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用于鉴定人体丝虫寄生虫的种特异性寡核苷酸探针。

Species-specific oligonucleotide probes for the identification of human filarial parasites.

作者信息

Williams S A, DeSimone S M, McReynolds L A

机构信息

Department of Biological Sciences, Smith College, Northampton, MA 01060.

出版信息

Mol Biochem Parasitol. 1988 Mar;28(2):163-9. doi: 10.1016/0166-6851(88)90064-3.

Abstract

Species-specific oligonucleotide probes have been constructed for the filarial parasites Brugia malayi and Brugia pahangi. Both parasites contain a 322 base pair repeated DNA sequence that is cleaved once by the restriction endonuclease HhaI. A consensus repeat sequence was determined from the DNA sequence of 15 cloned isolates of each species. Although the two repeats have an average homology of 89%, half the differences are clustered in a region of 66 nucleotides that has a homology of only 72%. Within this region, two probes, a 29-mer that is B. malayi specific and a 21-mer that is B. pahangi specific, were constructed. The sequence of both probes was chosen to obtain the maximum difference between the consensus sequences of the two species. The probes were also selected to be GC rich to increase their stability as a DNA hybrid. In a filter hybridization assay, the B. malayi probe has a 500-fold preference for B. malayi DNA versus B. pahangi DNA and a sensitivity of 200 pg. The B. pahangi probe has similar specificity and sensitivity for B. pahangi DNA. A rapid lysis procedure allows the probes to detect 1-2 third stage larvae of either B. malayi or B. pahangi in a filter hybridization assay.

摘要

已针对丝状寄生虫马来布鲁线虫和彭亨布鲁线虫构建了物种特异性寡核苷酸探针。这两种寄生虫都含有一段322个碱基对的重复DNA序列,该序列可被限制性内切酶HhaI切割一次。通过对每个物种的15个克隆分离株的DNA序列进行分析,确定了共有重复序列。尽管这两个重复序列的平均同源性为89%,但一半的差异集中在一个66个核苷酸的区域,该区域的同源性仅为72%。在该区域内,构建了两种探针,一种是29个核苷酸的马来布鲁线虫特异性探针,另一种是21个核苷酸的彭亨布鲁线虫特异性探针。两种探针的序列均经过选择,以使两个物种的共有序列之间的差异最大化。还选择了富含GC的探针,以提高其作为DNA杂交体的稳定性。在滤膜杂交试验中,马来布鲁线虫探针与彭亨布鲁线虫DNA相比,对马来布鲁线虫DNA的偏好性高500倍,灵敏度为200 pg。彭亨布鲁线虫探针对彭亨布鲁线虫DNA具有相似的特异性和灵敏度。一种快速裂解方法可使探针在滤膜杂交试验中检测到1-2条马来布鲁线虫或彭亨布鲁线虫的第三期幼虫。

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