Growth of Listeria monocytogenes at different pH values in uncultured whey or whey cultured with Penicillium camemberti

1988 ◽  
Vol 34 (6) ◽  
pp. 730-734 ◽  
Author(s):  
Elliot T. Ryser ◽  
Elmer H. Marth
Keyword(s):  
Listeria Monocytogenes ◽  
Penicillium Camemberti ◽  
Ph Values ◽  
Generation Times ◽  
Camembert Cheese

Wheys from making Camembert cheese were either uncultured or cultured with Penicillium camemberti, adjusted to pH 5.0, 5.2, 5.4, 5.6, 6.2, and 6.8, and filter sterilized. Whey samples were inoculated to contain 100 to 500 Listeria monocytogenes (strains Scott A, V7, CA, or OH) cfu/mL and incubated at 6 °C. Counts of L. monocytogenes were obtained by surface plating appropriate dilutions on Tryptose Agar. Listeria monocytogenes failed to grow at or below pH 5.4; except for strains Scott A and OH which grew in cultured whey at pH 5.4 and attained populations of 7.8 × 103 and 5.4 × 104 cfu/mL, respectively, after 35 d of storage. In uncultured whey at pH 5.6, 6.2, and 6.8, populations of L. monocytogenes increased from 7.20 to 7.81, 7.51 to 8.23, and 7.48 to 8.08 log10 cfu/mL, respectively, after 35 d of storage at 6 °C. In cultured whey at pH 5.6, 6.2, and 6.8, numbers of L. monocytogenes increased from 7.53 to 8.13, 7.82 to 8.55, and 7.95 to 8.80 log10 cfu/mL, respectively, after 35 d of storage. Generation times for L. monocytogenes at 6 °C in uncultured whey at pH 5.6, 6.2, and 6.8 ranged between 25.3 and 31.6 h, 14.8 and 21.1 h, and 14.0 and 19.4 h, respectively, depending on the Listeria strain. In contrast, generation times were significantly (p < 0.05) shorter in cultured whey and ranged between 16.6 and 27.4 h, 10.3 and 16.6 h, and 17.4 and 16.3 h at pH values of 5.6, 6.2, and 6.8, respectively.

Fate of Listeria monocytogenes During the Manufacture and Ripening of Camembert Cheese

1987 ◽  
Vol 50 (5) ◽  
pp. 372-378 ◽  
Author(s):  
ELLIOT T. RYSER ◽  
ELMER H. MARTH
Keyword(s):  
Listeria Monocytogenes ◽  
Fold Increase ◽  
Original Sample ◽  
Cheese Making ◽  
Penicillium Camemberti ◽  
Shaped Surface ◽  
Standard Procedures ◽  
Whole Milk ◽  
Camembert Cheese ◽  
Made In

The ability of Listeria monocytogenes to survive the Camembert cheese-making process and grow during ripening of the cheese was examined. Pasteurized whole milk was inoculated to contain about 500 L. monocytogenes [strain Scott A, V7, California, (CA) or Ohio (OH)] CFU/ml and made into Camembert cheese according to standard procedures. All wheels of cheese were ripened at 6°C following 10 d of storage at 15–16°C to allow proper growth of Penicillium camemberti. Duplicate wedge (pie-shaped), surface and interior cheese samples were analyzed for numbers of L. monocytogenes by surface-plating appropriate dilutions made in Tryptose Broth (TB) on McBride Listeria Agar (MLA). Initial TB dilutions were stored at 3°C and surface-plated on MLA after 2, 4, 6 or 8 weeks if the organism was not quantitated in the original sample. Selected Listeria colonies from duplicate samples were confirmed biochemically. Results showed that numbers of Listeria in cheese increased 5- to 10-fold 24 h after its manufacture. Listeria counts for strains Scott A, CA and OH decreased to &lt;10 to 100 CFU/g in all cheese samples taken during the first 18 d of ripening. In contrast, numbers of strain V7 remained unchanged during this period. All L. monocytogenes strains initiated growth in cheese after 18 d of ripening. Maximum Listeria counts of ca. 1 × 106 to 5 × 107 CFU/g were attained after 65 d of ripening. Generally, a 10- to 100-fold increase in numbers of Listeria occurred in wedge or surface as compared to interior cheese samples taken during the latter half of ripening. During this period, Listeria growth paralleled the increase in pH of the cheese during ripening.

