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通过基于聚合酶链反应(PCR)的对编码18S核糖体RNA的基因进行分析,来鉴定来自阿根廷利什曼病流行地区的白蛉种类。

The identification of sandfly species, from an area of Argentina with endemic leishmaniasis, by the PCR-based analysis of the gene coding for 18S ribosomal RNA.

作者信息

Barroso P A, Marco J D, Kato H, Tarama R, Rueda P, Cajal S P, Basombrío M A, Korenaga M, Taranto N J, Hashiguchi Y

机构信息

Department of Parasitology, Kochi Medical School, Kochi University, Kohasu, Okoh, Nankoku, Kochi 783-8505, Japan.

出版信息

Ann Trop Med Parasitol. 2007 Apr;101(3):247-53. doi: 10.1179/136485907X156988.

Abstract

The area around Río Blanco, in the Orán department in the north of the Argentinian province of Salta, is endemic for American tegumentary leishmaniasis. In an attempt to facilitate the identification of the Lutzomyia species in this area, sequences of the gene coding for the 18S ribosomal RNA (rRNA) of sandflies caught in a Shannon trap were explored, by a combination of PCR and analysis of restriction-fragment-length polymorphism (RFLP). The products from the PCR, which employed two primers developed specifically for this study (Lu.18S 1S and Lu.18S AR), were cloned into a commercial vector (pGEM-T Easy) so that their nucleotide sequences could be investigated. In the RFLP analysis, the products of single and double digestion with the AfaI and HapII restriction enzymes were separated by electrophoresis in 3% or 4% agarose. Taken together with the results of a morphological investigation of the flies, the resultant DNA fragment patterns were sufficient to identify most of the sandflies caught as Lu. neivai. Although two other species, Lu. cortelezzii and Lu. sallesi, were collected, they were relatively rare and only identified morphologically. A single digestion of the 18S-rRNA gene sequences with AfaI or HapII appeared sufficient and useful for the identification of Lu. neivai from the north of Salta province, and for several other Lutzomyia species.

摘要

阿根廷萨尔塔省北部奥兰县的里奥布兰科周边地区是美洲皮肤利什曼病的流行区。为便于鉴定该地区的罗蛉属物种,通过聚合酶链反应(PCR)与限制性片段长度多态性分析(RFLP)相结合的方法,对在香农诱捕器中捕获的白蛉18S核糖体RNA(rRNA)编码基因序列进行了研究。PCR产物使用专门为本研究设计的两种引物(Lu.18S 1S和Lu.18S AR)扩增,然后克隆到商业载体(pGEM-T Easy)中,以便研究其核苷酸序列。在RFLP分析中,用AfaI和HapII限制性内切酶进行单酶切和双酶切的产物,在3%或4%的琼脂糖凝胶中进行电泳分离。结合对白蛉的形态学研究结果,所得的DNA片段模式足以鉴定出大多数捕获的白蛉为内氏罗蛉。虽然还采集到了另外两个物种,即科氏罗蛉和萨氏罗蛉,但它们相对较少,仅通过形态学进行了鉴定。用AfaI或HapII对18S - rRNA基因序列进行单酶切,似乎足以且有助于从萨尔塔省北部鉴定内氏罗蛉以及其他几种罗蛉属物种。

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