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Isolation and Short-Term Persistence of Ehrlichia ewingii in Cell Culture

机译:细胞培养中埃文氏菌的分离和短期持久性

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摘要

Ehrlichia ewingii is the causative agent of human and canine granulocytic ehrlichiosis. Since its discovery in 1970, little work has been done to characterize the pathogen or study the transmission dynamics due to the inability to grow the agent in vitro. The aim of this study was to assess the suitability of multiple cell lines and media formulations for propagation of E. ewingii in cell culture. In this study, we present an overview of attempts to isolate E. ewingii from the buffy coat of goats naturally infected by Amblyomma americanum ticks, as well as a methodology for maintaining the pathogen for up to 16 weeks in culture. The most promising results were seen with HL-60 cells differentiated by the addition of 1.5% DMSO to the media and supplemented with 8mM l-glutamine. Cultures were passaged multiple times, and fluorescence and morulae were observed by indirect fluorescent antibody test and Diff-Quik staining. It is our hope that this information will provide a foundation for future attempts to propagate and maintain E. ewingii in cell culture.
机译:Ewinglichia ewingii是人和犬颗粒性大肠杆菌病的病原体。自从1970年被发现以来,由于无法在体外生长该病原体,因此几乎没有开展任何工作来表征病原体或研究传播动态。这项研究的目的是评估多种细胞系和培养基配方在细胞培养中对尤氏大肠杆菌的繁殖的适应性。在这项研究中,我们概述了尝试从自然感染美洲原虫tick的山羊绒毛大衣中分离出Ewingii的尝试,以及将病原体培养长达16周的方法。在向培养基中添加1.5%DMSO并补充8mM 1-谷氨酰胺分化的HL-60细胞中看到了最有希望的结果。将培养物传代多次,并通过间接荧光抗体试验和Diff-Quik染色观察荧光和桑ula。我们希望该信息将为将来尝试在细胞培养中繁殖和维持Ewingii提供基础。

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