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Evaluation of commercial methods to separate nucleic acids from intestinal tissues of pigs for diagnosis of porcine epidemic diarrhea

机译:评价商业方法与猪肠组织分离核酸以诊断猪流行性腹泻

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The article presents the results of evaluating commercial methods for extracting nucleic acids from pig intestinal tissues for the diagnosis of PED. The study was based on samples of small intestine tissues and faeces from 3–5 day old pigs which died from PED. Nucleic acid extraction was performed using commercial kits with different nucleic acid separation strategies based on: silicon-sorbent; silicate membrane fixed in a microcentrifuge column and magnetic balls. The studies were conducted in two stages. The first was a comparison of the results of the amplification of the obtained nucleic acid extracts from the homogenate of the intestines of piglets by using the above-mentioned commercial kits for the extraction of nucleic acids. For this purpose, samples of homogenate were used which in weight corresponded to the guideline for the application of the test kits. The second step was directed to determining the efficiency of extraction of DNA and RNA from homogenate samples with a weight of 10, 50, 100 and 200 mg. Determination of the optimal methodological strategy of nucleic acid extraction for the diagnosis of porcine epidemic diarrhea by PCR has been investigated. The results of the PCR studies of RNA of the PED virus and a unique pig DNA fragment indicate that the extraction of nucleic acids by commercial kits has different levels of efficiency and depends on different factors. According to the research, it was found that the most important of them are the adsorption capacity of the solid-phase sorbent, its configuration and nature, which binds RNA and DNA molecules, the type of sample from which extraction takes place, its volume, or the tissue mass used for extraction. Based on the obtained results, it has been found that the most effective PED virus RNA extraction is by “ArtBioTech”, “Bio Extract Column”, and “Viral DNA/RNA Extraction Kit”, and pig genomic DNA extraction by the “ArtBioTech” and “Viral DNA / RNA extraction Kit”.
机译:本文介绍了评价用于从猪肠组织中提取核酸以进行诊断的商业方法的结果。该研究基于小肠组织的样品,3-5天旧猪的粪便,从PED中死亡。使用具有不同核酸分离策略的商业试剂盒进行核酸提取,基于以下:硅 - 吸附剂;硅酸盐膜固定在微量加压柱和磁球中。这些研究是以两个阶段进行的。首先是通过使用上述商品试剂盒来提取核酸的商业试剂盒,首先是通过使用上述商品试剂盒来扩增所得核酸提取物从仔猪肠道的匀浆结果的比较。为此目的,使用匀浆样品,其重量与试验套件应用的指导相对应。涉及第二步,以确定从均质样品中提取DNA和RNA的效率,其重量为10,50,100和200mg。研究了PCR研究了PCR诊断猪疫情腹泻核酸萃取的最佳方法论策略。 PCRNA的PCR研究结果和独特的猪DNA片段表明,商业套件的核酸提取具有不同的效率水平,并取决于不同的因素。根据该研究,发现它们最重要的是固相吸附剂的吸附能力,其构造和性质结合RNA和DNA分子,提取的样品的类型,其体积,或用于提取的组织块。基于所得的结果,已经发现,最有效的PED病毒RNA提取是“Artbiotech”,“生物提取柱”和“病毒DNA / RNA提取试剂盒”,以及“Artbiotech”的猪基因组DNA提取和“病毒DNA / RNA提取套件”。

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