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用于饱血硬蜱的DNA提取和扩增技术比较

Comparison of DNA Extraction and Amplification Techniques for Use with Engorged Hard-Bodied Ticks.

作者信息

Reifenberger Gretchen C, Thomas Bryce A, Rhodes DeLacy V L

机构信息

Department of Biology, Berry College, Mount Berry, GA 30149, USA.

出版信息

Microorganisms. 2022 Jun 20;10(6):1254. doi: 10.3390/microorganisms10061254.

Abstract

Tick-borne infections are a serious threat to humans, livestock, and companion animals in many parts of the world, often leading to high morbidity and mortality rates, along with decreased production values and/or costly treatments. The prevalence of the microbes responsible for these infections is typically assessed by the molecular identification of pathogens within the tick vectors. Ticks sampled from animals are often engorged with animal blood, presenting difficulties in the amplification of nucleic acids due to the inhibitory effects of mammalian blood on the enzymes used in polymerase chain reactions (PCRs). This study tested two tick preparation methods, three methods of DNA extraction, and four commercially available DNA polymerases to determine the most reliable method of extracting and amplifying DNA from engorged ticks. Our study found that the phenol-chloroform extraction method yielded the highest concentration of DNA, yet DNA extracted by this method was amplified the least successfully. Thermo Scientific's Phusion Plus PCR Master Mix was the best at amplifying the tick 16s rRNA gene, regardless of extraction method. Finally, our study identified that using the Qiagen DNeasy Blood & Tissues kit for DNA extraction coupled with either Phusion Plus PCR Master Mix or GoTaq DNA polymerase Master Mix is the best combination for the optimized amplification of DNA extracted from engorged ticks.

摘要

蜱传感染对世界许多地区的人类、家畜和伴侣动物构成严重威胁,常常导致高发病率和死亡率,同时还会降低产值和/或增加治疗成本。通常通过对蜱传播媒介内病原体的分子鉴定来评估引起这些感染的微生物的流行情况。从动物身上采集的蜱通常饱食动物血液,由于哺乳动物血液对聚合酶链反应(PCR)中使用的酶具有抑制作用,因此在核酸扩增方面存在困难。本研究测试了两种蜱制备方法、三种DNA提取方法和四种市售DNA聚合酶,以确定从饱血蜱中提取和扩增DNA的最可靠方法。我们的研究发现,酚-氯仿提取法产生的DNA浓度最高,但用这种方法提取的DNA扩增成功率最低。无论采用何种提取方法,赛默飞世尔科技的Phusion Plus PCR预混液在扩增蜱16s rRNA基因方面表现最佳。最后,我们的研究确定,使用Qiagen DNeasy Blood & Tissues试剂盒进行DNA提取,再结合Phusion Plus PCR预混液或GoTaq DNA聚合酶预混液,是从饱血蜱中提取的DNA进行优化扩增的最佳组合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fff1/9228219/c8118479b348/microorganisms-10-01254-g001.jpg

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