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用于检测东南亚按蚊亚属中微小按蚊及四种相关疟疾媒介蚊种的多重PCR检测法。

Multiplex PCR assay for malaria vector Anopheles minimus and four related species in the Myzomyia Series from Southeast Asia.

作者信息

Phuc H K, Ball A J, Son L, Hanh N V, Tu N D, Lien N G, Verardi A, Townson H

机构信息

Liverpool School of Tropical Medicine, U.K.

出版信息

Med Vet Entomol. 2003 Dec;17(4):423-8. doi: 10.1111/j.1365-2915.2003.00462.x.

Abstract

Mosquitoes (Diptera: Culicidae) of the Anopheles (Cellia) Myzomyia Series are important malaria vectors in Africa, India and Southeast Asia. Among 10 named species of Myzomyia known from the Oriental Region, seven form the An. minimus group. Even for expert taxonomists, the adults of these species remain difficult to identify morphologically. For technical staff of malaria control programmes, confusion may extend to misidentification of species that are not formally within the minimus group. For identification of specimens from Indochina (Cambodia, Laos, Vietnam), we describe a multiplex polymerase chain reaction (PCR) assay, based on rDNA internal transcribed spacer 2 (ITS2) sequences, that employs a cocktail of primers to identify An. minimus Theobald sibling species A and C (sensu; Green et al., 1990) and three other species in the An. minimus group (An. aconitus Dönitz, An. pampanai Büttiker & Beales, An. varuna Iyengar), as well as An. jeyporiensis James, also belonging to the Myzomyia Series. As the test is DNA-based, it can be applied to all life stages of these mosquitoes for ecological investigations and vector incrimination studies. This PCR assay is simpler, quicker, cheaper and more readily interpreted than previous assays.

摘要

按蚊(塞利按蚊亚属)类疟蚊是非洲、印度和东南亚重要的疟疾传播媒介。在东洋区已知的10种指名疟蚊中,有7种构成微小按蚊复合体。即使对于专业分类学家而言,这些种类的成虫在形态上仍难以鉴别。对于疟疾防控项目的技术人员来说,混淆可能会延伸到对微小按蚊复合体以外种类的错误鉴定。为了鉴定来自印度支那(柬埔寨、老挝、越南)的标本,我们基于核糖体DNA内转录间隔区2(ITS2)序列描述了一种多重聚合酶链反应(PCR)检测方法,该方法使用一组引物来鉴定微小按蚊西奥博尔德种A和C(意义同;格林等人,1990)以及微小按蚊复合体中的其他三个种类(阿氏按蚊多尼茨、潘氏按蚊比蒂克和比尔斯、瓦鲁纳按蚊延加),还有同样属于类疟蚊的杰氏按蚊詹姆斯种。由于该检测基于DNA,它可应用于这些蚊子的所有生活阶段,用于生态调查和病媒判定研究。这种PCR检测方法比以前的检测方法更简单、更快捷、更便宜且更容易解读。

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