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用于快速检测和分离食品中沙门氏菌的新型培养基的评估

Evaluation of new culture media for rapid detection and isolation of salmonellae in foods.

作者信息

Pignato S, Marino A M, Emanuele M C, Iannotta V, Caracappa S, Giammanco G

机构信息

Istituto d'Igiene e Medicina Preventiva, Università di Catania, A. Mirri, Palermo, Italy.

出版信息

Appl Environ Microbiol. 1995 May;61(5):1996-9. doi: 10.1128/aem.61.5.1996-1999.1995.

Abstract

Conventional methods for Salmonella detection in foods can require up to 6 and at least 4 days. We have observed that the total analysis time can be reduced to 48 h by using Salmosyst broth as a liquid medium for both preenrichment and selective enrichment and Rambach agar (RA), a new selective plate medium. In samples of artificially contaminated ground beef Salmonella enteritidis was detected at a concentration of 0.4 CFU/g (10 CFU/25 g) by both a conventional method and the new method. Of 519 samples of foods for sale, 38 were Salmonella positive by both methods while 471 were negative. Nine samples which were negative by the conventional method were positive by the Salmosyst-RA method, while one sample positive by the first method was negative by the last. Therefore, the Salmosyst-RA method showed 97.9% sensitivity compared with the 81.2% sensitivity of the conventional method. The new method was also highly specific (98% specificity) in presumptive identification of Salmonella colonies. Furthermore, a 6-h preenrichment in Salmosyst broth has been proved sufficient for the repair of heat-injured Salmonella cells and for subsequent recovery by selective enrichment. In conclusion, the Salmosyst-RA method shows several advantages over both conventional and rapid noncultural methods: (i) only two media are required instead of the five media for conventional methods; (ii) in real time it is comparable to other rapid noncultural methods, which require 30 to 31 h; (iii) it is highly sensitive and specific; and (iv) it allows the isolation of Salmonella strains which can be characterized by appropriate phenotypic and genotypic typing methods for epidemiological investigations.

摘要

食品中沙门氏菌检测的传统方法可能需要长达6天,至少也需要4天。我们观察到,通过使用Salmosyst肉汤作为预增菌和选择性增菌的液体培养基以及一种新的选择性平板培养基——Rambach琼脂(RA),总分析时间可缩短至48小时。在人工污染的碎牛肉样本中,肠炎沙门氏菌的浓度为0.4 CFU/g(10 CFU/25 g)时,传统方法和新方法均能检测到。在519份待售食品样本中,两种方法均检测出38份沙门氏菌阳性,471份阴性。9份传统方法检测为阴性的样本,Salmosyst - RA方法检测为阳性,而1份传统方法检测为阳性的样本,Salmosyst - RA方法检测为阴性。因此,与传统方法81.2%的灵敏度相比,Salmosyst - RA方法的灵敏度为97.9%。在沙门氏菌菌落的初步鉴定中,新方法也具有高度特异性(98%的特异性)。此外,已证明在Salmosyst肉汤中进行6小时的预增菌足以修复热损伤的沙门氏菌细胞,并通过选择性增菌进行后续回收。总之,Salmosyst - RA方法相对于传统方法和快速非培养方法具有多个优点:(i)仅需两种培养基,而传统方法需要五种培养基;(ii)在实时性方面与其他需要30至31小时的快速非培养方法相当;(iii)具有高灵敏度和特异性;(iv)能够分离出沙门氏菌菌株,可通过适当的表型和基因型分型方法进行流行病学调查。

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