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Genes of Helicobacter pylori Regulated by Attachment to AGS Cells

机译:幽门螺杆菌的基因受AGS细胞附着的调控

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Reciprocal interactions between Helicobacter pylori and cells of the gastric epithelium to which it adheres may affect colonization. Changes in gene expression of H. pylori induced by adhesion to AGS gastric cancer cells by coculture were compared to changes in gene expression of H. pylori cultured without AGS cells by using cDNA filter macroarrays. Adhesion was quantitatively verified by confocal microscopy of green fluorescent protein-expressing bacteria. Four experiments showed that 22 and 21 H. pylori genes were consistently up- and down-regulated, respectively. The up-regulated genes included pathogenicity island, motility, outer membrane protein, and translational genes. The σ28 factor antagonist flgM, flgG, the stress response gene, flaA, omp11, and the superoxide dismutase gene (sodB) were down-regulated. The up-regulation of cag3, flgB, tonB, rho, and deaD was confirmed by quantitative PCR, and the up-regulation of lpxD, omp6, secG, fabH, HP1285, HP0222, and HP0836 was confirmed by reverse transcription (RT)-PCR. The down-regulation of flaA, sodB, and HP0874 was confirmed by quantitative PCR, and the down-regulation of omp11 was confirmed by RT-PCR. The alteration of gene expression in H. pylori after adhesion to gastric cells in vitro suggests that changes in motility, outer membrane composition, and stress responses, among other changes, may be involved in gastric colonization.
机译:幽门螺杆菌与其粘附的胃上皮细胞之间的相互作用可能会影响定植。 H基因表达的变化。比较了共培养对AGS胃癌细胞粘附的幽门螺杆菌与 H基因表达的变化。通过使用cDNA过滤器大阵列在无AGS细胞的情况下培养幽门螺杆菌。通过共聚焦显微镜观察表达绿色荧光蛋白的细菌来定量验证粘附力。四个实验表明22和21H。幽门螺杆菌基因分别持续上调和下调。上调的基因包括致病岛,运动性,外膜蛋白和翻译基因。 σ 28 因子拮抗剂 flgM flgG ,应激反应基因 flaA omp11 和超氧化物歧化酶基因( sodB )被下调。 cag3 flgB tonB rho deaD 的上调通过定量PCR证实,并且 lpxD omp6 secG fabH ,HP1285,通过逆转录(RT)-PCR确认了HP0222和HP0836。定量PCR证实了 flaA sodB 和HP0874的下调,而RT-证实了 omp11 的下调PCR。在 H基因表达的改变。幽门螺杆菌在体外粘附于胃细胞后提示,胃定植可能涉及运动性,外膜组成和应激反应等方面的变化。

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