沙眼衣原体培养中支原体去污:一种治疗方法。

IF 2.7 4区 医学 Q3 IMMUNOLOGY Pathogens and disease Pub Date : 2022-01-12 DOI:10.1093/femspd/ftab056
Madison Greer, Jacob H Elnaggar, Christopher M Taylor, Li Shen
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引用次数: 2

摘要

支原体对细胞培养物的污染是研究中的一个严重问题,从细胞繁殖的专性细胞内细菌中去除污染已被证明具有挑战性。在这里,我们提出了一个优化的方案,从污染的沙眼衣原体培养物中去除支原体。支原体去除的分步程序包括(i)在含非离子洗涤剂的溶液中孵育,(ii)通过荧光激活细胞分选(FACS)分离有活力的衣原体生物,然后使用焦点形成试验进行亚克隆。我们还采用了一种聚合酶链反应(PCR)方法,使用与沙眼衣原体相区别的通用和支原体特异性配对引物,结合Sanger测序来确定支原体16S rRNA基因的存在。这些综合方法允许完全去除支原体,正如改进的PCR检测所证实的那样,而不会损害活沙眼衣原体适应上皮细胞新感染的能力。讨论了支原体净化过程中的一些缺陷。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Mycoplasma decontamination in Chlamydia trachomatis culture: a curative approach.

Mycoplasma contamination of cell culture represents a serious problem in research and decontamination from cell-propagated obligate intracellular bacteria has proven challenging. Here, we presented an optimized protocol to remove Mycoplasma from contaminated Chlamydia trachomatis culture. A stepwise procedure of Mycoplasma removal entails (i) incubation in nonionic detergent-containing solution and (ii) separation of viable chlamydial organisms by fluorescence-activated cell sorting (FACS), followed by subcloning using a focus-forming assay. We also adapted a polymerase chain reaction (PCR) assay using paired universal and Mycoplasma-specific primers, which are distinguishable from the C. trachomatis counterparts, in combination with Sanger sequencing to determine the presence of mycoplasmas' 16S rRNA genes. These integrated approaches allow for full removal of Mycoplasma, as verified by the improved PCR assay, without compromising the capacity of viable C. trachomatis to adapt to new infection in epithelial cells. Some pitfalls during the Mycoplasma decontamination process are discussed.

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来源期刊
Pathogens and disease
Pathogens and disease IMMUNOLOGY-INFECTIOUS DISEASES
CiteScore
7.40
自引率
3.00%
发文量
44
期刊介绍: Pathogens and Disease publishes outstanding primary research on hypothesis- and discovery-driven studies on pathogens, host-pathogen interactions, host response to infection and their molecular and cellular correlates. It covers all pathogens – eukaryotes, prokaryotes, and viruses – and includes zoonotic pathogens and experimental translational applications.
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