Behavior of Listeria monocytogenes at 4 and 22°C in Whey and Skim Milk Containing 6 or 12% Sodium Chloride

1989 ◽  
Vol 52 (9) ◽  
pp. 625-630 ◽  
Author(s):  
DEMETRIOS K. PAPAGEORGIOU ◽  
ELMER H. MARTH
Keyword(s):  
Listeria Monocytogenes ◽  
Sodium Chloride ◽  
Skim Milk ◽  
Salt Tolerant ◽  
Ph Values ◽  
Generation Times ◽  
Order Of Magnitude ◽  
Entire Experiment

Autoclaved samples of skim milk and deproteinated whey were fortified with 6 or 12% NaCl, inoculated with Listeria monocytogenes strains Scott A or California (CA), to contain ca. 1.0 × 103 cfu/ml (in the products with 6% salt) or ca. 5.0 × 103 cfu/ml (in the products with 12% salt) and incubated at 4 and 22°C. The pH values of the 6% salted whey, 6% salted skim milk, 12% salted whey, and 12% salted skim milk were 5.65, 6.20, 5.50, and 6.00 respectively. These values remained relatively constant during the entire experiment. Listeria counts were obtained by surface-plating appropriate dilutions and/or undiluted samples on Trypticase Agar (TA). Samples in which L. monocytogenes was not detected, were re-examined after 2, 4, 6 and 8 weeks of cold-enrichment. Generation times of L. monocytogenes in 6% salted whey at 22°C (3.67 h and 3.56 h for strains Scott A and CA, respectively) were significantly shorter than those in 6% salted skim milk at 22°C (4.31 and 4.42 h for the two strains, respectively). Generation times in 6% salted products at 4°C ranged between 37.49 h and 49.43 h. Maximum populations reached at 22 and 4°C ranged from 7.58 to 8.10 Log10 cfu/ml, and were significantly higher in 6% salted whey than in 6% salted skim milk. In 12% salted whey and skim milk incubated at 22°C, L. monocytogenes gradually decreased in numbers. Strain CA was inactivated within 85 d in 12% salted skim milk or within 110 d in 12% salted whey, and was significantly less salt tolerant than strain Scott A which survived for more than 130 d under the same conditions. Loss of viability by both strains was similar in 12% salted whey and skim milk after 130 d of storage at 4°C, and the decreases in population were less than 0.7 order of magnitude.

Validation of Predictive Mathematical Models Describing the Growth of Listeria monocytogenes

1997 ◽  
Vol 60 (9) ◽  
pp. 1142-1145 ◽  
Author(s):  
ISABEL WALLS ◽  
VIRGINIA N. SCOTT
Keyword(s):  
Listeria Monocytogenes ◽  
Growth Rates ◽  
Microbial Growth ◽  
Lag Phase ◽  
Growth Data ◽  
Ph Values ◽  
Gompertz Equation ◽  
Generation Times ◽  
Different Temperatures ◽  
Good Agreement

Growth of Listeria monocytogenes and Listeria innocua in commercially available sterile homogeneous foods was investigated at different temperatures, pH values, and NaCl concentrations. Growth data were fitted to the Gompertz equation and the resulting growth kinetics were compared with predictions from the Pathogen Modeling Program and Food MicroModel. In general, good agreement was obtained when comparing growth rates and generation times for both models. Differences were observed when comparing lag phases, which ranged from 117 h shorter to 4.9 h longer than predicted for L. monocytogenes. Despite differences in lag phase, under most conditions, the models gave good predictions of microbial growth. Predictive modeling appears to be a useful tool in determining growth rates of Listeria in foods.

