antiserum exhibiting a specific recognition pattern for Mycobacterium tuberculosis proteins was used to screen an M. tuberculosis genomic library constructed in the expression vector lambda gt11. One clone, denominated C1:10, expressed M. tuberculosis-specific determinants as part of a large fusion protein with beta-galactosidase. The gene for this protein has been sequenced, and it encodes a protein of 134 amino acids (13.8 kDa) which did not display significant homology with any of the previously reported proteins in the data bases. Hybridization studies with restriction fragments of the cloned sequence revealed that it was not present in the genomes of related mycobacteria, namely, M. bovis, M. bovis BCG, M. flavescens, M. fortuitum, M. phlei, and M. vaccae. These findings suggest that we have detected a gene, or a fragment therefrom, unique for M. tuberculosis whose nucleotide and amino acid sequences could be useful tools in the design of an improved vaccine or a diagnostic method of greater accuracy for tuberculosis.

摘要

一种对结核分枝杆菌蛋白表现出特定识别模式的兔多克隆抗血清被用于筛选构建在表达载体λgt11中的结核分枝杆菌基因组文库。一个名为C1:10的克隆表达了结核分枝杆菌特异性决定簇,它是与β-半乳糖苷酶形成的一个大型融合蛋白的一部分。该蛋白的基因已被测序,它编码一个134个氨基酸(13.8 kDa)的蛋白,该蛋白与数据库中任何先前报道的蛋白均无显著同源性。用克隆序列的限制性片段进行杂交研究表明,它不存在于相关分枝杆菌的基因组中,即牛分枝杆菌、卡介苗、微黄分枝杆菌、偶然分枝杆菌、草分枝杆菌和母牛分枝杆菌。这些发现表明,我们检测到了一个结核分枝杆菌特有的基因或其片段,其核苷酸和氨基酸序列可能是设计改进疫苗或更准确的结核病诊断方法的有用工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf21/258900/bf6a04f8d809/iai00046-0081-a.jpg

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