Perelle S, Gibert M, Bourlioux P, Corthier G, Popoff M R
Unité des Toxines Microbiennes, Institut Pasteur, Paris, France.
Infect Immun. 1997 Apr;65(4):1402-7. doi: 10.1128/iai.65.4.1402-1407.1997.
A Clostridium difficile isolate was found to produce an actin-specific ADP-ribosyltransferase (CDT) homologous to the enzymatic components of Clostridium perfringens iota toxin and Clostridium spiroforme toxin (M. R. Popoff, E. J. Rubin, D. M. Gill, and P. Boquet, Infect. Immun. 56:2299-2306, 1988). The CDT locus from C. difficile CD196 was cloned and sequenced. It contained two genes (cdtA and cdtB) which display organizations and sequences similar to those of the iota toxin gene. The deduced enzymatic (CDTa) and binding (CDTb) components have 81 and 84% identity, respectively, with the corresponding components of iota toxin. CDTa and CDTb induced actin cytoskeleton alterations similar to those caused by other clostridial binary toxins. The lower level of production of binary toxin by CD196 than of iota toxin by C. perfringens was related to a lower transcript level, possibly due to a promoter region different from that of iota toxin genes. The cdtA and cdtB genes have been detected in 3 of 24 clinical isolates examined, and cdtB alone was found in 2 additional strains. One strain (in addition to CD196) was shown by Western blotting to produce CDTa and CDTb. These results indicate that some C. difficile strains synthesize a binary toxin that could be an additional virulence factor.
一株艰难梭菌分离株被发现能产生一种肌动蛋白特异性ADP - 核糖基转移酶(CDT),该酶与产气荚膜梭菌iota毒素和螺旋体梭菌毒素的酶组分同源(M. R. 波普夫、E. J. 鲁宾、D. M. 吉尔和P. 博凯,《感染与免疫》56:2299 - 2306,1988年)。对艰难梭菌CD196的CDT基因座进行了克隆和测序。它包含两个基因(cdtA和cdtB),其结构和序列与iota毒素基因相似。推导的酶组分(CDTa)和结合组分(CDTb)与iota毒素的相应组分分别有81%和84%的同源性。CDTa和CDTb诱导的肌动蛋白细胞骨架改变与其他梭菌二元毒素引起的改变相似。CD196产生二元毒素的水平低于产气荚膜梭菌产生iota毒素的水平,这与转录水平较低有关,可能是由于启动子区域与iota毒素基因不同。在检测的24株临床分离株中有3株检测到cdtA和cdtB基因,另外2株仅检测到cdtB基因。通过蛋白质印迹法显示,有一株(除CD196外)产生CDTa和CDTb。这些结果表明,一些艰难梭菌菌株合成一种二元毒素,它可能是一种额外的毒力因子。