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DNA FRAGMENTS, PRIMERS, KITS, AND METHODS FOR AMPLIFICATION THE DETECTION AND IDENTIFICATION OF CLINICALLY RELEVANT CANDIDA SPECIES

机译:DNA片段,起始位点,试剂盒和方法,用于扩增与临床相关的念珠菌属物种的检测和鉴定

摘要

The present invention describes a novel molecular method based on the polimerase chain reaction (PCR) in a multiplex variant in order to detect and identify Candida species with clinical relevance, namely C. albicans, C. glabrata, C. krusei, C. parapsilosis, C. tropicalis, C. guilliermondii, C. lusitaniae e C. dubliniensis. The strategy uses the existence of sequences, whether conserved or variable, in fungal ribosomal genes and in the use of a combination of universal primers, specific for fungi, and internal primers, specific for each one of the Candida species (Figure 1). In this sense, two fragments from the internal transcribed spacer (ITS) regions of the ribosomal RNA (rRNA) are amplified by multiplex PCR, allowing the easy identification of the Candida species in question. This methodology allows a rapid, effective and low-cost identification of Candida species with clinical relevance, bearing several advantages over the currently available diagnostic methods.
机译:本发明描述了一种基于多聚体变体中的聚合酶链反应(PCR)的新颖分子方法,以检测和鉴定具有临床相关性的念珠菌物种,即白色念珠菌,光滑念珠菌,克鲁斯梭菌,副念珠菌, C.tropicis,C.guilliermondii,C.lusitaniae和C.dubliniensis该策略利用真菌核糖体基因中存在的保守或可变序列,并结合使用针对真菌的通用引物和针对每种念珠菌物种的内部引物(图1)。从这个意义上讲,来自核糖体RNA(rRNA)内部转录间隔区(ITS)区域的两个片段通过多重PCR进行了扩增,从而可以轻松鉴定所讨论的念珠菌。这种方法可以快速,有效和低成本地鉴定具有临床相关性的念珠菌,与目前可用的诊断方法相比具有多个优点。

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