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Applied and Environmental Microbiology, February 2002, p. 602-607, Vol. 68, No. 2
0099-2240/02/$04.00+0 DOI: 10.1128/AEM.68.2.602-607.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
Effect of Commercial-Scale High-Temperature, Short-Time Pasteurization on the Viability of Mycobacterium paratuberculosis in Naturally Infected Cows' Milk
Irene R. Grant,1* Edward I. Hitchings,1 Alan McCartney,2 Fiona Ferguson,2 and Michael T. Rowe1,3
Department of Food Science (Food Microbiology), Queen's University of Belfast,1
Food Science Division, Department of Agriculture and Rural Development for Northern Ireland, Belfast,3
Loughry CollegeThe Food Centre, Department of Agriculture and Rural Development for Northern Ireland, Cookstown, County Tyrone, Northern Ireland, United Kingdom2
Received 25 June 2001/
Accepted 26 November 2001
Raw cows' milk naturally infected with Mycobacterium paratuberculosis was pasteurized with an APV HXP commercial-scale pasteurizer (capacity 2,000 liters/h) on 12 separate occasions. On each processing occasion, milk was subjected to four different pasteurization treatments, viz., 73°C for 15 s or 25 s with and without prior homogenization (2,500 lb/in2 in two stages), in an APV Manton Gaulin KF6 homogenizer. Raw and pasteurized milk samples were tested for M. paratuberculosis by immunomagnetic separation (IMS)-PCR (to detect the presence of bacteria) and culture after decontamination with 0.75% (wt/vol) cetylpyridinium chloride for 5 h (to confirm bacterial viability). On 10 of the 12 processing occasions, M. paratuberculosis was detectable by IMS-PCR, culture, or both in either raw or pasteurized milk. Overall, viable M. paratuberculosis was cultured from 4 (6.7%) of 60 raw and 10 (6.9%) of 144 pasteurized milk samples. On one processing day, in particular, M. paratuberculosis appeared to have been present in greater abundance in the source raw milk (evidenced by more culture positives and stronger PCR signals), and on this occasion, surviving M. paratuberculosis bacteria were isolated from milk processed by all four heat treatments, i.e., 73°C for 15 and 25 s with and without prior homogenization. On one other occasion, surviving M. paratuberculosis bacteria were isolated from an unhomogenized milk sample that had been heat treated at 73°C for 25 s. Results suggested that homogenization increases the lethality of subsequent heat treatment to some extent with respect to M. paratuberculosis, but the extended 25-s holding time at 73°C was found to be no more effective at killing M. paratuberculosis than the standard 15-s holding time. This study provides clear evidence that M. paratuberculosis bacteria in naturally infected milk are capable of surviving commercial high-temperature, short-time pasteurization if they are present in raw milk in sufficient numbers.
* Corresponding author. Mailing address: Department of Food Science (Food Microbiology), Queen's University Belfast, Newforge Ln., Belfast BT9 5PX, N. Ireland, United Kingdom. Phone: 44 28 9025 5299. Fax: 44 28 9025 5009. E-mail:
ireneRgrant{at}hotmail.com.
Applied and Environmental Microbiology, February 2002, p. 602-607, Vol. 68, No. 2
0099-2240/02/$04.00+0 DOI: 10.1128/AEM.68.2.602-607.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
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