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一种用于血液样本中布鲁氏菌属物种特异性检测和定量的快速DNA检测方法。

A rapid DNA assay for the species-specific detection and quantification of Brugia in blood samples.

作者信息

Poole C B, Williams S A

机构信息

Department of Biological Sciences, Smith College, Northampton, MA 01063.

出版信息

Mol Biochem Parasitol. 1990 Apr;40(1):129-36. doi: 10.1016/0166-6851(90)90086-2.

Abstract

This report describes a new assay for detecting filarial parasites of the genus Brugia in blood samples using labeled DNA probes. The sequences of these DNA probes are based on the HhaI repeat DNA family found in the genus Brugia. These DNA probes are species-specific and can detect the DNA from a single microfilaria in hybridization assays. To adapt this test for use on blood samples collected in the field, complex steps to separate microfilariae from blood cells and to purify parasite DNA were eliminated. We found that the most effective method was to filter blood samples through 5.0 microns pore nitrocellulose membranes, lyse the microfilariae on the membranes by proteinase K digestion, denature the parasite DNA with sodium hydroxide, and hybridize with the DNA probe. With this method, individual microfilariae can be visualized and counted on autoradiograms. The assay was evaluated in a mock field study using Brugia malayi-infected jirds and was found to be an efficient and accurate method for quantifying microfilariae in blood samples.

摘要

本报告描述了一种使用标记DNA探针检测血液样本中布鲁氏丝虫属丝状寄生虫的新检测方法。这些DNA探针的序列基于在布鲁氏丝虫属中发现的HhaI重复DNA家族。这些DNA探针具有种属特异性,在杂交检测中能够检测到单个微丝蚴的DNA。为使该检测方法适用于现场采集的血液样本,省去了从血细胞中分离微丝蚴以及纯化寄生虫DNA的复杂步骤。我们发现最有效的方法是将血液样本通过孔径为5.0微米的硝酸纤维素膜进行过滤,用蛋白酶K消化使膜上的微丝蚴裂解,用氢氧化钠使寄生虫DNA变性,然后与DNA探针杂交。通过这种方法,在放射自显影片上可以观察到单个微丝蚴并进行计数。该检测方法在一项使用感染马来布鲁氏丝虫的沙鼠的模拟现场研究中进行了评估,结果发现它是一种用于定量血液样本中微丝蚴的高效且准确的方法。

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