Priya Anshu, Kaur Kiranjeet, Bhattacharyya Shalmoli, Chakraborti Anuradha, Ghosh Sujata
Department of Experimental Medicine and Biotechnology, Post Graduate Institute of Medical Education & Research, Chandigarh 160012, India.
Department of Biophysics, Post Graduate Institute of Medical Education & Research, Chandigarh 160012, India.
J Med Microbiol. 2017 Mar;66(2):217-225. doi: 10.1099/jmm.0.000405. Epub 2017 Mar 6.
Enteroaggregative Escherichia coli (EAEC) is an emerging enteric pathogen causing diarrhoeal diseases in multiple epidemiological and clinical settings. However, understanding of the pathogenesis of the disease caused by this organism is still suboptimal. Studies have indicated that enteric bacteria induced cell cycle arrest and apoptosis in host intestinal epithelial cells might play a vital role in the pathogenesis caused by these organisms. In this study an attempt was made to assess EAEC-induced apoptosis and cell cycle modulation in human intestinal epithelial cell lines.
INT-407 and HCT-15 cells were infected with EAEC-T8 (clinical isolate) as well as plasmid cured variant of EAEC-T8 (EAEC-pT8). Propidium iodide staining was done to select the time of infection and the incubation period of the infected culture. Apoptosis was further assessed in EAEC infected both the cell lines by annexin-V-FLUOS & propidium iodide, cell death detection ELISA, DNA strand breaks and microscopic analysis. Further, the DNA content of the EAEC-infected cells at different phases of cell cycle was also monitored.
We have found that EAEC could induce apoptosis in human small intestinal as well as colonic epithelial cell lines, which was assessed by the expression of phosphatidylserine on host cell surface, internucleosomal cleavage of host cell DNA and microscopic analysis of the characteristic apoptotic features of these cells. EAEC was also found to arrest cells at S phase and G2-M phase of the cell cycle.
EAEC-T8 could induce maximum apoptosis and cell cycle modulation in both small intestinal and colonic epithelial cells. Further, we have observed that the plasmid of this organism had maximum contribution to these processes. The outcome of this study has undoubtedly led to a better understanding of the basic mechanism of pathogenesis caused by EAEC.
肠集聚性大肠杆菌(EAEC)是一种新出现的肠道病原体,在多种流行病学和临床环境中可引发腹泻疾病。然而,对该病原体所致疾病发病机制的了解仍不够完善。研究表明,肠道细菌诱导宿主肠道上皮细胞的细胞周期停滞和凋亡可能在这些病原体所致发病机制中起关键作用。本研究旨在评估EAEC对人肠道上皮细胞系凋亡和细胞周期的调节作用。
用EAEC-T8(临床分离株)以及EAEC-T8的质粒消除变异株(EAEC-pT8)感染INT-407和HCT-15细胞。通过碘化丙啶染色来选择感染时间和感染培养物的孵育期。通过膜联蛋白-V-荧光素和碘化丙啶、细胞死亡检测ELISA、DNA链断裂及显微镜分析,进一步评估EAEC感染的这两种细胞系中的凋亡情况。此外,还监测了EAEC感染细胞在细胞周期不同阶段的DNA含量。
我们发现EAEC可诱导人小肠及结肠上皮细胞系凋亡,这可通过宿主细胞表面磷脂酰丝氨酸的表达、宿主细胞DNA的核小体间切割以及这些细胞特征性凋亡特征的显微镜分析来评估。还发现EAEC可使细胞停滞在细胞周期的S期和G2-M期。
EAEC-T8可在小肠和结肠上皮细胞中诱导最大程度的凋亡和细胞周期调节。此外,我们观察到该病原体的质粒对这些过程的贡献最大。本研究结果无疑有助于更好地理解EAEC所致发病机制的基本原理。