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Identification of Candidate Agents Active against N. ceranae Infection in Honey Bees: Establishment of a Medium Throughput Screening Assay Based on N. ceranae Infected Cultured Cells

机译:蜜蜂中对中华绒螯蟹感染有活性的候选药物的鉴定:基于感染中华绒螯蟹的培养细胞的中等通量筛选方法的建立

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摘要

Many flowering plants in both natural ecosytems and agriculture are dependent on insect pollination for fruit set and seed production. Managed honey bees (Apis mellifera) and wild bees are key pollinators providing this indispensable eco- and agrosystem service. Like all other organisms, bees are attacked by numerous pathogens and parasites. Nosema apis is a honey bee pathogenic microsporidium which is widely distributed in honey bee populations without causing much harm. Its congener Nosema ceranae was originally described as pathogen of the Eastern honey bee (Apis cerana) but jumped host from A. cerana to A. mellifera about 20 years ago and spilled over from A. mellifera to Bombus spp. quite recently. N. ceranae is now considered a deadly emerging parasite of both Western honey bees and bumblebees. Hence, novel and sustainable treatment strategies against N. ceranae are urgently needed to protect honey and wild bees. We here present the development of an in vitro medium throughput screening assay for the identification of candidate agents active against N. ceranae infections. This novel assay is based on our recently developed cell culture model for N. ceranae and coupled with an RT-PCR-ELISA protocol for quantification of N. ceranae in infected cells. The assay has been adapted to the 96-well microplate format to allow automated analysis. Several substances with known (fumagillin) or presumed (surfactin) or no (paromomycin) activity against N. ceranae were tested as well as substances for which no data concerning N. ceranae inhibition existed. While fumagillin and two nitroimidazoles (metronidazole, tinidazole) totally inhibited N. ceranae proliferation, all other test substances were inactive. In summary, the assay proved suitable for substance screening and demonstrated the activity of two synthetic antibiotics against N. ceranae.
机译:自然生态系统和农业中的许多开花植物都依赖昆虫授粉来结实果实和生产种子。托管蜜蜂(Apis mellifera)和野生蜜蜂是提供这种不可或缺的生态和农业系统服务的主要授粉媒介。像所有其他生物一样,蜜蜂也受到许多病原体和寄生虫的攻击。 Nosema apis是一种蜜蜂致病性微孢子虫,广泛分布在蜜蜂种群中,不会造成太大危害。它的同种Nosema ceranae最初被描述为东方蜜蜂(Apis cerana)的病原体,但大约20年前从A. cerana跳到A. mellifera,并从A. mellifera溢出到Bombus spp。最近。如今,ceranae ceranae被认为是西方蜜蜂和大黄蜂的致命性寄生虫。因此,为保护蜂蜜和野蜂,迫切需要新颖且可持续的针对猪笼草的治疗策略。我们在这里介绍了一种体外培养基通量筛选测定方法的开发,用于鉴定对猪新孢子虫感染有活性的候选药物。这项新颖的检测方法基于我们最近开发的certaine。ceranae细胞培养模型,并结合了RT-PCR-ELISA方案来定量感染的cer.ae ceranae。该测定方法已适应96孔微孔板的形式,可以进行自动分析。测试了几种对已知烟曲霉具有(烟曲霉素)或推定(表面活性素)或无(巴龙霉素)活性的物质,以及不存在有关抑制cercerae的数据的物质。烟曲霉素和两种硝基咪唑(甲硝唑,替硝唑)完全抑制 N。 ceranae 增殖,其他所有测试物质均未激活。总而言之,该测定方法证明适用于物质筛选,并证明了两种合成抗生素对 N的活性。 ceranae

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