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Rapid and quantitative detection of viable emetic Bacillus cereus by PMA-qPCR assay in milk

机译:PMA-QPCR测定在牛奶中的快速和定量检测活性催吐性芽孢杆菌

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Emetic Bacillus cereus is one of the causative agents of foodborne diseases which can cause vomiting-type food poisoning after ingestion of contaminated food. To minimize B. cereus food poisoning, propidium monoazide (PMA) combined with quantitative polymerase chain reaction (qPCR) called PMA-qPCR was applied for detecting viable emetic B. cereus in milk. The cereulide synthetase gene of emetic B. cereus (cesB) was chosen for the primer, and PMA treatment was optimized at 3 mu g/mL to inhibit the PCR amplification of DNA from dead cells. Under optimized assay parameters, the limit of detection (LOD) using this method were 10(2) CFU/mL in both pure culture and in spiked milk matrix. The cycle threshold (Ct) values obtained for this assay was not significantly affected by the presence of non-target bacteria such as E. coli O157:H7 which indicated the high selectivity of the assay for emetic B. cereus. The PMA-qPCR assay used in this study has the potential for sensitive detection of viable emetic B. cereus in milk.
机译:Emetic Bacillus Cereus是食物中疾病的致病药物之一,可在摄入污染的食物后引起呕吐型食物中毒。为了最小化B.患者食物中毒,掺入定量聚合酶链反应(QPCR)的单氮化物(PMA)被称为PMA-QPCR的促进剂用于检测牛奶中的活催化B.培训。选择蜂鸣B.脑腺苷酸(CESB)的蜂窝状合成酶基因,为引物选择,PMA处理以3μg/ mL进行优化,以抑制来自死细胞的DNA的PCR扩增。在优化的测定参数下,使用该方法的检测极限(LOD)在纯培养和掺入乳基质中为10(2)CFU / mL。对于该测定法获得的循环阈值(CT)值没有显着影响非靶细菌的存在,例如大肠杆菌O157:H7,其表明eMETES B. CERES的测定选择性的高选择性。本研究中使用的PMA-QPCR测定具有对牛奶中可行性催化B.培养皿的敏感性检测的可能性。

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