Bona M, Nayak R, Wu M, Mincek M, Ellner J J
Division of Infectious Diseases, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106-4984, USA.
Tuber Lung Dis. 1997;78(2):133-41. doi: 10.1016/s0962-8479(98)80006-3.
This work describes the screening of a M. bovis BCG cosmid library in M. smegmatis with a hyperimmune rabbit anti-BCG serum. Cross-reactive antibodies interfere with the detection of BCG specific antigens in M. smegmatis culture filtrates. We, therefore, screened parallel western blots with serum adsorbed with a M. smegmatis cell lysate and unadsorbed serum. Comparison of the western blots allowed distinction between BCG specific and cross-reactive M. smegmatis antigens. Thirty-one cosmids expressed BCG specific antigens. One of them, a hitherto undescribed 100 kDa antigen was subcloned, sequenced and expressed in E. coli. It shows a high degree of homology to ClpB, a member of the Clp family of proteases and was immunologically reactive with the rabbit hyperimmune serum against M. bovis BCG. A positive signal was also obtained with sera of patients with tuberculosis. This antigen is a previously unrecognized target of the human immune response to mycobacteria.
这项工作描述了用超免疫兔抗卡介苗血清在耻垢分枝杆菌中筛选牛分枝杆菌卡介苗黏粒文库的过程。交叉反应抗体干扰了耻垢分枝杆菌培养滤液中卡介苗特异性抗原的检测。因此,我们用经耻垢分枝杆菌细胞裂解物吸附的血清和平行的未吸附血清筛选了蛋白质印迹。蛋白质印迹的比较使得能够区分卡介苗特异性抗原和耻垢分枝杆菌交叉反应抗原。31个黏粒表达了卡介苗特异性抗原。其中之一,一种迄今未描述的100 kDa抗原被亚克隆、测序并在大肠杆菌中表达。它与蛋白酶Clp家族成员ClpB具有高度同源性,并且与兔抗牛分枝杆菌卡介苗超免疫血清发生免疫反应。结核病患者的血清也获得了阳性信号。这种抗原是人类对分枝杆菌免疫反应先前未被识别的靶点。