首页> 美国卫生研究院文献>The American Journal of Tropical Medicine and Hygiene >High Throughput Multiplex Assay for Species Identification of Papua New Guinea Malaria Vectors: Members of the Anopheles punctulatus (Diptera: Culicidae) Species Group
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High Throughput Multiplex Assay for Species Identification of Papua New Guinea Malaria Vectors: Members of the Anopheles punctulatus (Diptera: Culicidae) Species Group

机译:高通量多重鉴定巴布亚新几内亚疟疾载体的物种:点按按蚊(双翅目:pt科)种组成员

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摘要

Malaria and filariasis are transmitted in the Southwest Pacific region by Anopheles punctulatus sibling species including An. punctulatus, An. koliensis, the An. farauti complex 1–8 (includes An. hinesorum [An. farauti 2], An. torresiensis [An. farauti 3]). Distinguishing these species from each other requires molecular diagnostic methods. We developed a multiplex polymerase chain reaction (PCR)–based assay specific for known species-specific nucleotide differences in the internal transcribed spacer 2 region and identified the five species most frequently implicated in transmitting disease (An. punctulatus, An. koliensis, An. farauti 1, An. hinesorum, and An. farauti 4). A set of 340 individual mosquitoes obtained from seven Papua New Guinea provinces representing a variety of habitats were analyzed by using this multiplex assay. Concordance between molecular and morphological diagnosis was 56.4% for An. punctulatus, 85.3% for An. koliensis, and 88.9% for An. farauti. Among 158 mosquitoes morphologically designated as An. farauti, 33 were re-classified by PCR as An. punctulatus, 4 as An. koliensis, 26 as An. farauti 1, 49 as An. hinesorum, and 46 as An. farauti 4. Misclassification results from variable coloration of the proboscis and overlap of An. punctulatus, An. koliensis, the An. farauti 4. This multiplex technology enables further mosquito strain identification and simultaneous detection of microbial pathogens.
机译:疟疾和丝虫病是由西南按蚊(An按蚊)同胞异种(包括An)传播的。准点科里安Farauti复合体1–8(包括An。hinesorum [An。farauti 2],A。torresiensis [An。farauti 3])。区分这些种类需要分子诊断方法。我们开发了一种基于多重聚合酶链反应(PCR)的检测方法,专门针对内部转录间隔区2区域内已知物种特异性核苷酸差异,并鉴定了与传播疾病最相关的五个物种(An。punctulatus,An。koliensis,An。 farauti 1,An。hinesorum和An。farauti 4)。使用这种多重分析法分析了从巴布亚新几内亚的七个省获得的代表各种栖息地的一组340只个体蚊子。 An的分子诊断与形态学诊断一致率为56.4%。点状,An占85.3%。 koliensis,An占88.9%。法鲁蒂。在158个蚊子中,形态上被称为 An。 PCR已将法拉第中的33个重新分类为 An。 punlatus ,以4作为 An。 koliensis ,26岁, An。 farauti 1,49 as An。 hinesorum ,以及46个 An。 farauti 4.错误分类归因于长吻舌的变色和 An的重叠。准点一个。 koliensis An farauti 4.这种多重技术可以进一步鉴定蚊子菌株并同时检测微生物病原体。

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