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通过新型实时TaqMan PCR检测法对法国科西嘉岛犬类和蚊子(双翅目:蚊科)体内的犬恶丝虫和匐行恶丝虫进行分子调查。

Molecular survey of Dirofilaria immitis and Dirofilaria repens by new real-time TaqMan PCR assay in dogs and mosquitoes (Diptera: Culicidae) in Corsica (France).

作者信息

Tahir Djamel, Bittar Fadi, Barré-Cardi Hélène, Sow Doudou, Dahmani Mustapha, Mediannikov Oleg, Raoult Didier, Davoust Bernard, Parola Philippe

机构信息

Research Unit of Emerging Infectious and Tropical Diseases (URMITE) UMR CNRS 7278 IRD 198 INSERM U1015 Aix-Marseille University, Marseille, France.

OCIC, Office de l'Environnement de la Corse, Corte, France.

出版信息

Vet Parasitol. 2017 Feb 15;235:1-7. doi: 10.1016/j.vetpar.2017.01.002. Epub 2017 Jan 8.

Abstract

Dirofilaria immitis and D. repens are filarioid nematodes of animals and humans, transmitted by the bite of infected mosquitoes. Domestic and wild canids are a major natural host and reservoir for these parasites. In this study, we designed a duplex real-time PCR protocol targeting the mitochondrial cytochrome c oxidase subunit I (COI) gene, detecting both D. immitis and D. repens using two primer pairs and two Dirofilaria-specific hydrolysable probes. The sensitivity and specificity of the primers and probes were tested in both experimental and naturally infected samples. The detection limits of this assay were evaluated using plasmid DNA from D. immitis and D. repens. No cross-reaction was observed when testing this system against DNA from other filarial nematodes. The detection limit of the real-time PCR system was one copy per reaction mixture containing 5μl of template DNA. Field application of the new duplex real-time assay was conducted in Corsica. The prevalence rate of D. immitis was 21.3% (20/94) in dogs. In a locality where most dogs with Dirofilaria spp. infection were found, D. immitis and D. repens were detected in 5% (20/389) and 1.5% (6/389) of the Aedes albopictus population, respectively. These results suggest that this sensitive assay is a powerful tool for monitoring dirofilariosis in endemic or high risk areas.

摘要

犬恶丝虫和匐行恶丝虫是寄生于动物和人类的类丝虫线虫,通过感染性蚊子的叮咬传播。家养和野生犬科动物是这些寄生虫的主要自然宿主和储存宿主。在本研究中,我们设计了一种针对线粒体细胞色素c氧化酶亚基I(COI)基因的双重实时荧光定量PCR方案,使用两对引物和两种恶丝虫特异性水解探针来检测犬恶丝虫和匐行恶丝虫。在实验感染和自然感染的样本中测试了引物和探针的敏感性和特异性。使用来自犬恶丝虫和匐行恶丝虫的质粒DNA评估了该检测方法的检测限。当用该系统检测来自其他丝虫线虫的DNA时,未观察到交叉反应。实时荧光定量PCR系统的检测限为每个含有5μl模板DNA的反应混合物1个拷贝。在科西嘉岛对新的双重实时荧光定量检测方法进行了现场应用。犬恶丝虫在犬中的感染率为21.3%(20/94)。在一个发现大多数感染恶丝虫属的犬的地区,白纹伊蚊群体中犬恶丝虫和匐行恶丝虫的检出率分别为5%(20/389)和1.5%(6/389)。这些结果表明,这种灵敏的检测方法是监测地方病流行区或高风险地区恶丝虫病的有力工具。

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