Navais Roberto, Méndez Jessica, Pérez-Pascual David, Cascales Desirée, Guijarro José A
Área de Microbiología; Departamento de Biología Funcional; Facultad de Medicina; IUBA; Universidad de Oviedo; Oviedo, Spain.
Virulence. 2014 Jul 1;5(5):619-24. doi: 10.4161/viru.29363. Epub 2014 May 27.
In an attempt to dissect the virulence mechanisms of Yersinia ruckeri two adjacent genes, yrpA and yrpB, encoding putative peptidases belonging to the U32 family, were analyzed. Similar genes, with the same genetic organization were identified in genomic analysis of human-pathogenic yersiniae. RT-PCR studies indicated that these genes form an operon in Y. ruckeri. Transcriptional studies using an yrpB::lacZY fusion showed high levels of expression of these genes in the presence of peptone in the culture medium, as well as under oxygen-limited conditions. These two factors had a synergic effect on gene induction when both were present simultaneously during bacterial incubation, which indicates the important role that environmental conditions in the fish gut can play in the regulation of specific genes. LD 50 experiments using an yrpA insertional mutant strain demonstrated the participation of this gene in the virulence of Y. ruckeri.
为了剖析鲁氏耶尔森菌的毒力机制,对两个相邻基因yrpA和yrpB进行了分析,这两个基因编码属于U32家族的假定肽酶。在对人类致病性耶尔森菌的基因组分析中鉴定出了具有相同基因组织的相似基因。逆转录聚合酶链反应(RT-PCR)研究表明,这些基因在鲁氏耶尔森菌中形成一个操纵子。使用yrpB::lacZY融合体进行的转录研究表明,在培养基中存在蛋白胨以及在氧限制条件下,这些基因有高水平表达。当在细菌培养期间这两个因素同时存在时,它们对基因诱导有协同作用,这表明鱼肠道中的环境条件在特定基因的调控中可能发挥的重要作用。使用yrpA插入突变株进行的半数致死剂量(LD50)实验证明了该基因参与鲁氏耶尔森菌的毒力。