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接种粪便浆液的牛胴体冷藏储存期间大肠杆菌生物型I和肠球菌属的复苏情况。

Recovery of Escherichia coli Biotype I and Enterococcus spp. during refrigerated storage of beef carcasses inoculated with a fecal slurry.

作者信息

Calicioglu M, Buege D R, Ingham S C, Luchansky J B

机构信息

Department of Animal Sciences, University of Wisconsin-Madison, 53706, USA.

出版信息

J Food Prot. 1999 Aug;62(8):944-7. doi: 10.4315/0362-028x-62.8.944.

Abstract

Three beef front quarters/carcasses were inoculated with a slurry of cattle manure. During storage at 4 degrees C, two sponge samples from each of three sites (i.e., 100 cm2 from each of two fat surfaces and 100 cm2 from a lean surface) were taken from each of the three carcasses on days 0, 1, 3, 7, and 10 after inoculation. The initial numbers of Escherichia coli averaged 2.0 log10 CFU/cm2 (1.21 to 2.47 log10 CFU/cm2) using the Petrifilm method and 2.09 log10 most probable number (MPN)/cm2 (0.88 to 2.96 log10 MPN/cm2) using the MPN method. The initial numbers of enterococci averaged 3.34 log10 CFU/cm2 (3.07 to 3.79 log10 CFU/cm2) using kanamycin esculin azide agar. In general, an appreciable reduction in the numbers of E. coli occurred during the first 24 h of storage; for the Petrifilm method an average reduction of 1.37 log10 CFU/cm2 (0.69 to 1.71 log10 CFU/cm2) was observed, and for the MPN method an average reduction of 1.52 log10 MPN/cm2 (0.47 to 2.08 log10 MPN/cm2) was observed. E. coli were not detected (<-0.12 log10 CFU/cm2) using Petrifilm on day 7 of the storage period on two (initial counts of 1.21 and 2.29 log10 CFU/cm2) of the three carcasses. However, viable E. coli cells were recovered from these two carcasses after a 24-h enrichment at 37 degrees C in EC broth. Viable E. coli cells were detected at levels of -0.10 log10 CFU/cm2 on the third carcass (initial count of 2.47 log10 CFU/cm2) after 7 days at 4 degrees C. No significant difference in recovery of viable cells was observed between the MPN and Petrifilm methods on days 0, 1, and 3 (P > 0.05). However, viable E. coli cells were recovered from all three carcasses by the MPN method on day 7 at an average of -0.29 log10 MPN/ cm2 (-0.6 to -0.1 log10 MPN/cm2). On day 10, viable cells were recovered by the MPN method from two of the three carcasses at -0.63 and -0.48 log10 MPN/cm2 but were not recovered from the remaining carcass (<-0.8 log10 MPN/cm2). Similar to E. coli, the greatest reduction (average of 1.26 log10 CFU/cm2, range = 1.06 to 1.45 log10 CFU/cm2) in the numbers of enterococci occurred during the first 24 h of storage. Because of higher initial numbers and a slightly slower rate of decrease, the numbers of Enterococcus spp. were significantly higher (P < 0.017) than the numbers of E. coli Biotype I after 3, 7, and 10 days of storage. These results suggest that enterococci may be useful as an indicator of fecal contamination of beef carcasses.

摘要

将三份牛前四分体/胴体接种牛粪悬液。在4℃储存期间,在接种后的第0、1、3、7和10天,从三个胴体中的每一个上的三个部位(即两个脂肪表面各100平方厘米和一个瘦肉表面100平方厘米)各取两个海绵样本。使用Petrifilm方法,大肠杆菌的初始数量平均为2.0 log10 CFU/平方厘米(1.21至2.47 log10 CFU/平方厘米),使用MPN方法为2.09 log10最可能数(MPN)/平方厘米(0.88至2.96 log10 MPN/平方厘米)。使用卡那霉素七叶苷叠氮化物琼脂,肠球菌的初始数量平均为3.34 log10 CFU/平方厘米(3.07至3.79 log10 CFU/平方厘米)。一般来说,在储存的前24小时内大肠杆菌数量有明显减少;对于Petrifilm方法,观察到平均减少1.37 log10 CFU/平方厘米(0.69至1.71 log10 CFU/平方厘米),对于MPN方法,观察到平均减少1.52 log10 MPN/平方厘米(0.47至2.08 log10 MPN/平方厘米)。在储存期的第7天,使用Petrifilm在三个胴体中的两个(初始计数分别为1.21和2.29 log10 CFU/平方厘米)上未检测到大肠杆菌(<-0.12 log10 CFU/平方厘米)。然而,在37℃的EC肉汤中富集培养24小时后,从这两个胴体中回收了活的大肠杆菌细胞。在4℃下放置7天后,在第三个胴体(初始计数为2.47 log10 CFU/平方厘米)上检测到活的大肠杆菌细胞,水平为-0.10 log10 CFU/平方厘米。在第0、1和3天,MPN方法和Petrifilm方法在回收活细胞方面没有观察到显著差异(P>0.05)。然而,在第7天,通过MPN方法从所有三个胴体中回收了活的大肠杆菌细胞,平均为-0.29 log10 MPN/平方厘米(-0.6至-0.1 log10 MPN/平方厘米)。在第10天,通过MPN方法从三个胴体中的两个中回收了活细胞,分别为-0.63和-0.48 log10 MPN/平方厘米,但从剩余的胴体中未回收(<-0.8 log10 MPN/平方厘米)。与大肠杆菌类似,肠球菌数量的最大减少(平均为1.26 log10 CFU/平方厘米,范围为1.06至1.45 log10 CFU/平方厘米)发生在储存的前24小时内。由于初始数量较高且下降速度稍慢,在储存3、7和10天后,肠球菌属的数量显著高于I型大肠杆菌的数量(P<0.017)。这些结果表明,肠球菌可能作为牛肉胴体粪便污染的指示菌。

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