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A组链球菌感染人二倍体细胞中L-变体的诱导

Induction of L-variants in human diploid cells infected by group A streptococci.

作者信息

Schmitt-Slomska J, Boué A, Caravano R

出版信息

Infect Immun. 1972 Mar;5(3):389-99. doi: 10.1128/iai.5.3.389-399.1972.

DOI:10.1128/iai.5.3.389-399.1972
PMID:4564563
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC422380/
Abstract

Human diploid cells in culture, infected with a balanced amount of living group A streptococci, were able to survive the infection and could be divided and propagated normally thereafter. The streptococci were rapidly phagocytized by the tissue culture cells. At the beginning, they kept their typical appearance, as well as their ability to fix dyes and group-specific immunoglobulins. After 1 to 2 days, the number of detectable streptococci decreased and they underwent important morphological changes. After some subsequent divisions of the cell line, streptococci persisted in cells only as large, isolated, swollen cocci, and no longer grew on suitable media. After six to eight divisions, a noticeable percentage of the tissue culture cells were very similar in appearance to the same cell line experimentally infected with "stable" L-variants. Cultures on L-phase media of supernatant fraction and cells, made 24 to 48 hr after inoculation, showed typical L-colonies. These grew well on media without antibiotics, as well as on media containing penicillin or vancomycin. They could be propagated on media with penicillin for months and were able to revert to group A streptococci after several subcultures on antibiotic-free media. Controls of uninoculated tissue culture cells never showed the presence of any microorganism. Group A streptococci inoculated into Eagle's basal medium, which was used for the tissue cultures, did not grow and never gave rise to L-colonies, even though the medium contained penicillin. Previous data suggest a biochemical explanation for this conversion, which otherwise is an occasional phenomenon.

摘要

在培养中的人二倍体细胞,感染了适量的活的A组链球菌后,能够在感染中存活下来,并且此后能够正常分裂和增殖。链球菌很快被组织培养细胞吞噬。一开始,它们保持着典型的外观,以及固定染料和群特异性免疫球蛋白的能力。1至2天后,可检测到的链球菌数量减少,并且它们发生了重要的形态变化。在细胞系随后进行了一些分裂后,链球菌仅以大的、孤立的、肿胀的球菌形式存在于细胞中,并且不再在合适的培养基上生长。经过六到八次分裂后,相当比例的组织培养细胞在外观上与实验感染“稳定”L-变体的同一细胞系非常相似。接种后24至48小时制备的上清液部分和细胞的L期培养基培养物显示出典型的L菌落。这些菌落在不含抗生素的培养基上以及含有青霉素或万古霉素的培养基上生长良好。它们可以在含有青霉素的培养基上繁殖数月,并且在无抗生素培养基上经过几次传代后能够回复为A组链球菌。未接种的组织培养细胞对照从未显示存在任何微生物。接种到用于组织培养的伊格尔基础培养基中的A组链球菌不生长,并且即使培养基含有青霉素也从未产生L菌落。先前的数据为这种转化提出了生化解释,否则这是一种偶然现象。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edb3/422380/91ea7dd245fd/iai00267-0128-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edb3/422380/dd055d64bb14/iai00267-0124-a.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edb3/422380/91ea7dd245fd/iai00267-0128-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edb3/422380/dd055d64bb14/iai00267-0124-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edb3/422380/abca6f097f6c/iai00267-0125-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edb3/422380/06f33cc18c0f/iai00267-0125-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edb3/422380/1483a5fc19d5/iai00267-0126-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edb3/422380/2746f7c60f73/iai00267-0128-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edb3/422380/91ea7dd245fd/iai00267-0128-b.jpg

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本文引用的文献

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Intracellular Production of Brucella L Forms I. Recovery of L Forms from Tissue Culture Cells Infected with Brucella abortus.布鲁氏菌L型的细胞内产生 一、从感染流产布鲁氏菌的组织培养细胞中回收L型
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