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[可引起小肠超微结构改变及侵袭HeLa细胞的经典肠致病性大肠杆菌血清型]

[Serotypes of classical enteropathogenic Escherichia coli that produce changes in the small bowel ultrastructure and invasion of HeLa cells].

作者信息

Fagundes Neto U, Scaletsky I, Schmitz L G, Freymuller E

机构信息

Disciplinas de Gastroenterologia Pediátrica, Universidade Federal de São Paulo, Brasilia.

出版信息

Rev Assoc Med Bras (1992). 1995 Sep-Oct;41(5):318-24.

PMID:8731594
Abstract

UNLABELLED

Enteropathogenic Escherichia coli (EPEC) is the main cause of diarrhea in infants up to one year of age in the majority of the developing countries. In vitro EPEC strains attach to HeLa or HEp-2 cells in a specific pattern called localized adherence (LA), which is correlated with 93% of the EPEC serotypes. In vivo, EPEC strains adhere intimately to cuplike projections of the apical enterocyte membrane causing localized destruction of the microvilli, described as an attaching and effacing lesion.

PURPOSE

We showed the attaching-effacing lesions and intracellular penetration in the ultrastructural study of the small intestinal cells as well as in the HeLa cell assay by the following EPEC serotypes: O111ab:H2, O119:H6 and O18ab:H14.

PATIENTS AND METHODS

These strains were isolated from the stools of three infants less than 2 years of age with watery diarrhea who were hospitalized for fluid and electrolyte repairment. In the three patients there were severe ultrastructural alterations of the enterocytes mainly shortening and destruction of the microvilli, and formation of cuplike pedestal lesions. There was also penetration of microorganisms into the cytoplasm of the enterocytes in the interior of endocytotic vesicles. The serotypes of EPEC were assayed with HeLa cells showing the formation of pedestals and penetration into the cytoplasm.

CONCLUSION

The ultrastructural alterations of the small bowel observed in these patients represent an important indication of the possibility of perpetuation of the diarrhea, owing to either a secretory mechanism or malabsorption of the nutrients.

摘要

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在大多数发展中国家,肠致病性大肠杆菌(EPEC)是1岁以下婴儿腹泻的主要病因。在体外,EPEC菌株以一种称为局部黏附(LA)的特定模式附着于HeLa或HEp-2细胞,这与93%的EPEC血清型相关。在体内,EPEC菌株紧密黏附于顶端肠细胞膜的杯状突起,导致微绒毛局部破坏,称为黏附和脱落性病变。

目的

我们通过以下EPEC血清型:O111ab:H2、O119:H6和O18ab:H14,在小肠细胞的超微结构研究以及HeLa细胞试验中展示了黏附和脱落性病变以及细胞内渗透情况。

患者和方法

这些菌株从3名2岁以下因水样腹泻住院进行液体和电解质补充的婴儿粪便中分离得到。在这3名患者中,肠细胞存在严重的超微结构改变,主要是微绒毛缩短和破坏,以及杯状基座病变的形成。在胞吞泡内部,微生物也渗透到肠细胞的细胞质中。用HeLa细胞检测EPEC血清型,显示基座形成和细胞质渗透情况。

结论

在这些患者中观察到的小肠超微结构改变是腹泻持续存在可能性的一个重要指标,这可能是由于分泌机制或营养物质吸收不良所致。

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