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Growth performance of Listeria monocytogenes and background microbiota from mushroom processing environments
被引:6
|作者:
Lake, Frank B.
[1
]
van Overbeek, Leo S.
[2
]
Baars, Johan J. P.
[3
]
Abee, Tjakko
[1
]
den Besten, Heidy M. W.
[1
]
机构:
[1] Wageningen Univ & Res, Food Microbiol, Bornse Weilanden 9, NL-6708 WG Wageningen, Netherlands
[2] Wageningen Univ & Res, Biointeract & Plant Hlth, Wageningen Plant Res, Droevendaalsesteeg 1, NL-6708 PB Wageningen, Netherlands
[3] Wageningen Univ & Res, Plant Breeding, Wageningen Plant Res, Droevendaalsesteeg 1, NL-6708 PB Wageningen, Netherlands
关键词:
Agaricus bisporus;
Mushroom medium;
Co-culture;
Spent mushroom medium;
pH effect;
Nutrient availability;
SPOILAGE-ASSOCIATED MICROBIOTA;
INTERNAL STIPE NECROSIS;
MIXED CULTURE BIOFILMS;
EWINGELLA-AMERICANA;
STAINLESS-STEEL;
AGARICUS-BISPORUS;
FOOD-INDUSTRY;
BACTERIA;
MEAT;
DYNAMICS;
D O I:
10.1016/j.ijfoodmicro.2023.110183
中图分类号:
TS2 [食品工业];
学科分类号:
0832 ;
摘要:
Interaction between Listeria monocytogenes and resident background microbiota may occur in food processing environments and may influence the survival of this pathogen in a factory environment. Therefore the aim of this study was to characterize the growth performance of microbiota isolated from the processing environments of frozen sliced mushrooms, and to investigate the competitive performance of L. monocytogenes when co-cultured with accompanying environmental microbiota. Acinetobacter, Enterobacteriaceae, Lactococcus and Pseudomonas were the most prominent background microbiota isolated from the processing environment of frozen sliced mushrooms. All individual microbiota strains were able to grow and form biofilm in filter-sterilized mushroom medium, with the mannitol-consumers Raoultella and Ewingella as top performers, reaching up to 9.6 and 9.8 log CFU/mL after 48 h incubation at room temperature. When L. monocytogenes mushroom isolates were co-cultured with the microbiota strains, L. monocytogenes counts ranged from 7.6 to 8.9 log CFU/mL after 24 h of incubation, while counts of the microbiota strains ranged from 5.5 to 9.0 log CFU/mL. Prolonged incubation up to 48 h resulted in further increase of L. monocytogenes counts when co-cultured with non-acidifying species Pseudomonas and Acinetobacter reaching 9.1 to 9.2 log CFU/mL, while a decrease of L. monocytogenes counts reaching 5.8 to 7.7 log CFU/mL was observed in co-culture with Enterobacteriaceae and acidifying Lactococcus representatives. In addition, L. monocytogenes grew also in spent mushroom media of the microbiota strains, except in acidified spent media of Lactococcus strains. These results highlight the competitive ability of L. monocytogenes during co-incubation with microbiota in fresh and in spent mushroom medium, indicative of its invasion and persistence capacity in food processing factory environments.
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