Effect of pH, Acidulant, Time, and Temperature on the Growth and Survival of Listeria monocytogenes

1989 ◽  
Vol 52 (8) ◽  
pp. 571-573 ◽  
Author(s):  
KENT M. SORRELLS ◽  
DAVIN C. ENIGL ◽  
JOHN R. HATFIELD
Keyword(s):  
Antimicrobial Activity ◽  
Acetic Acid ◽  
Lactic Acid ◽  
Listeria Monocytogenes ◽  
Citric Acid ◽  
Hydrochloric Acid ◽  
Malic Acid ◽  
Incubation Temperature ◽  
Growth And Survival ◽  
Ph Values

The effect of different acids, pH, incubation time, and incubation temperature on the growth and survival of four strains of Listeria monocytogenes in tryptic soy broth was compared. Hydrochloric acid (HCl), acetic acid (AA), lactic acid (LA), malic acid (MA), and citric acid (CA) were used to acidify tryptic soy broth to pH values 4.4, 4.6, 4.8, 5.0, and 5.2 pH. Incubation times were 1, 3, 7, 14, and 28 d at 10, 25, and 35°C. The inhibition of L. monocytogenes in the presence of high acidity appears to be a function of acid and incubation temperature. Based on equal pH values, the antimicrobial activity is AA &gt; LA &gt; CA ≥ MA &gt; HCl at all incubation times and temperatures. When based on equal molar concentration, the activity appeared to be CA ≥ MA &gt; LA ≥ AA &gt; HCl at 35 and 25°C, and MA &gt; CA &gt; AA ≥ LA &gt; HCl at 10°C. Greatest antimicrobial activity occurred at 35°C. Greatest survival occurred at 10°C and greatest growth occurred at 25°C. Final pH of the medium was as low as 3.8 in HCl at 28 d. All strains grew well at pH values lower than the minimum previously reported (5.5–5.6).

GROWTH RATES AND FERMENTATION PATTERNS OF LACTIC ACID BACTERIA ASSOCIATED WITH THE SAUERKRAUT FERMENTATION1

1971 ◽  
Vol 34 (11) ◽  
pp. 521-525 ◽  
Author(s):  
J. R. Stamer ◽  
B. O. Stoyla ◽  
B. A. Dunckel
Keyword(s):  
Lactic Acid ◽  
Lactic Acid Bacteria ◽  
Growth Rates ◽  
Leuconostoc Mesenteroides ◽  
Lactobacillus Brevis ◽  
Sensitive Species ◽  
Ph Values ◽  
Generation Times ◽  
Effects Of Ph ◽  
Early Phases

The effects of pH values and NaCl concentrations on the growth rates of five species of lactic acid bacteria commonly associated with the sauerkraut fermentation were determined in filter-sterilized cabbage juice. Growth rates of all cultures, with the exception of Pediococcus cerevisiae, were retarded by addition of salt, lower pH, or interaction of both pH and salt. Based upon lag and generation times, P. cerevisiae was the culture most tolerant to the pH and salt concentration employed, whereas Streptococcus faecalis was the most sensitive species. Of the heterofermentative cultures, Lactobacillus brevis was less subject to growth inhibition than Leuconostoc mesenteroides. Under conditions simulating those found during the initial phases of the sauerkraut fermentation (2.25% salt, pH 6.2), L. mesenteroides displayed the shortest lag and generation times of all cultures examined. This rapid growth rate coupled with a marked accelerated death rate may explain, in part, the reason this species is both the first to dominate and the first to die during the early phases of the sauerkraut fermentation. Although cabbage juice previously fermented by L. mesenteroides appears to inhibit growth of P. cerevisiae, it had no apparent inhibitory or stimulatory effects on the other cultures.

