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通过对聚合酶链反应扩增的微小环可变区序列进行分析,对来自南美洲和中美洲的克氏锥虫虫株进行分裂体分析。

Schizodeme analysis of Trypanosoma cruzi stocks from South and Central America by analysis of PCR-amplified minicircle variable region sequences.

作者信息

Avila H, Goncalves A M, Nehme N S, Morel C M, Simpson L

机构信息

Department of Biology, University of California, Los Angeles 90024-1606.

出版信息

Mol Biochem Parasitol. 1990 Sep-Oct;42(2):175-87. doi: 10.1016/0166-6851(90)90160-n.

Abstract

Kinetoplast DNA (kDNA) was isolated from 56 stocks of Trypanosoma cruzi isolated from human patients, animals and insects from Brazil, Venezuela, Colombia and Costa Rica. Comparison of the patterns of digested kDNA on acrylamide gels led to the grouping of several stocks into two schizodemes. Schizodeme analysis was also performed using a set of 330-bp fragments representing all the variable regions of the minicircle DNA molecules, which were obtained by PCR amplification of the kDNA using conserved region primers. The results of this analysis were consistent with the analysis using total kDNA, but the more informative restriction profiles allowed the construction of additional schizodemes. In addition, two oligomers were generated from variable region sequences of cloned minicircles from a Y and a Cl strain, and these were used as schizodeme-specific probes to detect homologous sequences in the amplified minicircle DNAs. The results indicate that a combination of restriction enzyme fingerprinting and hybridization of amplified variable region minicircle DNA with schizodeme-specific probes can be used for both sensitive detection and classification of T. cruzi.

摘要

从巴西、委内瑞拉、哥伦比亚和哥斯达黎加的人类患者、动物和昆虫体内分离出的56株克氏锥虫中提取动基体DNA(kDNA)。通过比较丙烯酰胺凝胶上消化后的kDNA图谱,可将几株虫株归为两个分裂体群。还使用一组代表微小环DNA分子所有可变区的330 bp片段进行分裂体分析,这些片段是通过使用保守区引物对kDNA进行PCR扩增获得的。该分析结果与使用总kDNA的分析结果一致,但信息量更大的限制性图谱允许构建更多的分裂体群。此外,从Y株和Cl株克隆的微小环可变区序列中生成了两种寡聚物,并将其用作分裂体特异性探针,以检测扩增的微小环DNA中的同源序列。结果表明,限制性酶切指纹图谱与扩增的可变区微小环DNA与分裂体特异性探针杂交相结合,可用于克氏锥虫的灵敏检测和分类。

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