Lobato-Márquez Damián, Moreno-Córdoba Inmaculada, Figueroa Virginia, Díaz-Orejas Ramón, García-del Portillo Francisco
1] Centro Nacional de Biotecnología-Consejo Superior de Investigaciones Científicas (CNB-CSIC). Darwin, 3. 28049 Madrid. Spain [2] Centro de Investigaciones Biológicas-CSIC (CIB-CSIC). Ramiro de Maeztu, 9. 28040 Madrid. Spain.
Centro de Investigaciones Biológicas-CSIC (CIB-CSIC). Ramiro de Maeztu, 9. 28040 Madrid. Spain.
Sci Rep. 2015 Mar 20;5:9374. doi: 10.1038/srep09374.
Toxin-antitoxin (TA) modules contribute to the generation of non-growing cells in response to stress. These modules abound in bacterial pathogens although the bases for this profusion remain largely unknown. Using the intracellular bacterial pathogen Salmonella enterica serovar Typhimurium as a model, here we show that a selected group of TA modules impact bacterial fitness inside eukaryotic cells. We characterized in this pathogen twenty-seven TA modules, including type I and type II TA modules encoding antisense RNA and proteinaceous antitoxins, respectively. Proteomic and gene expression analyses revealed that the pathogen produces numerous toxins of TA modules inside eukaryotic cells. Among these, the toxins HokST, LdrAST, and TisBST, encoded by type I TA modules and T4ST and VapC2ST, encoded by type II TA modules, promote bacterial survival inside fibroblasts. In contrast, only VapC2ST shows that positive effect in bacterial fitness when the pathogen infects epithelial cells. These results illustrate how S. Typhimurium uses distinct type I and type II TA modules to regulate its intracellular lifestyle in varied host cell types. This function specialization might explain why the number of TA modules increased in intracellular bacterial pathogens.
毒素-抗毒素(TA)模块有助于细菌在应激状态下形成非生长细胞。这些模块在细菌病原体中大量存在,但其大量存在的原因在很大程度上仍不清楚。以细胞内细菌病原体鼠伤寒沙门氏菌血清型鼠伤寒杆菌为模型,我们在此表明,一组特定的TA模块会影响真核细胞内细菌的适应性。我们对该病原体中的27个TA模块进行了表征,其中包括分别编码反义RNA和蛋白质类抗毒素的I型和II型TA模块。蛋白质组学和基因表达分析表明,该病原体在真核细胞内产生大量TA模块毒素。其中,由I型TA模块编码的毒素HokST、LdrAST和TisBST以及由II型TA模块编码的毒素T4ST和VapC2ST可促进细菌在成纤维细胞内的存活。相反,当病原体感染上皮细胞时,只有VapC2ST对细菌适应性表现出积极影响。这些结果说明了鼠伤寒沙门氏菌如何利用不同的I型和II型TA模块来调节其在不同宿主细胞类型中的细胞内生存方式。这种功能特化可能解释了细胞内细菌病原体中TA模块数量增加的原因。