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1.
J Food Prot ; 64(7): 994-9, 2001 Jul.
Article in English | MEDLINE | ID: mdl-11456209

ABSTRACT

The environment and products from two broiler abattoirs and processing plants and raw broiler pieces at the retail level were sampled for Listeria monocytogenes in order to evaluate the contamination level of the broiler carcasses and products. Sampling started in the slaughtering process and finished with raw broiler meat or ready-to-eat cooked product. Sampling sites positive for L. monocytogenes at the broiler abattoir were the air chiller, the skin-removing machine, and the conveyor belt leading to the packaging area. The L monocytogenes contamination rate varied from 1 to 19% between the two plants studied. Furthermore, 62% (38 of 61) of the raw broiler pieces, bought from retail stores, were positive for L. monocytogenes. Altogether, 136 L. monocytogenes isolates were obtained for serotyping and pulsed-field gel electrophoresis (PFGE) characterization performed with two rare-cutting enzymes (ApaI and AscI). Altogether three serotypes (1/2a, 1/2c, and 4b) and 14 different PFGE types were obtained using information provided from both ApaI and AscI patterns for discrimination basis. The two broiler abattoirs studied did not share the same PFGE types. However, the same PFGE types found in the raw broiler pieces at the retail level were also found in the broiler abattoirs where the broilers had been slaughtered.


Subject(s)
Food Contamination , Listeria monocytogenes/isolation & purification , Poultry Products/microbiology , Abattoirs , Animals , Chickens , Electrophoresis, Gel, Pulsed-Field , Food Handling , Food-Processing Industry , Hygiene , Listeriosis/epidemiology , Prevalence , Serotyping
2.
J Food Prot ; 63(9): 1204-7, 2000 Sep.
Article in English | MEDLINE | ID: mdl-10983793

ABSTRACT

Adherence of 3 persistent and 14 nonpersistent Listeria monocytogenes strains to stainless steel surfaces after short and long contact times was investigated. L. monocytogenes strains were obtained from poultry plants and an ice cream plant throughout several years. Adherence tests were performed in tryptic soy broth at 25 degrees C for 1, 2, and 72 h. Test surfaces were rinsed after the contact time, and attached cells were stained with acridine orange and enumerated with an epifluorescence microscope. The persistent poultry plant strains showed adherence 2- to 11-fold higher than the nonpersistent strains following 1- and 2-h contact times. The adherence of the persistent ice cream plant strain after 1- and 2-h contact times was higher than most of the nonpersistent strains. Seven of 12 nonpersistent ice cream strains showed an adherence of less than half that of the persistent strain. After 72 h, the differences in adherence were not as marked, since half the nonpersistent strains had reached adherence levels comparable with the persistent strains. In fact, three nonpersistent strains showed even higher adherence than the persistent strains. Thus, results of this study reveal that persistent L. monocytogenes strains show enhanced adherence at short contact times, promoting their survival in food processing facilities and possibly having an effect on initiation of persistent plant contamination.


Subject(s)
Bacterial Adhesion/physiology , Chickens/microbiology , Listeria monocytogenes/physiology , Stainless Steel , Animals , Colony Count, Microbial , Food Microbiology , Food-Processing Industry/standards , Ice Cream/microbiology , Listeria monocytogenes/genetics , Listeria monocytogenes/isolation & purification , Microscopy, Fluorescence/methods , Serotyping , Time Factors
3.
J Clin Microbiol ; 37(7): 2358-60, 1999 Jul.
Article in English | MEDLINE | ID: mdl-10364616

ABSTRACT

Febrile gastroenteritis in five healthy persons was associated with the consumption of vacuum-packed cold-smoked rainbow trout containing Listeria monocytogenes. L. monocytogenes isolates from the incriminated fish product lot and the stool samples were all of serotype 1/2a and were indistinguishable by pulsed-field gel electrophoresis employing AscI and SmaI.


Subject(s)
Disease Outbreaks , Food Microbiology , Gastroenteritis/epidemiology , Listeria monocytogenes/genetics , Listeriosis/epidemiology , Listeriosis/transmission , Oncorhynchus mykiss/microbiology , Adult , Animals , Child, Preschool , Electrophoresis, Gel, Pulsed-Field , Female , Fever , Finland/epidemiology , Food Handling , Gastroenteritis/microbiology , Humans , Listeria monocytogenes/classification , Listeria monocytogenes/isolation & purification , Listeriosis/microbiology , Male , Middle Aged , Molecular Epidemiology/methods , Serotyping
4.
Int J Food Microbiol ; 46(3): 187-92, 1999 Feb 18.
Article in English | MEDLINE | ID: mdl-10100898

ABSTRACT

One dominating strain of serotype 1/2b was found when serotyping and pulsed-field gel electrophoresis (PFGE) patterns were used for the characterization of 41 Listeria monocytogenes isolates originating from an ice cream plant. Samples were taken from the production environment, equipment and ice cream during the years 1990-1997. Serotyping divided the isolates into two serovars, 1/2b and 4b. Three rare-cutting enzymes (ApaI, AscI and SmaI) were used in the creation of PFGE patterns. AscI resulted in the best restriction enzyme digestion patterns (REDPs) for visual comparison. Eight different AscI REDPs were obtained, whereas ApaI produced six and SmaI seven banding patterns. When one-band differences are taken into account, 12 different PFGE types were distinguished based on information obtained with all three enzymes. The dominant PFGE type was found to have persisted in the ice cream plant for seven years. Improved and precisely targeted cleaning and disinfection practices combined with structural changes making for easier cleaning of the packaging machine, resulted in eradication of L. monocytogenes from this plant.


Subject(s)
Food Microbiology , Ice Cream/microbiology , Listeria monocytogenes/classification , Listeriosis/prevention & control , DNA Restriction Enzymes/chemistry , DNA, Bacterial/chemistry , Electrophoresis, Gel, Pulsed-Field , Food-Processing Industry/standards , Listeria monocytogenes/chemistry , Serotyping
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