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用于识别废水中微生物病原体的快速反向纯化DNA提取方法

Rapid Reverse Purification DNA Extraction Approaches to Identify Microbial Pathogens in Wastewater.

作者信息

Schurig Sarah, Kobialka Rea, Wende Andy, Ashfaq Khan Md Anik, Lübcke Phillip, Eger Elias, Schaufler Katharina, Daugschies Arwid, Truyen Uwe, Abd El Wahed Ahmed

机构信息

Institute of Animal Hygiene and Veterinary Public Health, Leipzig University, 04103 Leipzig, Germany.

Xpedite Diagnostics GmbH, 80687 Munich, Germany.

出版信息

Microorganisms. 2023 Mar 22;11(3):813. doi: 10.3390/microorganisms11030813.

DOI:10.3390/microorganisms11030813
PMID:36985386
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10056086/
Abstract

Wastewater monitoring became a promising solution in the early detection of outbreaks. Despite the achievements in the identification of pathogens in wastewater using real-time PCR, there is still a lack of reliable rapid nucleic acid extraction protocols. Therefore, in this study, samples were subjected to alkali, proteinase K and/or bead-beating followed by reverse purification magnetic beads-based separation. Wastewater samples spiked with , and were used as examples for Gram-positive and -negative bacteria and protozoa, respectively. All results were compared with a spin column technology as a reference method. Proteinase K with bead beating (vortexing with 0.1 mm glass beads for three minutes) was particularly successful for bacterial DNA extraction (three- to five-fold increase). The most useful extraction protocol for protozoa was pre-treatment with proteinase K (eight-fold increase). The selected methods were sensitive as far as detecting one bacterial cell per reaction for , ten bacterial cells for and two oocysts for . The extraction reagents are cold chain independent and no centrifuge or other large laboratory equipment is required to perform DNA extraction. A controlled validation trial is needed to test the effectiveness at field levels.

摘要

废水监测成为疾病暴发早期检测中一种很有前景的解决方案。尽管在利用实时聚合酶链反应(PCR)鉴定废水中的病原体方面取得了一些成果,但仍然缺乏可靠的快速核酸提取方案。因此,在本研究中,对样本进行碱处理、蛋白酶K处理和/或珠磨处理,然后采用基于磁珠反向纯化的分离方法。分别将添加了金黄色葡萄球菌、大肠杆菌和隐孢子虫的废水样本用作革兰氏阳性菌、革兰氏阴性菌和原生动物的示例。所有结果均与作为参考方法的离心柱技术进行比较。蛋白酶K结合珠磨处理(与0.1毫米玻璃珠涡旋三分钟)在提取细菌DNA方面特别成功(增加了三到五倍)。对原生动物最有效的提取方案是用蛋白酶K进行预处理(增加了八倍)。所选方法在检测每个反应中一个金黄色葡萄球菌细胞、十个大肠杆菌细胞和两个隐孢子虫卵囊时具有敏感性。提取试剂无需冷链,进行DNA提取也不需要离心机或其他大型实验室设备。需要进行一项对照验证试验来测试其在实际应用中的有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68a2/10056086/9bd864b1ccf9/microorganisms-11-00813-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68a2/10056086/a94e40120e2a/microorganisms-11-00813-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68a2/10056086/b9666ade7874/microorganisms-11-00813-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68a2/10056086/6f9212e118e1/microorganisms-11-00813-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68a2/10056086/8950917700a5/microorganisms-11-00813-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68a2/10056086/2440f25cf06c/microorganisms-11-00813-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68a2/10056086/9bd864b1ccf9/microorganisms-11-00813-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68a2/10056086/a94e40120e2a/microorganisms-11-00813-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68a2/10056086/b9666ade7874/microorganisms-11-00813-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68a2/10056086/6f9212e118e1/microorganisms-11-00813-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68a2/10056086/8950917700a5/microorganisms-11-00813-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68a2/10056086/2440f25cf06c/microorganisms-11-00813-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68a2/10056086/9bd864b1ccf9/microorganisms-11-00813-g006.jpg

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