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免疫层析法与TaqMan大肠杆菌O157:H7检测法用于检测苜蓿芽菜废灌溉水中及热烫后芽菜中大肠杆菌O157:H7的比较。

Comparison of an immunochromatographic method and the TaqMan E. coli O157:H7 assay for detection of Escherichia coli O157:H7 in alfalfa sprout spent irrigation water and in sprouts after blanching.

作者信息

Fratamico P M, Bagi L K

机构信息

Agricultural Research Service, Eastern Regional Research Center, U.S. Department of Agriculture, 600 East Mermaid Lane, Wyndmoor, PA 19038, USA.

出版信息

J Ind Microbiol Biotechnol. 2001 Aug;27(2):129-34. doi: 10.1038/sj.jim.7000134.

Abstract

An immunochromatographic-based assay (Quixtrade mark E. coli O157 Sprout Assay) and a polymerase chain reaction (PCR)-based assay (TaqMan E. coli O157:H7 Kit) were used to detect Escherichia coli O157:H7 strain 380-94 in spent irrigation water from alfalfa sprouts grown from artificially contaminated seeds. Ten, 25, 60, or 100 seeds contaminated by immersion for 15 min in a suspension of E. coli O157:H7 at concentrations of 10(6) or 10(8) cfu/ml were mixed with 20 g of non-inoculated seeds in plastic trays for sprouting. The seeds were sprayed with tap water for 15 s every hour and spent irrigation water was collected at intervals and tested. E. coli O157:H7 was detected in non-enriched water by both the TaqMan PCR (30 of 30 samples) and the immunoassay (9 of 24 samples) in water collected 30 h from the start of the sprouting process. However, enrichment of the spent irrigation water in brain heart infusion (BHI) broth at 37 degrees C for 20 h permitted detection of E. coli O157:H7 in water collected 8 h from the start of sprouting using both methods, even in trays containing as few as 10 inoculated seeds. The TaqMan PCR assay was more sensitive (more positive samples were observed earlier in the sprouting process) than the immunoassay; however, the immunoassay was easier to perform and was more rapid. At 72 h after the start of the sprouting process, the sprouts were heated at 100 degrees C for 30 s to determine the effectiveness of blanching for inactivation of E. coli O157:H7. All of the 32 samples tested with the TaqMan assay and 16 of 32 samples tested with the Quixtrade mark assay gave positive results for E. coli O157:H7 after enrichment of the blanched sprouts at 37 degrees C for 24 h. In addition, the organism was detected on Rainbow Agar O157 in 9 of 32 samples after 24 h of enrichment of the blanched sprouts. In conclusion, E. coli O157:H7 was detected in spent irrigation water collected from sprouts grown from artificially contaminated seeds by both the TaqMan and Quixtrade mark assays. The data also revealed that blanching may not be effective to completely inactivate all the E. coli O157:H7 that may be present in sprouts.

摘要

采用基于免疫层析的检测方法(Quixtrade商标大肠杆菌O157豆芽检测法)和基于聚合酶链反应(PCR)的检测方法(TaqMan大肠杆菌O157:H7试剂盒),检测人工污染种子培育的苜蓿芽菜用过的灌溉水中的大肠杆菌O157:H7菌株380 - 94。将10、25、60或100粒在浓度为10(6)或10(8) cfu/ml的大肠杆菌O157:H7悬液中浸泡15分钟而被污染的种子,与20克未接种的种子混合,置于塑料托盘中发芽。每隔一小时用自来水喷洒种子15秒,并定期收集用过的灌溉水进行检测。在发芽过程开始30小时收集的水中,通过TaqMan PCR(30个样本中的30个)和免疫测定法(24个样本中的9个)在未富集的水中检测到了大肠杆菌O157:H7。然而,将用过的灌溉水在37摄氏度的脑心浸液(BHI)肉汤中富集20小时后,使用这两种方法在发芽开始8小时收集的水中都能检测到大肠杆菌O157:H7,即使在仅含有10粒接种种子的托盘中也是如此。TaqMan PCR检测法比免疫测定法更灵敏(在发芽过程中更早观察到更多阳性样本);然而,免疫测定法操作更简便、速度更快。在发芽过程开始72小时后,将豆芽在100摄氏度加热30秒,以确定热烫对灭活大肠杆菌O157:H7的效果。用TaqMan检测法检测的32个样本以及用Quixtrade商标检测法检测的32个样本中的16个,在将热烫后的豆芽在37摄氏度富集24小时后,大肠杆菌O157:H7检测结果呈阳性。此外,在热烫后的豆芽富集24小时后,32个样本中有9个在彩虹O157琼脂上检测到了该菌。总之,通过TaqMan和Quixtrade商标检测法在人工污染种子培育的豆芽用过的灌溉水中检测到了大肠杆菌O157:H7。数据还表明,热烫可能无法有效完全灭活豆芽中可能存在的所有大肠杆菌O157:H7。

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