用于检测与 Akoya 珍珠贝黑斑病有关的 Tenacibaculum sp.菌株 Pbs-1 的 LAMP 抑制剂,以及降低抑制剂效果的添加剂。

IF 1.7 4区 生物学 Q4 BIOCHEMICAL RESEARCH METHODS
Akihiro Sakatoku , Takaya Suzuki , Kaito Hatano , Makoto Seki , Daisuke Tanaka , Shogo Nakamura , Nobuo Suzuki , Tadashi Isshiki
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引用次数: 0

摘要

黑斑病是一种尚未解决的病害,会降低珍珠质量并威胁珍珠牡蛎的生存。在之前的研究中,从患病的 Akoya 珍珠牡蛎 Pinctada fucata 中分离出了 Tenacibaculum sp.菌株 Pbs-1,并建立了一种快速、特异、灵敏的环介导等温扩增(LAMP)检测方法来检测这种病原体。这项技术在牡蛎孵化场和/或珍珠养殖场对菌株 Pbs-1 进行常规诊断方面具有相当大的潜力;因此,确定环境样本中可能会抑制 LAMP 的物质并找到能降低抑制作用的添加剂至关重要。在本研究中,我们以菌株 Pbs-1 的 DNA 为模板,研究了六种化学物质或蛋白质(又称传统 PCR 抑制剂)对 LAMP 的影响:腐植酸、尿素、六水合氯化铁 (III)、黑色素、肌红蛋白和乙二胺四乙酸二钠盐 (EDTA; pH 6.5)。接下来,为了减少已确定的抑制剂的影响,我们测试了在 LAMP 检测中添加牛血清白蛋白(BSA)或 T4 基因 32 蛋白(gp32)的方法。当使用 50 ng DNA 模板时,4 ng/μL 腐殖酸、0.05% 黑色素和 10 mM EDTA(pH 6.5)会抑制 LAMP 反应,而肌红蛋白、尿素和 FeCl3 则没有影响。当使用 50 pg DNA 模板时,4 ng/μL 腐殖酸、0.05% 黑色素、4 μg/μL 肌红蛋白、10 μg/μL 尿素和 10 mM EDTA 都会抑制 LAMP 反应。由此可见,在 LAMP 反应混合物中加入 BSA 或 gp32 可降低黑色素、腐植酸和尿素对基因扩增的抑制作用。该技术可作为防止珍珠贝大量死亡的方案的一部分;此外,该结果还增进了我们对抑制 LAMP 的物质和减少抑制作用的方法的了解,而这些物质和方法很少被报道。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibitors of LAMP used to detect Tenacibaculum sp. strain Pbs-1 associated with black-spot shell disease in Akoya pearl oysters, and additives to reduce the effect of the inhibitors

Black-spot shell disease is an unresolved disease that decreases pearl quality and threatens pearl oyster survival. In previous studies, the bacterium Tenacibaculum sp. strain Pbs-1 was isolated from diseased Akoya pearl oysters Pinctada fucata, and a rapid, specific, and sensitive loop-mediated isothermal amplification (LAMP) assay for detecting this pathogen was established. This technology has considerable potential for routine diagnosis of strain Pbs-1 in oyster hatcheries and/or pearl farms; therefore, it is vital to identify substances in environmental samples that might inhibit LAMP and to find additives that can reduce the inhibition. In this study, we investigated the effects of six chemicals or proteins, otherwise known as conventional PCR inhibitors, on LAMP, using the DNA of strain Pbs-1 as template: humic acid, urea, iron (III) chloride hexahydrate, melanin, myoglobin, and Ethylenediamine-N,N,N′,N′-tetraacetic acid, disodium salt, dihydrate (EDTA; pH 6.5). Next, to reduce the effects of identified inhibitors, we tested the addition of bovine serum albumin (BSA) or T4 gene 32 protein (gp32) to the LAMP assay. When 50 ng of DNA template was used, 4 ng/μL of humic acid, 0.05% melanin, and 10 mM of EDTA (pH 6.5) inhibited the LAMP reaction, whereas myoglobin, urea, and FeCl3 had no effect. When 50 pg of DNA template was used, 4 ng/μL of humic acid, 0.05% melanin, 4 μg/μL of myoglobin, 10 μg/μL of urea, and 10 mM of EDTA inhibited the LAMP reaction. Thus, it was shown that the gene-amplification inhibitory effect of melanin, humic acid, and urea could be reduced by adding BSA or gp32 to the LAMP reaction mixture. This technique could be applied as part of a protocol to prevent mass mortalities of pearl oysters; moreover, the results enhance our knowledge about substances that inhibit LAMP and methods to reduce the inhibition, which have rarely been reported.

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来源期刊
Journal of microbiological methods
Journal of microbiological methods 生物-生化研究方法
CiteScore
4.30
自引率
4.50%
发文量
151
审稿时长
29 days
期刊介绍: The Journal of Microbiological Methods publishes scholarly and original articles, notes and review articles. These articles must include novel and/or state-of-the-art methods, or significant improvements to existing methods. Novel and innovative applications of current methods that are validated and useful will also be published. JMM strives for scholarship, innovation and excellence. This demands scientific rigour, the best available methods and technologies, correctly replicated experiments/tests, the inclusion of proper controls, calibrations, and the correct statistical analysis. The presentation of the data must support the interpretation of the method/approach. All aspects of microbiology are covered, except virology. These include agricultural microbiology, applied and environmental microbiology, bioassays, bioinformatics, biotechnology, biochemical microbiology, clinical microbiology, diagnostics, food monitoring and quality control microbiology, microbial genetics and genomics, geomicrobiology, microbiome methods regardless of habitat, high through-put sequencing methods and analysis, microbial pathogenesis and host responses, metabolomics, metagenomics, metaproteomics, microbial ecology and diversity, microbial physiology, microbial ultra-structure, microscopic and imaging methods, molecular microbiology, mycology, novel mathematical microbiology and modelling, parasitology, plant-microbe interactions, protein markers/profiles, proteomics, pyrosequencing, public health microbiology, radioisotopes applied to microbiology, robotics applied to microbiological methods,rumen microbiology, microbiological methods for space missions and extreme environments, sampling methods and samplers, soil and sediment microbiology, transcriptomics, veterinary microbiology, sero-diagnostics and typing/identification.
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