Gao Daqing, Cheng Jing, Zheng Enjin, Li Yuhong, Shao Zeye, Xu Zeyan, Lu Chengping
Department of Pathogenic Microbiology and Immunology, Southeast University School of Medicine, Nanjing, China.
FEMS Microbiol Lett. 2014 Apr;353(2):132-40. doi: 10.1111/1574-6968.12420. Epub 2014 Apr 10.
Hemolysis causes major symptoms such as the reddening skin and systemic hemorrhagic septicemia of diseased fish infected by Edwardsiella tarda. Cytolysin A (ClyA) is a pore-forming cytotoxic protein encoded by the clyA gene in Escherichia coli K-12. In this study, we observed that the heterologous expression of the eha gene from E. tarda could confer hemolytic activity upon a hemolytic-silent E. coli strain. The transcription of clyA is positively controlled by the eha gene in E. tarda by RT-PCR. We cloned and purified Eha protein which had shown preferential binding ability to the clyA sequences in its promoter region, as evidenced by gel shift assay. The eha controls the transcriptional start predominantly at 72 bp upstream in the clyA promoter region, as determined by primer extension assays. We suggest that Eha protein is a new positive regulator found in E. tarda. In addition, we constructed the eha mutant and complementary strains of E. tarda. The hemolytic activity of the eha mutant was found to be attenuated compared with the wild-type strain. The complementary strains restored the hemolytic activity to levels between those of the wild type and the eha mutation. Our results indicate that the Eha protein is an important positive regulator in the hemolytic properties of E. tarda.
溶血会导致主要症状,如感染迟缓爱德华氏菌的患病鱼类出现皮肤发红和全身性出血性败血症。细胞溶素A(ClyA)是大肠杆菌K-12中由clyA基因编码的一种成孔细胞毒性蛋白。在本研究中,我们观察到迟缓爱德华氏菌的eha基因的异源表达可赋予溶血沉默的大肠杆菌菌株溶血活性。通过逆转录聚合酶链反应(RT-PCR)发现,迟缓爱德华氏菌中clyA的转录受eha基因的正向调控。我们克隆并纯化了Eha蛋白,凝胶迁移试验证明该蛋白对其启动子区域的clyA序列具有优先结合能力。通过引物延伸试验确定,eha主要在clyA启动子区域上游72 bp处控制转录起始。我们认为Eha蛋白是在迟缓爱德华氏菌中发现的一种新的正向调节因子。此外,我们构建了迟缓爱德华氏菌的eha突变体和互补菌株。与野生型菌株相比,发现eha突变体的溶血活性减弱。互补菌株将溶血活性恢复到野生型和eha突变体之间的水平。我们的结果表明,Eha蛋白是迟缓爱德华氏菌溶血特性中的一种重要正向调节因子。