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基于 SYBR Green 的多重实时 PCR 检测法用于快速检测和区分眼部细菌病原体。

A SYBR Green based multiplex Real-Time PCR assay for rapid detection and differentiation of ocular bacterial pathogens.

机构信息

Department of Biotechnology, Bharathiar University, Coimbatore, Tamil Nadu, India.

Aravind Eye Hospital and Postgraduate Institute of Ophthalmology, Coimbatore, Tamil Nadu, India.

出版信息

J Microbiol Methods. 2020 Apr;171:105875. doi: 10.1016/j.mimet.2020.105875. Epub 2020 Feb 19.

Abstract

PURPOSE

Ocular bacterial pathogenesis is a serious sight threatening infection due to several bacterial species like Staphylococcus aureus, Streptococcus pneumoniae and Pseudomonas aeruginosa which are predominant. It is necessary to expedite diagnosis of pathogens for early treatment. Hence, a SYBR Green based multiplex Real-Time PCR assay coupled with melting curve analysis has been developed for rapid detection and differentiation of Staphylococcus aureus, Streptococcus pneumoniae and Pseudomonas aeruginosa in a single reaction.

METHODS

The assay was designed for simultaneous detection and differentiation of pathogens based on their distinct melting curve. The analytical specificity, sensitivity and reproducibility of the assay were examined using various reference strains. Clinical validation was carried out with 100 ocular samples collected from patients suffering from ocular infections.

RESULT

Each reaction tested for the targets individually generated three non overlapping melting curves with well alienated peaks corresponding to each gene. Among 100 ocular samples tested, 40 samples diagnosed with positive results in RT-PCR. Thus assay showed 100% specificity with high sensitivity and reproducibility.

CONCLUSION

The developed assay consistently established as a rapid and accurate diagnosis of ocular bacterial pathogens compared to the conventional laboratory techniques. Such precise method would aid greatly in clinical management of devastating ocular infections.

摘要

目的

眼部细菌性发病机制是一种严重的威胁视力的感染,由金黄色葡萄球菌、肺炎链球菌和铜绿假单胞菌等几种主要细菌引起。为了进行早期治疗,需要加快对病原体的诊断。因此,开发了一种基于 SYBR Green 的多重实时 PCR 检测方法,结合熔解曲线分析,可在单次反应中快速检测和区分金黄色葡萄球菌、肺炎链球菌和铜绿假单胞菌。

方法

该检测方法基于病原体独特的熔解曲线,设计用于同时检测和区分病原体。使用各种参考菌株对检测方法的分析特异性、敏感性和可重复性进行了检验。用 100 份来自眼部感染患者的眼部样本进行临床验证。

结果

每个反应分别检测靶标,生成三个非重叠的熔解曲线,每个基因对应一个分离良好的峰。在 100 个眼部样本中,40 个样本在 RT-PCR 中检测为阳性。因此,该检测方法与传统实验室技术相比,具有 100%的特异性、高灵敏度和可重复性。

结论

与传统的实验室技术相比,该方法可快速、准确地诊断眼部细菌性病原体。这种精确的方法将极大地有助于严重眼部感染的临床管理。

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