Haque A, Bowe F, Fitzhenry R J, Frankel G, Thomson M, Heuschkel R, Murch S, Stevens M P, Wallis T S, Phillips A D, Dougan G
Immunology Unit, Department of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, Keppel St, London WC1E 7HT, UK.
Gut. 2004 Oct;53(10):1424-30. doi: 10.1136/gut.2003.037382.
Salmonella enterica serovar typhimurium (S typhimurium) causes invasive gastroenteritis in humans, a disease involving significant penetration of the intestinal mucosa. However, few studies have been undertaken to investigate this interaction directly using differentiated human gut tissue.
To investigate the early interactions of an enteropathogenic strain of S typhimurium with human intestinal mucosa using human intestinal in vitro organ culture (IVOC).
Wild-type and mutant derivatives of S typhimurium TML were used to compare interactions with cultured human epithelial cells, bovine ligated loops, and human intestinal IVOC.
S typhimurium TML was shown to attach to cultured Caco-2 brush border expressing cells and cause tissue damage and fluid accumulation in a ligated bovine loop model.S typhimurium TML bound predominantly to the mucus layer of human IVOC explants during the first four hours of IVOC incubation. From four to eight hours of IVOC incubation, small but characteristic foci of attaching and invading S typhimurium TML were detected as clusters of bacteria interacting with enterocytes, although there was no evidence for large scale invasion of explant tissues. Ruffling of enterocyte membranes associated with adherent Salmonella was visualised using electron microscopy.
Human IVOC can be used as an alternative model for monitoring the interactions between S typhimurium and human intestinal epithelium, thus potentially offering insight into the early stages of human Salmonella induced gastroenteritis.
鼠伤寒沙门氏菌(肠炎沙门氏菌鼠伤寒亚种)可引起人类侵袭性肠胃炎,这种疾病涉及肠道黏膜的显著穿透。然而,很少有研究直接使用分化的人类肠道组织来研究这种相互作用。
使用人类肠道体外器官培养(IVOC)研究鼠伤寒沙门氏菌致病菌株与人类肠道黏膜的早期相互作用。
使用鼠伤寒沙门氏菌TML的野生型和突变衍生物来比较与培养的人类上皮细胞、牛结扎肠袢和人类肠道IVOC的相互作用。
鼠伤寒沙门氏菌TML在结扎牛肠袢模型中显示可附着于培养的表达Caco-2刷状缘的细胞并导致组织损伤和液体蓄积。在IVOC培养的前四个小时,鼠伤寒沙门氏菌TML主要结合于人类IVOC外植体的黏液层。在IVOC培养四到八小时时,尽管没有证据表明外植体组织有大规模侵袭,但检测到有少量但特征性的附着和侵袭鼠伤寒沙门氏菌TML的病灶,表现为细菌与肠上皮细胞相互作用的簇状。使用电子显微镜观察到与黏附的沙门氏菌相关的肠上皮细胞膜褶皱。
人类IVOC可作为监测鼠伤寒沙门氏菌与人类肠道上皮之间相互作用的替代模型,从而有可能深入了解人类沙门氏菌诱导的肠胃炎的早期阶段。