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[A组链球菌与HEp-2细胞培养物的相互作用]

[Interaction of group A streptococci with a culture of HEp-2 cells].

作者信息

Grabovskaia K B, Totolian A A

出版信息

Zh Mikrobiol Epidemiol Immunobiol. 1977 Feb(2):32-6.

PMID:324184
Abstract

An initial stage of the interaction of the virulent (matt) and avirulent (glossy) strains of group A streptococcus with the human epithelial tissue (Hep-2) was studied. M+ and M- variants of three strains of group A streptococcus belonging to serological types 2 and 4 possessed different biological activity against the Hep-2 epithelial cells in the monolayer. M+-variant actively affected the great majority of the cells of the monolayer, multiplied of their surface and formed microcolonies. M--variant affected only an insignificant number of cells and failed to multiply on them. In difference from M+-streptococci, the activity of M+-variants is explained by their capacity to adhere to the surface of the animal cells irreversibly. This process started immediately and terminated by 1 1/2 hours of the microbial incubation in vitro with the Hep-2 monolayer. Trypsin treatment of M+-streptococci sharply diminished their capacity to adhesion, this apparently being the result of M-protein digestion. The data presented point to the important role played by M-protein in the phenomenon of the streptococci adhesion to the epithelial cells.

摘要

对A组链球菌的强毒株(粗糙型)和无毒株(光滑型)与人上皮组织(Hep-2)相互作用的初始阶段进行了研究。属于血清型2和4的三株A组链球菌的M +和M -变体对单层培养的Hep-2上皮细胞具有不同的生物活性。M +变体积极影响单层中的绝大多数细胞,在其表面增殖并形成微菌落。M -变体仅影响极少数细胞,并且无法在这些细胞上增殖。与M +链球菌不同,M +变体的活性归因于它们不可逆地粘附于动物细胞表面的能力。这个过程立即开始,并在体外与Hep-2单层微生物孵育1.5小时后终止。用胰蛋白酶处理M +链球菌会大大降低它们的粘附能力,这显然是M蛋白消化的结果。所呈现的数据表明M蛋白在链球菌粘附上皮细胞现象中发挥的重要作用。

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