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首页> 外文期刊>Journal of Clinical Microbiology >Rapid Visual Detection of Highly Pathogenic Streptococcus suis Serotype 2 Isolates by Use of Loop-Mediated Isothermal Amplification
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Rapid Visual Detection of Highly Pathogenic Streptococcus suis Serotype 2 Isolates by Use of Loop-Mediated Isothermal Amplification

机译:快速视觉检测的高致病性猪链球菌血清型2分离物通过使用环介导的等温扩增

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摘要

Streptococcus suis serotype 2 (S. suis 2) is an important zoonotic pathogen that causes considerable economic losses to the pig industry and significantly threatens public health worldwide. The highly pathogenic S. suis 2, which contains the 89K pathogenicity island (PAI), has caused large-scale outbreaks of infections in humans, resulting in high mortality rates. In this study, we established two loop-mediated isothermal amplification (LAMP)-based assays that can rapidly detect S. suis 2 and the 89K PAI and can be performed simultaneously under the same conditions. Further, based on the findings of these two LAMP assays and using the same set of serially diluted DNA samples, we compared the sensitivities of different LAMP product detection methods, including SYBR green detection, gel electrophoresis, turbidimetry, calcein assays, and hydroxynaphthol blue detection. The results suggest that target genes can be amplified and detected within 48 min under 63°C isothermal conditions. The sensitivity of tests for S. suis 2 detection varies between detection methods and reaction systems, indicating that for each LAMP reaction system, multiple detection methods should be performed to select the optimal one. The sensitivities of the optimized methods (7.16 copies/reaction) in the present study were identical to those of the real-time PCR assay, and the test results for reference strains and clinical samples showed that these LAMP systems have high specificities. Thus, since the LAMP systems established in this study are simple, fast, and sensitive, they may have good clinical potential for detecting the highly pathogenic S. suis 2.
机译:猪链球菌血清型2(猪链球菌2)是一种重要的人畜共患病原体,对养猪业造成可观的经济损失,并在全球范围内严重威胁公众健康。包含89K致病岛(PAI)的高致病性猪链球菌2已引起人类大规模感染爆发,导致高死亡率。在这项研究中,我们建立了两个基于环介导的等温扩增(LAMP)的检测方法,可以快速检测猪链球菌2和89K PAI,并且可以在相同条件下同时进行。此外,基于这两个LAMP分析的发现,并使用同一套连续稀释的DNA样品,我们比较了不同LAMP产品检测方法(包括SYBR绿检测,凝胶电泳,比浊法,钙黄绿素检测和羟萘酚蓝检测)的敏感性。 。结果表明,可以在63°C等温条件下48分钟内扩增和检测靶基因。猪链球菌2检测的检测灵敏度在检测方法和反应系统之间有所不同,这表明对于每个LAMP反应系统,应执行多种检测方法以选择最佳方法。本研究中优化方法的灵敏度(7.16拷贝/反应)与实时PCR分析的灵敏度相同,参考菌株和临床样品的测试结果表明这些LAMP系统具有很高的特异性。因此,由于本研究建立的LAMP系统简单,快速且灵敏,因此它们在检测高致病性猪链球菌2中可能具有良好的临床潜力。

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