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化脓性链球菌L型及脂磷壁酸对组织培养中人类细胞的影响。

Effect of L-form Streptococcus pyogenes and of lipoteichoic acid on human cells in tissue culture.

作者信息

DeVuono J, Panos C

出版信息

Infect Immun. 1978 Oct;22(1):255-65. doi: 10.1128/iai.22.1.255-265.1978.

DOI:10.1128/iai.22.1.255-265.1978
PMID:365747
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC422143/
Abstract

These studies showed the destruction of growing primary and established human cell lines with a predilection for the group A streptococci by an L-form of Streptococcus pyogenes adapted to grow in isotonic media. Also, this L-form was detected by fluorescent antibody for longer periods of time than by viable count in infected but recovered tissue culture monolayers. Additional studies with human heart cells showed changes in their protein profile and fatty acid content (but not composition) after L-form infection. This report is the first to show that the morphological changes and death of human kidney cells by this viable L-form were mimicked by the structurally different lipoteichoic acids from this organism and its parental streptococcus. These lipoteichoic acids were also equally effective in preventing attachment of S. pyogenes to human cell monolayers, but their deacylation obviated these two activities. Finally, the attachment of the isotonic L-form, as well as the parental streptococcus, to growing human kidney cells suggested that a rigid cell wall is not a prerequisite for host attachment in vitro.

摘要

这些研究表明,适应在等渗培养基中生长的化脓性链球菌L型对A组链球菌有偏好,可破坏正在生长的原代人类细胞系和已建立的人类细胞系。此外,在受感染但已恢复的组织培养单层中,通过荧光抗体检测到这种L型的时间比活菌计数法更长。对人类心脏细胞的进一步研究表明,L型感染后其蛋白质谱和脂肪酸含量(但不是组成)发生了变化。本报告首次表明,这种有活力的L型导致人类肾细胞的形态变化和死亡,可被来自该生物体及其亲本链球菌的结构不同的脂磷壁酸模拟。这些脂磷壁酸在防止化脓性链球菌附着于人类细胞单层方面同样有效,但其脱酰作用消除了这两种活性。最后,等渗L型以及亲本链球菌附着于正在生长的人类肾细胞表明,坚硬的细胞壁不是体外宿主附着的先决条件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8019/422143/2e5b40325de2/iai00202-0272-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8019/422143/3cfa273416a9/iai00202-0267-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8019/422143/9d6a687222d6/iai00202-0268-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8019/422143/ded4657275dc/iai00202-0269-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8019/422143/36ba17a58bca/iai00202-0270-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8019/422143/b9c21552bbae/iai00202-0271-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8019/422143/2e5b40325de2/iai00202-0272-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8019/422143/3cfa273416a9/iai00202-0267-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8019/422143/9d6a687222d6/iai00202-0268-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8019/422143/ded4657275dc/iai00202-0269-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8019/422143/36ba17a58bca/iai00202-0270-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8019/422143/b9c21552bbae/iai00202-0271-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8019/422143/2e5b40325de2/iai00202-0272-a.jpg

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