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用于定量蜜蜂相关样本中孢子的新型TaqMan PCR检测法。

Novel TaqMan PCR Assay for the Quantification of Spores in Bee-Related Samples.

作者信息

Kušar Darja, Papić Bojan, Zajc Urška, Zdovc Irena, Golob Majda, Žvokelj Lucija, Knific Tanja, Avberšek Jana, Ocepek Matjaž, Pislak Ocepek Metka

机构信息

Institute of Microbiology and Parasitology, Veterinary Faculty, University of Ljubljana, Gerbičeva 60, 1000 Ljubljana, Slovenia.

Institute of Pathology, Wild Animals, Fish and Bees, Veterinary Faculty, University of Ljubljana, Gerbičeva 60, 1000 Ljubljana, Slovenia.

出版信息

Insects. 2021 Nov 17;12(11):1034. doi: 10.3390/insects12111034.

Abstract

is the causative agent of American foulbrood (AFB), a devastating disease of honeybees. spore counts in bee-related samples correlate with the presence of AFB symptoms and may, therefore, be used to identify at-risk colonies. Here, we constructed a TaqMan-based real-time PCR (qPCR) assay targeting a single-copy chromosomal metalloproteinase gene for reliable quantification of . The assay was calibrated using digital PCR (dPCR) to allow absolute quantification of spores in honey and hive debris samples. The limits of detection and quantification were 8 and 58 spores/g for honey and 188 and 707 spores/mL for hive debris, respectively. To assess the association between AFB clinical symptoms and spore counts, we quantified spores in honey and hive debris samples originating from honeybee colonies with known severity of clinical symptoms. Spore counts in AFB-positive colonies were significantly higher than those in asymptomatic colonies but did not differ significantly with regard to the severity of clinical symptoms. For honey, the average spore germination rate was 0.52% (range = 0.04-6.05%), indicating poor and inconsistent in vitro germination. The newly developed qPCR assay allows reliable detection and quantification of in honey and hive debris samples but can also be extended to other sample types.

摘要

是美洲幼虫腐臭病(AFB)的病原体,这是一种对蜜蜂具有毁灭性的疾病。与蜜蜂相关样本中的孢子计数与AFB症状的存在相关,因此可用于识别有风险的蜂群。在此,我们构建了一种基于TaqMan的实时PCR(qPCR)检测方法,靶向单拷贝染色体金属蛋白酶基因,用于可靠定量。该检测方法使用数字PCR(dPCR)进行校准,以实现对蜂蜜和蜂巢碎片样本中孢子的绝对定量。蜂蜜和蜂巢碎片的检测限和定量限分别为8和58个孢子/克以及188和707个孢子/毫升。为了评估AFB临床症状与孢子计数之间的关联,我们对来自具有已知临床症状严重程度的蜜蜂蜂群的蜂蜜和蜂巢碎片样本中的孢子进行了定量。AFB阳性蜂群中的孢子计数显著高于无症状蜂群,但在临床症状严重程度方面没有显著差异。对于蜂蜜,平均孢子萌发率为0.52%(范围 = 0.04 - 6.05%),表明体外萌发较差且不一致。新开发的qPCR检测方法能够可靠地检测和定量蜂蜜和蜂巢碎片样本中的,但也可扩展到其他样本类型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca19/8621733/18bc9b11b4e5/insects-12-01034-g001.jpg

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