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环介导等温扩增法:用于定量检测弧菌科菌种以及粪栖弧菌和兰氏栖弧菌特异性菌种的简单快速检测方法的开发、验证及应用

Loop-mediated isothermal amplification: Development, validation and application of simple and rapid assays for quantitative detection of species of Arcobacteraceae family- and species-specific Aliarcobacter faecis and Aliarcobacter lanthieri.

作者信息

Khan I U H, Becker A, Cloutier M, Plötz M, Lapen D R, Wilkes G, Topp E, Abdulmawjood A

机构信息

Ottawa Research and Development Centre (ORDC), Agriculture and Agri-Food Canada, Ottawa, ON, Canada.

Institute of Food Quality and Food Safety, Research Center for Emerging Infections and Zoonoses (RIZ), University of Veterinary Medicine Foundation, Hannover, Germany.

出版信息

J Appl Microbiol. 2021 Jul;131(1):288-299. doi: 10.1111/jam.14926. Epub 2020 Dec 5.

Abstract

AIM

The family Arcobacteraceae formerly genus Arcobacter has recently been reclassified into six genera. Among nine species of the genus Aliarcobacter, Aliarcobacter faecis and Aliarcobacter lanthieri have been identified as emerging pathogens potentially cause health risks to humans and animals. This study was designed to develop/optimize, validate and apply Arcobacteraceae family- and two species-specific (A. faecis and A. lanthieri) loop-mediated isothermal amplification (LAMP) assays to rapidly detect and quantify total number of cells in various environmental niches.

METHODS AND RESULTS

Three sets of LAMP primers were designed from conserved and variable regions of 16S rRNA (family-specific) and gyrB (species-specific) genes. Optimized Arcobacteraceae family-specific LAMP assay correctly amplified and detected 24 species, whereas species-specific LAMP assays detected A. faecis and A. lanthieri reference strains as well as 91 pure and mixed culture isolates recovered from aquatic and faecal sources. The specificity of LAMP amplification of A. faecis and A. lanthieri was further confirmed by restriction fragment length polymorphism analysis. Assay sensitivities were tested using variable DNA concentrations extracted from simulated target species cells in an autoclaved agricultural water sample by achieving a minimum detection limit of 10 cells mL (10 fg). Direct DNA-based quantitative detection, from agricultural surface water, identified A. faecis (17%) and A. lanthieri (1%) at a low frequency compared to family-level (93%) with the concentration ranging from 2·1 × 10 to 2·2 × 10 cells 100 mL .

CONCLUSIONS

Overall, these three DNA-based rapid and cost-effective novel LAMP assays are sensitive and can be completed in less than 40 min. They have potential for on-site quantitative detection of species of family Arcobacteraceae, A. faecis and A. lanthieri in food, environmental and clinical matrices.

SIGNIFICANCE AND IMPACT OF THE STUDY

The newly developed LAMP assays are specific, sensitive, accurate with higher reproducibility that have potential to facilitate in a less equipped lab setting and can help in early quantitative detection and rate of prevalence in environmental niches. The assays can be adopted in the diagnostic labs and epidemiological studies.

摘要

目的

以前属于弓形杆菌属的弓形杆菌科最近被重新分类为六个属。在阿里弓形杆菌属的九个物种中,粪便阿里弓形杆菌和兰氏阿里弓形杆菌已被确定为新兴病原体,可能对人类和动物健康构成风险。本研究旨在开发/优化、验证和应用弓形杆菌科及两种特异性(粪便阿里弓形杆菌和兰氏阿里弓形杆菌)环介导等温扩增(LAMP)检测方法,以快速检测和定量各种环境生态位中的细胞总数。

方法与结果

从16S rRNA(科特异性)和gyrB(种特异性)基因的保守区和可变区设计了三组LAMP引物。优化后的弓形杆菌科特异性LAMP检测方法正确扩增并检测出24个物种,而种特异性LAMP检测方法检测出了粪便阿里弓形杆菌和兰氏阿里弓形杆菌参考菌株,以及从水生和粪便来源分离出的91株纯培养物和混合培养物。粪便阿里弓形杆菌和兰氏阿里弓形杆菌LAMP扩增的特异性通过限制性片段长度多态性分析进一步得到证实。通过对高压灭菌的农业水样中模拟目标物种细胞提取的不同DNA浓度进行检测,确定了检测灵敏度,最低检测限为10个细胞/毫升(10 fg)。从农业地表水进行基于DNA的直接定量检测发现,与科级水平(93%)相比,粪便阿里弓形杆菌(17%)和兰氏阿里弓形杆菌(1%)的检出频率较低,浓度范围为2.1×10至2.2×10个细胞/100毫升。

结论

总体而言,这三种基于DNA的快速且经济高效的新型LAMP检测方法灵敏,可在不到40分钟内完成。它们有潜力对食品、环境和临床样本中的弓形杆菌科、粪便阿里弓形杆菌和兰氏阿里弓形杆菌进行现场定量检测。

研究的意义和影响

新开发的LAMP检测方法具有特异性、灵敏性、准确性和更高的重现性,有潜力在设备较少的实验室环境中发挥作用,并有助于在环境生态位中进行早期定量检测和流行率评估。这些检测方法可应用于诊断实验室和流行病学研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d37/8359143/9be3b63a61b8/JAM-131-288-g001.jpg

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