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Antigens secreted from Mycobacterium tuberculosis: Identification by proteomics approach and test for diagnostic marker

结核分枝杆菌 抗原 肺结核 蛋白质组学 微生物学 生物 凝胶电泳 分子生物学 免疫印迹 大肠杆菌 化学 医学 免疫学 生物化学 基因 病理
作者
Young Yil Bahk,Suk Am Kim,Ji-Soo Kim,Hyung-Jin Euh,Gill Han Bai,Sung Rae Cho,Yu Sam Kim
出处
期刊:Proteomics [Wiley]
卷期号:4 (11): 3299-3307 被引量:134
标识
DOI:10.1002/pmic.200400980
摘要

Abstract Tuberculosis caused by mycobacteria, mainly Mycobacterium tuberculosis , is a major infectious disease of the respiratory system. An early diagnosis followed by chemotherapy is the major control strategy. In an effort to identify the antigens suitable for immunodiagnosis and vaccines, the proteins secreted in a culture medium from the M. tuberculosis K‐strain, which is the most prevalent among the clinical isolates in Korea and belongs to the Beijing family, were analyzed by two‐dimensional polyacrylamide gel electrophoresis (2‐D PAGE) and compared with those from the M. tuberculosis H37Rv and CDC1551 strains. Eight proteins, Rv0652, Rv1636, Rv2818c, Rv3369, Rv3865, Rv0566c, MT3304, and Rv3160, were identified by matrix‐assisted laser desorption/ionization‐time of flight‐mass spectrometry (MALDI‐TOF‐MS) or liquid chromatography‐electrospray ionization‐mass spectrometry (LC‐ESI‐MS) and found to be relatively abundant in the culture medium from the M. tuberculosis K‐strain but less so from the CDC1551 or H37Rv strains. In addition, Rv3874 (CFP‐10), Rv‐0560c and Rv3648c, which were expressed increasingly in the K and CDC1551 strains, were also identified using the same proteomics technology. All proteins were prepared by molecular cloning, expression in Escherichia coli followed by affinity purification. Among them, three proteins, rRv3369, rRv0566c, and rRv3874, were selected by prescreening and examined for their potential as serodiagnostic antigens using an enzyme‐linked immunosorbent assay. When 100 sera from tuberculosis patients and 100 sera from the healthy controls were analyzed, rRV3369, rRv3874, and rRv0566c showed a sensitivity of 60%, 74%, and 43%, and a specificity of 96%, 97%, and 84%, respectively. These results suggest that the rRv3369 and rRv3874 proteins, which were expressed more abundantly in the more recently obtained clinical isolates of M. tuberculosis than in the laboratory‐adapted H37Rv strain, are promising for use in the serodiagnosis of tuberculosis.
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