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核苷掺入L细胞株:类胸膜肺炎微生物的抑制作用

Nucleoside incorporation into strain L cells: inhibition by pleuropneumonia-like organisms.

作者信息

Nardone R M, Todd J, Gonzalez P, Gaffney E V

出版信息

Science. 1965 Sep 3;149(3688):1100-1. doi: 10.1126/science.149.3688.1100.

DOI:10.1126/science.149.3688.1100
PMID:5826523
Abstract

Contamination of Strain L cell cultures by pleuropneumonia-like organismtis (PPLO) resulted in a complete inhibition of the incorporation of tritiated thymnidine and uridine. Contanminated cultures were characterized by a concentration of PPLO along the margins of the cells and in the intercellular-spaces of the cultures. Autoracliograins of PPLO-contaminated cultures were characterized by exposed silver grains over the margins of the cells. Kanamnycin was efjective in the elimination of PPLO and the restoration of nucleoside incorporation.

摘要

类胸膜肺炎微生物(PPLO)污染L细胞培养物导致氚标记胸腺嘧啶核苷和尿苷的掺入完全受到抑制。受污染的培养物的特征是PPLO集中在细胞边缘和培养物的细胞间隙中。PPLO污染培养物的放射自显影片的特征是细胞边缘有银颗粒曝光。卡那霉素在消除PPLO和恢复核苷掺入方面有效。

相似文献

1
Nucleoside incorporation into strain L cells: inhibition by pleuropneumonia-like organisms.核苷掺入L细胞株:类胸膜肺炎微生物的抑制作用
Science. 1965 Sep 3;149(3688):1100-1. doi: 10.1126/science.149.3688.1100.
2
Lability of host-cell DNA in growing cell cultures due to Mycoplasma.支原体导致生长中的细胞培养物中宿主细胞DNA不稳定。
Science. 1965 Sep 3;149(3688):1098-9. doi: 10.1126/science.149.3688.1098.
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Incidence and detection of pleuropneumonia-like organisms in cell cultures by fluorescent antibody and cultural procedures.通过荧光抗体和培养程序在细胞培养物中检测类胸膜肺炎微生物的发生率和检测情况。
J Bacteriol. 1962 Jul;84(1):130-6. doi: 10.1128/jb.84.1.130-136.1962.
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ARGININE METABOLISM IN PLEUROPNEUMONIA-LIKE ORGANISMS ISOLATED FROM MAMMALIAN CELL CULTURE.从哺乳动物细胞培养物中分离出的类胸膜肺炎微生物中的精氨酸代谢
J Bacteriol. 1963 Aug;86(2):195-206. doi: 10.1128/jb.86.2.195-206.1963.
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The uptake of radioactivity of thymidine, uridine, formate, glycine and lysine into cultures of blood of normal human subjects. Relationships with mycoplasma infection.正常人血液培养物中胸苷、尿苷、甲酸、甘氨酸和赖氨酸的放射性摄取。与支原体感染的关系。
Haematologia (Budap). 1970;4(1):27-47.
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[Molecular cytology of the chronology and pattern of tritiated thymidine, uridine and leucine incorporation into normal human lymphocytes transformed in vitro].[氚标记胸腺嘧啶核苷、尿苷和亮氨酸掺入体外转化的正常人淋巴细胞的时间顺序和模式的分子细胞学]
Sangre (Barc). 1971;16(2):185-232.
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Inhibition of [3H]thymidine incorporation by Mycoplasma arginini-infected cells due to enzymatic cleavage of the nucleoside.精氨酸支原体感染的细胞因核苷的酶促裂解而抑制[3H]胸苷掺入。
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Antigenic properties of pleuropneumonia-like organisms from tissue cell cultures and the human genital area.来自组织细胞培养物及人类生殖器部位的类胸膜肺炎微生物的抗原特性。
J Bacteriol. 1961 Oct;82(4):542-7. doi: 10.1128/jb.82.4.542-547.1961.
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Growth of chick aortic endothelial cells: incorporation of tritiated uridine and thymidine.
Experientia. 1965 Nov 15;21(11):637-8. doi: 10.1007/BF02144051.

引用本文的文献

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Cell cycle parameters of 3T3 cells cultured as aggregates.作为聚集体培养的3T3细胞的细胞周期参数。
In Vitro. 1981 Feb;17(2):143-9. doi: 10.1007/BF02618072.
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Polyamine starvation prolongs the S and G2 phases of polyamine-dependent (arginase-deficient) CHO cells.多胺饥饿延长了多胺依赖性(精氨酸酶缺陷型)中国仓鼠卵巢细胞的S期和G2期。
Mol Cell Biol. 1984 May;4(5):915-22. doi: 10.1128/mcb.4.5.915-922.1984.
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Antibody-mediated neutralization of virus is abrogated by mycoplasma.支原体可消除抗体介导的病毒中和作用。
Infect Immun. 1980 Jun;28(3):649-53. doi: 10.1128/iai.28.3.649-653.1980.
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An autoradiographic method of detecting A. laidlawii and M. hyorhinis in cell cultures.一种在细胞培养物中检测莱氏无胆甾原体和猪鼻支原体的放射自显影方法。
In Vitro. 1981 Jul;17(7):563-9. doi: 10.1007/BF02618453.
6
Availability of bases and nucleosides as precursors of nucleic acids in L cells and in the agent of meningopneumonitis.L细胞及脑膜肺炎病原体中作为核酸前体的碱基和核苷的可用性。
J Bacteriol. 1966 Jun;91(6):2362-7. doi: 10.1128/jb.91.6.2362-2367.1966.
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Mycoplasmal deoxyribonuclease activity in virus-infected L-cell cultures.病毒感染的L细胞培养物中的支原体脱氧核糖核酸酶活性。
J Virol. 1969 Mar;3(3):313-7. doi: 10.1128/JVI.3.3.313-317.1969.
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Inhibition of thymidine kinase activity and deoxyribonucleic acid synthesis in L cells infected with the meningopneumonitis agent.对感染脑膜肺炎病原体的L细胞中胸苷激酶活性和脱氧核糖核酸合成的抑制作用
J Bacteriol. 1968 Dec;96(6):2054-65. doi: 10.1128/jb.96.6.2054-2065.1968.
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Proc Natl Acad Sci U S A. 1968 Jun;60(2):583-9. doi: 10.1073/pnas.60.2.583.
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In Vitro. 1971 Jul-Aug;7(1):26-41. doi: 10.1007/BF02619002.