Rapid and sensitive detection of Staphylococcus aureus via an all-in-one staggered strand exchange amplification platform

金黄色葡萄球菌 变性(裂变材料) DNA提取 聚合酶链反应 病菌 DNA 食物中毒 化学 微生物学 食品安全 色谱法 食品科学 生物 细菌 基因 生物化学 遗传学 核化学
作者
Jian Zhang,Xiangning Han,Ye Wang,Xiaofeng Mu,Chao Shi,Yong Li,Cuiping Ma
出处
期刊:Analyst [Royal Society of Chemistry]
卷期号:148 (9): 1970-1977 被引量:9
标识
DOI:10.1039/d2an02092k
摘要

Staphylococcus aureus is a common foodborne pathogen that causes food poisoning and infectious diseases in humans and animals. Rapid detection of S. aureus with high sensitivity is of great significance to prevent the spread of this pathogen. In this study, we developed a staggered strand exchange amplification (SSEA) method by refining denaturation bubble-mediated strand exchange amplification (SEA) to detect S. aureus at a constant temperature with high specificity and efficiency. This method employs a DNA polymerase and two sets of forward and reverse primers arranged in tandem that invade denaturation bubbles of double-stranded DNA. In comparison, the sensitivity of SSEA was 20 times that of SEA. Subsequently, magnetic bead (MB)-based DNA extraction was introduced into SSEA to establish an all-in-one SSEA platform that incorporated sample processing, amplification and detection in a single tube. The use of MBs further enhanced the sensitivity of SSEA by two orders of magnitude. Specificity tests showed that the all-in-one SSEA could specifically identify S. aureus and had no cross-reaction with other common foodborne pathogens. For artificially spiked meat samples, the method could detect 1.0 × 102 CFU g-1S. aureus in pork and 1.0 × 103 CFU g-1 in either duck or scallop samples without a bacterial enrichment step. The entire assay can be completed sample-to-answer within 1 h. Thus, we believe that this easy-to-operate diagnostic platform enables sensitive and accurate detection of S. aureus and holds great promise for the food safety industry.
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