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[用于新热带利什曼原虫分型的聚合酶链反应-限制性片段长度多态性分析及随机扩增多态性DNA分析]

[PCR-RFLP and RAPD for typing neotropical Leishmania].

作者信息

Montalvo Ana Margarita, Monzote Lianet, Fraga Jorge, Montano Ivón, Muskus Carlos, Marín Marcel, de Doncker Simonne, Vélez Iván Darío, Dujardin Jean Claude

机构信息

Departamento de Parasitología, Instituto Pedro Kourí, La Habana, Cuba.

出版信息

Biomedica. 2008 Dec;28(4):597-606.

Abstract

INTRODUCTION

The analysis of the PCR-restriction fragment length polymorphism and random amplified polymorphic DNA have been useful tools for Leishmania identification.

OBJECTIVES

Molecular procedures were demonstrated for identification and typing of reference strains of New World Leishmania and their applicability was validated for clinical samples.

MATERIALS AND METHODS

DNA was extracted from 16 reference strains of Latin American Leishmania as well as from clinical samples of leishmaniasis patients. A sequence coding for cysteine proteinase B was amplified by PCR and subjected to restriction fragment length polymorphism analysis. The enzyme used was Taq1. For eight of the reference strains, the random amplified polymorphic desoxyribonucleic acid technique (RAPD) was applied. Band patterns for Leishmania species differentiation were established each each method. The sample size of the clinical sample was of 5.

RESULTS

PCR products of the cysteine proteinase B gene were obtained for L. braziliensis, L. peruviana, L. panamensis and L. guyanensis. For the other species, L. mexicana, L. amazonensis, L. garnhami, L. lainsoni, L. chagasi, L. naiffi, no amplification occurred. The patterns of restriction fragments revealed band patterns in common for L. peruviana, L. guyanensis and L. panamensis, whereas L. braziliensis had a distinctive pattern. When human samples were examined, amplification occurred for all cases, and the profiles corresponded to the common profile of L. peruviana, L. guyanensis and L. panamensis. The RAPD technique demonstrated reproducible and distinctive patterns for each of the 8 reference strains, L. mexicana, L. amazonensis, L. garnhami, L. lainsoni, L. chagasi, L. naiffi, making possible to differentiate all them. The advantages and limitations of each procedure are discussed.

CONCLUSIONS

The combination of RFP and RAPD methodologies provide useful tools to identify medical important species of Leishmania by recognizing DNA sequences characteristic of each species.

摘要

引言

聚合酶链反应-限制性片段长度多态性分析(PCR-RFLP)和随机扩增多态性DNA分析(RAPD)是利什曼原虫鉴定的有用工具。

目的

展示用于鉴定新大陆利什曼原虫参考菌株及其分型的分子方法,并验证其在临床样本中的适用性。

材料与方法

从16株拉丁美洲利什曼原虫参考菌株以及利什曼病患者的临床样本中提取DNA。通过PCR扩增编码半胱氨酸蛋白酶B的序列,并进行限制性片段长度多态性分析。使用的酶是Taq1。对8株参考菌株应用随机扩增多态性脱氧核糖核酸技术(RAPD)。每种方法都建立了利什曼原虫物种区分的条带模式。临床样本的样本量为5。

结果

获得了巴西利什曼原虫、秘鲁利什曼原虫、巴拿马利什曼原虫和圭亚那利什曼原虫半胱氨酸蛋白酶B基因的PCR产物。对于其他物种,墨西哥利什曼原虫、亚马逊利什曼原虫、加恩哈米利什曼原虫、莱因索尼利什曼原虫、恰加斯利什曼原虫、奈菲利什曼原虫,未发生扩增。限制性片段模式显示秘鲁利什曼原虫、圭亚那利什曼原虫和巴拿马利什曼原虫有共同的条带模式,而巴西利什曼原虫有独特的模式。检查人类样本时,所有病例均发生扩增,图谱与秘鲁利什曼原虫、圭亚那利什曼原虫和巴拿马利什曼原虫的共同图谱一致。RAPD技术对8株参考菌株(墨西哥利什曼原虫、亚马逊利什曼原虫、加恩哈米利什曼原虫、莱因索尼利什曼原虫、恰加斯利什曼原虫、奈菲利什曼原虫)中的每一株都显示出可重复且独特的模式,从而能够区分所有菌株。讨论了每种方法的优缺点。

结论

RFP和RAPD方法的结合提供了有用的工具,通过识别每个物种特有的DNA序列来鉴定医学上重要的利什曼原虫物种。

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