Zhou Ze-Jun, Sun Li
Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of SciencesQingdao, China; Laboratory for Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and TechnologyQingdao, China; University of Chinese Academy of SciencesBeijing, China.
Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of SciencesQingdao, China; Laboratory for Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and TechnologyQingdao, China.
Front Cell Infect Microbiol. 2016 Jul 14;6:76. doi: 10.3389/fcimb.2016.00076. eCollection 2016.
Edwardsiella tarda is a Gram-negative bacterial pathogen that can infect a wide range of freshwater and marine fish. One salient feature of E. tarda is the ability to survive and replicate in various host cells. In this study, we observed that E. tarda replicated robustly in the zebrafish cell line ZF4, and that E. tarda-infected cells exhibited no detectable signs of apoptosis. Global transcriptome analysis and quantitative real-time RT-PCR revealed that E. tarda infection generally significantly downregulated pro-apoptotic genes and upregulated anti-apoptotic genes. To investigate the role of apoptosis in E. tarda infection, two upregulated anti-apoptotic genes (Fech and Prx3) and two downregulated pro-apoptotic genes (Brms1a and Ivns1a) were overexpressed in zebrafish. Subsequent infection study showed that Fech and Prx3 overexpression significantly promoted E. tarda dissemination in and colonization of fish tissues, while Brms1a and Ivns1a overexpression significantly reduced E. tarda dissemination and colonization. Consistently, when Fech and Prx3 were knocked down in zebrafish, E. tarda infection was significantly inhibited, whereas Brms1a and Ivns1a knockdown significantly enhanced E. tarda infection. These results indicate for the first time that E. tarda prevents apoptosis in teleost as a strategy for intracellular survival, and that some putative apoptotic genes of teleost function in the apoptosis pathway probably in a manner similar to that in mammalian systems.
迟缓爱德华氏菌是一种革兰氏阴性细菌病原体,可感染多种淡水和海水鱼类。迟缓爱德华氏菌的一个显著特征是能够在各种宿主细胞中存活和繁殖。在本研究中,我们观察到迟缓爱德华氏菌在斑马鱼细胞系ZF4中大量繁殖,且感染迟缓爱德华氏菌的细胞未表现出可检测到的凋亡迹象。全转录组分析和定量实时RT-PCR显示,迟缓爱德华氏菌感染通常会显著下调促凋亡基因并上调抗凋亡基因。为了研究凋亡在迟缓爱德华氏菌感染中的作用,在斑马鱼中过表达了两个上调的抗凋亡基因(Fech和Prx3)以及两个下调的促凋亡基因(Brms1a和Ivns1a)。随后的感染研究表明,过表达Fech和Prx3显著促进了迟缓爱德华氏菌在鱼组织中的传播和定植,而过表达Brms1a和Ivns1a则显著减少了迟缓爱德华氏菌的传播和定植。同样,当在斑马鱼中敲低Fech和Prx3时,迟缓爱德华氏菌感染受到显著抑制,而敲低Brms1a和Ivns1a则显著增强了迟缓爱德华氏菌感染。这些结果首次表明,迟缓爱德华氏菌通过阻止硬骨鱼凋亡作为细胞内存活策略,并且硬骨鱼的一些假定凋亡基因可能以与哺乳动物系统类似的方式在凋亡途径中发挥作用。