Smith Allen D, Yan Xianghe, Chen Celine, Dawson Harry D, Bhagwat Arvind A
Diet, Genomics and Immunology Laboratory, Beltsville Human Nutrition Research Center, USDA-ARS, 10300 Baltimore Ave., B307C, Rm. 228, BARC-E, Beltsville, MD, 20705, USA.
Environmental, Microbial, and Food Safety Laboratory, Beltsville Agriculture Research Center, USDA-ARS, Beltsville, MD, USA.
Arch Microbiol. 2016 May;198(4):353-62. doi: 10.1007/s00203-016-1191-y. Epub 2016 Feb 2.
Citrobacter rodentium (Cr) is a mouse pathogen that mimics many aspects of enteropathogenic Escherichia coli infections including producing attaching and effacing (A/E) lesions. Host-adapted (HA) Cr cells that are shed at the peak of infection have been reported to be hyper-infective. The exact mechanism underlying this phenomenon has remained elusive since the pathogen loses its HA 'status' immediately upon subculturing in laboratory media. We sequenced the entire transcriptome of Cr directly from the feces of infected mice and analyzed the gene expression pattern. We observed that the entire transcriptional machinery as well as several transcriptional regulators to be differentially expressed when compared with the transcriptome of cells grown on laboratory media. Major adhesion and effector genes, tir and eae, were highly expressed in HA along with many genes located on all five loci of enterocyte effacement regions (LEE 1-5). Notable absent among the HA expressed genes were 19 fimbrial operons and non-fimbrial adhesions and several non-LEE encoded effectors. These results demonstrate that host-adapted Cr has a unique transcriptome that is associated with increased host transmission.
鼠柠檬酸杆菌(Cr)是一种小鼠病原体,它模拟肠道致病性大肠杆菌感染的许多方面,包括产生紧密黏附并抹平损伤(A/E损伤)。据报道,在感染高峰期排出的宿主适应性(HA)Cr细胞具有高感染性。自从这种病原体在实验室培养基中继代培养后立即失去其HA“状态”以来,这一现象背后的确切机制一直难以捉摸。我们直接从感染小鼠的粪便中对Cr的整个转录组进行了测序,并分析了基因表达模式。我们观察到,与在实验室培养基上生长的细胞的转录组相比,整个转录机制以及几种转录调节因子存在差异表达。主要的黏附基因和效应子基因,tir和eae,在HA中高度表达,同时许多位于肠上皮细胞抹平区域(LEE 1-5)的所有五个位点上的基因也高度表达。在HA表达的基因中明显缺失的是19个菌毛操纵子和非菌毛黏附蛋白以及几种非LEE编码的效应子。这些结果表明,宿主适应性Cr具有独特的转录组,这与增加宿主传播有关。