RELATIONSHIP BETWEEN THE SPECTROMETRIC VALUES OF DNA, RNA, AND THE PCR PRESENCE OF A PATHOGEN IN SINGLE TICK SAMPLES

Gudrun Baersch
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Abstract

Aim. Ticks are the vectors of many pathogens, which cause diseases with fatal consequences. Polymerase chain reaction (PCR) was used to detect the presence of these different pathogens in ticks, but there is a need of isolated nucleic acid to conduct the molecular assays. In our previous research, we found that some ticks give huge yield of isolated nucleic acid during spectrometric measurements, therefore aim of this study is to find whether there is any relation between spectrometric values of DNA, RNA and presence of Borrelia burgdorferi as example pathogen in single tick samples. Methods. DNA and RNA were isolated with mini column method from single tick samples. They were run in real time as well as conventional PCR tests for the presence of Borrelia burgdorferi. The nucleic acid yields of isolated nucleic acid samples were measured with a spectrophotometer. Results. It was found that there were 47 ticks positive for Borrelia burgdorferi and 40 were negative. Average isolated DNA and RNA quantity was higher in pathogen positive ticks than those of negative ticks. There was no correlation between the yield of nucleic acid and presence of pathogen in a single tick, but there was tendency that pathogen positive tick gave higher yield of DNA and RNA during the isolation. Conclusions. This study shows some of Borrelia burgdorferi positive ticks give very high yield of DNA and RNA during the isolation. There is no correlation between presence of pathogen and nucleic acid in a single tick, but there is tendency that pathogen positive tick may have higher nucleic acid yield. Therefore, our recommendation is that laboratory should always measure the nucleic acid yield along with conducting the PCR tests.
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单个蜱虫样本中病原体的 DNA、RNA 和 PCR 光谱值之间的关系
目的。蜱虫是许多病原体的载体,这些病原体会导致致命的疾病。聚合酶链反应(PCR)被用来检测蜱虫体内是否存在这些不同的病原体,但进行分子检测需要分离核酸。在之前的研究中,我们发现一些蜱虫在光谱测量过程中会产生大量的分离核酸,因此本研究的目的是找出单个蜱虫样本中的 DNA、RNA 光谱值与作为病原体的博氏包虫病之间是否存在任何关系。研究方法用迷你柱法从单个蜱虫样本中分离 DNA 和 RNA。对它们进行实时检测和传统的 PCR 检测,以确定是否存在博氏包柔氏菌。用分光光度计测量分离核酸样本的核酸产量。结果显示结果发现,有 47 只蜱对布氏杆菌呈阳性反应,40 只呈阴性反应。病原体阳性蜱的 DNA 和 RNA 平均分离量高于阴性蜱。核酸产量与单只蜱体内是否存在病原体之间没有相关性,但在分离过程中,病原体阳性蜱的 DNA 和 RNA 产量较高。结论。这项研究表明,一些布氏包柔氏菌阳性的蜱虫在分离过程中DNA和RNA的产量非常高。病原体的存在与单个蜱虫的核酸之间没有相关性,但病原体阳性蜱虫的核酸产量可能更高。因此,我们建议实验室在进行 PCR 检测时,应始终测量核酸产量。
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