Growth of Listeria monocytogenes at 10°C in Milk Preincubated with Selected Pseudomonads1

1988 ◽  
Vol 51 (4) ◽  
pp. 277-282 ◽  
Author(s):  
DOUGLAS L. MARSHALL ◽  
RONALD H. SCHMIDT
Keyword(s):  
Listeria Monocytogenes ◽  
Skim Milk ◽  
Growth Curves ◽  
Milk Composition ◽  
Pseudomonas Fragi ◽  
Pseudomonas Spp ◽  
Generation Times ◽  
Whole Milk ◽  
Dry Milk ◽  
Stimulation Of

Preliminary studies involving co-inoculation of Listeria monocytogenes with Pseudomonas fragi into whole or skim milk demonstrated that neither inhibition nor stimulation of growth occurred for either organism. Additional investigations involved preincubation of whole milk, skim milk, and 10% reconstituted nonfat dry milk (NDM) for 3 d at 10°C with P. fragi, Pseudomonas fluorescens P26, P. fluorescens T25, or P. fluorescens B52, followed by inoculation with L. monocytogenes and further incubation at 10°C. Growth curves of L. monocytogenes were constructed for each treatment combination and generation times were statistically compared for differences. Results indicated that L. monocytogenes did not affect growth or survival of the preincubated Pseudomonas spp. However, growth rates of L. monocytogenes were significantly (P<0.05) enhanced in milks preincubated with pseudomonads. Doubling times of L. monocytogenes were reduced by up to 3 h when grown in milk preincubated with Pseudomonas spp. Three strains of P. fluorescens showed more stimulation of the growth rate of L. monocytogenes compared to P. fragi in preincubated whole or skim milk but not in preincubated NDM. Milk composition had little effect on growth of either genus when incubated alone. Results of this study indicate that L. monocytogenes can grow in the presence of Pseudomonas spp. either as a co-inoculant or following preincubation in milk at 10°C. Furthermore, data suggest that the presence of the pseudomonads may enhance growth of L. monocytogenes in milk.

Growth of Listeria monocytogenes in Skim, Whole and Chocolate Milk, and in Whipping Cream during Incubation at 4, 8, 13, 21 and 35°C

1987 ◽  
Vol 50 (6) ◽  
pp. 452-459 ◽  
Author(s):  
EILEEN M. ROSENOW ◽  
ELMER H. MARTH
Keyword(s):  
Listeria Monocytogenes ◽  
Low Temperatures ◽  
Incubation Temperature ◽  
Growth Curves ◽  
Interactive Effects ◽  
Chocolate Milk ◽  
Refrigerated Storage ◽  
Generation Times ◽  
Whole Milk ◽  
Doubling Times

Autoclaved samples of skim, whole, and chocolate milk and of whipping cream were inoculated with Listeria monocytogenes (one to four strains were tested individually, depending on the experiment) and incubated at 4, 8, 13, 21 or 35°C. Growth curves were then derived and generation times and maximum populations calculated for each combination of strain, product, and temperature. The growth rate of L. monocytogenes was similar in all four products at a given incubation temperature and increased with an increase in temperature. Doubling times over all products and strains were 41 min (35°C), 1 h 43 min-1 h 55 min (21°C), 4 h 27 min-6 h 55 min (13°C), 8 h 40 min-14 h 33 min (8°C), and 29 h 44 min-45 h 33 min (4°C). In each instance, maximum populations reached were at least 107 cells/ml, with highest numbers consistently produced in chocolate milk (at least 10 times greater than in skim or whole milk or cream at any temperature). Little decrease in final numbers occurred with extended storage at the incubation temperature being studied. All results were analyzed statistically to determine magnitude and source of variation. Observed differences in data resulted from interactive effects between strain, product, and temperature. Therefore, no single factor can be considered as the sole cause of a particular finding. That L. monocytogenes can attain such high populations at low temperatures should be of concern. Since refrigerated storage is no guarantee of protection against growth of L. monocytogenes, every precaution should be taken to prevent contamination of certain foods by this organism.

