利用环路介导等温扩增技术对鲑鱼鱼立克次体进行快速诊断和基因分型的进展。

IF 4 2区 生物学 Q2 MICROBIOLOGY Frontiers in Microbiology Pub Date : 2024-09-24 eCollection Date: 2024-01-01 DOI:10.3389/fmicb.2024.1392808
Adolfo Isla, Marcelo Aguilar, Sandra N Flores-Martin, Claudia A Barrientos, Genaro Soto-Rauch, Jorge Mancilla-Schulz, Felipe Almendras, Jaime Figueroa, Alejandro J Yañez
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引用次数: 0

摘要

导言:鲑鱼鱼立克次体病(Piscirickettsia salmonis)是鲑鱼鱼立克次体病的病原体,对智利水产养殖业构成重大威胁,每年造成巨大经济损失。该病原体于 1992 年首次被确定为种属,并分为两个基因组:LF-89 和 EM-90,它们具有不同的表型死亡率和致病性。传统的基因分型方法(如多重 PCR)虽然有效,但受限于成本、设备要求和对专业知识的需求:方法:本研究验证了环路介导等温扩增(LAMP)是诊断沙门氏菌感染的一种快速、特异的替代方法。我们开发了首个以物种保守的 tonB 受体基因(tonB-r,WP_016210144.1)为目标的 qPCR 和 LAMP 检测方法,用于特异性地鉴定 P. salmonis 的物种水平。此外,我们还设计了两种基因分型 LAMP 检测方法,利用 LF-89 的独特编码序列硝酸单加氧酶(WP_144420689.1)和 EM-90 的独特编码序列酸性磷酸酶(WP_016210154.1)来区分 LF-89 和 EM-90 基因组:结果:LAMP 检测法的灵敏度和特异性与实时 PCR 相当,而且具有结果快速、成本较低和操作简便等优点,因此特别适合野外使用。通过检测其他鲑鱼病原体,如鲑鱼肾杆菌、鲑鱼弧菌、鲑鱼嗜黄杆菌、鲑鱼天牛杆菌和鲑鱼气单胞菌,证实了其特异性,未发现交叉反应:可视检测方法和基因组之间的精确区分凸显了 LAMP 作为水产养殖业可靠诊断工具的潜力。在鲑鱼疫病的物种检测(qPCR 和 LAMP)和基因分型方面取得的这一进展标志着水产养殖业在疾病管理方面向前迈出了重要一步。LAMP 的实施有望加强疾病监测、早期检测和改进管理策略,最终使鲑鱼养殖业受益。
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Advancements in rapid diagnostics and genotyping of Piscirickettsia salmonis using Loop-mediated Isothermal Amplification.

Introduction: Piscirickettsia salmonis, the causative agent of Piscirickettsiosis, poses a significant threat to the Chilean aquaculture industry, resulting in substantial economic losses annually. The pathogen, first identified as specie in 1992, this pathogen was divided into two genogroups: LF-89 and EM-90, associated with different phenotypic mortality and pathogenicity. Traditional genotyping methods, such as multiplex PCR, are effective but limited by their cost, equipment requirements, and the need for specialized expertise.

Methods: This study validates Loop-mediated Isothermal Amplification (LAMP) as a rapid and specific alternative for diagnosing P. salmonis infections. We developed the first qPCR and LAMP assay targeting the species-conserved tonB receptor gene (tonB-r, WP_016210144.1) for the specific species-level identification of P. salmonis. Additionally, we designed two genotyping LAMP assays to differentiate between the LF-89 and EM-90 genogroups, utilizing the unique coding sequences Nitronate monooxygenase (WP_144420689.1) for LF-89 and Acid phosphatase (WP_016210154.1) for EM-90.

Results: The LAMP assays demonstrated sensitivity and specificity comparable to real-time PCR, with additional benefits including rapid results, lower costs, and simplified operation, making them particularly suitable for field use. Specificity was confirmed by testing against other salmonid pathogens, such as Renibacterium salmoninarum, Vibrio ordalii, Flavobacterium psychrophilum, Tenacibaculum maritimum, and Aeromonas salmonicida, with no cross-reactivity observed.

Discussion: The visual detection method and precise differentiation between genogroups underscore LAMP's potential as a robust diagnostic tool for aquaculture. This advancement in the specie detection (qPCR and LAMP) and genotyping of P. salmonis represents a significant step forward in disease management within the aquaculture industry. The implementation of LAMP promises enhanced disease surveillance, early detection, and improved management strategies, ultimately benefiting the salmonid aquaculture sector.

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来源期刊
CiteScore
7.70
自引率
9.60%
发文量
4837
审稿时长
14 weeks
期刊介绍: Frontiers in Microbiology is a leading journal in its field, publishing rigorously peer-reviewed research across the entire spectrum of microbiology. Field Chief Editor Martin G. Klotz at Washington State University is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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