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金黄色葡萄球菌在培养的肠上皮细胞内的存活情况。

Intracellular survival of Staphylococcus aureus within cultured enterocytes.

作者信息

Hess D J, Henry-Stanley M J, Erickson E A, Wells C L

机构信息

Department of Surgery, University of Minnesota, Minneapolis, Minnesota 55455, USA.

出版信息

J Surg Res. 2003 Sep;114(1):42-9. doi: 10.1016/s0022-4804(03)00314-7.

Abstract

BACKGROUND

Little is known about the mechanisms involved in bacterial translocation from the intestinal lumen to extraintestinal sites. Because Staphylococcus aureus can colonize the intestinal tract, and because the intestinal tract is a reservoir for antibiotic resistant S. aureus, experiments were designed to clarify the interactions of S. aureus with cultured intestinal epithelial cells, and assays included measurements of bacterial internalization, enterocyte apoptosis, and epithelial barrier function.

METHODS AND RESULTS

Mature, confluent enterocytes were incubated 1 h with S. aureus, and the gentamicin protection assay was used to quantify intracellular bacterial survival at various time intervals up to 120 h later. Enterocyte apoptosis was assessed using Annexin V, and the permeability of confluent enterocyte cultures was measured by transepithelial electrical resistance and by transmigration of Escherichia coli across confluent enterocytes.S. aureus was internalized by cultured enterocytes and remained viable for up to 120 h within both HT-29 and Caco-2 enterocytes. S. aureus intracellular survival was associated with enterocyte apoptosis and with decreased transepithelial electrical resistance across confluent Caco-2 enterocytes. S. aureus intracellular survival over time was also associated with increased E. coli transmigration across confluent Caco-2, but not HT-29, enterocytes.

CONCLUSIONS

S. aureus appeared to survive within cultured enterocytes for prolonged time periods, up to several days. Survival of S. aureus within host eukaryotic cells, such as enterocytes, might facilitate persistence of S. aureus in infected tissue despite appropriate antibiotic therapy.

摘要

背景

关于细菌从肠腔转移至肠外部位的机制,目前了解甚少。由于金黄色葡萄球菌可在肠道定植,且肠道是耐抗生素金黄色葡萄球菌的储存库,因此设计了实验以阐明金黄色葡萄球菌与培养的肠上皮细胞之间的相互作用,检测项目包括细菌内化、肠上皮细胞凋亡和上皮屏障功能的测定。

方法与结果

将成熟的融合肠上皮细胞与金黄色葡萄球菌孵育1小时,采用庆大霉素保护试验在长达120小时的不同时间间隔定量细胞内细菌存活情况。使用膜联蛋白V评估肠上皮细胞凋亡,通过跨上皮电阻和大肠杆菌跨融合肠上皮细胞的迁移来测量融合肠上皮细胞培养物的通透性。金黄色葡萄球菌被培养的肠上皮细胞内化,并在HT - 29和Caco - 2肠上皮细胞内长达120小时仍保持存活。金黄色葡萄球菌在细胞内的存活与肠上皮细胞凋亡以及融合的Caco - 2肠上皮细胞跨上皮电阻降低有关。随着时间推移,金黄色葡萄球菌在细胞内的存活还与大肠杆菌跨融合的Caco - 2而非HT - 29肠上皮细胞的迁移增加有关。

结论

金黄色葡萄球菌似乎能在培养的肠上皮细胞内存活较长时间,长达数天。金黄色葡萄球菌在宿主真核细胞(如肠上皮细胞)内的存活可能有助于其在感染组织中持续存在,尽管进行了适当的抗生素治疗。

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