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以12S rDNA作为遗传标记对蓖麻硬蜱血餐来源进行分子鉴定。

Molecular identification of bloodmeal source in Ixodes ricinus ticks using 12S rDNA as a genetic marker.

作者信息

Humair Pierre-François, Douet Véronique, Morán Cadenas Francisca, Schouls Leo M, Van De Pol Ingrid, Gern Lise

机构信息

Laboratory of Eco-Epidemiology, Institute of Biology, University of Neuchâtel, 2009 Neuchâtel, Switzerland.

出版信息

J Med Entomol. 2007 Sep;44(5):869-80. doi: 10.1603/0022-2585(2007)44[869:miobsi]2.0.co;2.

Abstract

We developed an efficient molecular method for the identification of the bloodmeal sources in the tick Ixodes ricinus (L.), the European vector of the agents of Lyme borreliosis and tick-borne encephalitis. An approximately 145-bp orthologous fragment of the vertebrate mitochondrial 12S rDNA was used as a molecular marker to discriminate host vertebrate species. The method consists of a single run polymerase chain reaction amplification of the 12S rDNA molecular marker by using nondegenerate primers followed by a reverse line blot hybridization assay by using specific oligonucleotide probes. The palette of probes allowed us to distinguish major groups of host vertebrates (e.g., mammals, small rodents, artiodactyls, birds, lizards) and to identify the bloodmeal sources at the genus or species level. External primers were designed and used to sequence the 12S rDNA molecular marker of a broad range of known or potential host vertebrate species (n = 60), including mammal (n = 28), bird (n = 31), and reptile (n = 1) species. The use of this technique coupled with known methods for identification of tick-borne pathogens (e.g., Borrelia burgdorferi sensu lato) allowed us to determine the source of infective bloodmeal and to identify reservoir species. The present method was successfully used to identify the source of bloodmeals in all feeding I. ricinus ticks and in half of questing field-collected I. ricinus ticks. Moreover, the bloodmeal source was identified in 65% of ticks infected with B. burgdorferi sensu lato. Further development of this technique may be envisaged for the detection of other vector-borne pathogens and their reservoir hosts.

摘要

我们开发了一种高效的分子方法,用于鉴定蓖麻硬蜱(Ixodes ricinus (L.))体内的血餐来源。蓖麻硬蜱是莱姆病螺旋体和蜱传脑炎病原体的欧洲传播媒介。脊椎动物线粒体12S rDNA约145 bp的直系同源片段被用作分子标记,以区分宿主脊椎动物物种。该方法包括使用非简并引物对12S rDNA分子标记进行单次聚合酶链反应扩增,随后使用特异性寡核苷酸探针进行反向线印迹杂交检测。探针组合使我们能够区分主要的宿主脊椎动物群体(如哺乳动物、小型啮齿动物、偶蹄目动物、鸟类、蜥蜴),并在属或种水平上鉴定血餐来源。设计了外部引物,并用于对广泛的已知或潜在宿主脊椎动物物种(n = 60)的12S rDNA分子标记进行测序,包括哺乳动物(n = 28)、鸟类(n = 31)和爬行动物(n = 1)物种。将该技术与已知的蜱传病原体(如广义伯氏疏螺旋体(Borrelia burgdorferi sensu lato))鉴定方法相结合,使我们能够确定感染性血餐的来源并鉴定储存宿主物种。本方法成功用于鉴定所有正在吸血的蓖麻硬蜱以及一半野外采集的正在寻觅宿主的蓖麻硬蜱体内的血餐来源。此外,在65%感染广义伯氏疏螺旋体的蜱中鉴定出了血餐来源。可以设想进一步开发该技术以检测其他媒介传播的病原体及其储存宿主。

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