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[Experimental toxoplasmosis in mice. Comparative activity of clindamycin, midecamycin, josamycin, spiramycin, pyrimethamine-sulfadoxine, and trimethoprim-sulfamethoxazole].[小鼠实验性弓形虫病。克林霉素、麦迪霉素、交沙霉素、螺旋霉素、乙胺嘧啶-磺胺多辛及甲氧苄啶-磺胺甲恶唑的比较活性]
Ann Pediatr (Paris). 1984 Nov;31(10):841-5.
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Chemotherapeutic implications of polyamine biosynthesis inhibition.多胺生物合成抑制的化疗意义。
Clin Pharmacol Ther. 1984 Mar;35(3):287-300. doi: 10.1038/clpt.1984.33.
3
New micromethod to study the effect of antimicrobial agents on Toxoplasma gondii: comparison of sulfadoxine and sulfadiazine individually and in combination with pyrimethamine and study of clindamycin, metronidazole, and cyclosporin A.研究抗菌药物对刚地弓形虫作用的新微量法:磺胺多辛和磺胺嘧啶单独及与乙胺嘧啶联合使用的比较以及克林霉素、甲硝唑和环孢素A的研究
Antimicrob Agents Chemother. 1984 Jul;26(1):26-30. doi: 10.1128/AAC.26.1.26.
4
Inhibition of growth of Giardia lamblia by difluoromethylornithine, a specific inhibitor of polyamine biosynthesis.二氟甲基鸟氨酸(一种多胺生物合成的特异性抑制剂)对蓝氏贾第鞭毛虫生长的抑制作用。
J Protozool. 1984 Feb;31(1):161-3. doi: 10.1111/j.1550-7408.1984.tb04308.x.
5
[Spiramycin ; therapeutic value in humans. (author's transl)].[螺旋霉素;对人类的治疗价值。(作者译)]
Sem Hop. 1982 Feb 4;58(5):289-97.
6
[Theoretical bases of the prevention by spiramycin of congenital toxoplasmosis in pregnant women].[螺旋霉素预防孕妇先天性弓形虫病的理论基础]
Presse Med (1893). 1968 Dec 7;76(48):2266.
7
Congenital toxoplasmosis. A prospective study of 378 pregnancies.先天性弓形虫病。对378例妊娠的前瞻性研究。
N Engl J Med. 1974 May 16;290(20):1110-6. doi: 10.1056/NEJM197405162902003.
8
Difluoromethylornithine and formycin B in toxoplasmosis.二氟甲基鸟氨酸和间型霉素B治疗弓形虫病
J Infect Dis. 1985 Nov;152(5):1101. doi: 10.1093/infdis/152.5.1101.
9
Enzyme immunoassay for evaluation of Toxoplasma gondii growth in tissue culture.用于评估组织培养中弓形虫生长的酶免疫测定法。
J Clin Microbiol. 1985 Jan;21(1):88-91. doi: 10.1128/jcm.21.1.88-91.1985.
10
Comparison of the biological effects of four irreversible inhibitors of ornithine decarboxylase in two murine lymphocytic leukemia cell lines.两种小鼠淋巴细胞白血病细胞系中四种鸟氨酸脱羧酶不可逆抑制剂的生物学效应比较
Cancer Res. 1986 Mar;46(3):1148-54.

酶免疫测定法评估抗菌剂对组织培养中弓形虫的作用。

Enzyme immunoassay to assess effect of antimicrobial agents on Toxoplasma gondii in tissue culture.

作者信息

Derouin F, Chastang C

机构信息

Laboratoire de Parasitologie-Mycologie, Hôpital, Saint-Louis, Paris, France.

出版信息

Antimicrob Agents Chemother. 1988 Mar;32(3):303-7. doi: 10.1128/AAC.32.3.303.

DOI:10.1128/AAC.32.3.303
PMID:3284458
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC172164/
Abstract

Toxoplasma gondii grown on MRC5 fibroblasts in 96-well tissue culture plates was tested for susceptibility to five antimicrobial agents. T. gondii growth was quantitated by an enzyme-linked immunosorbent assay, which was performed directly on the fixed cultures, using a rabbit anti-T. gondii immunoglobulin G as the first antibody and a phosphatase-labeled anti-rabbit immunoglobulin G as the second antibody. Optical density values were highly correlated with the number of T. gondii organisms in the Giemsa-stained cultures (r = 0.89), and an enzyme-linked immunosorbent assay was used to assess the effect of antimicrobial agents at various concentrations. For each drug, regression models were used to quantify the relationship between optical density values and antimicrobial agent concentrations in the cultures. A significant inhibitory effect was found with pyrimethamine and sulfadoxine for concentrations greater than or equal to 0.05 and 30 micrograms/ml, respectively. With spiramycin, a progressive increase in inhibition of T. gondii was observed for increasing concentrations from 1 to 100 micrograms/ml. Ornidyl (difluoromethylornithine) and (2R,5R)-6-heptyne-2,5-diamine, which are ornithine decarboxylase inhibitors, were found to have a marked inhibitory effect for concentrations greater than or equal to 25 and 2 mM, respectively. This proposed method was sensitive and easy to perform and does not require the use of radiolabeled compounds; since it allows experimental design on replicate cultures and can be partially automated, it thus may prove useful for the systematic screening of the activity of new compounds against T. gondii.

摘要

对在96孔组织培养板中MRC5成纤维细胞上生长的刚地弓形虫进行了5种抗菌药物的敏感性测试。刚地弓形虫的生长通过酶联免疫吸附测定法定量,该测定直接在固定培养物上进行,使用兔抗刚地弓形虫免疫球蛋白G作为一抗,磷酸酶标记的抗兔免疫球蛋白G作为二抗。光密度值与吉姆萨染色培养物中刚地弓形虫生物体的数量高度相关(r = 0.89),并使用酶联免疫吸附测定法评估不同浓度抗菌药物的效果。对于每种药物,使用回归模型来量化培养物中光密度值与抗菌药物浓度之间的关系。发现乙胺嘧啶和磺胺多辛分别在浓度大于或等于0.05和30微克/毫升时具有显著的抑制作用。对于螺旋霉素,随着浓度从1微克/毫升增加到100微克/毫升,观察到对刚地弓形虫的抑制作用逐渐增强。鸟氨酸脱羧酶抑制剂奥尼地尔(二氟甲基鸟氨酸)和(2R,5R)-6-庚炔-2,5-二胺分别在浓度大于或等于25和2毫摩尔时具有显著的抑制作用。该方法灵敏且易于操作,不需要使用放射性标记化合物;由于它允许对重复培养物进行实验设计并且可以部分自动化,因此可能被证明对系统筛选新化合物对刚地弓形虫的活性有用。