Sporadic case of listeriosis associated with the consumption of a Listeria monocytogenes-contaminated ‘Camembert’ cheese

1997 ◽  
Vol 35 (2) ◽  
pp. 195-197 ◽  
Author(s):  
P. Gilot ◽  
C. Hermans ◽  
M. Yde ◽  
J. Gigi ◽  
M. Janssens ◽  
...  
Keyword(s):  
Listeria Monocytogenes ◽  
Sporadic Case ◽  
Camembert Cheese

Some Chemical and Bacteriological Characteristics of Regional Cheeses from Asturias, Spain

1996 ◽  
Vol 59 (5) ◽  
pp. 509-515 ◽  
Author(s):  
ABELARDO MARGOLLES ◽  
ANA RODRIGUEZ ◽  
CLARA G. de los REYES-GAVILAN
Keyword(s):  
Listeria Monocytogenes ◽  
Listeria Innocua ◽  
Chemical Characteristics ◽  
Salmonella Spp ◽  
Cheese Making ◽  
Ph Values ◽  
Plate Counts ◽  
Coagulase Positive Staphylococci ◽  
Enrichment Methods

One hundred and one samples of six representative short-ripened cheeses (five homemade and one industrially manufactured) were collected over 1 year in several supermarkets in Asturias and analyzed for mesophilic plate counts, coliforms, enterobacteria, coagulase-positive staphylococci, the presence of species of Salmonella and Listeria, pH, moisture, NaCl, and aw. Chemical characteristics varied, largely depending on the type of cheese. The percentages of moisture and NaCl ranged from 36.11 to 48.91 and from 1.16 to 2.08 respectively. The aw values were between 0.95 and 0.99. Acidification was quite efficient, all cheeses having mean pH values between 4.56 and 5.39. None of the samples yielded Salmonella spp. Coagulase-positive staphylococci were detected in two cheeses, in one reaching levels up to 106 CFU/g. Listeria spp. contaminated 11.8% of the cheeses, with Listeria monocytogenes isolated from 8.91 % and Listeria innocua from 4.95% of the samples. The distribution of Listeria spp. varied largely depending on the type of cheese: 41% of the samples contaminated with L. monocytogeneswere obtained from one type of cheese which had the lowest pH and NaCl values and the highest aw and moisture levels of the cheeses analyzed. However, L. monocytogenes was absent from another type of cheese, which showed intermediate chemical characteristics. High levels of coliforms and enterobacteria (4 to 5 log CFU/ml) were detected in the five homemade cheeses and were statistically associated with the presence of Listeria spp. and L. monocytogenes. Cold enrichment was unsuccessful for the recovery of Listeria spp. from the cheeses analyzed, while a combination of different enrichment methods resulted in the best procedure for detecting all positive samples. This study shows that L. monocytogenes and coagulase-positive staphylococci are present in short-ripened cheeses consumed in Asturias. Adequate measures to prevent contamination during cheese making will probably result in safer products.

Control of Listeria monocytogenes by Monoglycerides in Foods

1997 ◽  
Vol 60 (2) ◽  
pp. 131-138 ◽  
Author(s):  
LIH-LING WANG ◽  
ERIC A. JOHNSON
Keyword(s):  
Antimicrobial Activity ◽  
Lactic Acid ◽  
Listeria Monocytogenes ◽  
Culture Media ◽  
Cottage Cheese ◽  
Minimally Processed ◽  
Chemical Factors ◽  
Lipid Compounds ◽  
Camembert Cheese ◽  
Increased Activity

Monoglycerides (MCs) including MC10, MC12, and coconut MCs were tested for inhibitory activity against Listeria monocytogenes strain Scott A in culture media and in several foods. MCs were inhibitory to L. monocytogenes in certain foods including beef frank slurries (pH 5.0 and 5.5) and seafood salad (pH 4.9) at 4°C, but were less active at 12 than at 4°C. MCs were less inhibitory to L. monocytogenes in other foods tested including turkey frank slurries (pH 5.5), imitation crabmeat, cooked shrimp, summer sausage, yogurt, cottage cheese, and Camembert cheese. Combinations of MCs, particularly MC10 and MC12, showed increased activity in certain foods. The combination of MC10 (250 to 500 μg/ml) and MC12 (250 to 500 μg/ml) or a mixture of coconut-derived MCs (500 to 1,000 μg/ml) were inhibitory against L. monocytogenes in beef and turkey frank slurries. Certain Chemical factors affected the degree of inhibition by the lipid compounds including pH, acidulants such as lactic acid, certain antioxidants, and lipid carriers. The results suggest that MCs could be used as preservatives in certain classes of minimally processed refrigerated foods when intrinsic antimicrobial activity is inadequate.

