De Rycke J, Nougayrede J P, Oswald E, Mazars P
Laboratoire INRA Associé de Microbiologie Moléculaire, Toulouse, France.
Adv Exp Med Biol. 1997;412:363-6. doi: 10.1007/978-1-4899-1828-4_58.
Cytotoxic necrotizing factors (CNF) constitute a group a cell-associated proteic toxins of 110-115 kDa produced by some clinical isolates of Escherichia coli from man and animals. Purified CNFs are known to exacerbate actin polymerization in exposed cells, a property that has been ascribed to their ability to modify rho a small GTP-protein involved in the regulation of the cytoskeleton. We speculated that, in spite of their lack of excretion in broth culture supernatants, CNF might be expressed upon direct interaction of organisms with infected cells. To test this hypothesis, we set up a model of interaction using epithelial cell line HeLa and the CNF1-producing strain BM2-1, which is adherent to Hela cells. An interaction of four hour duration triggers the progressive development of a dose-dependent cytopathic effect (CPE) with following characteristics: (1) intense cell enlargement with formation of a dense network of stress fibers, (2) inhibition of cell mitosis due to an irreversible block in G2/M transition phase, (3) nucleus swelling and fragmentation, and (4) cell death starting five days after infection. The three last features clearly differentiate CPE from the effect produced by CNF1 alone. In addition CPE, was not produced by cell-free culture supernatants nor abolished by an antiserum neutralizing CNF1. Tn5::PhoA insertion in the 3' end of cnf1 structural gene abolished CPE, which was not restored by trans complementation with cloned cnf1. These results demonstrate that CNF1-producing E. coli exert a specific pathogenic effect in HeLa cells, which is determined by cnf1 and at least one additional gene, located downstream cnf1.
细胞毒性坏死因子(CNF)是由人和动物的一些大肠杆菌临床分离株产生的一组与细胞相关的蛋白质毒素,分子量为110 - 115 kDa。已知纯化的CNF会加剧暴露细胞中的肌动蛋白聚合,这一特性归因于它们修饰rho的能力,rho是一种参与细胞骨架调节的小GTP蛋白。我们推测,尽管CNF在肉汤培养上清液中不分泌,但在生物体与感染细胞直接相互作用时可能会表达。为了验证这一假设,我们建立了一个使用上皮细胞系HeLa和产生CNF1的菌株BM2 - 1的相互作用模型,该菌株可粘附于HeLa细胞。持续4小时的相互作用会引发剂量依赖性细胞病变效应(CPE)的逐步发展,其具有以下特征:(1)细胞强烈肿大并形成致密的应力纤维网络;(2)由于G2/M转换期的不可逆阻滞导致细胞有丝分裂受到抑制;(3)细胞核肿胀和碎片化;(4)感染后五天开始细胞死亡。最后三个特征明显将CPE与单独由CNF1产生的效应区分开来。此外,CPE不是由无细胞培养上清液产生的,也不会被中和CNF1的抗血清所消除。在cnf1结构基因的3'端插入Tn5::PhoA消除了CPE,通过克隆的cnf1进行反式互补也无法恢复CPE。这些结果表明,产生CNF1的大肠杆菌在HeLa细胞中发挥特定的致病作用,这是由cnf1和位于cnf1下游的至少一个其他基因决定的。