Avelino-Flores Fabiola, Soria-Bustos Jorge, Saldaña-Ahuactzi Zeus, Martínez-Laguna Ygnacio, Yañez-Santos Jorge A, Cedillo-Ramírez María L, Girón Jorge A
Centro de Investigación en Ciencias Microbiológicas, Benemérita Universidad Autónoma de Puebla, Puebla 72570, Mexico.
Instituto de Ciencias de la Salud, Universidad Autónoma del Estado de Hidalgo, Pachuca 42160, Mexico.
Microorganisms. 2022 Apr 9;10(4):792. doi: 10.3390/microorganisms10040792.
The flagella of enteropathogenic (EPEC) O127:H6 E2348/69 mediate adherence to host proteins and epithelial cells. What environmental and nutritional signals trigger or down-regulate flagella expression in EPEC are largely unknown. In this study, we analyzed the influence of pH, oxygen tension, cationic and anionic salts (including bile salt), carbon and nitrogen sources, and catecholamines on the expression of the flagellin gene ( of E2348/69. We found that sodium bicarbonate, which has been shown to induce the expression of type III secretion effectors, down-regulated flagella expression, explaining why E2348/69 shows reduced motility and flagellation when growing in Dulbecco's Minimal Essential Medium (DMEM). Further, growth under a 5% carbon dioxide atmosphere, in DMEM adjusted to pH 8.2, in M9 minimal medium supplemented with 80 mM glucose or sucrose, and in DMEM containing 150 mM sodium chloride, 0.1% sodium deoxycholate, or 30 µM epinephrine significantly enhanced transcription to different levels in comparison to growth in DMEM alone. When EPEC was grown in the presence of HeLa cells or in supernatants of cultured HeLa cells, high levels (4-fold increase) of transcription were detected in comparison to growth in DMEM alone. Our data suggest that nutritional and host signals that EPEC may encounter in the intestinal niche activate expression in order to favor motility and host colonization.
肠致病性大肠杆菌(EPEC)O127:H6 E2348/69的鞭毛介导对宿主蛋白和上皮细胞的黏附。在EPEC中,哪些环境和营养信号触发或下调鞭毛表达在很大程度上尚不清楚。在本研究中,我们分析了pH值、氧张力、阳离子和阴离子盐(包括胆盐)、碳源和氮源以及儿茶酚胺对E2348/69鞭毛蛋白基因表达的影响。我们发现,已被证明可诱导III型分泌效应子表达的碳酸氢钠下调了鞭毛表达,这解释了为什么E2348/69在杜氏改良伊格尔培养基(DMEM)中生长时运动性和鞭毛形成减少。此外,与仅在DMEM中生长相比,在5%二氧化碳气氛下、在pH值调至8.2的DMEM中、在补充有80 mM葡萄糖或蔗糖的M9基本培养基中以及在含有150 mM氯化钠、0.1%脱氧胆酸钠或30 µM肾上腺素的DMEM中生长,显著增强了不同水平的flhDC转录。当EPEC在HeLa细胞存在下或在培养的HeLa细胞上清液中生长时,与仅在DMEM中生长相比,检测到高水平(增加4倍)的flhDC转录。我们的数据表明,EPEC在肠道生态位中可能遇到的营养和宿主信号激活flhDC表达,以利于运动性和宿主定殖。