多重PCR法测定药品样品中指示菌

S. FARAJNIA, M. HASSAN, S. HALLAJ NEZHADI, L. MOHAMMADNEJAD, M. MILANI, F. LOTFIPOUR
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引用次数: 19

摘要

快速、灵敏的指示性病原体检测技术在制药行业具有重要意义。然而,常用的检测方法依赖于细菌培养与生化试验相结合,这一过程通常需要5-6天才能完成。因此,本研究的目的是建立一种多重聚合酶链反应(mPCR)方法,用于在单一反应中同时检测和鉴定四种指示致病菌。采用大肠杆菌、金黄色葡萄球菌、铜绿假单胞菌、沙门氏菌等指示菌的特异性引物同时检测,并测定每对引物的敏感性和特异性。在混合DNA样品的mPCR中,同时检测到相应细菌的特异性条带。琼脂糖凝胶电泳结果显示,在预期大小的单条带中,mPCR的特异性为100%。低水平的微生物污染低于10 cfu每毫升或克的产品被检测使用mPCR法。4种指示致病菌的检测均在8 h内完成,而传统的美国药典方法和单链PCR分别需要5 ~ 6 d和27 h。在医药工业中,应用mPCR法对非无菌药品进行微生物质量控制是一种经济、及时的方法。大肠杆菌、金黄色葡萄球菌、沙门氏菌和铜绿假单胞菌的致病指标检测是非无菌药品微生物质量的强制性检测之一;因此,快速、灵敏地检测污染物对产品放行具有重要意义。本研究结果表明,利用mPCR法可以同时检测制药成品中4种主要潜在致病菌的低水平,具有较好的成本效益和及时性,在制药行业具有潜在的应用前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DETERMINATION OF INDICATOR BACTERIA IN PHARMACEUTICAL SAMPLES BY MULTIPLEX PCR

ABSTRACT

Rapid and sensitive detection techniques for indicator pathogens are important in pharmaceutical industry. However, common detection methods rely on bacterial culture in combination with biochemical tests, a process that typically takes 5–6 days to complete. Thus, the aim of this study was to develop a multiplex polymerase chain reaction (mPCR) assay for simultaneous detection and identification of four indicator pathogenic bacteria in a single reaction. Specific primers for indicator bacteria, namely Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosaand Salmonella, were applied to allow simultaneous detection of them, and the sensitivity and specificity of each primer pairs were determined. In the mPCR with mixed DNA samples, specific bands for corresponding bacteria were simultaneously detected. Agarose gel electrophoresis of PCR products revealed 100% specificity of mPCR with single bands in the expected sizes. Low levels of microbial contamination less than 10 cfu per milliliter or gram of product were detected using mPCR assay. The detection of all four indicator pathogenic bacteria were completed in less than 8 h with this novel mPCR method, whereas the conventional United States Pharmacopeia methods and uniplex PCR required 5–6 days and 27 h for completion, respectively. Using mPCR assay, the microbial quality control of nonsterile pharmaceutical products can be performed in a cost-effective and timely manner in pharmaceutical industry.

PRACTICAL APPLICATIONS

Detection of pathogenic indicatiors of Escherichia coli, Staphylococcus aureus, Salmonella and Pseudomonas aeruginosa is one of the mandatory tests in microbial quality of nonsterile pharmaceutical products; therefore, rapid and sensitive detection of the contaminations is of great importance for product release. According to the results of the present study, simultaneous detection of low levels of four major potential pathogenic bacteria in pharmaceutical finished products can be performed using mPCR in a cost-effective and timely manner, and upon these properties of the mPCR assay it could have potential applications in pharmaceutical industry.

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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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