Psychrotrophic Growth and Thermal Inactivation of Listeria monocytogenes as a Function of Milk Composition

1986 ◽  
Vol 49 (12) ◽  
pp. 994-998 ◽  
Author(s):  
CATHERINE W. DONNELLY ◽  
ELIZABETH H. BRIGGS
Keyword(s):  
Listeria Monocytogenes ◽  
Thermal Resistance ◽  
Thermal Inactivation ◽  
Skim Milk ◽  
Raw Milk ◽  
Milk Composition ◽  
Cellular Growth ◽  
Whole Milk ◽  
Serotype 1 ◽  
Serotype 4B

Listeria monocytogenes strains 19111, 19113, 19115, F5027 and F5069 were grown in 11% nonfat milk solids, skim milk and whole milk at 4, 10, 22, and 37°C to determine the influence of temperature and milk composition on growth and thermal resistance. Milk composition affected cellular growth. The psychrotrophic growth of L. monocytogenes serotype 4b strains was enhanced in whole milk when compared to skim milk or 11% NFMS. This enhancement of psychrotrophic growth was not observed for serotype 1 or 3 strains. The stimulatory effect of whole milk on serotype 4b L. monocytogenes strains was most dramatic at 10°C where cells increased from 7.9 × 10° to 5.8 × 106 CFU/ml within 48 h. Milk composition did not affect the thermal resistance of L. monocytogenes. All strains used in this study had a D62.7°C value of 1.0 min or less, therefore, pasteurization as defined by current FDA guidelines should eliminate this organism from raw milk with a large margin of safety. Post-pasteurization contamination of dairy products with L. monocytogenes must be eliminated since the psychrotrophic nature of this organism ensures survival and proliferation during refrigerated storage.

Growth of Listeria monocytogenes at 4, 32, and 40°C in Skim Milk and in Retentate and Permeate from Ultrafiltered Skim Milk

1991 ◽  
Vol 54 (5) ◽  
pp. 338-342 ◽  
Author(s):  
FATHY E. EL-GAZZAR ◽  
HANS F. BOHNER ◽  
ELMER H. MARTH
Keyword(s):  
Listeria Monocytogenes ◽  
Skim Milk ◽  
Growth Curves ◽  
Generation Times

Pasteurized skim milk and retentate (concentrated fivefold or twofold by volume) and permeate from ultrafiltered skim milk were inoculated with Listeria monocytogenes strains California or V7 and incubated at 4, 32, or 40°C. Changes in populations of the pathogen were determined, growth curves were derived, and generation times and maximum populations calculated for each combination of strain, product, and temperature. Both strains grew faster and achieved higher (ca. 1 to 2 orders of magnitude) populations at 4°C in retentate of either concentration than in skim milk. The pathogen grew in permeate at 4°C and attained maximum populations of ca. 106 to 107/ml. Tyndallized samples of skim milk and retentate and permeate from ultrafiltered skim milk were inoculated with the same strains of L. monocytogenes and incubated at 32 or 40°C. Populations achieved by the pathogen at these temperatures, ca. 107 to 108/ml, were similar in skim milk, retentate, and permeate.

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.

Oxidation of Cholesterol in Commercially Processed Cow's Milk

1987 ◽  
Vol 50 (10) ◽  
pp. 867-871 ◽  
Author(s):  
MAE Z. CLEVELAND ◽  
NATHOLYN D. HARRIS
Keyword(s):  
Skim Milk ◽  
Milk Lipid ◽  
Oxidized Cholesterol ◽  
Heated Milk ◽  
Whole Milk ◽  
Dry Milk ◽  
Liquid Milk ◽  
Milk Lipids ◽  
And Storage ◽  
Layer Chromatography

Pasteurized whole milk, ultra-high temperature heated milk, canned evaporated milk, skim milk and instant nonfat dry milk were analyzed for presence of oxidized cholesterol compounds. Effects of heating whole milk and storage of whole milk lipid extracts were also examined. Analytical thin-layer chromatography data indicate that cholesterol in liquid milk was stable during commercial pasteurization, sterilization and evaporation. However, instant non-fat dry milk contained 7-hydroxy-cholesterol. Heating whole milk for 12 h at 85°C did not produce oxysterols, but GC-MS analysis indicate that storage of whole milk lipids may have produced steroidal ketones.

Thermal Resistance of Listeria monocytogenes Scott A in Ultrafiltered Milk as Related to the Effect of Different Milk Components

2010 ◽  
Vol 73 (11) ◽  
pp. 2110-2115 ◽  
Author(s):  
KINGA SZLACHTA ◽  
SUSANNE E. KELLER ◽  
ARLETTE SHAZER ◽  
STUART CHIRTEL
Keyword(s):  
Listeria Monocytogenes ◽  
Thermal Resistance ◽  
Milk Fat ◽  
Milk Powder ◽  
Skim Milk ◽  
Skim Milk Powder ◽  
Single Measure ◽  
Total Solids ◽  
Whole Milk ◽  
Milk Components

