Donaghy J A, Totton N L, Rowe M T
Agriculture, Food and Environmental Science Division (Food Microbiology Branch), Department of Agriculture and Rural Development for N. Ireland, Newforge Lane, Belfast BT9 5PX, N. Ireland, United Kingdom.
Appl Environ Microbiol. 2004 Aug;70(8):4899-905. doi: 10.1128/AEM.70.8.4899-4905.2004.
Model Cheddar cheeses were prepared from pasteurized milk artificially contaminated with high 10(4) to 10(5) CFU/ml) and low (10(1) to 10(2) CFU/ml) inocula of three different Mycobacterium paratuberculosis strains. A reference strain, NCTC 8578, and two strains (806PSS and 796PSS) previously isolated from pasteurized milk for retail sale were investigated in this study. The manufactured Cheddar cheeses were similar in pH, salt, moisture, and fat composition to commercial Cheddar. The survival of M. paratuberculosis cells was monitored over a 27-week ripening period by plating homogenized cheese samples onto HEYM agar medium supplemented with the antibiotics vancomycin, amphotericin B, and nalidixic acid without a decontamination step. A concentration effect was observed in M. paratuberculosis numbers between the inoculated milk and the 1-day old cheeses for each strain. For all manufactured cheeses, a slow gradual decrease in M. paratuberculosis CFU in cheese was observed over the ripening period. In all cases where high levels (>3.6 log(10)) of M. paratuberculosis were present in 1-day cheeses, the organism was culturable after the 27-week ripening period. The D values calculated for strains 806PSS, 796PSS, and NCTC 8578 were 107, 96, and 90 days, respectively. At low levels of contamination, M. paratuberculosis was only culturable from 27-week-old cheese spiked with strain 806PSS. M. paratuberculosis was recovered from the whey fraction in 10 of the 12 manufactured cheeses. Up to 4% of the initial M. paratuberculosis load was recovered in the culture-positive whey fractions at either the high or low initial inoculum.
切达干酪模型由经巴氏杀菌的牛奶制成,这些牛奶被三种不同副结核分枝杆菌菌株的高接种量(10⁴至10⁵CFU/ml)和低接种量(10¹至10²CFU/ml)人工污染。本研究调查了一株参考菌株NCTC 8578以及之前从零售巴氏杀菌牛奶中分离出的两株菌株(806PSS和796PSS)。所制作的切达干酪在pH值、盐分、水分和脂肪成分方面与市售切达干酪相似。在27周的成熟期间,通过将均质化的奶酪样品接种到添加了抗生素万古霉素、两性霉素B和萘啶酸的HEYM琼脂培养基上(无需去污步骤)来监测副结核分枝杆菌细胞的存活情况。对于每个菌株,在接种牛奶和1日龄奶酪之间观察到了副结核分枝杆菌数量的浓度效应。对于所有制作的奶酪,在成熟期间观察到奶酪中副结核分枝杆菌CFU缓慢逐渐减少。在1日龄奶酪中副结核分枝杆菌含量高(>3.6 log₁₀)的所有情况下,经过27周的成熟后该微生物仍可培养。计算得出806PSS、796PSS和NCTC 857菌株的D值分别为107天、96天和90天。在低污染水平下,仅从接种了806PSS菌株的27周龄奶酪中可培养出副结核分枝杆菌。在12个制作的奶酪中有10个从乳清部分中检测到了副结核分枝杆菌。在高初始接种量或低初始接种量的情况下,在培养阳性的乳清部分中回收了高达4%的初始副结核分枝杆菌载量。