环介导的等温扩增检测大西洋鳕鱼沙门氏气单胞菌引起的非典型真菌病

AMOD KULKARNI, CHRISTOPHER MARLOWE A. CAIPANG, MONICA F. BRINCHMANN, KJETIL KORSNES, VISWANATH KIRON
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引用次数: 12

摘要

建立了一种环介导等温扩增(LAMP)检测大西洋鳕鱼(Gadus morhua)中沙门氏气单胞菌引起的非典型真菌病的方法。选择致病菌DNA螺旋酶B亚基编码基因gyrB,设计了5组引物,分别针对该基因的侧翼区域。该引物对沙门氏菌的检测具有特异性,与大西洋鳕鱼常见的其他致病菌如鳗弧菌、鱼酸Francisella、ruckeri耶尔森菌及大西洋鳕鱼肠道内的一些内源性细菌无交叉反应。该试验的检测限为1 picogram of bacterial DNA mL - 1,而在黏液作为抑制剂存在时,检测限降低了1 log稀释。由于其特异性和敏感性,LAMP可被认为是水产养殖系统常规监测计划中监测大西洋鳕鱼和其他海洋物种非典型疖病的有用工具。LAMP是一种有潜力的诊断技术,可用于快速和早期检测大西洋鳕鱼中引起真菌病的非典型沙门氏菌气单胞菌。该技术不需要复杂的设备,可以在等温条件下进行。该检测方法高度敏感,能够在感染发生之前检测到病原体,因此,可以采取缓解措施,以防止养殖种群的重大损失。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
LOOP-MEDIATED ISOTHERMAL AMPLIFICATION – AN ASSAY FOR THE DETECTION OF ATYPICAL FURUNCULOSIS CAUSED BY AEROMONAS SALMONICIDA IN ATLANTIC COD, GADUS MORHUA

ABSTRACT

A loop-mediated isothermal amplification (LAMP)-based assay was developed for the detection of atypical furunculosis, caused by Aeromonas salmonicida in Atlantic cod, Gadus morhua. Gene gyrB encoding the B subunit of DNA gyrase present in the pathogen was selected for designing five sets of primers targeting the flanking regions of the gene. The primers were specific for the detection of A. salmonicida with no cross reactions to other bacterial pathogens commonly infecting Atlantic cod, e.g., Vibrio anguillarum, Francisella piscicida, Yersinia ruckeri and some endogenous bacteria found in the gut of Atlantic cod. The detection limit of the assay was 1 picogram of bacterial DNA mL−1, whereas there was a decrease in detection limit by 1 log dilution in the presence of mucus as inhibitor. Because of its specificity and sensitivity, LAMP can be considered a useful tool in routine surveillance programs in aquaculture systems for monitoring atypical furunculosis in Atlantic cod and other marine species.

PRACTICAL APPLICATIONS

LAMP is a potential diagnostic technique that can be used for the rapid and early detection of atypical Aeromonas salmonicida, the causative agent of furunculosis in Atlantic cod. This technique does not require sophisticated equipment and can be performed under isothermal conditions. The assay is highly sensitive to enable detection of the pathogen prior to the onset of infection, thus, mitigating measures can be applied to prevent heavy losses of the cultured stock.

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来源期刊
Journal of Rapid Methods and Automation in Microbiology
Journal of Rapid Methods and Automation in Microbiology 生物-生物工程与应用微生物
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