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采用酶免疫测定法(衣原体酶检测法)快速测定15种抗衣原体药物的最低抑菌浓度。

Rapid determination of MICs of 15 antichlamydial agents by using an enzyme immunoassay (Chlamydiazyme).

作者信息

Bianchi A, Scieux C, Salmeron C M, Casin I, Perol Y

机构信息

Laboratoire de Bactériologie-Virologie, Hôpital Saint-Louis, Université Paris VII, France.

出版信息

Antimicrob Agents Chemother. 1988 Sep;32(9):1350-3. doi: 10.1128/AAC.32.9.1350.

Abstract

An enzyme immunoassay (EIA), Chlamydiazyme (Abbott Laboratories), was evaluated for its determination of MICs of 15 antimicrobial agents against Chlamydia trachomatis (MRC-1, LB, TRIC/GB/MRC-1 Gf [ATCC VR-1]). The inoculum size, incubation time, and enhancers were defined for the assessment of chlamydial antigen synthesis in HeLa 229 cells seeded as monolayers in 96-well plates. MICs were determined and defined as the lowest antibiotic concentrations required to inhibit, after 24 or 48 h of incubation, antigen production as determined by the EIA. The MICs (after 48 h) were similar to those determined by the peroxidase-antiperoxidase staining of inclusions. MIC determinations after 24 h were suitable for screening the activities of quinolones, but less so for measuring the susceptibility of C. trachomatis to macrolides and tetracyclines. MIC determination by EIA was rapid, appropriate for standardization, and less cumbersome than determination by quantification of inclusions.

摘要

对一种酶免疫测定法(EIA)——衣原体酶检测法(雅培实验室)进行了评估,以确定15种抗菌剂对沙眼衣原体(MRC - 1、LB、TRIC/GB/MRC - 1 Gf [ATCC VR - 1])的最低抑菌浓度(MIC)。确定了接种量、孵育时间和增强剂,用于评估接种于96孔板单层培养的HeLa 229细胞中衣原体抗原的合成。测定MIC,并将其定义为在孵育24或48小时后,通过EIA测定抑制抗原产生所需的最低抗生素浓度。(48小时后的)MIC与通过包涵体过氧化物酶 - 抗过氧化物酶染色法测定的结果相似。24小时后的MIC测定适用于筛选喹诺酮类药物的活性,但不太适合测定沙眼衣原体对大环内酯类和四环素类药物的敏感性。通过EIA测定MIC快速、适合标准化,且比通过包涵体定量测定更简便。

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