Detection of Listeria monocytogenes in Samples Containing Listeria innocua

1994 ◽  
Vol 57 (12) ◽  
pp. 1048-1051 ◽  
Author(s):  
MICHAEL S. CURIALE ◽  
CATHERINE LEWUS
Keyword(s):  
Listeria Monocytogenes ◽  
Growth Rates ◽  
Environmental Samples ◽  
Listeria Innocua ◽  
Enrichment Broth ◽  
Selective Media ◽  
Common Culture ◽  
Generation Times ◽  
Secondary Enrichment ◽  
Culture Procedure

A common culture procedure for the detection of Listeria monocytogenes in meats and environmental samples was evaluated in a multilaboratory study using samples inoculated with both Listeria monocytogenes and Listeria innocua. Listeria monocytogenes was recovered from 5.4% of beef broth samples containing between 140 and 1400 L. monocytogenes cells per 25-ml sample in the presence of twice as many L. innocua cells; whereas L. innocua was recovered from all of the samples. Listeria monocytogenes was isolated from 100% of the samples when L. innocua was absent. Similar results were obtained for swab samples containing both L. monocytogenes and L. innocua. Listeria monocytogenes was recovered from 31% of the swabs containing 4.8 L. monocytogenes cells per swab and from 0% of the swabs containing the same number of L. monocytogenes cells and 4 L. innocua cells per swab. When the ratios of L. monocytogenes to L. innocua were 12:1, 120:1 and 1200:1, L. monocytogenes was isolated from 38%, 92% and 85% of the swabs, respectively. The recovery rates were consistent with the differences in growth rates for the two organisms in selective media. The generation times for L. monocytogenes were 74 min in primary enrichment broth and 105 min in modified secondary enrichment broth. Listeria innocua posted generation times of 53 and 81 min in the same two enrichment broths.

Behavior of Listeria monocytogenes in the Presence of Cocoa, Carrageenan, and Sugar in a Milk Medium Incubated With and Without Agitation

1990 ◽  
Vol 53 (1) ◽  
pp. 30-37 ◽  
Author(s):  
LAURA J. PEARSON ◽  
ELMER H. MARTH
Keyword(s):  
Listeria Monocytogenes ◽  
Linear Relationship ◽  
Skim Milk ◽  
Type A ◽  
Cane Sugar ◽  
Sugar Concentration ◽  
Chocolate Milk ◽  
Type B ◽  
Cocoa Powder ◽  
Generation Times

Enhanced growth of Listeria monocytogenes strain V7 in chocolate milk rather than skim milk was further investigated by testing various concentrations of cocoa powder (two types of Dutch-process, designated A and B), cane sugar, and sodium carrageenan in skim milk at 13 and 30°C with and without agitated incubation. Increasing sugar concentrations (0, 6.5, and 12.0%) were marginally significant (p = 0.06) in shortening generation times (5.17, 5.07, and 5.05 h, respectively) of the pathogen. Maximum populations attained by the pathogen were greater when cocoa (0.75% type A or B) and sugar (6.5 or 12.0%) were present. Sugar concentration affected growth of L. monocytogenes in an approximately linear relationship (8.41, 8.67, 8.82 log10 CFU/ml for 0, 6.5, and 12.0% sugar, respectively) except in samples containing only carrageenan. In this instance, presence of 6.5 and 12.0% sugar resulted in equivalent maximum populations (8.54 and 8.52 log10 CFU/ml). Three factors enhanced growth of the pathogen at 30°C: addition of cocoa, addition of sugar, and agitated rather than quiescent incubation. Without cocoa, generation times of L. monocytogenes were longer (1.04 h) compared to presence of type A (0.87 h) or B (0.90 h) cocoa. L. monocytogenes in agitated samples had shorter (0.82 h) generation times than in quiescent cultures (0.95 h). Highest populations were attained in agitated samples containing sugar and type A (9.21 log10 CFU/ml) or type B (9.22 log10 CFU/ml) cocoa compared to lowest populations in quiescent samples of skim milk (8.56 log10 CFU/ml).

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