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Applied and Environmental Microbiology, January 1999, p. 150-155, Vol. 65, No. 1
Department of Food and Environmental Hygiene,
Received 24 June 1998/Accepted 8 October 1998
Sites of Listeria monocytogenes contamination in a
cold-smoked rainbow trout (Oncorhynchus mykiss) processing
plant were detected by sampling the production line, environment, and
fish at different production stages. Two lots were monitored. The
frequency of raw fish samples containing L. monocytogenes was low. During processing, the frequency of fish
contaminated with L. monocytogenes clearly rose after
brining, and the most contaminated sites of the processing plant were
the brining and postbrining areas. A total of 303 isolates from the raw
fish, product, and the environment were characterized by pulsed-field
gel electrophoresis (PFGE). PFGE yielded nine pulsotypes, which formed
four clusters. The predominating L. monocytogenes pulsotypes of the final product were associated with brining and slicing, whereas contaminants of raw fish were not detected in the
final product. Air-mediated contamination in the plant could not be
proved. In accordance with these results, an L. monocytogenes eradication program was planned. The use of hot
steam, hot air, and hot water seemed to be useful in eliminating
L. monocytogenes. None of the control samples taken in
the 5 months after the eradication program was implemented contained
L. monocytogenes.
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Sources of Listeria monocytogenes Contamination in a
Cold-Smoked Rainbow Trout Processing Plant Detected by Pulsed-Field
Gel Electrophoresis Typing
*
Corresponding author. Mailing address: Department of
Food and Environmental Hygiene, Faculty of Veterinary Medicine,
P.O. Box 57, FIN-00014 Helsinki University, Finland. Phone:
358-9-70849766. Fax: 358-9-70849718. E-mail:
tiina.jo.autio{at}helsinki.fi.
Applied and Environmental Microbiology, January 1999, p. 150-155, Vol. 65, No. 1
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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