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产志贺毒素大肠杆菌重组枯草杆菌蛋白酶细胞毒素变体的细胞毒性和凋亡作用

Cytotoxic and apoptotic effects of recombinant subtilase cytotoxin variants of shiga toxin-producing Escherichia coli.

作者信息

Funk J, Biber N, Schneider M, Hauser E, Enzenmüller S, Förtsch C, Barth H, Schmidt H

机构信息

Institute of Food Science and Biotechnology, Department of Food Microbiology and Hygiene, University of Hohenheim, Stuttgart, Germany.

Institute of Pharmacology and Toxicology, University of Ulm Medical Center, Ulm, Germany.

出版信息

Infect Immun. 2015 Jun;83(6):2338-49. doi: 10.1128/IAI.00231-15. Epub 2015 Mar 30.

Abstract

In this study, the cytotoxicity of the recently described subtilase variant SubAB2-2 of Shiga toxin-producing Escherichia coli was determined and compared to the plasmid-encoded SubAB1 and the chromosome-encoded SubAB2-1 variant. The genes for the respective enzymatic active (A) subunits and binding (B) subunits of the subtilase toxins were amplified and cloned. The recombinant toxin subunits were expressed and purified. Their cytotoxicity on Vero cells was measured for the single A and B subunits, as well as for mixtures of both, to analyze whether hybrids with toxic activity can be identified. The results demonstrated that all three SubAB variants are toxic for Vero cells. However, the values for the 50% cytotoxic dose (CD50) differ for the individual variants. Highest cytotoxicity was shown for SubAB1. Moreover, hybrids of subunits from different subtilase toxins can be obtained which cause substantial cytotoxicity to Vero cells after mixing the A and B subunits prior to application to the cells, which is characteristic for binary toxins. Furthermore, higher concentrations of the enzymatic subunit SubA1 exhibited cytotoxic effects in the absence of the respective B1 subunit. A more detailed investigation in the human HeLa cell line revealed that SubA1 alone induced apoptosis, while the B1 subunit alone did not induce cell death.

摘要

在本研究中,测定了最近描述的产志贺毒素大肠杆菌枯草杆菌蛋白酶变体SubAB2-2的细胞毒性,并与质粒编码的SubAB1和染色体编码的SubAB2-1变体进行比较。扩增并克隆了枯草杆菌蛋白酶毒素各自的酶活性(A)亚基和结合(B)亚基的基因。表达并纯化了重组毒素亚基。测定了单个A和B亚基以及两者混合物对Vero细胞的细胞毒性,以分析是否能鉴定出具有毒性活性的杂种。结果表明,所有三种SubAB变体对Vero细胞均有毒性。然而,各个变体的50%细胞毒性剂量(CD50)值有所不同。SubAB1表现出最高的细胞毒性。此外,可获得来自不同枯草杆菌蛋白酶毒素的亚基杂种,在将A和B亚基混合后应用于细胞之前,它们对Vero细胞具有显著的细胞毒性,这是二元毒素的特征。此外,在没有相应B1亚基的情况下,较高浓度的酶亚基SubA1表现出细胞毒性作用。在人HeLa细胞系中进行的更详细研究表明,单独的SubA1诱导细胞凋亡,而单独的B1亚基不诱导细胞死亡。

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