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一种多重PCR检测方法,可将红带锥蝽与粗壮锥蝽隐存种复合体(半翅目:猎蝽科)的成员区分开来。

A multiplex PCR assay that separates Rhodnius prolixus from members of the Rhodnius robustus cryptic species complex (Hemiptera: Reduviidae).

作者信息

Pavan M G, Monteiro F A

机构信息

Departamento de Medicina Tropical, Instituto Oswaldo Cruz, FIOCRUZ, Rio de Janeiro, Brazil.

出版信息

Trop Med Int Health. 2007 Jun;12(6):751-8. doi: 10.1111/j.1365-3156.2007.01845.x.

DOI:10.1111/j.1365-3156.2007.01845.x
PMID:17550472
Abstract

Rhodnius prolixus is one of the most important primary vectors of human Chagas disease in Latin America. Its morphology is, however, identical to that of the members of the Rhodnius robustus cryptic species complex, which includes secondary vectors. The correct identification of these taxa with differential vector competence is, therefore, of great epidemiological relevance. We used the alignment of 26 mitochondrial cytochrome b haplotypes (663 bp) to select for PCR-amplifiable species-specific regions. We designed one forward primer on a region conserved across all haplotypes, and three reverse primers that anneal to species-specific regions and amplify fragments of different lengths for R. prolixus (285 bp) and for members of the two major R. robustus lineages: group I (349 bp) and groups II-IV (239 bp). These fragments were easily identifiable on regular 1.5% agarose gels. This multiplex PCR assay was successfully tested on 81 specimens from six Latin American countries, and used to determine the phylogeographic boundaries for each species. It is a simple, objective, and cost-effective assay. Its PCR-based nature makes it applicable to any insect developmental stage, as well as to dried specimens, and insect remains. It should be particularly useful in areas where representatives of these Rhodnius species occur in sympatry.

摘要

红带锥蝽是拉丁美洲人类恰加斯病最重要的主要传播媒介之一。然而,它的形态与包括次要传播媒介的强壮锥蝽隐存种复合体成员的形态相同。因此,正确识别这些具有不同传播媒介能力的分类群具有重大的流行病学意义。我们利用26种线粒体细胞色素b单倍型(663 bp)的比对来选择可进行PCR扩增的物种特异性区域。我们在所有单倍型保守的区域设计了一条正向引物,以及三条反向引物,它们与物种特异性区域退火,并为红带锥蝽(285 bp)以及强壮锥蝽两个主要谱系的成员扩增不同长度的片段:第一组(349 bp)和第二至四组(239 bp)。这些片段在常规的1.5%琼脂糖凝胶上很容易识别。这种多重PCR检测方法在来自六个拉丁美洲国家的81个标本上成功进行了测试,并用于确定每个物种的系统地理边界。它是一种简单、客观且经济高效的检测方法。其基于PCR的特性使其适用于任何昆虫发育阶段,以及干燥标本和昆虫残骸。在这些锥蝽物种的代表同域分布的地区,它应该会特别有用。

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