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Technical Note: Improved Method for Rapid DNA Extraction of Mastitis Pathogens Directly from Milk

机译:技术说明:直接从牛奶中快速提取乳腺炎病原体DNA的改进方法

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Efficient control against bovine mastitis requires sensitive, rapid, and specific tests to detect and identify the main bacteria that cause heavy losses to the dairy industry. Molecular detection of pathogenic microorganisms is based on DNA amplification of the target pathogen. Therefore, efficient extraction of DNA from pathogenic bacteria is a major step. In this study, we aimed to develop a specific, sensitive, and rapid method to extract DNA directly from the main gram-positive bacteria known to cause bovine mastitis (Staphylococ-cus aureus, Streptococcus agalactiae, Streptococcus dys-galactiae, and Streptococcus uberis) found in milk samples. The DNA extraction method is based on the lysing and nuclease-inactivating properties of the chaotropic agent, guanidinium thiocyanate, together with the nucleic acid-binding properties of the silica particles. An efficient protocol consisting of 6 basic steps (3 of which were done twice) was developed and applied directly to milk samples. Absence of PCR inhibitors and DNA quality were evaluated by PCR amplification of the species-specific DNA sequences of the target bacteria. The level of sensitivity achieved in our experiments is applicable to milk sample analysis without sample enrichment.
机译:要有效控制牛乳腺炎,需要进行灵敏,快速且特定的测试,以检测和识别对乳业造成重大损失的主要细菌。病原微生物的分子检测基于目标病原体的DNA扩增。因此,从致病菌中有效提取DNA是重要的一步。在这项研究中,我们旨在开发一种特异性,灵敏和快速的方法,直接从已知会引起牛乳腺炎的主要革兰氏阳性细菌(金黄色葡萄球菌,无乳链球菌,dys-半乳链球菌和乳房链球菌)中提取DNA。在牛奶样品中发现。 DNA提取方法基于离液剂硫氰酸胍的裂解和核酸酶灭活特性,以及二氧化硅颗粒的核酸结合特性。制定了包括6个基本步骤(其中3个步骤进行了两次)的有效规程,并将其直接应用于牛奶样品。通过PCR扩增靶细菌的物种特异性DNA序列来评估PCR抑制剂的缺乏和DNA质量。在我们的实验中达到的灵敏度水平适用于无需样品富集的牛奶样品分析。

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