Pasteurization parameters for grade A milk are well established and set by regulation. However, as solids levels increase, an increased amount of heat is required to destroy any pathogens present. This effect is not well characterized. In this work, the effect of increased dairy solids levels on the thermal resistance of Listeria monocytogenes was examined through the use of ultrafiltered (UF) milk, reconstituted milk powder, and the milk components lactose and caseinate. From the results obtained, lactose and caseinate did not appear to affect thermal resistance. In addition, the level of milk fat, up to 10% of the total solids in UF whole milk, did not result in statistically significant changes to thermal resistance when compared with UF skim milk. Reconstituted skim milk powder at 27% total solids (D62-value = 1.16 ± 0.2 [SD] min, z = 5.7) did result in increased thermal resistance, as compared with reconstituted skim milk powder at 17.5% (D62-value = 0.86 ± 0.02 min, z = 5.57) and UF whole milk at 27% total solids (D62-value = 0.66 ± 0.07 min, z = 5.16). However, that increase appeared to be due to the increase in salt levels, not to increases in caseinate, fat, or lactose. Consequently, total solids, as a single measure, could not be used to predict increased thermal resistance of L. monocytogenes in concentrated milk.

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).

Combined Effects of NaCl, NaOH, and Biocides (Monolaurin or Lauric Acid) on Inactivation of Listeria monocytogenes and Pseudomonas spp.

2001 ◽  
Vol 64 (9) ◽  
pp. 1442-1445 ◽  
Author(s):  
C. VASSEUR ◽  
N. RIGAUD ◽  
M. HÉBRAUD ◽  
J. LABADIE
Keyword(s):  
Acetic Acid ◽  
Listeria Monocytogenes ◽  
Lauric Acid ◽  
Bacterial Species ◽  
Early Stationary Phase ◽  
Pseudomonas Fragi ◽  
Pseudomonas Spp ◽  
Log Reduction ◽  
Processing Plants ◽  
Low Efficiency

This study highlighted combinations of chemical stresses that could decrease or eliminate Listeria monocytogenes and Pseudomonas spp. surviving in food processing plants. Strains of L. monocytogenes, Pseudomonas fragi, and Pseudomonas fluorescens isolated from processing environments (meat and milk) were grown at 20°C up to the early stationary phase. The strains were then subjected to 30 min of physicochemical treatments. These treatments included individual or combined acid (acetic acid), alkaline (NaOH), osmotic (NaCl), and biocides (fatty acids) challenges. Survival of the strains was studied after individual or combined acid (acetic acid), alkaline (NaOH), osmotic (NaCl), and biocides (monolaurin, lauric acid) challenges. Individual pH shocks had lower efficiencies than those used in combinations with other parameters. The treatment pH 5.4 followed by pH 10.5 had a low efficiency against L. monocytogenes. The opposite combination, pH 10.5 followed by pH 5.4, led to a 3-log reduction of the L. monocytogenes population. Pseudomonas spp. strains were much more sensitive than L. monocytogenes, and population reductions of 5 and 8 log (total destruction), respectively, were observed after the same treatments. As for L. monocytogenes, the combination pH 10.5 followed by pH 5.4 is more deleterious than the opposite. Whatever the bacterial species, the most efficient treatments were combinations of alkaline, osmotic, and biocide shocks. For instance, the combination pH 10.5 and 10% NaCl plus biocides showed reductions of 5 to 8 log for both bacteria. The origins of the observed lethal effects are discussed.

Competitive Growth of Listeria monocytogenes and Yersinia enterocolitica in Milk

1993 ◽  
Vol 56 (6) ◽  
pp. 528-532 ◽  
Author(s):  
EBO BUDU-AMOAKO ◽  
SYED TOORA ◽  
RICHARD F. ABLETT ◽  
JIM SMITH
Keyword(s):  
Listeria Monocytogenes ◽  
Yersinia Enterocolitica ◽  
Skim Milk ◽  
Competitive Growth ◽  
No Inhibition ◽  
Whole Milk ◽  
Uninoculated Control ◽  
Control Samples

Sterile whole milk and skim milk were inoculated with cultures of Yersinia enterocolitica (10 CFU/ml) and Listeria monocytogenes (15 CFU/ml) either separately or together and incubated at 4, 10, and 22°C. Unlike uninoculated control samples, growth of Y. enterocolitica with or without L. monocytogenes in whole milk or skim milk at 22°C and in whole milk at 10°C led to the development of off-odors with coagulation after heating to 80°C. Growth of Y. enterocolitica alone in whole milk and in skim milk at 4°C and in skim milk at 10°C did not result in any odor changes or coagulation. Similar or lower populations did not result in any character changes in trials with L. monocytogenes. In the presence of Y. enterocolitica, the growth of L. monocytogenes was found to be competitively inhibited in whole milk at temperatures of 10 and 22°C, but not at 4°C, whereas in skim milk no inhibition was observed at all the temperatures investigated.

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