2</sup>CFU?mL<sup>-1</sup> ; 20d 穩(wěn)定性實驗顯示 6×10<sup>3</sup> CFU mL<sup>-1</sup> 菌懸液的Ct值變異系數(shù)為 1.89% ,穩(wěn)定性良好。在對20份市售樣品的檢測中,兩種方法陽性檢出率完全一致。TaqMan法單樣檢測耗時較國標法縮短至 50h ,但需依賴核酸擴增設備。結論:TaqMan實時熒光PCR適用于大批量樣本初篩,建議與噬菌體裂解技術聯(lián)用實現(xiàn)活菌檢測;國標法作為確認方法對陽性樣本進行復核評估,可以確保檢測合規(guī)。研究證實建立“分子初篩-培養(yǎng)確認”的聯(lián)合檢測體系可提升檢測效率,為食品微生物快檢技術標準化及生食水產(chǎn)品安全監(jiān)管提供數(shù)據(jù)支撐。-龍源期刊網(wǎng)" />

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生食動物性水產(chǎn)品中單增李斯特氏菌TaqMan實時熒光PCR檢測法和國標法的比較研究

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Comparative Study Between TaqMan Real-Time Fluorescence PCR Assay and National Standard Method for the Detection of Listeria monocytogenes in Raw Animal Aquatic Products

LIUAifang,ZHENG Ermei,WANGHanzheng,MAO Zhanhua, ZHU Weizhi (Zhejiang Gongzheng Testing Center, Hangzhou 31oooo, China)

Abstract: Objective: To systematically compare the technical characteristics of TaqMan real-time fluorescent PCR and national standard assays for the detection of Listeria monocytogenes in raw animal aquatic products,in order to optimize the detection processand improve the effciency of foodbome pathogen monitoring.Method:The optimal primer probe combinations of the TaqMan detection system were screened by specificity experiments to validate its sensitivityand detection stability; five types ofcommercially available raw aquatic products (mud snail, ready-to-eat jellyfish threads,choking crab,Arctic shrimp,and salmon) were detected toevaluate the diferences in detection eficacy between the two methods.Result: The optimal primer probe combination for LIS2 was obtained by screening,and its detection sensitivity reached 6×102 CFU mL-1 ,and the 20-day stability test showed that the coefficient of variation of the Ct value of the 6×103 CFU mL-1 bacterial suspension was 1.89% ,which demonstrated good stability.In20 commercially available samples,the positive detection rates were identical for both methods, and the TaqMan method took up to 50h less time than the national standard method for a single sample,but relied on nucleic acid amplification equipment. Conclusion: TaqMan real-time fluorescent PCR is suitable for the primary screening of large quantities of samples,and it is recommended to be combined with phage lysis technology to achievelive bacteria detection.The national standard method was used as a confirmation method to review and evaluate the positive samples to ensure that the detection was inaccordance with the regulations.The studyconfirmed that the establishment of a joint detection system of“molecular preliminary screening-culture confirmation”can improve the detection efficiency and provide data support for the standardization of food microbiological rapid detection technology and the safety supervision of raw aquatic products.

Keywords: Listeria monocytogenes; TaqMan real-time fluorescent PCR; raw animal aquatic products; national standard method

在全球飲食文化相互滲透、不斷交融的時代浪潮中,刺身、牡蠣、生腌海鮮等生食動物性水產(chǎn)品,以其別具一格的風味和口感,在消費市場中迅速走紅,深受廣大消費者喜愛。(剩余8876字)

目錄
monitor