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Barcoding blood meals: New vertebrate-specific primer sets for assigning taxonomic identities to host DNA from mosquito blood meals

机译:条码血粉:新的脊椎动物特异性引物组用于分配分类学身份以容纳蚊血粉中的DNA

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摘要

The transmission dynamics of mosquito-vectored pathogens are, in part, mediated by mosquito host-feeding patterns. These patterns are elucidated using blood meal analysis, a collection of serological and molecular techniques that determine the taxonomic identities of the host animals from which blood meals are derived. Modern blood meal analyses rely on polymerase chain reaction (PCR), DNA sequencing, and bioinformatic comparisons of blood meal DNA sequences to reference databases. Ideally, primers used in blood meal analysis PCRs amplify templates from a taxonomically diverse range of vertebrates, produce a short amplicon, and avoid co-amplification of non-target templates. Few primer sets that fit these requirements are available for the cytochrome c oxidase subunit I (COI) gene, the species identification marker with the highest taxonomic coverage in reference databases. Here, we present new primer sets designed to amplify fragments of the DNA barcoding region of the vertebrate COI gene, while avoiding co-amplification of mosquito templates, without multiplexed or nested PCR. Primers were validated using host vertebrate DNA templates from mosquito blood meals of known origin, representing all terrestrial vertebrate classes, and field-collected mosquito blood meals of unknown origin. We found that the primers were generally effective in amplifying vertebrate host, but not mosquito DNA templates. Applied to the sample of unknown mosquito blood meals, > 98% (60/61) of blood meals samples were reliably identified, demonstrating the feasibility of identifying mosquito hosts with the new primers. These primers are beneficial in that they can be used to amplify COI templates from a diverse range of vertebrate hosts using standard PCR, thereby streamlining the process of identifying the hosts of mosquitoes, and could be applied to next generation DNA sequencing and metabarcoding approaches.
机译:蚊媒病原体的传播动力学部分是由蚊子宿主的摄食模式介导的。使用血粉分析阐明了这些模式,血粉分析是一种血清学和分子技术的集合,这些技术确定了衍生出血粉的宿主动物的分类学身份。现代血粉分析依赖于聚合酶链反应(PCR),DNA测序以及血粉DNA序列与参考数据库的生物信息学比较。理想情况下,用于血粉分析PCR的引物可从分类学多样的脊椎动物中扩增模板,产生短扩增子,并避免非靶标模板的共同扩增。细胞色素C氧化酶亚基I(COI)基因(在参考数据库中具有最高分类学覆盖率的物种识别标记)几乎没有适合这些要求的引物集。在这里,我们提出了新的引物集,旨在扩增脊椎动物COI基因的DNA条形码区域的片段,同时避免了蚊子模板的共同扩增,而无需多重或嵌套式PCR。使用来自已知来源的蚊血粉的宿主脊椎动物DNA模板验证了引物,该模板代表了所有陆生脊椎动物类别,并且现场采集了未知来源的蚊血粉。我们发现引物通常在扩增脊椎动物宿主方面有效,但对蚊子DNA模板无效。将其应用于未知蚊子血粉样品中,可以可靠地鉴定出≥98%(60/61)的血粉样品,这证明了使用新引物鉴定蚊子宿主的可行性。这些引物的优势在于,可以使用标准PCR将其用于从多种脊椎动物宿主中扩增COI模板,从而简化了蚊子宿主的鉴定过程,并可以应用于下一代DNA测序和元条形码方法。

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