Department of Microbiology & Immunology, University of Texas Medical Branch, Galveston, TX 77555-1070, USA.
Gene. 2012 May 1;498(2):280-7. doi: 10.1016/j.gene.2012.02.024. Epub 2012 Feb 23.
Aeromonas hydrophila is both a human and animal pathogen, and the cytotoxic enterotoxin (Act) is a crucial virulence factor of this bacterium because of its associated hemolytic, cytotoxic, and enterotoxic activities. Previously, to define the role of some regulatory genes in modulating Act production, we showed that deletion of a glucose-inhibited division gene (gidA) encoding tRNA methylase reduced Act levels, while overproduction of DNA adenine methyltransferase (Dam) led to a concomitant increase in Act-associated biological activities of a diarrheal isolate SSU of A. hydrophila. Importantly, there are multiple GATC binding sites for Dam within an upstream sequence of the gidA gene and one such target site in the act gene upstream region. We showed the dam gene to be essential for the viability of A. hydrophila SSU, and, therefore, to better understand the interaction of the encoding genes, Dam and GidA, in act gene regulation, we constructed a gidA in-frame deletion mutant of Escherichia coli GM28 (dam(+)) and GM33 (∆dam) strains. We then tested the expressional activity of the act and gidA genes by using a promoterless pGlow-TOPO vector containing a reporter green fluorescent protein (GFP). Our data indicated that in GidA(+) strains of E. coli, constitutive methylation of the GATC site(s) by Dam negatively regulated act and gidA gene expression as measured by GFP production. However, in the ∆gidA strains, irrespective of the presence or absence of constitutively active Dam, we did not observe any alteration in the expression of the act gene signifying the role of GidA in positively regulating Act production. To determine the exact mechanism of how Dam and GidA influence Act, a real-time quantitative PCR (RT-qPCR) assay was performed. The analysis indicated an increase in gidA and act gene expression in the A. hydrophila Dam-overproducing strain, and these data matched with Act production in the E. coli GM28 strain. Thus, the extent of DNA methylation caused by constitutive versus overproduction of Dam, as well as possible conformation of DNA influence the expression of act and gidA genes in A. hydrophila SSU. Our results indicate that the act gene is under the control of both Dam and GidA modification methylases, and Dam regulates Act production via GidA.
嗜水气单胞菌既是人类病原体也是动物病原体,细胞毒性肠毒素(Act)是该细菌的重要毒力因子,因为其具有相关的溶血、细胞毒性和肠毒性活性。以前,为了确定一些调节基因在调节 Act 产生中的作用,我们表明,缺失编码 tRNA 甲基酶的葡萄糖抑制分裂基因(gidA)会降低 Act 水平,而 DNA 腺嘌呤甲基转移酶(Dam)的过度产生会导致嗜水气单胞菌腹泻分离株 SSU 的 Act 相关生物学活性同时增加。重要的是,gidA 基因上游序列中有多个 GATC 结合位点用于 Dam,而 act 基因上游区域中有一个这样的靶位点。我们表明 dam 基因对嗜水气单胞菌 SSU 的生存能力至关重要,因此,为了更好地理解编码基因 Dam 和 GidA 在 act 基因调控中的相互作用,我们构建了大肠杆菌 GM28(dam(+))和 GM33(∆dam)菌株的 gidA 框内缺失突变体。然后,我们使用含有报告绿色荧光蛋白(GFP)的无启动子 pGlow-TOPO 载体测试了 act 和 gidA 基因的表达活性。我们的数据表明,在大肠杆菌 GidA(+) 菌株中,Dam 通过 GATC 位点的组成性甲基化负调控 act 和 gidA 基因的表达,如 GFP 产生所测量的。然而,在 ∆gidA 菌株中,无论是否存在组成性激活的 Dam,我们都没有观察到 act 基因表达的任何改变,这表明 GidA 正向调节 Act 的产生。为了确定 Dam 和 GidA 如何影响 Act 的的确切机制,进行了实时定量 PCR(RT-qPCR)测定。分析表明,在嗜水气单胞菌 Dam 过表达菌株中 gidA 和 act 基因的表达增加,这些数据与大肠杆菌 GM28 菌株中的 Act 产生相匹配。因此,组成性或过表达 Dam 引起的 DNA 甲基化程度以及 DNA 的可能构象影响了嗜水气单胞菌 SSU 中 act 和 gidA 基因的表达。我们的结果表明,act 基因受 Dam 和 GidA 修饰甲基酶的共同控制,并且 Dam 通过 GidA 调节 Act 的产生。