Meštrović Tomislav, Virok Dezső P, Ljubin-Sternak Sunčanica, Raffai Tímea, Burián Katalin, Vraneš Jasmina
University North, University Centre Varaždin, Varaždin, Croatia.
Clinical Microbiology and Parasitology Unit, Polyclinic "Dr. Zora Profozić", Zagreb, Croatia.
Methods Mol Biol. 2019;2042:33-43. doi: 10.1007/978-1-4939-9694-0_5.
Obligate intracellular localization of Chlamydia trachomatis (C. trachomatis) complicates antimicrobial sensitivity testing efforts that we are so accustomed to in routine bacteriology. Cell culture systems with immunofluorescence staining, to identify cellular inclusions in the presence of various concentrations of antimicrobial drugs, are still the most pervasive techniques, but more specific and sensitive nucleic acid concentration measuring methods are increasingly being used. Here we describe how to approach antimicrobial susceptibility/resistance screening in C. trachomatis by using a McCoy cell culture system, optimized by a research group from Croatia, and direct qPCR-based monitoring of chlamydial growth, optimized by a research group from Hungary.
沙眼衣原体(C. trachomatis)的专性胞内定位使我们在常规细菌学中习以为常的抗菌药敏试验变得复杂。利用免疫荧光染色的细胞培养系统,在不同浓度抗菌药物存在的情况下识别细胞内包涵体,仍然是最普遍使用的技术,但越来越多地采用更特异、更灵敏的核酸浓度测量方法。在此,我们描述如何通过使用由克罗地亚一个研究小组优化的 McCoy 细胞培养系统,以及由匈牙利一个研究小组优化的基于直接定量聚合酶链反应(qPCR)的衣原体生长监测,来进行沙眼衣原体的抗菌药敏/耐药性筛查。