2</sup>CFU?mL<sup>-1</sup> ; 20d 穩(wěn)定性實(shí)驗(yàn)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(duì)20份市售樣品的檢測(cè)中,兩種方法陽(yáng)性檢出率完全一致。TaqMan法單樣檢測(cè)耗時(shí)較國(guó)標(biāo)法縮短至 50h ,但需依賴核酸擴(kuò)增設(shè)備。結(jié)論:TaqMan實(shí)時(shí)熒光PCR適用于大批量樣本初篩,建議與噬菌體裂解技術(shù)聯(lián)用實(shí)現(xiàn)活菌檢測(cè);國(guó)標(biāo)法作為確認(rèn)方法對(duì)陽(yáng)性樣本進(jìn)行復(fù)核評(píng)估,可以確保檢測(cè)合規(guī)。研究證實(shí)建立“分子初篩-培養(yǎng)確認(rèn)”的聯(lián)合檢測(cè)體系可提升檢測(cè)效率,為食品微生物快檢技術(shù)標(biāo)準(zhǔn)化及生食水產(chǎn)品安全監(jiān)管提供數(shù)據(jù)支撐。-龍?jiān)雌诳W(wǎng)" />

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生食動(dòng)物性水產(chǎn)品中單增李斯特氏菌TaqMan實(shí)時(shí)熒光PCR檢測(cè)法和國(guó)標(biāo)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(shí)代浪潮中,刺身、牡蠣、生腌海鮮等生食動(dòng)物性水產(chǎn)品,以其別具一格的風(fēng)味和口感,在消費(fèi)市場(chǎng)中迅速走紅,深受廣大消費(fèi)者喜愛。(剩余8876字)

目錄
monitor